Pharmacy Jobs

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.

Roles & Responsibilities: • Perform routine and advanced quality control analysis of raw materials, in-process samples, and finished products. • Conduct stability studies in accordance with ICH guidelines. • Ensure strict compliance with GLP, GMP, and data integrity requirements. • Maintain accurate analytical documentation, laboratory records, and reports. • Support internal and external regulatory audits and inspections. • Operate and handle QC laboratory instruments and analytical techniques. Qualification: • B.Sc / M.Sc / B.Pharm / M.Pharm Experience: • 1–3 years of Quality Control experience in a regulated pharmaceutical industry. Skills: • Hands-on exposure to QC analysis and stability testing. • Strong understanding of GLP practices and GMP compliance. • Knowledge of regulatory guidelines (USFDA / WHO-GMP preferred). • Good documentation and data integrity awareness. • Ability to work in a regulated, audit-driven environment. About the Organisation: Emcure Pharmaceuticals Ltd. is a leading Indian pharmaceutical company with a strong presence in regulated markets, known for its focus on quality, compliance, and innovation, offering stable career growth and exposure to global regulatory standards. Email your application to:bhavik.parekh@emcure.com

Roles & Responsibilities: Quality Control: • Perform routine QC testing of raw materials, in-process samples, and finished products. • Conduct analytical testing as per approved specifications and SOPs. • Maintain accurate documentation, test records, and data integrity. • Support stability studies and sample management activities. • Follow GMP, GLP, and safety guidelines strictly. • Assist during audits, inspections, and compliance activities. Formulation Production: • Assist in formulation manufacturing operations as per Batch Manufacturing Records (BMR). • Support granulation, blending, compression, coating, and packing activities. • Ensure adherence to GMP guidelines and production SOPs. • Maintain production records, logbooks, and documentation accurately. • Follow safety procedures and work in shift-based operations. • Support equipment cleaning, area maintenance, and production readiness. Qualification: • Quality Control: M.Sc. (Analytical Chemistry) / B.Pharm / M.Pharm • Formulation Production: D.Pharm / ITI / Diploma (relevant discipline) Experience: • Fresher only (Pass-out candidates).Walk-in Interview Details: • Date: 31-01-2026 (Saturday) • Venue: Ahmedabad Management Association (AMA), ATIRA Campus, Dr. Vikram Sarabhai Marg, Near Panjrapol Cross Roads, Ahmedabad – 401506 • Candidates should carry updated CV, relevant education documents, Aadhaar card, and recent photographs. • Smart phone required for online registration and assessment.About the Organisation: Macleods Pharmaceuticals is one of India’s fastest-growing pharmaceutical companies with a strong presence across multiple therapeutic segments, ranked among the top pharma companies, and committed to excellence in quality, innovation, and manufacturing through its world-class facilities and Centre of Excellence training programs.

Roles & Responsibilities: • Manage day-to-day medical coding operations. • Assign accurate diagnosis and procedure codes to patient charts. • Maintain a minimum of 95% quality on production. • Adhere to internal and external coding compliance policies and client requirements. • Improve performance based on feedback from reporting managers. • Follow organizational policies related to information security, HIPAA, and HR compliance. Qualification: • Life Science or Paramedical graduate. • No backlogs with complete academic documentation. Skills: • Strong analytical and logical thinking skills. • High attention to detail and accuracy. • Average written and spoken English communication skills. • Ability to understand medical terminology and coding standards. Assessment / Interview Process: • HR Interview. • Online Assessment – Anatomy & Physiology. • Medical Transcription (MT) Training. • MT-cleared candidates will be onboarded into Medical Coding training batch. Compensation & Benefits: • Competitive remuneration. • Annual performance-based bonus. • Standard industry benefits. • Relocation package as per company policy (for candidates outside base city). About the Organisation: AGS Health is a global leader in healthcare revenue cycle management, combining AI-enabled technologies with expert services to support leading U.S. health systems, physician groups, and academic medical centers, with 12,000+ professionals serving 100+ clients worldwide.

