Job Title: Executive – Corporate Quality Assurance (CQA) Department: Quality Assurance Experience: 2–9 Years Location: Nandesari Industry: Pharmaceuticals Key Responsibilities: Ensure compliance with cGMP, regulatory guidelines (USFDA, MHRA, EU-GMP, etc.). Review and approve validation protocols, SOPs, batch records, and quality documents. Coordinate internal audits and support regulatory inspections. Monitor CAPA, change controls, deviations, and market complaints. Provide support to manufacturing sites for quality system implementation. Track quality KPIs and assist in continuous improvement initiatives. Qualifications: B.Pharm / M.Pharm / M.Sc in relevant field. 2–9 years of experience in QA/QMS, preferably in a regulated pharma environment. Knowledge of regulatory requirements and audit handling. Job Type: Full-time Pay: ₹20,069.80 - ₹65,314.17 per month Benefits: Food provided Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person

Job Summary: We are looking for a proactive and detail-oriented Electrical Purchase Officer to handle procurement activities related to electrical equipment, materials, and services for our pharmaceutical manufacturing facility. The ideal candidate should have a background in electrical purchasing, strong negotiation skills, and knowledge of pharma industry standards. Key Responsibilities: Source and procure electrical items such as transformers, panels, cables, circuit breakers, UPS systems, motors, etc., based on project and maintenance requirements. Evaluate vendor quotations and negotiate terms to obtain cost-effective deals without compromising on quality and compliance. Maintain vendor relationships, track supplier performance, and onboard new vendors as per company policy. Ensure timely delivery of materials and follow up with vendors to avoid delays in production or project schedules. Prepare and maintain procurement-related documentation including purchase orders (POs), GRNs, quotations, comparison sheets, etc. Work closely with engineering, maintenance, and project teams to understand technical specifications and ensure the procurement of the right materials. Comply with cGMP, safety standards, and internal quality policies while purchasing materials. Assist in conducting vendor audits and ensuring adherence to quality and compliance standards. Maintain inventory levels of critical electrical spares to avoid stockouts or overstocking. Use ERP systems (SAP / Oracle / etc.) for purchase requisitions, order tracking, and reporting. Job Type: Full-time Pay: ₹13,094.77 - ₹20,410.84 per month Benefits: Food provided Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person

Job Title: Executive – Corporate Quality Assurance (CQA) Department: Quality Assurance Experience: 2–9 Years Location: Nandesari Industry: Pharmaceuticals Key Responsibilities: Ensure compliance with cGMP, regulatory guidelines (USFDA, MHRA, EU-GMP, etc.). Review and approve validation protocols, SOPs, batch records, and quality documents. Coordinate internal audits and support regulatory inspections. Monitor CAPA, change controls, deviations, and market complaints. Provide support to manufacturing sites for quality system implementation. Track quality KPIs and assist in continuous improvement initiatives. Qualifications: B.Pharm / M.Pharm / M.Sc in relevant field. 2–9 years of experience in QA/QMS, preferably in a regulated pharma environment. Knowledge of regulatory requirements and audit handling. Job Type: Full-time Pay: ₹20,069.80 - ₹65,314.17 per month Benefits: Food provided Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person

Job Summary: We are looking for a proactive and detail-oriented Electrical Purchase Officer to handle procurement activities related to electrical equipment, materials, and services for our pharmaceutical manufacturing facility. The ideal candidate should have a background in electrical purchasing, strong negotiation skills, and knowledge of pharma industry standards. Key Responsibilities: Source and procure electrical items such as transformers, panels, cables, circuit breakers, UPS systems, motors, etc., based on project and maintenance requirements. Evaluate vendor quotations and negotiate terms to obtain cost-effective deals without compromising on quality and compliance. Maintain vendor relationships, track supplier performance, and onboard new vendors as per company policy. Ensure timely delivery of materials and follow up with vendors to avoid delays in production or project schedules. Prepare and maintain procurement-related documentation including purchase orders (POs), GRNs, quotations, comparison sheets, etc. Work closely with engineering, maintenance, and project teams to understand technical specifications and ensure the procurement of the right materials. Comply with cGMP, safety standards, and internal quality policies while purchasing materials. Assist in conducting vendor audits and ensuring adherence to quality and compliance standards. Maintain inventory levels of critical electrical spares to avoid stockouts or overstocking. Use ERP systems (SAP / Oracle / etc.) for purchase requisitions, order tracking, and reporting. Job Type: Full-time Pay: ₹13,094.77 - ₹20,410.84 per month Benefits: Food provided Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person

