QA Executive

Role & responsibilitiesThe Executive QA Validation will be responsible for executing and ensuring compliance of validation activities in the Injectable (Sterile) manufacturing facility, including equipment, utilities, cleaning, process, computerized systems, and analytical methods. The role requires adherence to cGMP, regulatory guidelines, and internal SOPs...

JOB SUMMARY:Senior Scientific Officer- Validation (QA) shall be responsible for ensuring the quality and efficacy of vaccine formulations (Vaccine Drug Product Plant,Baddi). This position will be responsible for overseeing the Qualification/ validation of various Equipment/ System like HVACFilling line, Autoclave, Tunnel, Utilitiy systems,...

Quality Control ManagerJob Profile:To carry out testing of all raw, Finish, Packing material as required for day to day production of any formulation unit having Liquid Orals, External Application, Tablet, Hard Gelatin Capsule, Dry Syrup, Injectables etc. on his own and through his team of analyst and MicrobiologistTo run, train & guide team of analyst &...

Continuous Improvement Lead (CI) - VDSP, Lalru & VDPP, BaddiReports To: Strategic Project Manager (SPM)Department: COO – VaccineJob Location:VDSP, Lalru & VDPP, BaddiRole Summary:To lead and institutionalize continuous improvement (CI) initiatives across the WHO prequalified vaccine manufacturing facility by driving cost reduction, waste elimination,...

Job Title: Operations Analyst (OA)- VDSP, Lalru & VDPP, BaddiLocation: Baddi, Himachal Pradesh & Lalru, PunjabRole Summary:To enable data-driven decision-making and support operational excellence across Drug Substance and Drug Product manufacturing by developing performance dashboards, conducting variance analyses, and ensuring strict adherence to WHO-GMP...

Job Title: Digital & Automation Support (DAS) - VDSP, Lalru & VDPP, BaddiReports to: Dotted Line – COO, Vaccine: Direct – CIODepartment: COO – VaccineLocation: Baddi, Himachal Pradesh & Lalru, PunjabRole Summary:The Digital & Automation Support (DAS) professional will coordinate with IT, QA and Engineering and support the implementation and integration...

Company DescriptionCPF - Center of Pharma Force is a professional platform fostering learning, growth, and collaboration among pharmaceutical industry professionals. Through CPF, individuals can share insights, thoughts, and updates on regulations relevant to India and global markets. The platform emphasizes mentorship, encouraging industry experts to train...

DivisionDepartmentSub Department 1Job PurposePrepare, update and review the specifications, SOPs, policy and operating documents for analysis of materials in order to ensure alignment to predefined quality parameters and compliance to respective standards / pharmacopeia and cGMP requirementsKey Accountabilities (1/6)Prepare documents like SOPs,...

Position - Group Leader API – Analytical DevelopmentQualification - PhD in Analytical ChemistryAdditional Qualification - Research experience from Analytical R&D center of reputed API companyExperience Years in APIsPosition Objective & ResponsibilitiesPosition Summary:The Group Leader – ARD will be responsible for leading the analytical research and...

Job SummaryWe are seeking a dynamic individual to lead our engineering function for OSD. The role involves ensuring equipment and plant reliability, driving maintenance efficiency, and upholding safety standards. Responsibilities include budget management, energy efficiency projects, new facility design, and leading engineering during regulatory audits. ...