Pharmacy Jobs

Roles & Responsibilities • Implement marketing strategies and promotional campaigns for medical device, pharma, and OTC products • Drive product promotion through effective in-clinic presentations to doctors • Identify and promote the right products for the right doctors and institutions • Monitor retail chemist prescription audits and secondary sales • Lead, guide, and motivate a team of ABMs and MRs to achieve business objectives • Ensure timely reporting, territory reviews, and performance tracking • Achieve assigned value and volume targets for the region Qualifications • B.Sc or B.Pharm Experience • Minimum 1 year experience as a 2nd line manager • Proven experience handling a team of ABMs and MRs • Exposure to OTC and Pharma segments is mandatory • Experience in medical devices will be an added advantage Skills • Strong people management and leadership skills • Effective communication, presentation, and negotiation abilities • Strategic thinking with strong execution capability • Target-driven with proven regional performance About the Organisation APLE Pharma is a growing pharmaceutical organization with a presence across pharma, OTC, and medical device segments, focused on ethical promotion, innovation, and building strong relationships with healthcare professionals.

Roles & Responsibilities • Implement marketing strategies and promotional campaigns for assigned products • Promote products to doctors through effective in-clinic presentations • Identify and promote the right products to the right doctors • Conduct retail chemist prescription audits and collect market feedback • Ensure timely reporting of daily field activities • Achieve assigned value and volume sales targets Qualifications • B.Sc or B.Pharm Experience • Minimum 1 year experience in pharmaceutical ethical selling • Experience in Derma and/or Disinfectant segment preferred Skills • High energy level and strong field orientation • Effective communication, presentation, and convincing skills • Strong relationship-building ability • Proven track record of achieving sales targets About the Organisation A growing pharmaceutical organization with a strong focus on ethical promotion and a developing presence in the Derma and Disinfectant segments, committed to quality products and long-term partnerships with healthcare professionals.

Roles & Responsibilities: • Implement marketing strategies and promotional campaigns for assigned products • Conduct effective in-clinic product presentations to doctors • Identify and promote the right products to the right doctors • Generate prescriptions through ethical promotion practices • Conduct retail chemist prescription audits • Ensure timely reporting of field activities • Achieve assigned value and volume sales targets Qualifications: • B.Sc or B.Pharma Experience: • Minimum 1 year experience in pharma ethical selling preferred Skills: • Strong communication, presentation, and convincing skills • High energy level with result-oriented approach • Ability to build strong relationships with doctors and chemists • Proven track record of achieving sales targets About the Organization: APLE PHARMA is a growing pharmaceutical company engaged in marketing quality healthcare products across multiple therapeutic segments, with a strong focus on ethical promotion and field excellence.

Role & Responsibilities • Contribute to a culture of process improvement and operational excellence • Review and process Serious Adverse Events (SAEs), spontaneous ADRs, and safety data • Perform safety review of clinical and diagnostic data • Ensure case processing accuracy as per SOPs, study procedures, regulatory and sponsor requirements • Maintain and review safety tracking systems for data quality and compliance • Liaise with investigational sites, reporters, sponsors, and cross-functional teams on safety issues • Attend project team meetings and sponsor teleconferences as required • Serve as a safety resource for investigational sites and internal teams • Assist in training and mentoring junior Drug Safety Associates • Support generation of study-specific procedures and identify out-of-scope activities • Act as Lead Drug Safety Associate for local or regional projects • Support MSS Functional Lead under supervision • Travel up to 10% (domestic/international) as required Qualification • Life Sciences / Pharmacy / Healthcare background preferred Experience • 4–10 years of experience in Pharmacovigilance / Drug Safety • Experience in Pharma, Biotech, CRO, or Clinical Research environments Skills • Strong knowledge of Pharmacovigilance processes • Hands-on experience with Oracle Argus • Knowledge of EudraVigilance and global safety databases • Exposure to aggregate reporting activities • Strong attention to detail and data quality focus • Effective communication and stakeholder coordination skills • Ability to work independently and lead safety activities About the Company • Covalent Trainings specialises in pharmacovigilance training and industry placements, Supports global PV projects across pharma, biotech, and CRO sectors

