Medical Lab Technician Jobs
Browse the latest opportunities in Medical Lab Technician Jobs.
Why This Role MattersAnalytical Development plays a critical role in pharmaceutical product lifecycle management. From method development and validation to stability data interpretation, the Analytical Development Laboratory (ADL) ensures product quality, regulatory compliance, and scientific integrity.This Walk-In Drive, organized by Gowrie Research Pvt. Ltd. under B&S Group, is a dedicated hiring initiative for women professionals, offering growth opportunities in R&D and regulatory-focused domains.The ADL team supports formulation development, scale-up activities, and regulatory submissions by generating scientifically sound analytical data. Professionals joining this function contribute directly to quality assurance, regulatory acceptance, and successful product commercialization.Job DescriptionB&S Group – Gowrie Research Pvt. Ltd., Vadodara, is conducting a Walk-In Drive for Women Professionals from 23rd to 27th February 2026. The organization is hiring experienced candidates for the Analytical Development Laboratory (ADL) across standard and special product segments.The selected candidates will be responsible for analytical method development, validation, stability studies, instrument handling, and regulatory documentation support. The role requires strong technical knowledge, regulatory awareness, and the ability to work in a structured R&D environment.Key Features of the Role• Direct involvement in analytical method development and validation• Exposure to regulated market documentation standards• Hands-on experience with advanced analytical instruments• Opportunity to work on special product development projects• Participation in stability studies and data interpretation• Women-focused hiring initiative promoting leadership and growth• Strong career pathway in R&D and regulatory complianceResponsibilities RequiredAnalytical Method Development & Validation• Develop and optimize analytical methods for pharmaceutical formulations• Perform method validation as per ICH guidelines• Ensure accuracy, precision, robustness, and reproducibility of analytical methods• Prepare validation protocols and reports• Troubleshoot analytical challenges and provide scientific solutionsStability Studies & Data Analysis• Conduct stability studies as per regulatory requirements• Analyze stability samples and interpret data trends• Identify out-of-specification (OOS) or out-of-trend (OOT) results• Support stability report preparation and documentation• Collaborate with formulation teams for stability improvementsInstrument Handling & Laboratory Operations• Operate and maintain analytical instruments such as HPLC, GC, UV-Visible Spectrophotometer, and related equipment• Perform system suitability testing and calibration checks• Maintain proper documentation and ensure data integrity• Follow laboratory safety and GMP practices• Ensure proper maintenance of analytical recordsRegulatory Documentation Support• Prepare analytical sections for regulatory submissions• Support dossier compilation for regulated and semi-regulated markets• Maintain documentation aligned with GMP and data integrity standards• Assist during audits and regulatory inspections• Coordinate with QA and regulatory teams for compliance verificationSpecial Products (Senior Role)• Lead analytical activities for complex or special product portfolios• Provide technical guidance to junior team members• Oversee method transfer and cross-functional coordination• Support strategic R&D initiatives• Drive continuous improvement in analytical processesQualificationsCandidates must possess strong analytical expertise, regulatory understanding, and laboratory discipline. The role demands scientific accuracy, documentation excellence, and problem-solving ability.For senior-level positions, leadership capability and experience handling complex projects are essential.Educational RequirementsResearch Associate / Sr. Research Associate – ADL• M.Sc/ B.Pharm / M.PharmSenior Research Associate – ADL (Special Products)• M.Pharm (Mandatory)Specialization in Pharmaceutical Analysis or related discipline preferred.Experience and SkillsExperience• 3–8 years for Research Associate / Sr. Research Associate• 8–10 years for Special Products Senior Role• Experience in regulated market exposure preferredTechnical Skills• Strong knowledge of analytical method development• Experience in method validation as per ICH guidelines• Stability study execution and interpretation• Hands-on experience with HPLC, GC, UV, and related instruments• Knowledge of GMP and data integrity requirements• Familiarity with regulatory documentation standardsBehavioral Skills• Strong analytical and troubleshooting skills• Detail-oriented documentation practices• Ability to manage multiple projects• Effective communication and collaboration• Leadership capability (for senior roles)• Proactive and quality-focused mindsetSalary Insights• Estimated salary range (3–8 years experience): ₹5 LPA – ₹9 LPA• Estimated salary range (8–10 years senior role): ₹9 LPA – ₹14 LPA• Compensation may vary depending on expertise in special products and regulatory exposure• Performance-based incentives may be applicableAdditional Benefits• Performance-based incentives• Professional growth in R&D and regulatory domains• Exposure to special product development projects• Women-focused empowerment hiring initiative• Opportunity to work in structured, compliance-driven environmentCompany OverviewGowrie Research Pvt. Ltd., part of B&S Group, is a pharmaceutical research-driven organization specializing in formulation development, analytical research, quality systems, and regulatory-focused operations.Located in Vadodara, the organization emphasizes scientific innovation, regulatory excellence, and operational quality. It provides strong career growth opportunities in R&D, QA, and project management domains, especially for professionals seeking exposure to regulated market standards.Walk-In & Application ProcessWalk-In Dates: 23rd to 27th February 2026Location: VadodaraInterested candidates should:• Attend the walk-in interview during the specified dates• Carry updated resume and educational documents• Reach early due to limited vacanciesFAQsIs this walk-in drive only for women professionals?Yes, this is a dedicated hiring initiative for women professionals.Is regulated market experience required?Preferred but not mandatory for mid-level roles; highly desirable for senior positions.What instruments experience is required?Hands-on experience with HPLC, GC, UV, and similar analytical instruments.Are freshers eligible?No, relevant experience is required for these roles.Is leadership experience required for the senior role?Yes, the Special Products Senior role requires leadership and advanced analytical expertise.Application Tips• Clearly mention analytical instruments handled• Highlight method validation and stability study experience• Include regulatory submission exposure• Quantify number of methods developed or validated• Mention experience in special or complex product handling• Carry all academic and experience certificates during walk-inThis walk-in opportunity is ideal for experienced women professionals looking to advance their careers in Analytical Development and regulated pharmaceutical research domains.
