Pharmacy Jobs

Roles & Responsibilities Microbiology (Executive/Sr. Executive) • Ensure sterility assurance and environment monitoring • Supervise environment monitoring activities • Prepare Rational and Risk assessment documents • Perform MLT validations, BET validations, Sterility test validation, and microbial method validations QA – QMS (Assistant Manager/Deputy Manager) • Handle investigations, root cause analysis, change control, incident/deviation, CAPA, market complaints, recall QA – IPQA (Executive/Sr. Executive) • Manage line clearance for production manufacturing QA – Validation Injectable (Executive/Sr. Executive) • Handle injectable equipment like filling, Lyo, and Autoclave Qualification • B.Pharm / M.Pharm / M.Sc (depending on role) Experience • Microbiology: 8–12 years • QA-QMS: 12–16 years • QA-IPQA: 5–10 years • QA Validation Injectable: 3–10 years Skills • Formulation injectable experience mandatory • Knowledge of sterility assurance, validations, QA/QMS processes • Strong documentation, investigation, and problem-solving skills About the Company SP Accure Labs is a globally recognized pharmaceutical organization specializing in high-quality injectable formulations, committed to innovation, patient safety, and maintaining international regulatory standards in manufacturing and quality assurance. Note: Male candidates preferred. Bring resume, recent increment letter, 3 months payslips, 3 months bank statement, educational certificates, Aadhaar & PAN card.

Roles & Responsibilities Production (Technical Staff/Executive/Senior Executive) • Allocate manpower and manage production workstations. • Ensure GMP compliance and maintain production documentation. • Record/verify process parameters and support validation activities. • Monitor machine parameters, BMR submission, and output reporting. • Perform in-process checks, equipment calibration, MIS reporting. • Ensure workplace safety, discipline, and ERP reporting. Packing (Technical Staff/Executive) • Supervise line operations and manpower allocation. • Conduct in-process checks, line clearance, CAPA, and SAP reporting. • Follow cGMP, GDP, SOPs, and safety guidelines. • Handle deviations, rejections, minor mechanical issues, and cleaning. • Ensure expected output and report issues promptly. Qualification • B.Pharm, B.Sc., M.Sc. (Chemistry), or relevant Diploma Experience • Production: 2–6 years • Packing: 1–5 years Skills • Pharma manufacturing & machine operation knowledge • Strong GMP, cGMP, GDP, SOP compliance • Manpower management & line coordination • Documentation, reporting, ERP/SAP familiarity • Good communication & problem-solvingWalk-in Interview Details Date: February 1, 2026 (Sunday)  Timing: 9:00 AM – 3:00 PM Walk-in Venue: The Red Maple Mashal, Hoomer Jhat, Rasal Pura, Rau, Indore, Madhya Pradesh 453446Note: Bring updated resume, educational certificates, experience letters, latest increment letter, and passport-size photographs. About the Organization Piramal Pharma Limited is a leading global CDMO delivering innovative, high-quality patient-centric pharmaceutical solutions with operations in North America, Europe, and Asia.

Roles & Responsibilities: • Perform end-to-end pharmacovigilance case processing for clinical trial safety cases • Collect, assess, process, and submit adverse event (AE) and serious adverse event (SAE) reports • Ensure timely and accurate data entry in LSMV (LifeSphere MultiVigilance) database • Maintain compliance with global pharmacovigilance regulations (ICH-GCP, GVP, FDA, EMA) • Support signal detection activities and risk management assessments • Collaborate with cross-functional teams on safety queries and investigations • Stay updated with current drug safety guidelines and industry standards Qualification: • Bachelor’s degree in Life Sciences, Pharmacy, or related discipline Experience: • Minimum 2+ years of experience in pharmacovigilance case processing • Hands-on experience in Clinical Trial Safety Cases OR LSMV / Argus / Safety Databases Skills: • Strong analytical skills with high attention to detail • Excellent written and verbal communication skills • Proven commitment to quality, compliance, and patient safety About the Organisation: ICON plc is a global leader in healthcare intelligence and clinical research, dedicated to advancing patient safety and delivering high-quality clinical development solutions across the pharmaceutical and biotech industries.