Roles & Responsibilities: • Manage day-to-day medical coding operations. • Assign accurate diagnosis and procedure codes to patient charts. • Maintain a minimum of 95% quality on production. • Adhere to internal and external coding compliance policies and client requirements. • Improve performance based on feedback from reporting managers. • Follow organizational policies related to information security, HIPAA, and HR compliance. Qualification: • Life Science or Paramedical graduate. • No backlogs with complete academic documentation. Skills: • Strong analytical and logical thinking skills. • High attention to detail and accuracy. • Average written and spoken English communication skills. • Ability to understand medical terminology and coding standards. Assessment / Interview Process: • HR Interview. • Online Assessment – Anatomy & Physiology. • Medical Transcription (MT) Training. • MT-cleared candidates will be onboarded into Medical Coding training batch. Compensation & Benefits: • Competitive remuneration. • Annual performance-based bonus. • Standard industry benefits. • Relocation package as per company policy (for candidates outside base city). About the Organisation: AGS Health is a global leader in healthcare revenue cycle management, combining AI-enabled technologies with expert services to support leading U.S. health systems, physician groups, and academic medical centers, with 12,000+ professionals serving 100+ clients worldwide.

Roles & Responsibilities: • Manage day-to-day medical coding operations. • Assign accurate diagnosis and procedure codes to patient charts. • Maintain minimum 95% quality and productivity standards. • Ensure adherence to internal and client-specific coding compliance policies. • Implement feedback provided by reporting managers to improve performance. • Follow organizational policies related to information security, HIPAA, and HR compliance. Qualification: • Life Science or Paramedical graduate. • No backlogs with complete semester mark sheets. Experience: • Freshers only. • Passed out between 2022 and 2024. • Immediate joiners preferred. Skills: • Strong analytical and logical thinking skills. • High attention to detail and accuracy. • Average written and spoken English communication skills. • Ability to learn medical coding standards and healthcare workflows. Assessment / Interview Process: • HR Interview. • Online Assessment – Anatomy & Physiology. • Medical Transcription (MT) Training. • MT-cleared candidates will be onboarded into Medical Coding training batch. Compensation & Benefits: • Competitive remuneration. • Annual performance-based bonus. • Standard industry benefits. • Relocation package as per company policy (for outstation candidates). About the Organisation: AGS Health is a global leader in healthcare revenue cycle management, combining AI-enabled technologies with expert services to support leading U.S. health systems, physician groups, and academic medical centers, with a global workforce of 12,000+ professionals serving over 100 clients across diverse care settings.

Roles & Responsibilities: • Prepare and compile CTD dossiers for pharmaceutical product registration and renewals in the UAE. • Ensure full compliance with UAE MOH regulations and regulatory guidelines. • Monitor and stay updated on regulatory requirements for pharmaceutical products. • Coordinate with internal teams on documentation, labeling, and submission activities. • Support pharmacovigilance activities including adverse event reporting. • Liaise with UAE MOH and other regulatory authorities for approvals, queries, and follow-ups. • Assist during regulatory audits and inspections. • Maintain accurate records of submissions, approvals, and regulatory correspondence. Qualification: • B.Pharmacy or D.Pharmacy Experience: • Minimum 2 years of experience in the UAE pharmaceutical industry. • Hands-on experience in CTD dossier preparation and submissions. • Working knowledge of UAE MOH regulations and pharmacovigilance requirements. Skills: • Strong understanding of UAE regulatory frameworks and CTD documentation. • Good coordination and communication skills. • High attention to detail and compliance orientation. • Ability to manage multiple submissions and deadlines. • Proficiency in documentation and record management. About the Organisation: Microsynergy Pharmaceuticals is a pharmaceutical company focused on regulatory compliance, product registration, and lifecycle management, supporting the timely approval and safe marketing of pharmaceutical products within the UAE market.