Laboratory Assistant - National Forensic Sciences University (NFSU)
Why This Role MattersThe Laboratory Assistant position at National Forensic Sciences University (NFSU) plays a critical role in supporting scientific, forensic, and technical operations across various laboratories of this Institution of National Importance under the Ministry of Home Affairs, Government of India. Laboratory Assistants contribute to the efficient functioning of forensic science laboratories by assisting in practical, analytical, and research-based activities. Their role ensures that scientific investigations, academic training, and research outputs maintain high standards of accuracy, integrity, and compliance.Given the growing importance of forensic science in criminal justice, cybersecurity, narcotics testing, and scientific investigation, Laboratory Assistants form the backbone of laboratory operations. They support faculty members, scientific officers, and researchers in conducting experiments, maintaining laboratory equipment, handling samples, and ensuring procedural compliance. The role demands discipline, scientific aptitude, and adherence to institutional and regulatory guidelines.This position is ideal for candidates with a strong academic foundation in life sciences, physical sciences, forensic science, or pharmacy who aspire to build a career in forensic laboratories, government research institutes, or scientific technical services.Job DescriptionThe Laboratory Assistant will assist in routine laboratory operations, sample handling, documentation, and technical support functions in accordance with institutional policies and scientific standards. The role requires working in a structured laboratory environment and supporting forensic and scientific activities as assigned by senior officials.Selection for this post is based on merit of marks obtained in the Written Test and/or Skill Test.Key Features of the Role• Position Title: Laboratory Assistant• Pay Level: Level 5• Total Posts: 24• Recruitment Type: Direct Recruitment• Institution: National Forensic Sciences University (NFSU)• Ministry: Ministry of Home Affairs, Government of India• Selection Mode: Written Test and/or Skill Test• Posting: Any campus of NFSU (transferable across campuses)• Probation Period: Two Years as per University normsResponsibilitiesAlthough specific task allocation will depend on the assigned laboratory, the Laboratory Assistant will be expected to:• Assist in preparation, organization, and maintenance of laboratory equipment and materials• Support scientific officers and faculty members during practical sessions and research activities• Handle, label, and manage laboratory samples carefully• Maintain laboratory records, documentation, and registers• Ensure cleanliness, safety, and proper functioning of laboratory infrastructure• Follow institutional safety protocols and quality standards• Support testing, analysis, and routine laboratory procedures• Assist in written test/skill-based practical demonstrations as part of institutional requirements• Comply with University rules, policies, and procedural instructions• Work collaboratively in a scientific and research-oriented environmentRequired QualificationsCandidates must fulfill the eligibility conditions as specified in the advertisement.Educational RequirementsThe candidate must possess a Bachelor’s Degree from a recognized University or Institute in any one of the following disciplines:• Forensic Science , Criminology, Physics , Botany , Zoology , Microbiology , Biotechnology , Physical Anthropology , Genetics , Chemistry , Biochemistry , Pharmacology , PharmacyThe degree must be obtained from a recognized University or Institute.Experience and SkillsNo prior mandatory experience is specified for this post in the advertisement. However, candidates are expected to possess:• Basic laboratory handling knowledge• Understanding of scientific principles relevant to their discipline• Ability to maintain records and documentation• Awareness of laboratory safety standards• Practical aptitude for handling equipment and samples• Discipline and adherence to institutional protocols• Ability to work in a team-based laboratory environmentSelection will be based on merit in the Written Test and/or Skill Test, indicating that technical competence and practical ability are key evaluation criteria.Age Eligibility• Minimum Age: 18 Years• Maximum Age: 27 YearsAge relaxation provisions:• Relaxable for Government Servants up to 40 years as per Central Government instructions• Age relaxation for SC/ST/OBC/Disabled/Ex-servicemen candidates as per Government of India RulesProof of age must be supported by Matriculation or Higher Secondary School Examination Certificate issued by the concerned Board.Salary Insights• Pay Level: Level 5 (as per applicable Government norms)• Salary will be structured as per University and Government of India pay matrix rules• Additional benefits and allowances will be as per University norms• Application Fee (General/EWS/OBC): ₹500/- + GST & transaction charges• SC/ST, PwBD and Women candidates are exempted from application feeThe application fee is non-refundable.Company OverviewNational Forensic Sciences University (NFSU) is an Institution of National Importance under the Ministry of Home Affairs, Government of India. Headquartered in Gandhinagar, Gujarat, the University operates multiple campuses across India including Gandhinagar, Delhi, Goa, Agartala, Bhopal, Dharwad, Guwahati, Bhubaneswar, Raipur, Nagpur, Chennai, and Jaipur.The University specializes in forensic science education, research, and scientific services. It contributes to national security, criminal justice systems, cyber defense, narcotics testing, forensic psychology, and advanced scientific investigations.Appointments are transferable across all campuses of the University.FAQs1. What is the selection process for Laboratory Assistant?Selection is based on merit of marks obtained in the Written Test and/or Skill Test.2. Is prior experience mandatory?No specific prior experience is mentioned as mandatory for this post.3. What is the age limit?Candidates must be between 18 and 27 years, with applicable relaxations as per Government rules.4. Can Government employees apply?Yes, with age relaxation provisions and required documentation such as NOC at the time of verification.5. Is the post transferable?Yes, selected candidates may be placed at any campus of NFSU and the appointment is transferable.Application Tips• Ensure you meet educational qualification criteria before applying• Apply only through the official Samarth Portal• Submit separate applications if applying for multiple posts• Keep required documents ready for verification• Ensure accuracy while filling the online form as changes are not permitted after submission• Submit the application well before the deadline to avoid technical issuesThe portal for online application will be opened from 23.02.2026 (IST 12:00 PM). The last date for submission of the online application is 23.03.2026 (IST 11:59 PM).
ADL (Analytical Development Laboratory)
Roles & Responsibilities• Perform analytical method development for sterile and injectable products• Optimize, validate, and verify analytical methods as per regulatory guidelines• Provide analytical testing support for formulation and production teams• Execute technology transfer activities from development to manufacturing• Operate and maintain analytical instruments including HPLC/UPLC, GC, UV-Visible Spectrophotometer, and Dissolution Apparatus• Prepare and review analytical documentation in compliance with GMP and regulatory standards• Troubleshoot analytical issues and ensure timely resolution• Maintain laboratory records, protocols, and reports as per quality systemsQualification• M.Sc, B.Pharm (Bachelor of Pharmacy), or M.Pharm (Master of Pharmacy) in Analytical Chemistry or Pharmaceutical SciencesExperience• 1–5 years of experience in analytical method development• Experience in sterile/injectable formulation analysis preferredSkills• Strong knowledge of analytical method development and validation• Hands-on experience with HPLC/UPLC, GC, UV-Vis, and dissolution testing• Understanding of GMP, regulatory compliance, and documentation practices• Technical troubleshooting and problem-solving abilities• Good analytical thinking and attention to detailAbout the CompanyAculife Healthcare Private Limited, a part of the reputed Nirma Group, is a leading sterile pharmaceutical manufacturer specializing in parenteral products and advanced Blow-Fill-Seal (BFS) technology, known for its strong quality systems and global regulatory compliance.Walk-In Interview DetailsDate: 25 February 2026 (Wednesday)Time: 08:00 AM – 11:00 AMVenue: Aculife Healthcare Private Limited (formerly known as Nirlife), Near Railway Crossing (Sanand–Viramgam Highway), Village: Sachana, Taluka: Viramgam, District: Ahmedabad – 382150, Gujarat
Clinical Data Manager
Roles & Responsibilities• Perform end-to-end clinical data management activities for assigned studies• Review and evaluate clinical trial imaging and clinical data for accuracy and compliance• Collaborate with project teams to define study-specific edit checks• Run, review, and resolve data queries and discrepancies• Support study setup including database structure, specifications, and TF design• Coordinate receipt, integration, and processing of external and electronic clinical data• Maintain complete, accurate, and audit-ready study documentation• Track open data issues and ensure timely resolution• Ensure CDM activities comply with regulatory guidelines and internal SOPs• Participate in client meetings and cross-functional discussions• Continuously enhance technical and industry knowledge through trainingQualification• Bachelor’s degree in Life Sciences, Computer Science, or a related discipline• Equivalent clinical data management experience will be consideredExperience• Minimum 1 year of experience in Clinical Data Management (Pharma, Biotech, or CRO)Skills• Strong understanding of clinical trial terminology and CDM processes• Working knowledge of relational databases and data validation• SAS knowledge is desirable• Proficiency in MS Word, Excel, and Access• Strong analytical skills with high attention to detail• Excellent documentation, organizational, and communication skills• Ability to work independently and effectively in fast-paced team environmentsAbout the OrganisationClario is a global leader in clinical trial endpoint technology, delivering innovative imaging, cardiac safety, and digital endpoint solutions to support clinical trials worldwide. The company partners with leading pharmaceutical, biotech, and medical device organizations, offering professionals exposure to global studies, advanced technology platforms, and diverse therapeutic areas.