Roles & Responsibilities: Production FP (Officer / Executive) • Handle production planning and filling activities in compliance with cGMP standards • Operate and maintain equipment like Lyophilizer, Aseptic Media fills, HPHV • Follow SOPs, DO, IQ, PQ, OQ protocols and preventive maintenance schedules • Ensure proper handling of filter integrities and other critical production processes Packing (Jr Executive / Executive) • Operate labeling machines and printers • Supervise packing lines and ensure smooth operations • Maintain Quality Management System (QMS) compliance during packing Qualification: • B. Pharm / M. Pharm / M. Sc Experience: • Production FP: 2 – 10 Years • Packing: 3 – 5 Years Skills: • Hands-on exposure to pharmaceutical operations, especially aseptic processing and equipment handling • Knowledge of cGMP, SOPs, and preventive maintenance • Ability to supervise production or packing lines effectively About the Organisation: Hetero Biopharma, part of the renowned Hetero Group, is a leading biopharmaceutical company specializing in biologics manufacturing, committed to producing high-quality medicines in a certified and innovative environment.Interested candidates should send their updated resume to Praveen.ko@hetero.com.

Roles & Responsibilities: • Develop and execute business strategy aligned with the company’s growth aspirations in ME markets • Lead and mentor a team, setting clear goals and ensuring high performance • Drive revenue growth by meeting and exceeding sales targets • Strengthen internal processes to enhance operational efficiency • Ensure continuous customer engagement and build long-term relationships • Collaborate with cross-functional teams to ensure smooth execution of business strategies • Oversee budgeting and execution to achieve business objectives • Travel extensively to key markets, understanding customer needs and market trends Qualification: • Science background (M.Sc., PhD, M.Pharm) or Engineering followed by an MBA Experience: • 15+ years in Sales, Marketing, and Business Development • Cross-functional exposure in Manufacturing / R&D / Quality / Regulatory is a plus • Proven expertise in handling the ME Market • Strong leadership experience managing and motivating large teams Skills: • Strong technical acumen to provide solutions to customers effectively • Exceptional communication, negotiation, and strategic thinking skills About the Organisation: Hetero Biopharma is a leading global pharmaceutical company specializing in generic formulations and active pharmaceutical ingredients, committed to delivering affordable and high-quality medicines worldwide.

Roles & Responsibilities: • Prepare demand forecasts based on sales inputs, historical data, and market trends • Convert demand plans into supply plans in coordination with production, procurement, and SCM teams • Monitor inventory levels to ensure optimum stock availability and minimize excess or obsolescence • Coordinate with sales, marketing, and plant teams to align demand and supply plans • Track order fulfillment, identify risks, and proactively address supply gaps • Prepare and analyze MIS reports, dashboards, and planning metrics using Excel • Work extensively on SAP for demand planning, MRP, inventory management, and reporting • Participate in monthly S&OP meetings and support decision-making with data-driven insights • Ensure compliance with internal processes and pharmaceutical industry standards Qualification: • Bachelor’s degree in Pharmacy, Supply Chain, Operations, or related discipline • MBA is preferred Experience: • 3 – 6 Years in Demand & Supply Planning, preferably within the Pharma industry Skills: • Strong hands-on experience with SAP (Demand Planning / Supply Planning / MRP modules) • Advanced proficiency in MS Excel (pivot tables, formulas, dashboards) • Sound understanding of pharmaceutical supply chain processes • Strong analytical, coordination, and stakeholder management skills • Ability to work in a fast-paced, cross-functional corporate environment About the Organisation: Hetero Biopharma is a leading global pharmaceutical company specializing in generic formulations and active pharmaceutical ingredients, committed to delivering affordable and high-quality medicines worldwide.

