Department: Regulatory Affairs (Formulation) Location: Kandivali - West, Mumbai Role: Responsible for regulatory activity related to clinical section for US, EU, WHO, Canada, Australia, New Zealand and South Africa Markets Key Responsibilities: Preparation of bioequivalence related sections of ANDA product dossiers as per current regulatory guidelines Ensure timely preparation of amendments related to bioequivalence to expedite approvals Review of BE protocol for all market including ROW market Review of bio-waiver information and clinical strategy before start of clinical study. Confirmation of reference product for EU countries for clinical study Review and Preparation of 2.4 (non-clinical review) and 2.5 (clinical review) module for EU submissions Review of SmPC, PIL, Labeling for US, EU and other markets with reference product to keep the generic product labeling up to date. Key Activities: Review of technical documents (clinical) on receipt from various Departments before inclusion in dossiers. Discuss and coordinate with cross-functional teams for finalization of documents Preparation and review of clinical section of product dossiers for ANDA filing. Preparing response of queries for USFDA & UK related to clinical section to facilitate product approval. Attend meetings with QPPV for SmPC and PIL related changes. Key Competencies: Qualification Essential : B. Pharm/M. Pharm/Ph D. Desirable : M.Pharma in Pharmacology/Ph D Experience Essential :10 years and above Desirable : 12 years and above Show more Show less

Job Location : Mumbai Qualification : Graduate · Experience : 1 - 2 yrs Job Profile: Executing the export orders in internal system once the order is received. Raising & following up on Artwork Initiation form for first time export to Clients or export of Products for the first time Follow up for Packing List & COA’s from Plant Make the Shipping instructions for ready orders and effect shipment Follow up with parties for outstanding& overdue payment & coordinating with the Finance dept as soon as payment is received by the client. Generating Co-payment Request forms & Uploading Invoices on supplier portal with respect to one Client- The Global Fund. Arranging inspections for shipments- coordinate with Inspection Agency, Plant & Logistics for the same. Follow up with the Logistic dept & Nominated agents to ensure that shipment leaves country on time. Keep updated data of Export Purchase Order (EPO’s) raised and Shipments made. Generate Monthly requirements to be sent to Planning & Production team Generate Monthly Projections of sales To look after Commissions for various agents Co-ordination with Country Managers and Customers for registration of products in various countries Show more Show less

Job Title : Production/Packing Officer &Executive Qualification: B.Pharm/ M.Pharm Experience: 2 to 7years Job Location - Jorethang (South Sikkim) Job Description: Accountability to ensure production planning & timely delivery of high productivity and low cost products and with compliance to cGMP. Responsible for handling CAPA, Deviation, Change Control, URS, Contingency Plan and Investigation report. Responsibilities: Maintain the CGMP in working area Ensure shop floor observation compliance from QA (if any) investigate the matter and compliance.Verify environmental conditions i.e. Temp.,RH & DP of area as per SOP and BPR requirement and record the same Ensure shop floor observation compliance from QA (if any) investigate the matter and compliance. Responsible for line clearance activity manufacturing and packing activity Filling of daily logs,online documents and in process checks in granulation area.If any deviation occurs during process immediately inform to section incharge / department Head. Show more Show less

Position: Trainee Job Location: Kandivli, Mumbai Education: Any Graduate. Post Graduation not required Experience: 0 to 1 year Key Responsibilities: Maintaining Database Assisting the Dept in Day-to-Day activities Coordination within Departments Assisting in recruitment activities Interested applicants please share resume at neha.jaybhaye@ipca.com Show more Show less

Walk-in At Vapi Dt. 09.10.2022 Vacancy : Officer Quality Control Job Location: Athal Designation : Officer / Sr. Officer Department : Quality Control Qualification : D.Pharm/ B.Sc/ B.Pharm Experience : 1 to 7 years Responsibilities : Relevant Experience in IPQA, QMS & Validations of QA Activities.

Vacancy : Officer / Sr. Officer Functional Area : Quality Control Job Location: Kandla Qualification : BSC / B Pharma Experience : 4 - 6 Years Must : Preferred candidates from pharmaceutical industry only Job Profile: · Handling of troubleshooting of HPLC and GC analysis in Chromeleon Software. · To ensure that work performs as per SOP/STP/CSOP/GTP including GLP and EHS norms with Laboratory discipline. · To review/ ensure all the related log books and records of wet Laboratory and to ensure timely up-dation. · To ensure the completion of daily activities / targets. · Responsible for HPLC column management activities. · Handling of LIMS,LMS,IMS,SCM, Software. · To identity the gaps of SOPs/ Analytical worksheets/ STP/GTP etc and to take the initiative for up-dation the respective documents. · To maintain all QC. SOP IN dISPLAY Copy. · Perform the calibration activity of all QC instruments as per schedule. · To maintain the GLP working area. · To perform and maintain the calibration of HPLC. · Monitoring of column management. · Analysis of in process, finished product and stability samples by instrument HPLC.