Senior Medical Writer (Medical Information Writing)
Why This Role MattersMedical writing plays a central role in translating complex clinical and scientific data into clear, compliant, and impactful communication for healthcare professionals, regulators, and patients. As a Senior Medical Writer at Syneos Health, you will directly support global pharmaceutical and biotech organizations by developing scientifically accurate and regulatory-compliant content. This role contributes to accelerating therapy delivery, enhancing scientific communication quality, and ensuring patient-centric information dissemination. Through high-quality medical information writing, this position strengthens evidence-based decision-making across clinical, regulatory, and medical affairs functions.Job DescriptionThe Senior Medical Writer will serve as a lead contributor on medical information writing projects, supporting global standard scientific response documents, FAQs, guidance materials, manuscripts, and publication deliverables. The role requires coordination with cross-functional teams including data management, regulatory affairs, biostatistics, and medical affairs. The candidate will respond to escalated scientific queries from healthcare professionals and internal stakeholders while ensuring adherence to journal, congress, and company regulatory standards. The position demands scientific accuracy, attention to detail, leadership in mentoring junior writers, and familiarity with literature search and publication planning tools.Key Features of the Role:• Remote full-time opportunity• Leadership role within medical writing function• Exposure to global publication and medical information projects• Cross-functional collaboration with regulatory and clinical teams• Opportunity to mentor junior medical writers• Involvement in scientific figure development and publication planningResponsibilities• Lead assigned medical information writing projects• Mentor and guide less experienced medical writers• Develop and update global scientific response communications (gSSRCs)• Respond to escalated scientific queries from HCPs and stakeholders• Conduct literature searches using PubMed and client databases• Develop manuscripts, abstracts, posters, and oral presentations• Ensure adherence to regulatory and journal guidelines• Review documents for scientific accuracy and referencing quality• Coordinate with regulatory, medical affairs, and biostatistics teams• Support publication planning using tools such as Datavision and PubConnect• Create scientific figures using GraphPad Prism and Adobe Illustrator• Maintain compliance with SOPs and client templates• Monitor project timelines and budget specifications• Serve as peer reviewer for internal document quality checksRequired Qualifications• Strong experience in medical information writing or publication writing• Familiarity with regulatory standards and journal guidelines• Experience handling scientific documentation and literature analysis• Ability to work independently with minimal supervision• Strong project management capabilitiesEducational Requirements:• Advanced degree in Life Sciences, Pharmacy, Medicine, Biotechnology, or related discipline preferred• Equivalent relevant experience consideredExperience and Skills:• Experience in clinical manuscript and publication development• Strong scientific writing and editing expertise• Familiarity with figure creation and data visualization tools• Knowledge of publication planning platforms• Excellent analytical and literature review skills• Strong communication and stakeholder coordination skills• Attention to detail and high-quality documentation standards• Ability to work within budget and timeline constraints• Leadership and mentoring capabilitiesAge Eligibility:No specific age criteria mentioned. Candidates must meet educational and professional qualification requirements.Salary InsightsCompensation is competitive and aligned with industry standards for senior medical writing roles. Salary may vary based on experience, therapeutic expertise, and project leadership exposure. Additional benefits may include career progression programs, training opportunities, and performance incentives.Company OverviewSyneos Health is a fully integrated biopharmaceutical solutions organization operating in over 110 countries with approximately 29,000 employees globally. The organization accelerates clinical development, medical affairs, and commercialization strategies for pharmaceutical and biotech clients. Known for its patient-centric Clinical Development model, Syneos Health supports the majority of recently approved FDA and EMA products. The company promotes diversity, professional growth, and a collaborative culture under its “Work Here Matters Everywhere” philosophy.FAQsIs prior medical writing experience required?Yes, senior-level experience in medical writing is expected.Is the role fully remote?Yes, this position is remote-based in Pune/Pimpri-Chinchwad Area.Does the role involve travel?Minimal travel may be required (less than 25%).What type of documents will be handled?Medical information documents, manuscripts, abstracts, posters, and scientific responses.Are regulatory guidelines important for this role?Yes, adherence to journal, regulatory, and SOP standards is critical.Application Tips• Highlight publication and medical information writing experience clearly• Showcase manuscript, abstract, and scientific communication exposure• Mention familiarity with PubMed, regulatory guidelines, and figure tools• Quantify project leadership or mentoring experience• Emphasize compliance, accuracy, and document quality standards• Tailor your resume to highlight therapeutic area expertise and writing portfolio
Materiovigilance Programme of India (MvPI)
Why This Role MattersThis internship under the Materiovigilance Programme of India (MvPI) offers students a rare opportunity to gain structured exposure to India’s national medical device safety monitoring framework. In a healthcare ecosystem where patient safety and regulatory vigilance are becoming increasingly critical, materiovigilance plays a key role in identifying, documenting, and preventing adverse events related to medical devices. This role allows interns to understand how real-world safety data is evaluated at a national level and how regulatory systems function within the public health infrastructure. By participating in this program, students contribute to strengthening healthcare safety standards while building foundational expertise in regulatory science and public health systems.Job DescriptionThe internship provides hands-on exposure to materiovigilance activities under the coordination of the Indian Pharmacopoeia Commission. Interns will assist in data evaluation, documentation processes, adverse event monitoring related to medical devices, and public health reporting activities. The role involves structured learning combined with practical assignments that align with national safety monitoring objectives. Interns will work closely with professionals involved in regulatory documentation, reporting systems, and compliance processes to understand real-time safety evaluation mechanisms.Key Features of the Role:• Practical exposure to materiovigilance systems• Real-time evaluation of medical device safety data• Government-recognized internship certification• Experience within a national healthcare regulatory framework• Skill development in documentation and analysis• Opportunity to contribute to public health safety initiativesResponsibilities• Assist in monitoring and reviewing medical device-related adverse event reports• Support documentation and reporting processes• Participate in data compilation and evaluation activities• Assist in maintaining regulatory records and compliance documentation• Contribute to research and analytical assignments• Support preparation of public health reports• Observe and learn national coordination center operations• Participate in structured training sessions and workshopsRequired Qualifications• Enrolled in Pharmacy, Biomedical Sciences/Engineering, Public Health, Nursing, Biotechnology, Microbiology, or related healthcare disciplines• Strong academic background• Interest in regulatory affairs and patient safety• Basic