Roles & Responsibilities: • Perform bioanalytical sample analysis using LC-MS/MS techniques. • Conduct method development and method validation as per regulatory guidelines. • Operate and troubleshoot AB Sciex LCMS instruments. • Ensure compliance with GLP, GCP, and regulatory standards. • Prepare and review bioanalytical reports and documentation. • Maintain laboratory records, SOPs, and calibration logs. • Support audits and inspections when required. Qualification: • M.Sc / M.Pharm / B.Pharm or equivalent Life Sciences qualification. Experience: • 2–6 years of hands-on experience in a Bioanalytical Laboratory. Skills: • Strong hands-on experience in LCMS bioanalysis. • Knowledge of method development, validation, and sample processing. • Familiarity with AB Sciex platforms preferred. • Candidates only from the Bioanalytical domain will be considered. About the Organisation: Navitas Lifesciences is a globally recognized clinical research and bioanalytical services organization, providing regulated bioanalytical and clinical research solutions across global projects, with a strong focus on scientific excellence and regulatory compliance.

Roles & Responsibilities: • Analyze and interpret operational data to provide actionable insights. • Troubleshoot issues via phone, email, or software to identify root causes. • Maintain data accuracy and integrity across all platforms. • Research, sort, and validate information from multiple data sources. • Identify and resolve discrepancies in incomplete records. • Escalate unresolved issues as required and ensure timely closure. • Ensure compliance with project standards and reporting requirements. Qualification: • Graduate in Life Sciences, Pharma, Healthcare, or any related discipline. Experience: • 0–3 years of experience in data entry, customer operations, or healthcare analytics. Skills: • Strong written and verbal communication skills. • Proficiency in MS Office (Excel, Word, Outlook). • Knowledge of US Healthcare domain preferred. • Excellent problem-solving and time management skills. • Ability to work independently and under pressure. • Familiarity with ticketing tools or data entry systems is an advantage. About the Organisation: A leading global healthcare support organization committed to delivering high-quality operational solutions and data-driven insights to improve healthcare outcomes across the United States.

Roles & Responsibilities • Perform end-to-end ICSR case processing for marketed products as per global regulations. • Assess seriousness, expectedness and causality and ensure timely global reporting. • Process literature ICSRs and maintain compliance with monitoring requirements. • Support aggregate reporting activities including PSURs and DSURs. • Maintain safety database integrity with hands-on experience in LSMV preferred. • Perform reconciliation activities and support KPI and SLA tracking. • Collaborate with medical, clinical and cross-functional teams on safety evaluations. • Support signal detection, risk management activities and identification of safety trends. • Participate in regulatory audits and inspections. • Train and mentor junior pharmacovigilance associates. • Review SOPs and contribute to continuous process improvement. Qualification • B.Pharm / M.Pharm, Pharm.D, BDS, B.Sc Nursing / M.Sc Nursing, BAMS / BHMS Experience • Minimum 4+ years of pharmacovigilance case processing experience. • Mandatory experience in Post-Marketing Surveillance (PMS). Skills • Strong knowledge of global pharmacovigilance regulations. • Hands-on experience with safety databases (LSMV preferred). • Expertise in ICSR processing for marketed products. • Experience with PSUR / DSUR and aggregate reports. • Familiarity with SDEA concepts and SLA / KPI management. • Audit and inspection readiness. • Excellent analytical, communication and documentation skills. • Proficiency in Microsoft Office tools. About the Company ICON plc is a global healthcare intelligence and clinical research organization delivering outsourced development and commercialization services to the pharmaceutical, biotechnology and medical device industries, supporting innovation and patient safety across the product lifecycle worldwide.