Roles & Responsibilities: • Provide compliance and operational oversight of the CCDS and Global Labeling processes. • Support inspections and audits related to CCDS and labeling activities. • Monitor and manage labeling change control metrics with focus on safety-related changes. • Oversee labeling operations activities within internal systems (e.g., EAGLE, CCTA). • Support global RA Labeling and CCDS activities to ensure timely, high-quality, and compliant submissions. • Support global oversight of labeling submissions and approvals. • Ensure country-level compliance with global labeling procedures. • Maintain internal systems in line with company policies and procedures. • Ensure quality compliance of marketed products and timely labeling submissions. • Support review, development, and training on RA labeling tools, systems, practices, and policies. • Support GxP audits and inspections related to CCDS and labeling. • Conduct quality self-inspections and audits to ensure SOP compliance. • Drive process efficiency, optimization, and global technical alignment for labeling. • Coordinate training activities to ensure capability building and compliance. • Contribute to global RA collaboration and establishment of best practices. Qualification: • Master’s degree in Pharmacy or other Life Science discipline (or equivalent experience). Experience: • Minimum 8 years of experience in Regulatory Affairs within a global environment. • Experience managing projects and working in a matrixed organization. • Strong knowledge of regulatory landscape, systems, and procedures for CCDS and labeling. Skills: • Proficiency in English language. • Excellent communication, influencing, planning, and problem-solving skills. • Ability to build and manage strong stakeholder relationships. • Strong collaboration skills without direct reporting authority. • Leadership mindset with focus on shared accountability and quality culture. About the Organisation: Astellas is a global pharmaceutical company focused on turning innovative science into value for patients, delivering high-quality medicines across therapeutic areas through strong regulatory, quality, and compliance frameworks worldwide.

Roles & Responsibilities: • Perform local safety case receipt, processing, data entry, QC tracking, and ICSR follow-up in line with agreed timelines. • Manage generic and client-specific safety email inboxes. • Register, triage, assign, and coordinate processing of vigilance cases. • Perform follow-up with local reporters for missing or additional information. • Respond to queries from clients and reporters. • Conduct periodic reconciliations to ensure complete and compliant handling of safety reports. • Support local pharmacovigilance activities as required. • Participate in audits, inspections, and implementation of corrective action plans. Qualification: • Bachelor’s or Master’s degree in Medicine, Pharmacy, Nursing, or a science-related field (or equivalent experience). Experience: • 2+ years of experience in Pharmacovigilance within a service provider environment. • Hands-on experience in safety case data entry and QC. • Experience working to strict timelines and managing client communications. • Knowledge of UK and EU PV regulations. • Strong pharmaceutical background with understanding of GVP, GCP, FDA, and drug safety regulations. • In-depth knowledge of PV principles, adverse event reporting, and causality assessment. Skills: • Excellent organizational and interpersonal skills. • Strong team-working capability. • Effective time management and prioritization skills. • High level of accountability and autonomy. • Process-oriented with strong attention to detail. • Clear written and verbal communication skills to explain complex concepts. • Flexible and adaptable in a dynamic work environment. • Ability to work under pressure and meet deadlines. • Safety database experience preferred. About the Organisation: ProductLife Group is a global life sciences consulting and services company delivering end-to-end solutions across pharmacovigilance, regulatory affairs, quality, and compliance, supporting pharmaceutical, biotechnology, and medical device companies worldwide throughout the full product lifecycle.

Roles & Responsibilities: • Perform quality control of vigilance cases. • Conduct medical evaluation of safety reports. • Data entry of vigilance cases into agreed databases/formats. • Follow-up of vigilance cases via phone and email. • Pre-analysis of complex cases prior to data entry. • Medical evaluation of files including coding, causality assessment, expectedness, and seriousness of events. • Identify submission requirements for each case. • Validate documents prepared by Data Managers/Vigilance Associates. • Close vigilance case files in compliance with regulations. • Define and implement ICSR/MLM filters and applicable changes. • Analyze inclusion/exclusion of EV/MHRA cases. • Provide medical information support and handle safety-related calls. • Review medical information queries and quality complaints to identify safety information. • Act as key contact for specific clients and prepare quality documents as required. Qualification: • Doctor of Pharmacy / Pharmacist Experience: • 1–3 years of experience in a similar Pharmacovigilance role • Knowledge of Pharmacovigilance is an advantage Skills: • Experience with safety databases preferred • Knowledge of current PV regulations • Process-oriented, detail-focused, and team player • Proficient in Microsoft Office tools • Strong multitasking and flexibility • Excellent communication skills in French and English About the Organisation: ProductLife Group is a global life sciences consulting and services company providing integrated solutions across pharmacovigilance, regulatory affairs, quality, and compliance, supporting pharmaceutical, biotechnology, and medical device companies worldwide throughout the entire product lifecycle.