understanding of healthcare systemsEducational Requirements:• Undergraduate or postgraduate student in healthcare or life sciences stream• Candidates must be currently pursuing or recently completed relevant courseworkExperience and Skills:• Basic knowledge of healthcare documentation processes• Strong analytical and observational skills• Good written and verbal communication skills• Attention to detail• Interest in regulatory and public health systems• Ability to work in a structured professional environment• Basic computer proficiencyAge Eligibility:No specific age criteria mentioned. Applicants must meet academic eligibility requirements.Salary InsightsThis is a structured internship program. Fees are applicable based on duration. The program offers professional exposure and certification rather than salaried employment.Company OverviewThe Materiovigilance Programme of India operates under the Indian Pharmacopoeia Commission, Ministry of Health & Family Welfare, Government of India. It serves as the national coordination center for monitoring adverse events associated with medical devices. The program aims to ensure patient safety by systematically collecting, analyzing, and responding to safety data. Through structured frameworks and regulatory oversight, MvPI contributes to strengthening India’s healthcare quality and safety standards.FAQsIs this a paid internship?No, this is a structured internship with applicable fees depending on duration.Who can apply?Students from pharmacy, biomedical sciences, public health, nursing, biotechnology, microbiology, and related healthcare streams.What is the duration?3 months, 6 months, or 1 year options are available.Will a certificate be provided?Yes, a government-recognized internship certificate is provided upon completion.Is this relevant for pharmacovigilance careers?Yes, it provides foundational exposure relevant to regulatory affairs and pharmacovigilance.Application Tips• Highlight your interest in regulatory affairs and patient safety• Mention any coursework related to pharmacovigilance or medical devices• Demonstrate analytical and documentation skills• Keep your resume concise and structured• Apply within the specified deadline• Ensure all required documents are submitted correctly
Pharmacovigilance Associate
Why This Role MattersPharmacovigilance plays a critical role in protecting patient safety by monitoring, detecting, and preventing adverse drug reactions. As a Pharmacovigilance Associate at Tata Consultancy Services, you will contribute directly to global drug safety operations, ensuring regulatory compliance and supporting pharmaceutical clients in maintaining high-quality safety standards. This role is essential in strengthening patient trust, maintaining regulatory integrity, and supporting life sciences innovation through structured safety monitoring and reporting.Job DescriptionTata Consultancy Services is hiring Pharmacovigilance Associates to support adverse event case processing, safety data management, and regulatory compliance activities. The selected candidate will be responsible for reviewing and processing Individual Case Safety Reports (ICSRs), performing drug safety data entry and validation, and ensuring accurate and timely submission of regulatory reports. The role requires hands-on experience with safety databases such as Argus or ARISg and strong knowledge of global pharmacovigilance regulations.Key Features of the Role:• Exposure to global pharmacovigilance operations• Opportunity to work with leading pharmaceutical clients• Hands-on experience with Argus Safety and ARISg databases• Involvement in signal detection and risk assessment support• Cross-functional collaboration within life sciences teams• Competitive salary structure aligned with industry standardsResponsibilities• Process and review adverse event case reports• Perform drug safety data entry and validation• Ensure compliance with global pharmacovigilance regulations• Work on safety databases such as Argus or ARISg• Conduct case follow-ups and resolve safety queries• Prepare and review case narratives• Maintain accuracy and completeness of safety data• Collaborate with cross-functional teams for safety reporting• Support signal detection and risk assessment activities• Participate in audits and regulatory inspections• Maintain documentation as per SOPs and guidelines• Ensure timely submission of regulatory reports• Identify discrepancies and resolve safety data issues• Assist in quality control and compliance checksRequired Qualifications• University Graduate (Life Sciences, Pharmacy, Biotechnology, Nursing, or related field preferred)• 2–4 years of experience in pharmacovigilance or drug safety• Experience in ICSR processing and case management• Hands-on knowledge of Argus Safety or ARISgEducational Requirements:• Bachelor’s degree in Pharmacy, Life Sciences, Biotechnology, or related discipline• Relevant certification in Pharmacovigilance preferredExperience and Skills:• Strong understanding of pharmacovigilance and drug safety processes• Expertise in ICSR case processing• Knowledge of global regulatory compliance requirements• Proficiency in Argus Safety or ARISg• Good understanding of medical terminology• Strong analytical and data review skills• Attention to detail and quality-focused mindset• Effective communication and documentation skills• Ability to work within defined timelines and SOP frameworksAge Eligibility:No specific age criteria mentioned. Candidates must meet educational and experience requirements.Salary Insights₹4,00,000 – ₹8,00,000 per annum (based on experience and expertise). Compensation may vary depending on candidate profile, project allocation, and skill level.Company OverviewTata Consultancy Services (TCS) is a global IT services, consulting, and business solutions organization delivering technology-driven solutions to leading enterprises worldwide. With a strong presence in life sciences and healthcare domains, TCS supports pharmaceutical and biotech organizations in pharmacovigilance, regulatory operations, clinical research, and digital transformation initiatives. TCS operates across multiple countries and is known for innovation, operational excellence, and client-centric solutions.FAQs1. Is experience in Argus mandatory?Experience in Argus or ARISg is strongly preferred.2. Is this a client-facing role?The role involves collaboration with internal and external stakeholders in safety reporting.3. Is remote work available?Location is specified as Mumbai / Pune; work model depends on project allocation.4. What growth opportunities are available?Career progression may include Senior PV Associate, Drug Safety Specialist, or Quality Reviewer roles.Application Tips• Highlight ICSR processing and case narrative experience clearly• Mention safety database expertise (Argus/ARISg) prominently• Showcase knowledge of global PV regulations• Quantify case volume handled per month if possible• Emphasize audit experience and compliance adherence• Tailor your CV specifically for pharmacovigilance keywords
Pharmacist