Roles & Responsibilities • Manage end-to-end scientific writing and publication workflows using Pub Connect. • Create and maintain publication plans, author approvals, versions and checklists. • Coordinate journal and congress submissions including pre-submission inquiries and dummy submissions. • Track submission requirements, guideline updates and provide status updates to stakeholders. • Prepare and collate metadata and complete submission packages. • Ensure accurate documentation from kick-off through review, sign-off and approvals. • Support system activities such as uploads, reference linking and workflow monitoring. • Ensure compliance with journal/congress guidelines, SOPs, client standards and templates. • Perform literature searches and provide ad-hoc operational support as required. • Manage assigned tasks within budgeted hours and defined timelines. Qualification • Master’s degree in Life Sciences, Pharmacy, Medicine or related discipline. Experience • Relevant experience as a Medical Writer or Publication Project Coordinator in a medical communications or biopharmaceutical environment. Skills • Strong experience in scientific writing and publication planning. • Hands-on knowledge of Pub Connect and publication planning tools such as Datavision, Veeva Vault PromoMats or MedComms systems. • Understanding of journal and congress submission processes and regulatory guidelines. • Strong documentation, organizational and project management skills. • Ability to manage multiple workflows and coordinate with cross-functional and sponsor teams. • Strong communication and stakeholder management skills. About the Company Syneos Health® is a leading fully integrated biopharmaceutical solutions organization supporting clinical development, medical affairs and commercial functions worldwide, partnering with global life sciences companies to accelerate the delivery of therapies through innovation, collaboration and a people-centric culture.

Roles & Responsibilities • Manage end-to-end scientific writing and publication workflows using Pub Connect. • Create and maintain publication plans, author approvals, pre-submission queries and submission activities. • Assign and monitor workflows in Pub Connect with real-time updates on project status, versions and checklists. • Maintain accurate documentation from pre-kick-off through review cycles, sign-off and author approvals. • Capture and validate full publication plans and related documents in Pub Connect. • Coordinate journal submissions and congress activities. • Recommend appropriate target journals and manage pre-submission inquiries when required. • Perform dummy submissions to ensure readiness and review journal/congress websites for updated guidelines. • Collate metadata and prepare complete submission packages for journals and congresses. • Provide timely submission status updates to stakeholders. • Offer ad-hoc operational support including uploads in systems as required. • Create placeholders, upload versions, manage reference linking, anchoring and workflow monitoring. • Ensure compliance with journal/congress guidelines, SOPs, client standards and approved templates. • Perform online clinical literature searches as applicable. • Stay aligned with budgeted hours and communicate changes to medical writing leadership. • Complete administrative tasks within defined timelines. • Minimal travel as required (less than 25%). Qualification • Master’s degree in Life Sciences, Pharmacy, Medicine or related discipline. Experience • Relevant experience as a Medical Writer or Publication Project Coordinator in medical communications or biopharmaceutical environment. Skills • Strong experience in publication planning and scientific writing. • Hands-on knowledge of Pub Connect and publication planning tools such as Datavision, Veeva Vault PromoMats or MedComms systems. • Understanding of journal and congress submission processes and guidelines. • Strong documentation, organizational and project management skills. • Ability to coordinate with cross-functional and sponsor teams. • Strong attention to detail with ability to manage multiple projects simultaneously. • Good communication and stakeholder management skills. About the Company Syneos Health® is a fully integrated biopharmaceutical solutions organization operating across clinical development, medical affairs and commercial services, partnering with global life sciences companies to accelerate therapy development and delivery, with a strong global presence and a people-centric, inclusive culture.