Roles & Responsibilities: • Meet doctors and chemists to promote pharmaceutical products • Handle general and multi-specialty segment product promotion • Build and maintain strong relationships with doctors, chemists, and distributors • Achieve sales targets and ensure effective product positioning • Collect market feedback and share insights with management • Ensure regular follow-ups and complete territory coverage Qualifications: • B.Sc, B.Pharma, or any graduate preferred Experience: • 0–3 years experience in meeting doctors and chemists • Freshers with strong communication skills can also apply Skills: • Strong communication and presentation skills • Sales and negotiation abilities • Relationship-building with healthcare professionals • Willingness to travel within assigned territory • Self-motivated and result-oriented About the Organization: L K Saddi Associates is a pharmaceutical marketing and recruitment organization focused on promoting quality pharma products through strong doctor and chemist engagement across multiple segments.

Roles & Responsibilities: • Develop and implement innovative solutions using analytical and problem-solving skills • Collaborate with cross-functional teams to achieve business objectives • Conduct market research and analyze data to identify trends and opportunities • Provide customer service and support to clients and stakeholders • Stay updated with industry developments and emerging technologies • Participate in training and skill development programs Qualifications: • D Pharma, B Pharma, B.Sc, M.Sc, or B.Tech Experience: • 0–4 years in Pharma, Biotech, or Life Sciences industry preferred Skills: • Strong knowledge of pharmaceutical and life sciences concepts • Excellent communication and interpersonal skills • Strong analytical and problem-solving abilities • Ability to work in a fast-paced environment and meet deadlines • Familiarity with medical terminology and healthcare practices • Knowledge of chemical compounds and food products • Innovative mindset and critical thinking ability About the Organization: Leading Client is a reputed organization operating in the pharmaceutical and life sciences sector, focused on innovation, quality, and delivering value-driven healthcare solutions in a dynamic and collaborative work environment.

Roles & Responsibilities: • Ensure MAH pharmacovigilance compliance with EU GVP Modules and UK MHRA requirements • Act as operational PV representative for UK and EU markets • Support QPPV / UK QPPV in maintaining PV system oversight • Ensure PV agreements with partners, distributors, and service providers are in place • Provide oversight of outsourced PV providers (ICSRs, literature, signals, aggregate reports) • Monitor vendor performance against KPIs and SLAs and lead governance meetings • Ensure timely and compliant ICSR reporting to EudraVigilance, MHRA, and partners • Oversee PSUR/PBRERs, RMPs, signal management, and benefit–risk evaluations • Maintain MAH PV Quality Management System and ensure SOP compliance • Support PV inspections and audits (MHRA, EMA, partners) and manage CAPAs • Act as PV contact for Regulatory, Quality, and Commercial teams • Ensure safety information is accurately reflected in SmPC, PIL, and submissions Qualifications: • M.Pharma in Pharmacy Experience: • Proven pharmacovigilance experience within UK and/or EU • Experience working in an MAH environment • Hands-on experience managing outsourced/third-party PV providers Skills: • Strong regulatory and compliance mindset • Excellent vendor and stakeholder management skills • Strong documentation, review, and inspection readiness abilities • Ability to work independently and manage multiple priorities • Experience in generics and post-marketing PV • Exposure to global PV operations and EudraVigilance systems About the Organization: B&S Group is a global distribution and supply chain organization operating across pharmaceuticals and healthcare, with a strong focus on regulatory compliance, quality, and patient safety across international markets.