Why This Role MattersThe Part-Time Pharmacist at Chemist Discount Centre Boronia plays a critical role in ensuring medication safety and continuity of care for nursing home residents and community patients. This position focuses on Dose Administration Aids (DAAs), which are essential in supporting medication adherence, reducing errors, and improving patient outcomes.By overseeing nursing home and community pack preparation, this role directly contributes to patient safety, regulatory compliance, and high-quality pharmacy service delivery. It is an ideal opportunity for a detail-oriented pharmacist who values accuracy, structured workflows, and meaningful patient impact.Job DescriptionChemist Discount Centre Boronia is seeking a motivated and detail-focused Part-Time Pharmacist to support nursing home and community DAA operations. The role will primarily involve preparing and checking medication packs, managing medication changes, and ensuring compliance with safety standards.You will work closely with the dispensary team while taking ownership of DAA-related processes. Flexibility with rostered hours is required, including alternate Saturdays and occasional Sunday or public holiday coverage if needed.This is a 12-month contract position with the possibility of extension based on operational requirements.Key Features of the Role• Focused responsibility on nursing home and community DAA services• Part-time structured roster with consistent weekly hours• Opportunity to work within a supportive pharmacy group• Competitive hourly rate with higher weekend pay• 12-month contract with potential continuation• Collaborative and team-based working environmentResponsibilities• Prepare and accurately check nursing home and community Dose Administration Aids (DAAs)• Manage medication orders and process medication changes efficiently• Ensure compliance with regulatory standards and patient safety requirements• Maintain high levels of accuracy in all DAA-related work• Support the dispensary team when required• Communicate effectively with nursing homes and healthcare providers• Assist with workflow coordination to ensure timely medication supply• Cover shifts when other staff members are on leaveRequired Qualifications• Current AHPRA registration as a Pharmacist• Legal right to work in Australia• Strong understanding of medication safety and compliance standardsEducational Requirements• Bachelor of Pharmacy (B.Pharm) or equivalent qualification• Completion of internship and registration requirements• Ongoing CPD complianceExperience and SkillsExperience• Previous experience with nursing home packs and community DAAs highly desirable• Experience in community pharmacy practice preferredSkills• Strong attention to detail and accuracy• Excellent organisational and time management skills• Ability to manage medication changes efficiently• Strong communication skills with healthcare professionals and staff• Ability to work independently and within a team• Flexibility with rostered hours and shift coverageSalary Insights• Competitive hourly rate: $46–$52 per hour + super (based on experience)• Higher rates applicable for Saturdays and Sundays• Stable part-time hours with structured roster• Potential continuation beyond 12-month contractCompany OverviewChemist Discount Centre Boronia is part of a strong and supportive pharmacy group focused on delivering quality healthcare and exceptional customer service. The pharmacy is committed to fostering a positive workplace culture, supporting professional growth, and maintaining high standards of patient care within the community.FAQsIs prior DAA experience mandatory?It is highly desirable but not strictly mandatory for the right candidate.Are weekend shifts required?Yes, alternate Saturdays are required, with potential Sunday or public holiday shifts if needed.Is this a permanent role?It is a 12-month contract with the possibility of extension.What are the working hours?The tentative roster includes Monday, Tuesday, Thursday, Friday, and alternate Saturdays.Is flexibility important for this role?Yes, flexibility with start and finish times and covering shifts is required.Application Tips• Clearly mention your AHPRA registration status• Highlight experience with nursing home packs and DAAs• Emphasize accuracy, attention to detail, and medication safety experience• Mention availability for alternate Saturdays and shift flexibility• Demonstrate strong teamwork and communication skills
Physiotherapist
Why This Role MattersThe Physiotherapist role at Kurrajong is vital in helping clients with disability and functional challenges improve mobility, manage pain, achieve physical goals, and participate fully in daily life. Working within a multidisciplinary team, the physiotherapist provides evidence‑based interventions, rehabilitation programs, and therapeutic support across diverse settings — including clinic, home, school, and community environments. This role contributes directly to client independence, quality of life, and overall health outcomes, supporting Kurrajong’s mission to empower people with disability to live fulfilling, active lives. Job DescriptionThe Physiotherapist will assess, plan, implement, and evaluate physiotherapy interventions tailored to clients’ functional needs and goals. The role involves providing direct therapy sessions, developing rehabilitation programs, supporting client participation in daily activities, collaborating with families and multidisciplinary teams, and monitoring progress using outcome measures. Physiotherapy services may be delivered in clinics, homes, schools, or community settings depending on client requirements. Key Features of the Role• Position: Physiotherapist• Company: Kurrajong• Location: Wagga Wagga, NSW, Australia• Employment Type: Full‑Time• Salary Range: Up to AUD 155,000 per year + superannuation, bonuses, and salary packaging • Work Environment: Allied health (disability and community support)• Focus: Client‑centred physiotherapy, rehabilitation, functional independence, multidisciplinary collaboration Responsibilities• Conduct thorough physiotherapy assessments for clients of all ages with varying disabilities • Develop, implement, and evaluate tailored physiotherapy and rehabilitation programs • Deliver direct therapy sessions in clinic, home, school, or community settings • Collaborate with families, carers, and multidisciplinary teams to achieve consistent, coordinated care • Monitor client progress and adjust therapy plans according to outcomes • Maintain accurate clinical documentation and reports • Contribute to continuous quality improvement and best‑practice service delivery Required QualificationCandidates must meet essential educational and professional requirements to practise physiotherapy in Australia and provide services in a disability support context. Educational Requirement• Bachelor’s or Master’s Degree in Physiotherapy from a recognised institution • Current registration as a Physiotherapist with AHPRA • NSW Working with Children Check and NDIS Worker Screening Check (or willingness to obtain prior to employment) • Class C Driver’s Licence for travel to client locations Important Remarks• Role involves supporting clients across the Riverina Murray region, delivering services in multiple environments. • Salary packaging, bonuses, incentives and flexible working arrangements are included. • Kurrajong offers professional development, mentoring, and a supportive work culture. Experience and SkillsExperience Required• Experience in physiotherapy practice is preferred; motivated early‑career clinicians and new graduates with placement experience may apply. Key Skills Expected• Clinical assessment and treatment planning expertise • Strong communication and teamwork skills for multidisciplinary collaboration • Ability to adapt to varied clinical environments • Sound knowledge of evidence‑based physiotherapy practice and rehabilitation • Competence in documentation, outcome measurement and client progress monitoring Age Eligibility• Not specified; candidates must meet Australian professional registration and employment requirements.Salary Insights• Up to AUD 155,000 per year plus super, bonuses, and salary packaging. Company OverviewKurrajong is a long‑standing not‑for‑profit organisation supporting people with disability in the Riverina Murray region. Kurrajong delivers therapy, allied health, community engagement, and support services, focusing on person‑centred care and promoting independence, inclusion, and functional participation in everyday life.FAQsIs AHPRA registration mandatory?Yes — current registration with AHPRA as a Physiotherapist is required.Can new graduates apply?Yes — applicants with placement experience and relevant qualifications are encouraged to apply.What salary package is offered?Up to AUD 155,000 per year plus super, bonuses, and salary packaging. Is the role full‑time?Yes — full‑time with flexible arrangements. Where will I work?Services may be delivered in clinic, home, school, or community settings across the Riverina Murray region. Application Tips• Highlight your AHPRA registration and physiotherapy qualifications.• Emphasise experience or placement work across different settings and age groups.• Showcase communication, assessment, and treatment planning skills.• Include relevant checks (Working with Children, NDIS Screening) in your application.• Attach a tailored cover letter describing your person‑centred care approach and fit with Kurrajong’s mission.