Roles & Responsibilities: • Conduct experimental research and development in assigned project areas. • Design and execute research protocols and experiments. • Maintain accurate records of laboratory data and reports. • Collaborate with multidisciplinary teams to achieve project objectives. • Support publication and presentation of research findings. Qualification: • M.E / M.Tech / M.Pharm Skills: • Strong experimental and analytical skills. • Proficiency in laboratory techniques related to agri-food biotechnology. • Good documentation and reporting skills. • Ability to work collaboratively in a research environment. Age Limit: • Minimum: 21 years • Maximum: 40 years Walk-in Details: • Walk-in Interview: 03-02-2026 • Venue: NABI, Knowledge City, Sector-81, Mohali, Punjab – 140306 About the Organisation: National Agri-Food Biotechnology Institute (NABI) is a premier research institute focused on agri-food biotechnology. And it works on innovative solutions for agriculture and food security. It promotes cutting-edge research, technology development, and translational science.Application formClick HereOfficial NotificationClick Here

Roles & Responsibilities • Support and independently execute research activities under ongoing projects at NABI. • Design, plan, and conduct experiments related to life sciences, biotechnology, or pharmaceutical research. • Analyze experimental data and prepare technical reports, presentations, and documentation. • Maintain laboratory records, project documentation, and ensure data integrity. • Assist in coordination of project activities, timelines, and deliverables. • Ensure compliance with laboratory safety guidelines, SOPs, and institutional policies. • Support procurement, inventory management, and maintenance of laboratory equipment. • Mentor junior research staff and provide technical guidance when required. • Participate in meetings, reviews, and scientific discussions related to project progress. Qualification • MD / MS, M.V.Sc, B.Pharm, MDS (from a recognized university / institution) Experience • Relevant research or project experience in life sciences, biotechnology, pharmaceutical sciences, or allied fields is preferred. • Experience in handling laboratory techniques, data analysis, and research documentation is desirable. Skills • Strong understanding of research methodologies and experimental design. • Good analytical, documentation, and reporting skills. • Ability to work independently and in a multidisciplinary team environment. • Proficiency in MS Office and basic research data tools. • Effective communication and coordination skills. Age Limit • Minimum Age: 21 Years • Maximum Age: 40 Years • Age relaxation as per NABI / Government of India norms. Walk-in Interview Details • Date: 03-02-2026 • Venue: National Agri-Food Biotechnology Institute (NABI), Knowledge City, Sector-81, Mohali, Punjab – 140306 About the Organisation National Agri-Food Biotechnology Institute (NABI) is an autonomous institute under the Department of Biotechnology, Government of India, dedicated to translational research in agri-food biotechnology to improve human nutrition, food security, and agricultural sustainability.Application formClick HereOfficial NotificationClick Here

Role & Responsibilities • Perform quality control (QC) of pharmacovigilance cases • Conduct medical evaluation of adverse event reports • Enter vigilance case data into agreed databases and formats • Perform follow-up of cases via phone and email • Pre-analyse complex cases prior to data entry • Evaluate cases for medical coding as per applicable dictionaries • Assess causality between suspect product and reported events • Determine seriousness and expectedness of events • Identify regulatory submission requirements for each case • Validate documents prepared by Vigilance Associates or Data Managers • Close vigilance case files in compliance with timelines • Support setup and review of ICSR / MLM filters • Analyse inclusion or exclusion of EV / MHRA cases • Provide medical input to the Medical Information division • Support client-specific pharmacovigilance activities within the business unit Qualification • Doctor (MBBS or equivalent) or Pharmacist by training Experience • Minimum 3 years’ experience with service providers in pharmacovigilance • Hands-on experience in QC of safety cases • Experience with SafetyEasy database (mandatory) Skills • Strong knowledge of global pharmacovigilance regulations • Experience working with safety databases • Process-oriented and detail-focused approach • Ability to multitask and manage multiple priorities • Proficiency in Microsoft Office tools • Excellent written and verbal communication skills in English • Strong teamwork and collaboration skills • Flexible and adaptable in a dynamic environment About the Company • ProductLife Group is a global life sciences consulting and services company , Supports pharmaceutical, biotech, and medical device companies across the product lifecycle.