Roles & Responsibilities: • Report safety information from India and India cluster (South Asia countries) to Global Safety • Follow up with reporters for additional safety information • Review and manage safety mailbox for incoming reports • Perform monthly reconciliation and compliance checks from a pharmacovigilance perspective • Prepare and submit Periodic Safety Update Reports (PSURs) to regulatory authorities as per regulations • Gather requirements and prepare regulatory dossiers for new products, clinical trials, variations, and renewals • Prepare responses to regulatory authority queries and coordinate with global teams • Support preparation for regulatory authority and expert committee meetings • Prepare and follow up on regulatory submissions for South Asia countries • Prepare and update product labeling materials • Review promotional materials for compliance with approved product registrations • Ensure timely updates to regulatory databases • Update and maintain local SOPs • Update and renew safety agreements with partners, manufacturers, and distributors • Coordinate price updates and ensure timely entry into NPPA pricing database • Manage lifecycle maintenance activities and update commercial teams on key milestones Qualifications: • Bachelor’s degree in Pharmacy, Life Sciences, Microbiology, Chemistry, or related field Experience: • Minimum 1+ year experience in India Regulatory Affairs and Pharmacovigilance • Experience within pharmaceutical or biotechnology industry preferred Skills: • Knowledge of Indian regulatory and pharmacovigilance requirements • Strong documentation and dossier preparation skills • Ability to coordinate with global and cross-functional teams • Good communication and regulatory compliance understanding • Attention to detail and ability to manage multiple submissions About the Organization: Ferring Therapeutics is a global, research-driven biopharmaceutical company committed to developing innovative treatments in areas of high unmet medical need. The company focuses on maintaining the highest standards of quality, regulatory compliance, and patient safety while delivering life-changing therapies worldwide.

Roles & Responsibilities: • Perform medical assessments of client’s product ranges and evaluate adverse events • Conduct medical reviews of aggregate reports and prepare clinical expert statements • Detect signals for client’s medicinal products and manage risk management plans • Provide guidance and participate in follow-up of adverse events, offering backup medical support • Interact with staff at various levels to resolve issues during reviews • Contribute to enhancing pharmacovigilance processes and writing SOPs • Ensure compliance with local regulations and global pharmacovigilance requirements • Assist in developing SOPs for the department and clients, and communicate with clients and regulatory agencies if needed Qualifications: • Relevant degree in Life Sciences, Pharmacy, or related field Experience: • 0–1 year in pharmacovigilance or related field Skills: • Knowledge of local and national pharmacovigilance requirements • Strong communication and client interaction skills • Ability to work effectively with staff at various levels and functional areas • Marketing, business generation, direct sales, and client servicing skills About the Organization: This organization is a dynamic employment and recruitment services firm providing specialized healthcare and pharmacovigilance staffing solutions. They focus on regulatory compliance, quality processes, and client satisfaction while fostering a collaborative environment for professional growth.

Roles & Responsibilities: • Dispense and manage medications as per prescriptions and organizational protocols • Maintain accurate records of drug inventory, storage, and distribution • Ensure compliance with standard operating procedures (SOPs) and regulatory guidelines • Counsel patients or staff on proper medication usage and safety • Support clinical and research teams in medication-related tasks • Report discrepancies, adverse reactions, or anomalies to supervisors Qualifications: • B. Pharm, D. Pharm, or 12th Pass with relevant pharmacy training Skills: • Knowledge of pharmacy operations and medication management • Strong attention to detail and record-keeping skills • Ability to work collaboratively in a team environment • Understanding of regulatory standards and patient safety practices Age Limit: • Minimum: 21 Years • Maximum: 45 Years • Age relaxation as per DSHM norms Important Date: • Application Deadline: 07-02-2026 About the Organization: DSHM is a leading healthcare and public health organization dedicated to providing high-quality medical services and ensuring the safe and effective management of medications. The organization fosters a collaborative environment for professionals to contribute to healthcare delivery and patient safety.Official NotificationClick Here