Pharmacist (AHPRA Registered)
Why This Role MattersThe Pharmacist (AHPRA Registered) position in Toowoomba is a vital community healthcare role focused on delivering ethical, outcome-driven health solutions. This is more than a dispensing position — it is a clinician-focused opportunity to provide direct patient care, vaccinations, MedsChecks, and medication management services that genuinely improve community health outcomes.Working in an independent, locally owned pharmacy gives you direct engagement with decision-makers, access to modern clinical resources, and the opportunity to practice pharmacy with professional autonomy and integrity.Job DescriptionThe pharmacy is seeking a confident and motivated AHPRA-registered Pharmacist for a Full-Time or Permanent Part-Time position in Toowoomba, Queensland. The role suits an enthusiastic Early Career Pharmacist (ECP) seeking mentorship and structured learning, or an experienced pharmacist looking for flexible, well-remunerated working hours.The pharmacy operates 365 days a year from 8:00 AM to 10:00 PM. At times, you may work as the sole pharmacist, supported by an experienced Dispensary Manager, senior dispensary technicians, and the Managing Partner/Pharmacist Manager.The pharmacy features modern technology platforms, two consulting and vaccination rooms, a full compounding laboratory, and private consultation areas. The practice actively participates in 8CPA Practice Incentive Programs and extended Scope of Practice initiatives, with CPD and additional clinical training support provided.Key Features of the Role• Independent pharmacy – no banner group or franchise affiliation• Modern, purpose-designed premises• Two consulting and vaccination rooms• Full compounding laboratory• Participation in 8CPA and Extended Scope of Practice programs• Mentored and supportive team environment• Flexible full-time or permanent part-time options• Open 365 days with structured shifts• Relocation assistance available (where applicable)• On-site undercover parking providedResponsibilities• Dispense and check prescriptions accurately in compliance with regulations• Provide patient counselling and medication advice• Conduct MedsChecks and medication reviews• Administer vaccinations within scope of practice• Prepare and manage community Dose Administration Aids (DAA’s)• Engage confidently with patients to deliver outcome-driven care• Collaborate with dispensary staff and pharmacy management• Participate in 8CPA Practice Incentive Programs• Support extended Scope of Practice services• Maintain professional standards and accurate documentationRequired Qualifications• Current AHPRA registration as a Pharmacist (essential)• Legal right to work in Australia• Strong patient engagement and communication skillsEducational Requirements• Bachelor of Pharmacy (B.Pharm) or equivalent qualification• Completion of internship and full registration requirements• Vaccination accreditation preferred• Commitment to ongoing CPDExperience and SkillsExperience• Suitable for Early Career Pharmacists or experienced pharmacists• Community pharmacy experience preferred• Experience with MedsChecks and vaccinations desirable• Experience using Fred Dispense Plus, Fred Office Plus, and Webstercare MMS highly favourableSkills• Strong customer service and counselling abilities• Confident clinical decision-making• Ability to work independently when required• Effective time management• Professional communication and teamwork skills• Adaptability to expanded scope servicesSalary Insights• Salary package of approximately $130,000 per annum• Flexible working arrangements• Relocation expenses available where applicable• Professional development and CPD supportCompany OverviewThis is a locally owned, independent community pharmacy based in Toowoomba, Queensland. The pharmacy operates with long-serving experienced staff and provides a professional, service-driven healthcare environment. With modern facilities and direct owner engagement, the workplace supports ethical practice, mentorship, and clinical growth.Toowoomba is a thriving regional Queensland city located approximately 90 minutes west of Brisbane. Known for its elevated position along the Great Dividing Range and scenic views, Toowoomba offers a high quality of life with strong education, healthcare, business, and recreational infrastructure.FAQsIs this role suitable for Early Career Pharmacists?Yes, mentorship and structured support are available.Is sole pharmacist experience required?Not mandatory, but confidence in independent practice is important.Is experience with Fred systems essential?Not essential, but highly favourable.Are relocation expenses provided?Yes, where reasonable and applicable.Are public holidays included in the roster?Yes, as the pharmacy operates 365 days per year.Application Tips• Clearly mention your AHPRA registration status• Highlight MedsCheck and vaccination experience• Include dispensing system proficiency if applicable• Demonstrate strong patient engagement skills• Be prepared to discuss availability for weekends and public holidays• Mention willingness to relocate if applicable
Pharmacist
Why This Role MattersAs a Pharmacist at Slade Pharmacy New Town, you play an essential role in delivering safe, patient-centred care to the local community. This position goes beyond dispensing medications — it focuses on building trusted relationships, supporting aged care residents, and providing personalized health advice that improves long-term outcomes. Your expertise directly contributes to medication safety, continuity of care, and overall community wellbeing.Job DescriptionThe Pharmacist is responsible for delivering professional community pharmacy services while maintaining compliance with Australian regulatory and safety standards. The role includes prescription dispensing, medication counselling, aged care medication supply, and non-sterile compounding.Approximately 50% of each shift is spent in the dispensary, including prescription checking and customer service. The role requires collaboration with healthcare professionals to ensure coordinated and high-quality patient care.Key Features of the Role• Community-focused pharmacy environment• Balanced mix of dispensary and patient interaction duties• Involvement in aged care medication services• Exposure to non-sterile compounding• Supportive and collaborative team culture• Opportunities for professional growth within a national healthcare networkResponsibilities• Accurately dispense and check prescriptions in accordance with regulations• Provide clear counselling on prescription and OTC medications• Deliver personalized health advice to patients• Manage approximately 50% of shift duties within the dispensary• Supply medications to nursing homes and aged care facilities• Support medication chart management and documentation• Perform non-sterile compounding where required• Maintain compliance with professional and safety standards• Collaborate with doctors, nurses, and healthcare teams• Build strong relationships with patients and community membersRequired Qualifications• Current AHPRA registration as a Pharmacist• Eligibility to practice in Australia• Strong understanding of community pharmacy operationsEducational Requirements• Bachelor of Pharmacy (B.Pharm) or equivalent qualification• Completion of internship and registration requirements• Additional certifications in compounding or aged care (desirable)Experience and SkillsExperience• Experience in community pharmacy preferred• Experience in non-sterile compounding desirable• Exposure to aged care medication services advantageousSkills• Strong communication and interpersonal abilities• High level of accuracy and attention to detail• Effective time management skills• Strong clinical knowledge and counselling capability• Team-oriented mindset• Ability to work efficiently in a fast-paced settingSalary Insights• Competitive remuneration aligned with Australian community pharmacy standards• Salary based on experience and expertise• Potential professional development and career progression opportunitiesCompany OverviewIcon Group is Australia’s largest integrated provider of cancer care, operating across Australia, New Zealand, Asia, and the United Kingdom. The organization integrates oncology, pharmacy, compounding, and research services to deliver comprehensive, patient-centred care. With thousands of healthcare professionals and a strong national presence, Icon Group is committed to improving access to world-class healthcare close to home.FAQsIs aged care experience mandatory?Aged care experience is preferred but not compulsory.Is compounding experience required?Non-sterile compounding experience is desirable but not essential.Will I work independently or in a team?You will work both independently and collaboratively within a supportive team environment.Are there growth opportunities?Yes, career development pathways are available within the broader healthcare network.What type of patients will I serve?You will support community patients and aged care residents.Application Tips• Ensure your AHPRA registration is active and clearly mentioned in your resume• Highlight community pharmacy and patient counselling experience• Mention compounding and aged care exposure if applicable• Demonstrate teamwork and communication strengths• Prepare for scenario-based interview questions focusing on patient safety and medication management