Job Title: Front Desk Executive / Receptionist Department: Administration Location: Farmson Basic Drugs Pvt. Ltd., Plot No. 14, GIDC Industrial Estate, Nandesari, Vadodara – 391340, Gujarat, India Experience: 2–5 years (preferably in hospital, healthcare, or insurance handling roles) Qualification: Graduate (Any discipline); Diploma in Hospital or Healthcare Administration preferred Job Purpose: To efficiently manage the front desk and reception area while supporting patient/visitor handling, insurance-related coordination, and administrative operations aligned with healthcare and pharma environments. Key Responsibilities: Greet and guide visitors, clients, and patients in a professional and courteous manner. Handle telephone calls, direct inquiries, and maintain appointment schedules. Manage visitor entry, security protocols, and ID verification procedures. Coordinate with internal departments and medical professionals for appointments and visitor flow. Assist with patient insurance verification, document collection, and follow-up with insurance companies or TPA (Third-Party Administrators). Ensure proper filing and documentation of insurance-related records, including pre-authorization forms and claim submissions (where applicable). Coordinate between patients and HR/insurance team for internal employee health claims or policy coverage. Track and update internal employee medical insurance records (if applicable). Maintain confidentiality in handling sensitive medical and insurance data. Support administrative duties such as data entry, courier handling, email correspondence, and supply coordination. Job Type: Full-time Pay: ₹300,000.00 - ₹606,779.90 per year Benefits: Food provided Health insurance Provident Fund Schedule: Day shift Work Location: In person

Job Title: Front Desk Executive / Receptionist Department: Administration Location: Farmson Basic Drugs Pvt. Ltd., Plot No. 14, GIDC Industrial Estate, Nandesari, Vadodara – 391340, Gujarat, India Experience: 2–5 years (preferably in hospital, healthcare, or insurance handling roles) Qualification: Graduate (Any discipline); Diploma in Hospital or Healthcare Administration preferred Job Purpose: To efficiently manage the front desk and reception area while supporting patient/visitor handling, insurance-related coordination, and administrative operations aligned with healthcare and pharma environments. Key Responsibilities: Greet and guide visitors, clients, and patients in a professional and courteous manner. Handle telephone calls, direct inquiries, and maintain appointment schedules. Manage visitor entry, security protocols, and ID verification procedures. Coordinate with internal departments and medical professionals for appointments and visitor flow. Assist with patient insurance verification, document collection, and follow-up with insurance companies or TPA (Third-Party Administrators). Ensure proper filing and documentation of insurance-related records, including pre-authorization forms and claim submissions (where applicable). Coordinate between patients and HR/insurance team for internal employee health claims or policy coverage. Track and update internal employee medical insurance records (if applicable). Maintain confidentiality in handling sensitive medical and insurance data. Support administrative duties such as data entry, courier handling, email correspondence, and supply coordination. Job Type: Full-time Pay: ₹300,000.00 - ₹606,779.90 per year Benefits: Food provided Health insurance Provident Fund Schedule: Day shift Work Location: In person