Roles & Responsibilities • Prepare ANDA Annual Reports, supplements and amendments in compliance with US FDA guidelines. • Support change control evaluations and review supporting documents including batch manufacturing records, analytical methods, specifications and validation documents. • Maintain regulatory databases, trackers and submission logs in real time. • Assist senior regulatory staff in FDA filing determinations and submission strategies. • Ensure approved applications remain compliant with FDA regulations throughout the product lifecycle. • Participate in cross-functional regulatory and quality projects as assigned. Qualification • M.Pharm in Regulatory Affairs or Quality Assurance (preferred). Experience • Minimum 2 years of experience in Regulatory Affairs, OR • Experience in QC, Analytical, R&D, Manufacturing or Pharmaceutical Production with regulatory exposure. Skills • Strong knowledge of FDA regulations and ANDA processes. • Hands-on experience with regulatory documentation and submissions. • Proficiency in MS Word, Excel and regulatory documentation tools. • Strong written and verbal communication skills. • High attention to detail with ability to manage multiple priorities. • Ability to work independently and collaborate with cross-functional teams. About the Company Teva Pharmaceuticals is a global leader in generic and specialty medicines, committed to improving patient health by delivering high-quality, affordable healthcare solutions, with a strong global presence and robust regulatory and compliance systems supporting markets worldwide.

Roles & Responsibilities • Coordinate with global R&D sites to provide end-to-end support for stability testing. • Perform routine analysis and testing for new product formats using analytical instruments in cGMP labs. • Develop, optimize and validate analytical methods. • Troubleshoot analytical instrumentation and support transfer of analytical methods and new technologies. • Drive operational excellence initiatives to simplify and improve technical processes using statistical approaches and experimental design. • Maintain, calibrate, qualify and troubleshoot laboratory instrumentation. • Ensure accurate, updated and compliant laboratory documentation following ALCOA+ principles. Qualification • M.Sc in Analytical Science / Organic Chemistry or related discipline. • Masters in Pharmacy. Experience • Minimum 2 years of total experience. • At least 1 year of hands-on experience with HPLC / GC in a cGMP environment. Skills • Strong expertise in chromatography techniques (HPLC / GC). • Experience working as an analytical scientist in a multinational Pharma / FMCG organization. • Hands-on exposure to stability testing. • Thorough knowledge of ICH / WHO / FDA guidelines, cGMP requirements and ALCOA+ principles. • Ability to support analytical method validation, forced degradation studies and documentation. Preferred Skills • Experience with OpenLab software and compliance with 21 CFR Part 11 (electronic records). • Knowledge of eLN and LIMS systems. • Strong analytical thinking, decision-making and problem-solving skills. • Good business presentation and communication skills. • Ability to handle assigned programs independently with minimal supervision. About the Company Colgate-Palmolive Company is a global consumer products organization operating in over 200 countries, specializing in Oral Care, Personal Care, Home Care, Skin Care and Pet Nutrition, driven by its core values of Caring, Inclusive and Courageous, and committed to building a healthier future for people, pets and the planet.

Roles & Responsibilities • Develop tabulations and summaries using Excel, VBA, SQL and Python. • Write complex SQL queries to extract, merge and transform datasets. • Perform data processing, statistical analysis and modeling using Python. • Build, review and maintain analytics reports and dashboards for clients. • Translate business questions into analytical problem statements. • Define, track and analyze KPIs for omnichannel initiatives. • Conduct market research and secondary data analysis. • Develop forecasting models including pharma inline forecasts. • Present data-driven insights to internal and external stakeholders. • Own analytics projects end-to-end with minimal supervision. • Apply consulting frameworks and best practices in analytics delivery. Qualification • BTech + MBA / MTech. • MPharm / PharmD with analytics certifications. Experience • Data Analyst: 1 to 2 years of relevant analytics experience. Skills • Python for data analysis, modeling and automation. • Strong SQL for data extraction and transformation. • Advanced Excel for reporting and analysis. • Knowledge of statistics and data science (good to have). • Strong communication and presentation skills. • Understanding of life sciences / pharma market preferred. About the Company Indegene is a global healthcare solutions company that enables healthcare organizations to be future-ready through data-driven and technology-enabled services, with strong capabilities across analytics, omnichannel engagement, medical affairs and digital transformation, supporting life sciences companies across global markets.