Job Title - Sr. Officer - EHS Job Location - Athal Department - EHS Qualification : B.Sc / M.Sc/ Diploma in Safety / B.E/ Any Safety Course Experience: 3 - 4 years Job Role :- ETP Legal Compliance Environment Monitoring

Ipca Laboratories Ltd is seeking an Executive/Officer for the Administration Department in Mumbai. The primary responsibility entails Air Ticket Booking & Billing. Ideal candidates should possess 3 to 4 years of experience in Air Ticket Booking & Billing. To apply, please send your resume to neha.jaybhaye@ipca.com

Company Description Ipca Laboratories Limited, a consumer-led global pharmaceutical company, has been creating healthy doses of life since 1949. Operating in over 120 countries across six continents, Ipca is a fully-integrated pharmaceutical company that manufactures over 350 formulations and 80 APIs for various therapeutic segments. We are among the world's largest suppliers of over a dozen APIs, produced at fully-automated manufacturing facilities approved by top global regulatory authorities. Ipca maintains high-quality standards and prioritizes the safety and dignity of people and consumers. Role Description This is a full-time on-site role for a QC Microbiology Executive/Sr. Executive located in Gandhidham. The responsibilities include performing daily microbiological testing and analysis, ensuring compliance with regulatory standards, maintaining microbiological documentation, and conducting environmental monitoring. The role also involves participating in audits, reviewing SOPs, and coordinating with various departments to ensure quality control standards are met. Company: Ipca Laboratories Ltd. Department: Quality Control – Microbiology Location: Gandhidham Gujarat. Position: QC – Microbiology Executive / Sr. Executive Experience: 6 to 8 Years Qualification: B.Sc / M.Sc – Microbiology or related field Industry: Pharmaceuticals / Formulations Job Description: We are looking for experienced and motivated candidates to join our Quality Control – Microbiology team. The ideal candidate should have hands-on experience in: * Microbial analysis of raw materials, finished products, and water samples. * Environmental monitoring and handling of EM instruments. * Maintenance and calibration of microbiological instruments. * Documentation as per cGMP guidelines. * Knowledge of regulatory audits (USFDA, WHO, MHRA, etc.) will be an added advantage. Skills Required: * Strong microbiological technical skills * Good knowledge of cGMP and GLP * Attention to detail and strong documentation skills * Ability to work in shifts How to Apply: Interested candidates can share their updated resume at avneesh.patel@ipca.com with the subject line “Application for QC – Micro (6-8 Years)”. Thanks & Regard Avneesh patel Sr. Officer - HRD avneesh.patel@ipca.com Ipca Laboratories Ltd, - Gandhidham

Exciting Opportunity at Ipca Laboratories Ltd, Mumbai! Are you a Science graduate with a Master's in Pharmacy or Management? We are looking for a Marketing Manager to join our dynamic team in Mumbai. Key Requirements: - 10 years of extensive experience in Product Management - Previous roles as PE/PM/Sr PM - Preferably experienced in Diabetes, Cardiac Therapy, or General Medicine Therapy - Age range: 35 to 38 years - Mumbai-based candidates only - Ideally leading a Product Management team currently Interested in this role? Share your resume at neha.jaybhaye@ipca.com

Job Title: Executive - Manager (Medical Affairs) Department: Medical Affairs Location: Kandivali (West), Mumbai Qualification & Experience: · MD Pharmacology / MBS/ MDS / BDS / PharmD with 1 - 2 years experience in medico-marketing. Key Responsibilities: · Scientific support for New Product launches and established brands · Train medical representatives · Handling queries / complaints Key Activities: · Train the medical representatives · Prepare training manuals & training presentations · Making medical News letters and product monographs · Prepare presentation for doctor meets aligned to TA. · Scientific literatures support to marketing for brand promotion · Provide scientific support for New Product launches · Approvals of promotional inputs for correctness from scientific and ethical perspective with Senior guidance · Answer queries of the doctors and field staff · KOL development · Attending CME, Conference and symposium as speaker/delegate MUST · Knowledge of Medical Concepts & Terminology · Knowledge of Latest Developments & Current Affairs · Training