Roles & Responsibilities: • Prepare and review clinical study protocols, clinical study reports (CSRs), investigator brochures (IBs), and other clinical trial documents in line with regulatory guidelines and industry standards • Collaborate with cross-functional teams, including clinical operations, regulatory affairs, and biostatistics, to ensure accuracy and completeness of deliverables • Interpret and summarize clinical trial data from study reports, statistical analyses, and scientific literature • Assist in preparation of regulatory submissions (INDs, NDAs, BLAs, MAAs) with high-quality medical writing support • Participate in project meetings, provide updates on medical writing activities, and contribute to project planning and timelines • Stay current with developments in medical writing, regulatory requirements, and therapeutic areas relevant to projects • Mentor junior medical writers and provide guidance on best practices for document preparation Qualifications: • Bachelor’s degree in Life Sciences, Pharmacy, or related field; advanced degree (MD, PhD, PharmD) preferred Experience: • Minimum 5 years of experience in medical writing within pharmaceutical, biotechnology, or CRO industry • Proficiency in interpreting clinical trial data, including statistical analyses and safety reports • Strong understanding of regulatory guidelines (ICH, FDA, EMA) for clinical trial documents and submissions Skills: • Excellent written and verbal communication skills • Detail-oriented with strong organizational and time management abilities • Ability to work independently and collaboratively in multidisciplinary teams • Proficiency in Microsoft Office Suite and familiarity with document management systems (e.g., SharePoint) About the Organization: MS Clinical Research Pvt Ltd is a dynamic and innovative clinical research organization specializing in clinical trials and comprehensive medical writing services. The company is committed to advancing medical research, supporting regulatory submissions, and improving patient outcomes through high-quality, scientifically accurate documentation and collaborative project execution.

Roles & Responsibilities: • Lead the planning and execution of clinical studies across Skin, Hair, and Oral domains • Ensure studies are conducted in alignment with organizational goals, timelines, and budgets • Oversee day-to-day operations of the Clinical Operations team • Develop study plans, timelines, and resource allocation strategies • Ensure all study activities are executed as per protocol schedules and client expectations • Review study documents including protocols, CRFs, questionnaires, and monitoring plans • Identify operational risks and implement mitigation strategies • Conduct Site Initiation Visits (SIVs), monitoring visits, and close-out activities • Ensure proper delegation of study responsibilities and oversight at all sites • Maintain strong relationships with investigators and site personnel • Oversee completion of protocol, SOP, and GCP training for internal teams and site staff • Monitor adherence to regulatory requirements and internal quality standards • Act as primary point of contact for study-related communication with sponsors • Coordinate multisite studies, ensuring consistency in execution, data quality, and reporting • Ensure timely completion of study documentation and support audit readiness • Drive continuous improvement in clinical operational processes Qualifications: • Master’s/Bachelor’s degree in Life Sciences, Pharmacy, Cosmetic Technology, or related field Experience: • 5–10+ years in clinical trials with at least 2–3 years in a supervisory/managerial role • Experience in cosmetic/dermatology clinical studies highly desirable Skills: • Strong knowledge of clinical research processes, GCP, and regulatory guidelines • Expertise in managing Skin, Hair, Cosmetic, or Dermatology-based clinical studies (preferred) • Excellent communication and stakeholder management skills • Ability to lead teams and manage multiple projects simultaneously • Strong analytical thinking, documentation, and problem-solving skills About the Organization: The organization specializes in conducting high-quality clinical trials in cosmetic, dermatology, and life sciences domains. It focuses on regulatory compliance, operational excellence, and delivering innovative clinical solutions while fostering a collaborative and professional work environment.

Roles & Responsibilities: • Conduct site initiation, routine monitoring, and close-out visits to ensure compliance with study protocols, GCP, and regulatory requirements • Build and maintain strong relationships with investigative sites, investigators, and study coordinators • Perform routine monitoring visits to assess site performance, data integrity, and regulatory compliance • Ensure timely resolution of data queries and issues identified during monitoring visits • Ensure all study activities are conducted according to approved protocols, SOPs, and regulatory guidelines • Collaborate with investigators to address and resolve protocol-related queries • Assist in preparation and submission of regulatory documents to ethics committees and regulatory authorities • Collaborate with data management teams for accurate and timely data collection and entry • Perform source data verification and data validation activities • Monitor and report adverse events as per regulatory and safety reporting procedures • Provide training and support to site staff on study protocols, data collection, and regulatory compliance • Act as a resource for investigators and site staff throughout the study Qualifications: • Bachelor’s degree in Life Sciences or a related field Experience: • Minimum 3 years as a Clinical Research Associate with proven site management and monitoring experience • Familiarity with regulatory requirements and guidelines governing clinical trials Skills: • Excellent verbal and written communication skills • Strong organizational and time management skills with attention to detail • Ability to work effectively in cross-functional teams and independently • Willingness to travel to investigative sites as required About the Organization: MS Clinical Research Pvt Ltd is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. The company focuses on conducting high-quality clinical trials, ensuring regulatory compliance, and supporting the development of innovative medical solutions in a collaborative and dynamic environment.