Company Overview Farmson is a global leader in API paracetamol manufacturing, with an annual capacity of ~52,000 MTPA and operations across 60+ countries. Their Nandesari campus houses multiple units (Units I, II & IV), including integrated R&D and analytical labs farmson.com+3farmson.com+3farmson.com+3. Role Overview You’ll join Farmson’s Nandesari Process Development Lab to develop, optimize, and scale new and existing APIs—starting from bench-scale experiments through to pilot/commercial batches—ensuring quality, efficiency, and regulatory compliance. Key Responsibilities Design and execute bench-scale reaction protocols for paracetamol and emerging APIs (caffeine, glacial acetic acid, etc.) farmson.com Conduct feasibility studies, DoE-based optimization, and lab validation Manage impurity synthesis, analytical method development (HPLC, UPLC, GC, FTIR) Support scale-up to pilot/commercial plants (Units I–IV) through tech-transfer collaboration with production engineers Troubleshoot process issues during scale-up or pilot batches Generate technical documentation: batch records, SOPs, validation reports Enforce GLP/GMP, EHS policies, and safety standards Coordinate with QC, manufacturing, and regulatory teams across units Contribute to sustainable process development initiatives Required Qualifications B.Tech / M.Sc / Ph.D. in Chemical Engineering, Chemistry, or related discipline 3–5 years in process development within pharmaceutical/API sectors Expertise in reaction engineering, purification, DoE, and scale-up principles Hands-on experience with reactors, autoclaves, vacuum dryers, HPLC/GC/FTIR, etc. Familiarity with GLP/GMP and documentation standards Strong problem-solving, organizational, and communication skills Ability to work both independently and collaboratively across teams Job Type: Full-time Pay: ₹300,000.00 - ₹500,000.00 per month Benefits: Food provided Health insurance Provident Fund Work Location: In person

Job Title: Quality Control Executive – Finished Product (Chemical Testing) Department: Quality Control (QC) Location: [Insert Location] Reports to: QC Manager / Quality Head Experience Required: 2–5 years in pharmaceutical/chemical industry Qualification: B.Sc. / M.Sc. (Chemistry), B.Pharm / M.Pharm Job Purpose: Responsible for sampling and chemical analysis of finished pharmaceutical products, ensuring compliance with standard operating procedures (SOPs), regulatory standards (ICH), and internal quality specifications using techniques such as HPLC, UHPLC, GC, and wet chemistry. Key Responsibilities:1. Sampling & Testing Perform sampling of finished products as per approved SOPs. Conduct chemical analysis using validated analytical methods (wet chemistry and instrumental methods like HPLC, UHPLC, GC). Ensure all tests are conducted in accordance with Analytical Data Sheets and test methods . 2. Documentation & Compliance Prepare and maintain test records, COAs (Certificate of Analysis) , WRS (Working Reference Standards) logbooks, and Analytical Data Sheets . Maintain raw data and ensure timely review and approval of results. Adhere to ICH Q2/Q6 guidelines for method validation and product specifications. 3. Investigation & Reporting Handle OOS (Out of Specification) and OOC (Out of Trend) results, including root cause analysis, CAPA implementation, and documentation. Participate in Deviation, Change Control (DC), and Corrective/Preventive Actions (CAPA) processes. 4. Instrument Operation & Calibration Operate and troubleshoot HPLC, UHPLC, GC , UV, and other analytical instruments. Ensure instruments are calibrated and maintained as per AMC (Annual Maintenance Contract) schedules. 5. Stability & Regulatory Compliance Perform stability studies on finished products as per ICH guidelines and ensure timely reporting. Contribute to CSR (Comparative Study Report) and regulatory documentation when required. 6. Review & Audit Conduct peer reviews of analytical documents. Assist during internal and external audits (e.g., USFDA, WHO, MHRA). Ensure GMP and GLP compliance in the QC lab. Required Skills: In-depth knowledge of analytical techniques (HPLC, GC, wet chemistry) Understanding of ICH guidelines , GMP/GLP , OOS/OOC handling Good documentation practices and data integrity awareness Proficient in analytical software (Empower, LabSolutions, Chromeleon preferred) Job Types: Full-time, Permanent Pay: ₹300,000.00 - ₹600,000.00 per year Benefits: Food provided Health insurance Provident Fund