Roles & Responsibilities Quality Control – • Officer to Executive: Perform analytical testing including Assay, Dissolution, CU, BU, RC, PSD etc. • Operate and handle HPLC, UPLC, GC, FTIR, KF Titrator instruments. • Analytical troubleshooting and shift handling activities. Quality Control – • Assistant Manager: Handle OOS/OOT investigations and perform root cause analysis. • Implement CAPA and ensure compliance with cGMP, GLP, GDP and data integrity (ALCOA+). • Audit trail review and laboratory incident investigations. Manufacturing – • Officer to Executive: Operate granulation, coating, compression, capsule filling and bottle packing operations. • Handle RMG, FBE, auto coaters, bottle packing line and track & trace systems. • Ensure OSD manufacturing activities as per cGMP guidelines. Qualification • B.Sc / M.Sc / M.Pharm for Quality Control roles. • ITI / Diploma / B.Sc / B.Pharm for Manufacturing roles. Experience • Quality Control Officer to Executive: 2–6 years. • Quality Control Assistant Manager: 10–12 years. • Manufacturing Officer to Executive: 3–6 years. Skills • Strong knowledge of analytical techniques and laboratory instruments. • OOS/OOT handling, CAPA, cGMP, GLP, GDP and data integrity practices. • Granulation, coating, compression, packing operations in regulated pharma environment. Walk-in Interview Details • Date: Sunday, 8 February 2026. • Time: 9:00 AM onwards (candidates are advised to arrive early). • Venue: Hampton by Hilton, Alkapuri, 14, Friends Co-operative Society, Vadodara, Gujarat – 390007. • Carry updated resume and relevant documents. About the Company Amneal Pharmaceuticals is a leading global biopharmaceutical company listed on the NYSE (AMRX) with over 7,500 employees worldwide, engaged in the development, manufacturing and distribution of high-quality generic and specialty medicines, offering strong career growth opportunities in a regulated pharmaceutical environment.

Role & Responsibilities • Lead and manage medical writing assignments, including protocols, clinical study reports, regulatory documents, manuscripts, abstracts, and presentations • Mentor and supervise junior and mid-level medical writers, providing developmental feedback, training, and quality review • Ensure consistency, clarity, and scientific accuracy across all documents • Review and approve materials related to clinical trial registration (e.g., CTRI entries) and ethics committee submissions • Guide the team on best practices for literature review, referencing, and scientific integrity using sources like PubMed, NIH Library, and NLM databases • Provide strategic input on publication planning, conference material development, and stakeholder communications • Collaborate closely with cross-functional teams including researchers, project managers, and external consultants to align on deliverables • Maintain up-to-date knowledge of global regulatory writing standards (e.g., ICH-GCP, GPP3, CONSORT) • Recommend and implement process improvements, templates, and SOPs for documentation • Provide oversight for version control, formatting, and adherence to SOP MSCR/GEN/03-03 Qualification • PhD/MD/MPharm/MSc in Life Sciences, Medicine, or Pharmacy Experience • Minimum 10 years of medical writing experience, preferably in a CRO or clinical/preclinical research setting • Demonstrated experience managing or mentoring a team of writers • Strong command of written English and scientific communication • Proficiency with referencing tools (e.g., EndNote) and document management systems • Excellent organizational and project management skills Skills • Experience in preclinical (in-vitro/in-vivo) and clinical trial documentation • Exposure to publication strategy and submission to peer-reviewed journals • Familiarity with tools like CTD structure, CTRI submission portals, and regulatory publishing platforms About The Company • MS Clinical Research (MSCR) is a clinical research organization (CRO) focused on providing comprehensive services in medical writing, regulatory affairs, and pharmacovigilance.