Designation : AGM / DGM - Formulation & Development. Qualification : M. Pharma / PhD. Experience : 15 to 20 yrs of experience in Formulation & development of Ophthalmic / Liquid oral dosage form for Regulated Market. Must have filed 10-15 products for US/EU market. Team handling,

Position - Executive / Senior Executive Department - Corporate Quality Assurance Pharmacovigilance Job Location - Kandivali - West, Mumbai Qualification - M Pharm Experience - 4 - 6 years Job Role: To ensure compliance with SOPs of Corporate Pharmacovigilance cell as well as Corporate Qualifty Assurance To assist Corporate pharmacovigilance cell in overseeing vendor complaince with periodic review and vendor audit To act as a liaison with internal and external auditors and assume responsibility for ensuring corrective actions with their specification To persuade Corporate pharmacovigilance cell staff to adopt and incorporate quality methods in to their work To conduct internal pharmacovigilance audit To perform CAPA management To review change control process, deviation and related QMS documents. The role demands travel for audits at corporate and various plants.

Job Title: Incentive Finance Executive / Analyst Department: Internal Audit Location: Kandivali - West, Mumbai Qualification & Experience: Role - CA Qualification - Chartered Accountant Vacancy - 1 no. Preferable Experience - 1-3 years (preferably in MIS, Audit, Finance, or Sales Incentive roles) AND Role - CA Inter Qualification - CA Inter (Both Groups Cleared) Vacancy - 2 nos. Preferable Experience - 1-2 years experience in Finance/Audit /MIS/Sales Incentive roles Skills & Competencies: Good knowledge of Excel (pivot, formulas, excel advance, macros); Power BI or analytics tools is a plus Working knowledge of any ERP/SAP systems and sales data structure is a plus Good analytical, planning, and number-crunching ability Proactive in handling data inconsistencies and process gaps Good interpersonal skills for working with Marketing/& Sales High attention to detail and strong documentation ability Time management and commitment to monthly closure timelines. Job Description 1. Incentive Calculation & Disbursement (Monthly) 2. Incentive Scheme Designing 3. Mid-Year New Product launch Based Scheme Planning/ Designing 4. Data Analytics & Reporting 5. Incentive Process Improvement 6. Incentive Provisioning & Accounting 7. Cross-functional Coordination.

Position: Product Executive / Product Manager / Senior Product Manager Location : Mumbai Segment: Rheumatology Experience : Product Manager - minimum 2-3 years into Brand Management Senior Product Manager - minimum 5-6 years into Brand Management Role & Responsibilities : Brand Management Product strategies and execution Assess promotional needs of the products Conducting market research, Drive market growth, Data Analysis Product launch Brand Audit at regular intervals Train and guide field staff Handle product related queries Carry out events ( Domestic & International) Design trade activities Conducting Cycle / Briefing meets, Managing conferences Functional Knowledge / Skills: General Product Knowledge Market dynamics & competitive behavior Data analysis Goal oriented Specialized Managing brand expenses Strategic and tactical implication for better performance ROI strategy Awareness of competitors & market trends Key Competencies: Excellent communicator Should be able to work well with a wide range of people Able to inspire others Should be able to manage different projects Should be energetic and passionate about work/product Good presentation skills Able to work well under pressure Organized and methodical Deadline-driven, creative Interested applicants please share resume at neha.jaybhaye@ipca.com

As a Senior Executive/ Assistant Manager in the Corporate Quality Assurance Pharmacovigilance department, located in Kandivali - West, Mumbai, your primary responsibility will be to ensure compliance with SOPs of the Corporate Pharmacovigilance cell and Corporate Quality Assurance. You will be expected to assist the Corporate pharmacovigilance cell in overseeing vendor compliance through periodic reviews and vendor audits. In this role, you will act as a liaison with internal and external auditors, taking responsibility for ensuring corrective actions are implemented according to their specifications. Your duties will also include persuading Corporate pharmacovigilance cell staff to adopt and incorporate quality methods into their work processes. As part of your responsibilities, you will be required to conduct internal pharmacovigilance audits, perform CAPA management, and review the change control process, deviations, and related Quality Management System (QMS) documents. Additionally, the role involves travel for conducting audits at corporate offices and various plants. The ideal candidate for this position should hold an M Pharm qualification and possess 4 to 6 years of relevant experience in the field. Effective communication skills, attention to detail, and the ability to work collaboratively with internal and external stakeholders are crucial for success in this role.,