ob Title: Microbiologist – Quality Control / Microbiology Lab Department: Quality Control / Microbiology Location: [Insert Location] Reports to: QC Manager / Microbiology Head Experience Required: 2–5 years in pharmaceutical/food/chemical industry microbiology Qualification: M.Sc. Microbiology / B.Sc. Microbiology / B.Pharm / M.Pharm Job Purpose: To perform microbiological testing, preparation of media, sterilization of glassware, and analysis of finished products and water samples. Ensure compliance with regulatory guidelines and support HVAC validation and calibration activities (DQ/IQ/OQ/PQ). Key Responsibilities:1. Microbiological Testing Conduct microbiological testing of finished products and water samples as per SOPs and regulatory standards. Perform environmental monitoring including HVAC system checks. 2. Media Preparation & Sterilization Prepare microbiological media and reagents accurately according to prescribed methods. Sterilize glassware, media, and equipment using autoclaves and other sterilization methods ensuring no contamination. 3. Validation & Calibration Support HVAC system validation activities including Design Qualification (DQ) , Installation Qualification (IQ) , Operational Qualification (OQ) , and Performance Qualification (PQ) . Assist in preparation and review of User Requirement Specifications (URS) . Participate in calibration of laboratory instruments and equipment as per schedule. 4. Documentation & Compliance Maintain accurate records of microbiological testing, sterilization logs, calibration certificates, and validation reports. Ensure adherence to GMP, GLP , and regulatory requirements. Assist during regulatory audits and inspections. 5. Regulatory and Quality Support Support quality assurance activities related to microbiological aspects. Handle deviations, CAPA, and change controls related to microbiology and sterilization processes. Required Skills: Good understanding of microbiological techniques and sterility testing. Experience with media preparation and sterilization procedures. Knowledge of HVAC systems and their validation. Familiarity with DQ, IQ, OQ, PQ protocols. Strong documentation and data integrity awareness. Ability to work under GMP/GLP guidelines. Good communication and teamwork skills. Job Types: Full-time, Permanent Pay: ₹300,000.00 - ₹600,000.00 per year Benefits: Food provided Health insurance Paid sick time Provident Fund

ob Title: Microbiologist – Quality Control / Microbiology Lab Department: Quality Control / Microbiology Location: [Insert Location] Reports to: QC Manager / Microbiology Head Experience Required: 2–5 years in pharmaceutical/food/chemical industry microbiology Qualification: M.Sc. Microbiology / B.Sc. Microbiology / B.Pharm / M.Pharm Job Purpose: To perform microbiological testing, preparation of media, sterilization of glassware, and analysis of finished products and water samples. Ensure compliance with regulatory guidelines and support HVAC validation and calibration activities (DQ/IQ/OQ/PQ). Key Responsibilities:1. Microbiological Testing Conduct microbiological testing of finished products and water samples as per SOPs and regulatory standards. Perform environmental monitoring including HVAC system checks. 2. Media Preparation & Sterilization Prepare microbiological media and reagents accurately according to prescribed methods. Sterilize glassware, media, and equipment using autoclaves and other sterilization methods ensuring no contamination. 3. Validation & Calibration Support HVAC system validation activities including Design Qualification (DQ) , Installation Qualification (IQ) , Operational Qualification (OQ) , and Performance Qualification (PQ) . Assist in preparation and review of User Requirement Specifications (URS) . Participate in calibration of laboratory instruments and equipment as per schedule. 4. Documentation & Compliance Maintain accurate records of microbiological testing, sterilization logs, calibration certificates, and validation reports. Ensure adherence to GMP, GLP , and regulatory requirements. Assist during regulatory audits and inspections. 5. Regulatory and Quality Support Support quality assurance activities related to microbiological aspects. Handle deviations, CAPA, and change controls related to microbiology and sterilization processes. Required Skills: Good understanding of microbiological techniques and sterility testing. Experience with media preparation and sterilization procedures. Knowledge of HVAC systems and their validation. Familiarity with DQ, IQ, OQ, PQ protocols. Strong documentation and data integrity awareness. Ability to work under GMP/GLP guidelines. Good communication and teamwork skills. Job Types: Full-time, Permanent Pay: ₹300,000.00 - ₹600,000.00 per year Benefits: Food provided Health insurance Paid sick time Provident Fund