Why This Role MattersThis role supports patients and families during one of the most sensitive and complex stages of healthcare decision-making. As part of the Voluntary Assisted Dying (VAD) service, the pharmacist plays a crucial role in ensuring safe, compliant, and compassionate medication management.Beyond technical dispensing responsibilities, this position requires empathy, professionalism, and strong ethical judgement. The role directly contributes to patient dignity, quality of care, and seamless coordination across healthcare settings.Job DescriptionThe Clinical Pharmacist – VAD Services is responsible for the safe preparation, dispensing, and management of medications associated with Voluntary Assisted Dying across the district.The position involves coordination with multidisciplinary healthcare teams across acute and community settings, providing education to patients and carers, and ensuring compliance with legislative and clinical governance frameworks.This is a highly specialised role requiring strong communication skills, emotional resilience, and sound clinical judgement.Key Features of the Role• Specialised Voluntary Assisted Dying (VAD) service• District-wide coordination across hospital and community settings• Strong multidisciplinary collaboration• Focus on patient dignity and compassionate care• Clinical governance and regulatory compliance responsibilities• Education and advisory componentResponsibilities• Dispense and manage VAD medications in accordance with legislation and clinical protocols• Ensure safe storage, documentation, and distribution of VAD medications• Maintain strict compliance with regulatory and ethical frameworks• Coordinate patient care across acute and community healthcare settings• Liaise with medical practitioners, nursing staff, and allied health professionals• Provide education to patients, carers, and healthcare teams regarding VAD processes• Support medication counselling with sensitivity and professionalism• Maintain accurate documentation and reporting standards• Participate in quality improvement and governance activities• Contribute to a collaborative and supportive team environmentEducational and Registration Requirements• Bachelor of Pharmacy (or equivalent qualification)• Eligibility for registration with the Australian Health Practitioner Regulation Agency (AHPRA) – MandatoryExperience and SkillsExperience:• Clinical pharmacy or hospital pharmacy experience preferred• Experience working in multidisciplinary healthcare settings desirableTechnical Skills:• Strong clinical knowledge and medication safety expertise• Understanding of legislative and regulatory frameworks• Documentation accuracy and compliance management• Risk assessment and medication governance capabilityBehavioral Skills:• Exceptional communication skills, particularly regarding sensitive topics such as death and dying• Emotional resilience and professionalism• Strong critical thinking and clinical judgement• Conflict resolution and ethical decision-making capability• Ability to work collaboratively within a team-based healthcare modelWork Environment• Collaborative, multidisciplinary healthcare team• Supportive and growth-oriented culture• Exposure to complex clinical and ethical care scenarios• Opportunity to contribute meaningfully to patient-centred servicesSalary and Benefits• Competitive remuneration aligned with NSW public health awards• Access to professional development and continuing education• Opportunities for career progression within the public health system• Supportive workplace culture focused on patient-centred careCompany OverviewNSW Health is the largest public health system in Australia, delivering safe and high-quality healthcare services across New South Wales. The organisation is recognised for its commitment to clinical excellence, innovation, training, and patient-centred care.FAQsIs prior VAD experience required?While prior experience is beneficial, strong clinical judgement and the ability to manage sensitive discussions are essential.Is this a hospital-based role?The role involves coordination across both acute and community healthcare settings.What type of team will I work with?You will collaborate with doctors, nurses, allied health professionals, and district healthcare teams.What personal qualities are important for this role?Empathy, professionalism, emotional resilience, and strong communication skills are critical.Is AHPRA registration mandatory?Yes, eligibility for AHPRA registration is required.Application Tips• Highlight clinical or hospital pharmacy experience• Emphasise experience handling sensitive patient interactions• Demonstrate strong documentation and compliance knowledge• Provide examples of multidisciplinary collaboration• Showcase critical thinking and ethical decision-making skills
Occupational Therapist
Why This Role MattersThe Occupational Therapist role at Kurrajong in Wagga Wagga, NSW is a meaningful allied health position that directly supports people with disability and diverse functional needs to participate in everyday life with confidence, independence, and purpose. Working within a multidisciplinary team, Occupational Therapists help clients of all ages — from children to adults — to build functional skills, improve daily living participation and achieve personalised goals through evidence‑based therapy and community engagement. This work enhances quality of life, contributes to inclusive communities, and supports long‑term independence.Job DescriptionThe Occupational Therapist will provide comprehensive assessment, planning, implementation and evaluation of occupational therapy interventions across individual and group settings. The role involves working collaboratively with clients, families, carers and allied health professionals to support meaningful, goal‑focused participation in daily activities such as self‑care, play, work, learning and community engagement. Service delivery may occur in clinic, school, home or community environments depending on client needs.Key Features of the Role• Position: Occupational Therapist• Company: Kurrajong• Location: Wagga Wagga, NSW, Australia• Employment Type: Full‑Time• Salary Range: Up to AUD 155,000 per year + superannuation + salary packaging & bonuses • Work Environment: Allied health (disability and community support)• Focus: Client‑centred occupational therapy, goal‑based intervention, multidisciplinary collaborationResponsibilities• Conduct detailed occupational therapy assessments across age groups and functional areas • Develop, implement and evaluate individualised therapy plans based on client goals and needs • Use evidence‑based intervention strategies to support engagement in daily living activities such as self‑care, learning, play and productivity • Engage with families, carers and other professionals to support consistent, coordinated care • Provide services in multiple settings including clinics, homes, schools and community environments • Maintain accurate clinical documentation and progress reports • Monitor outcome measures, adjust therapy plans and support