Roles & Responsibilities: • Conduct clinical trials in compliance with ICH-GCP and protocol guidelines • Support study start-up activities and assist with site initiation • Participate in recruitment and retention of study subjects • Complete and maintain source documents, CRFs, and logs accurately • Compile and update the Site Master File • Manage Investigational Products (IP), including accountability and shipping • Coordinate submissions and communication with the Ethics Committee • Update sponsors on study progress and prepare for monitoring visits • Perform other responsibilities assigned by management Qualifications: • Graduates/postgraduates in Life Sciences, Pharmacy, Biotechnology, or related fields • Freshers with a completed Clinical Research course can also apply Experience: • 2–4 years in clinical research or relevant field (freshers with certification considered) Skills: • Strong interest in clinical trials and regulatory compliance • Excellent organizational, communication, and documentation skills About the Organization: This organization is dedicated to conducting high-quality clinical trials with a focus on regulatory compliance and data integrity. They provide a collaborative environment where professionals can grow their careers in clinical research and contribute to innovative healthcare solutions.

Roles & Responsibilities: • Conduct clinical trials as per ICH-GCP guidelines, study protocols, and SOPs • Operate, handle, and maintain lab instruments as per SOPs and manuals • Document instrument data accurately and maintain calibration records • Perform routine instrument calibration and ensure proper record keeping • Coordinate with floor teams to ensure smooth execution of study activities • Assist in scheduling study subjects and ensure adherence to timelines • Submit study-related data on time for analysis • Report deviations, anomalies, or concerns to line manager and escalate when needed Qualifications: • Bachelor’s degree or diploma in Life Sciences, Pharmacy, or related field Experience: • Prior experience in clinical research or laboratory environment preferred Skills: • Knowledge of ICH-GCP and clinical trial procedures • Strong attention to detail and documentation accuracy • Good communication and coordination skills • Ability to work collaboratively in a fast-paced research environment About the Organization: MS Clinical Research Pvt Ltd is a leading clinical research organization focused on conducting high-quality clinical trials. The company is committed to maintaining international standards, ensuring data integrity, and supporting innovative healthcare solutions.

Role & Responsibilities • Perform signal detection activities across global safety databases • Conduct medical review and assessment of aggregate safety reports (PSUR, PBRER, DSUR) • Perform medical evaluation of Individual Case Safety Reports (ICSRs) • Support benefit–risk evaluation and safety decision-making • Ensure compliance with global pharmacovigilance regulations and guidelines • Collaborate with pharmacovigilance, regulatory, and cross-functional teams • Maintain high standards of documentation and medical review quality Qualification • MBBS or MD (mandatory) • Registered medical practitioner in India Experience • Minimum 1 year of experience in pharmacovigilance or drug safety • Hands-on exposure to signal detection and aggregate reporting preferred Skills • Strong knowledge of signal detection methodologies • Experience with aggregate safety reports (PSUR, PBRER, DSUR) • Understanding of global PV guidelines (ICH, GVP) • Good analytical and medical writing skills • High attention to detail and compliance orientation Availability • Immediate joiners or candidates with up to 1 month notice period preferred About the Company • OrciMed Life Sciences is a growing pharmacovigilance and life sciences services organisation