Job Title: Quality Control Executive – Finished Product (Chemical Testing) Department: Quality Control (QC) Location: [Insert Location] Reports to: QC Manager / Quality Head Experience Required: 2–5 years in pharmaceutical/chemical industry Qualification: B.Sc. / M.Sc. (Chemistry), B.Pharm / M.Pharm Job Purpose: Responsible for sampling and chemical analysis of finished pharmaceutical products, ensuring compliance with standard operating procedures (SOPs), regulatory standards (ICH), and internal quality specifications using techniques such as HPLC, UHPLC, GC, and wet chemistry. Key Responsibilities:1. Sampling & Testing Perform sampling of finished products as per approved SOPs. Conduct chemical analysis using validated analytical methods (wet chemistry and instrumental methods like HPLC, UHPLC, GC). Ensure all tests are conducted in accordance with Analytical Data Sheets and test methods . 2. Documentation & Compliance Prepare and maintain test records, COAs (Certificate of Analysis) , WRS (Working Reference Standards) logbooks, and Analytical Data Sheets . Maintain raw data and ensure timely review and approval of results. Adhere to ICH Q2/Q6 guidelines for method validation and product specifications. 3. Investigation & Reporting Handle OOS (Out of Specification) and OOC (Out of Trend) results, including root cause analysis, CAPA implementation, and documentation. Participate in Deviation, Change Control (DC), and Corrective/Preventive Actions (CAPA) processes. 4. Instrument Operation & Calibration Operate and troubleshoot HPLC, UHPLC, GC , UV, and other analytical instruments. Ensure instruments are calibrated and maintained as per AMC (Annual Maintenance Contract) schedules. 5. Stability & Regulatory Compliance Perform stability studies on finished products as per ICH guidelines and ensure timely reporting. Contribute to CSR (Comparative Study Report) and regulatory documentation when required. 6. Review & Audit Conduct peer reviews of analytical documents. Assist during internal and external audits (e.g., USFDA, WHO, MHRA). Ensure GMP and GLP compliance in the QC lab. Required Skills: In-depth knowledge of analytical techniques (HPLC, GC, wet chemistry) Understanding of ICH guidelines , GMP/GLP , OOS/OOC handling Good documentation practices and data integrity awareness Proficient in analytical software (Empower, LabSolutions, Chromeleon preferred) Job Types: Full-time, Permanent Pay: ₹300,000.00 - ₹600,000.00 per year Benefits: Food provided Health insurance Provident Fund

Job Summary: We are seeking a dedicated and detail-oriented Executive / Sr. Executive – CLM to manage and streamline the end-to-end lifecycle of contracts across the organization. The ideal candidate will ensure timely contract creation, negotiation, execution, renewal, and compliance as per internal policies and external regulatory frameworks. Key Responsibilities: Contract Drafting & Review: Draft, review, and revise a wide range of contracts such as vendor agreements, NDAs, supply agreements, service contracts, and purchase orders. Contract Management System (CLM): Maintain and update the digital contract repository. Monitor contract timelines, renewals, expirations, and compliance obligations. Coordination & Communication: Liaise with internal stakeholders (procurement, finance, legal, etc.) and external vendors/partners to ensure contract accuracy and alignment with business terms. Ensure that contracts are aligned with company policies and legal standards. Compliance & Risk Management: Identify contractual risks and suggest appropriate risk mitigation measures. Ensure all contracts comply with statutory and regulatory requirements. Reporting & Documentation: Prepare and maintain accurate documentation and reports for audits and internal reviews. Track KPIs related to contract lifecycle stages and timelines. Qualifications: Education: Graduate / Postgraduate in Law, Commerce, or related field(LLB / LLM preferred but not mandatory) Experience: 2 to 5 years of experience in Contract Lifecycle Management or similar roles.Prior experience in the pharmaceutical or manufacturing industry will be an added advantage. Skills Required: Strong knowledge of contract laws and legal terms. Excellent written and verbal communication skills. Proficiency in MS Office, CLM software/tools (preferred). Detail-oriented with strong organizational skills. Job Types: Full-time, Permanent Pay: ₹500,000.00 - ₹634,778.51 per year Benefits: Food provided Health insurance Provident Fund Work Location: In person