long‑term participation goals • Contribute to quality improvement and best‑practice service delivery within the therapy teamRequired QualificationCandidates must meet essential educational and professional requirements to practise occupational therapy in Australia and work in a disability support context.Educational Requirement• Bachelor’s or Master’s Degree in Occupational Therapy from a recognised institution • Current registration as an Occupational Therapist with the Australian Health Practitioner Regulation Agency (AHPRA)• Current NSW Working with Children Check and NDIS Worker Screening Check (or willingness to obtain prior to employment) • Class C Driver’s Licence (required for travel to client locations)Important Remarks• Role involves working with clients with disability across the Riverina Murray region with flexible delivery settings, including clinics, schools, and homes. • Generous salary packaging, incentives, bonuses and flexible working arrangements are part of the total rewards package. • Positive work culture, professional development opportunities and staff wellbeing initiatives are offered by Kurrajong.Experience and SkillsExperience Required• Experience in occupational therapy practice is preferred, but motivated early‑career clinicians and new graduates with relevant placement experience may also be considered.Key Skills Expected• Excellent clinical assessment and intervention planning skills • Strong interpersonal and communication skills for working with clients, families and multidisciplinary teams • Ability to work independently and and adapt to varied service environments • Sound knowledge of family‑centred practice and person‑centred support models • Competence in documentation, therapy evaluation and outcome monitoringSalary Insights• Up to AUD 155,000 per year plus superannuation, bonuses and salary packaging components, making it a highly competitive allied health salary in the region.Company OverviewKurrajong is a long‑standing community‑based not‑for‑profit organisation supporting people with disability across the Riverina Murray region. With over 60 years of service, Kurrajong provides a wide range of disability supports including therapy services (Occupational Therapy, Physiotherapy, Speech Pathology), social participation, employment preparation and community engagement programs. The organisation emphasises inclusive practice, personalised support and empowering individuals to live fulfilling lives.FAQsIs AHPRA registration mandatory?Yes — current registration with AHPRA as an Occupational Therapist is required.Can new graduates apply?Yes — applicants with placement experience and relevant qualifications are encouraged to apply.What salary package is offered?Up to AUD 155,000 per year plus super, bonuses and salary packaging.Is the role full‑time?Yes — this is a full‑time opportunity with flexible working arrangements.Where will I work?Services may be delivered in clinic, home, school and community settings across the Riverina Murray region.Application Tips• Highlight your AHPRA registration status and Occupational Therapy qualifications in your CV.• Emphasise experience or placement work with clients across different settings and age groups.• Demonstrate strong communication, assessment and goal‑planning skills.• Include any relevant checks (Working with Children, NDIS Screening) in your application.• Attach a tailored cover letter outlining your person‑centred therapy philosophy and fit with Kurrajong’s mission.
Community Pharmacist
Why This Role MattersThis role offers pharmacists the opportunity to practice beyond traditional dispensing by combining evidence-based medicine with integrative and holistic health solutions. In a community-focused setting, you will directly impact patient wellbeing through counselling, preventative care, and professional health services.Working within an established pharmacy that values innovation and natural health, this position allows you to align your clinical expertise with a wellness-driven healthcare model while advancing your professional development.Job DescriptionFull-time and part-time Pharmacist positions are available at Wholelife Pharmacy & Healthfoods Currimundi. The successful candidate will join a team of four rostered pharmacists, including the owner, in a professional services-focused environment.The role involves delivering high-quality dispensing and clinical services, supervising pharmacy support staff, ensuring compliance with professional standards, and actively contributing to integrative healthcare initiatives.Flexible weekday and weekend shifts are available to promote work–life balance. Future partnership opportunities may be considered for suitable candidates.Key Features of the Role• Full-time and part-time positions available• Professional services-focused practice• Integrative healthcare model combining pharmacy and natural health• Mentorship from experienced leadership team• Flexible roster to support work–life balance• Future partnership potential• Above-award hourly rate starting from $60 per hour• Sign-on bonus and relocation assistanceResponsibilities• Dispense prescription medicines accurately and safely• Provide counselling on prescription and OTC medications using evidence-based practice• Deliver professional health services, including 7CPA initiatives• Supervise and mentor pharmacy assistants and interns• Manage pharmacy programs and ensure compliance with QCPP standards• Process and manage 7CPA claims accurately• Maintain high standards of regulatory and professional compliance• Collaborate with the multidisciplinary team to optimise patient outcomes• Promote integrative health solutions aligned with customer needs• Contribute to a positive, supportive, and professional workplace cultureEducational and Registration Requirements• Bachelor of Pharmacy – Mandatory• Current General Registration with the Australian Health Practitioner Regulation Agency (AHPRA) – MandatoryExperience and SkillsExperience:• Open to newly registered and experienced pharmacists• Community pharmacy experience preferred• Experience delivering professional services advantageousTechnical Skills:• Proficiency in dispensing software systems• Understanding of 7CPA initiatives and claiming processes• Knowledge of QCPP compliance standards• Vaccination accreditation desirable but not essentialBehavioral Skills:• Strong clinical focus with patient-centred approach• Excellent communication and time-management skills• Ability to work collaboratively within a multidisciplinary team• Leadership capability for mentoring support staff• Interest in holistic and integrative healthcare modelsWork Schedule• Flexible weekday and weekend shifts• Full-time and part-time options availableSalary and Benefits• Above-award pay starting from $60 per hour (negotiable based on experience and performance)• Sign-on bonus• Relocation assistance• Supportive, team-first culture• Ongoing professional development• Mentorship from experienced pharmacy leadership• Future partnership opportunity (subject to mutual agreement)Company OverviewWholelife Pharmacy & Healthfoods is Australia’s first retail pharmacy group to integrate traditional pharmacy services with a comprehensive range of organic and natural health products. The Currimundi store has served its local community for over 24 years, delivering evidence-based healthcare alongside holistic wellness solutions in a trusted, locally owned environment.FAQsAre both full-time and part-time roles available?Yes, flexible employment options are available.Is vaccination accreditation mandatory?It is desirable but not essential.Is this suitable for newly registered pharmacists?Yes, both early-career and experienced pharmacists are encouraged to apply.Are there career growth opportunities?Yes, mentoring, professional development, and potential future partnership pathways are available.Is relocation support provided?Yes, relocation assistance and a sign-on bonus are offered.Application Tips• Clearly mention AHPRA registration details• Highlight experience with 7CPA initiatives and QCPP compliance• Emphasise counselling and professional services experience• Demonstrate interest in holistic and integrative healthcare• Mention vaccination accreditation if applicable