Roles & Responsibilities Production • Handle solid dosage manufacturing operations • Maintain BMRs, logbooks, and production documentation • Ensure cGMP-compliant production as per SOPs • Support routine production activities and shift operations Formulation R&D • Solid oral formulation development and optimization • Process validation and scale-up activities • Troubleshooting during development and technology transfer • Lifecycle management and MSAT exposure Quality Assurance • Process and cleaning validation activities • Deviation handling, CAPA implementation, and change control • Support internal and external audits • Ensure GMP/GDP compliance across operations • Qualification of equipment, systems, and processesQualification & Experience Production • Designation: Officer / Senior Officer / Executive • Experience: 3 to 8 Years • Qualification: B.Pharm / M.Pharm Formulation R&D • Designation: Research Associate to Deputy Manager • Experience: 3 to 15 Years • Qualification: M.Pharm Quality Assurance (QA) • Designation: Executive to Assistant Manager • Experience: 3 to 10 Years • Qualification: M.Sc / M.Pharm Desired Candidate Profile • Strong knowledge of pharmaceutical manufacturing and regulatory practices • Experience in regulated plant environments • Good documentation and compliance mindset • Willingness to work in shifts (as applicable)Walk-In Interview Details Date: 1st February 2026 Time: 09:30 AM to 05:30 PM Venue: Hotel – Red Maple, Jhoomer Ghat, Rasalpura, Rau, Indore – 453 446, Madhya Pradesh, IndiaAbout the Organisation NAARI pharma is a fast-growing pharmaceutical organization dedicated to excellence in manufacturing, formulation development, and quality systems. With a strong focus on compliance, innovation, and inclusive growth, NAARI offers professionals the opportunity to work in regulated environments while building long-term careers across Production, R&D, and Quality functions.

Roles & Responsibilities: • Develop, program, and validate ADaM datasets as per CDISC standards. • Create Tables, Listings, and Figures (TLFs) using SAS and/or R. • Implement Statistical Analysis Plans (SAP) and Statistical Programming Plans (SPP). • Ensure compliance with regulatory and industry standards (CDISC – SDTM, ADaM). • Collaborate closely with biostatisticians and clinical teams to ensure data accuracy. • Develop reusable macros and automate programming processes for efficiency. • Perform independent QC checks on statistical outputs and deliverables. • Support programming activities across multiple therapeutic areas including Oncology, Neuroscience, and Immunology. Qualifications • Graduate / Postgraduate in Life Sciences, Engineering, Statistics, or related disciplines.Experience: • 3 to 12 years of experience in clinical or biostatistical programming. • Hands-on experience in ADaM, TLF development, and clinical trial data analysis. Skills: • Strong expertise in SAS and/or R programming. • In-depth knowledge of CDISC standards (SDTM, ADaM). • Experience working with clinical trial protocols and regulatory guidelines. • Proficiency in TLF generation and data manipulation techniques. • Strong analytical, problem-solving, and attention-to-detail skills. • Exposure to additional tools such as Python or SQL (preferred). • Basic understanding of machine learning concepts applied to clinical data (preferred). About the Organisation: The organization is a leading clinical research and data analytics-driven company supporting global clinical trials across multiple therapeutic areas, offering a collaborative work environment, exposure to regulatory-compliant projects, and long-term career growth opportunities in statistical and clinical programming.

Roles & Responsibilities: • Carry out API production activities as per SOPs and batch manufacturing records. • Handle day-to-day production operations in a regulated pharmaceutical environment. • Follow GMP, safety, and quality standards during manufacturing processes. • Support smooth shift operations and documentation activities. • Coordinate with team members to ensure timely production targets. Qualification: • B.Sc / M.Sc / B.Pharmacy Experience: • 0 to 6 years of experience in API / pharmaceutical production • Freshers with strong subject knowledge can also apply Skills: • Basic knowledge of API and pharmaceutical manufacturing processes. • Understanding of production operations and documentation practices. • Willingness to work in rotational shifts. • Good learning attitude and team coordination skills. Walk-In Interview Details: • Date: January 30 & 31, 2026 • Time: 09:30 AM to 04:00 PM • Venue: Honour Lab Limited – Unit-IX, Sy.No. 332, 335, 336 & 341, Veliminedu, Chityala (M), Nalgonda (Dt.), Telangana – 508114 • Documents to Carry: Updated resume, educational certificates, experience letters (if applicable), and recent photographs. • Contact: 9949043874 / 9154840911 About the Organisation: Established in Hyderabad, Telangana, Honour Lab Limited is a leading pharmaceutical manufacturer specializing in APIs and intermediates, operating multiple manufacturing units with global regulatory approvals and offering stable career growth in a quality-driven, regulated environment.