Roles & Responsibilities • Perform end-to-end ICSR processing from spontaneous, clinical, literature, and solicited sources • Handle case intake, triage, data entry, MedDRA and WHO-DD coding, narrative writing, QC, and follow-ups • Conduct systematic literature surveillance and generate compliant literature ICSRs • Ensure timely regulatory submissions to global health authorities (USFDA, EMA, MHRA, PMDA, etc.) • Support aggregate safety reports including PSUR, PBRER, and DSUR • Maintain compliance with global PV regulations, internal SOPs, and client procedures • Support internal, client, and regulatory audits including CAPA activities • Assist in signal detection and ongoing safety data review • Perform regulatory intelligence and safety trend monitoring • Collaborate with cross-functional and client teams in a consulting environment Qualification • Graduate or Postgraduate in Life Sciences • B.Pharm / M.Pharm / Biotechnology / Biology / Chemistry or related disciplines • Master’s degree preferred Experience • 1–5 years of experience in Pharmacovigilance or Drug Safety • Experience in global PV projects and regulatory submissions preferred Skills • Hands-on experience with safety databases such as Argus, ArisG, Veeva, or similar • Strong knowledge of global pharmacovigilance regulations (ICH, GVP, USFDA, EMA, MHRA) • Excellent communication, analytical, and documentation skills • Ability to work in a fast-paced consulting and client-facing environment About the Organisation Amarant Lifesciences Private Limited is a regulatory and pharmacovigilance consulting organization providing end-to-end drug safety and compliance solutions to global pharmaceutical and biotechnology clients, offering strong exposure to international regulatory projects and career growth opportunities.

Roles & Responsibilities • Respond to medical information queries from healthcare professionals, patients, and internal stakeholders via calls and emails • Provide accurate, balanced, and compliant scientific responses • Document and track medical inquiries as per SOPs and regulatory guidelines • Ensure adherence to quality standards, audit readiness, compliance, and turnaround time (TAT) • Coordinate with Pharmacovigilance, Quality Assurance, Regulatory Affairs, and Medical Affairs teams • Maintain data integrity, confidentiality, and regulatory compliance in a global pharma environment Qualification • B.Pharm / M.Pharm / PharmD • B.Sc / M.Sc (Life Sciences) Experience • Experience in Medical Information, MICC, Pharmacovigilance, Drug Safety, or Voice / Call Center process • Candidates from non-core voice process backgrounds with pharma education are encouraged to apply Skills • Strong verbal and written communication skills • Understanding of SOPs, compliance, and quality systems • Ability to handle scientific discussions with HCPs and patients • Experience working with global or international clients is an added advantage About the Organisation Mitocon Biopharma Pvt. Ltd. is a growing pharmaceutical and biotechnology company focused on innovation, regulatory compliance, and global healthcare solutions. The organization provides strong career-transition opportunities for pharmacy professionals to move into core pharmacovigilance and medical information roles.

Roles & Responsibilities • Assist in product development and pharmaceutical formulation activities • Perform laboratory trials and accurately document experimental data • Prepare, update, and maintain Standard Operating Procedures (SOPs) • Conduct literature surveys to support formulation and development work • Coordinate with analytical R&D teams for testing and validation • Ensure adherence to quality, safety, and regulatory guidelines • Support senior scientists in day-to-day R&D operations Qualification • B.Pharm / D.Pharm • B.Sc (Chemistry, Microbiology, Biochemistry, Biology, Zoology, Botany) • B.Tech / B.E (Biotechnology, Biomedical, Chemical Engineering) • Diploma in Chemical / Pharmacy • M.Pharm (Any Specialization) • M.Sc (Chemistry, Microbiology, Nursing, Chemical Engineering) • MS / DM (Any Specialization) Experience • Freshers to 4 years of experience in pharmaceutical R&D or laboratory environment • Academic project or internship experience in formulation or R&D will be an advantage Skills • Strong foundational knowledge in pharmaceutical research and development • Basic understanding of formulation development processes • Familiarity with laboratory instruments and technical documentation • Good communication and coordination skills • Willingness to learn and adapt in a regulated pharmaceutical environment About the Organisation Stedman Pharmaceuticals is a growing pharmaceutical company focused on research-driven product development. The organization offers a learning-oriented environment with hands-on exposure to formulation R&D, regulatory practices, and quality standards, supporting long-term career growth in the pharmaceutical industry.