QA - Trainee Officer / Officer Aneta Pharmaceuticals

0.0 - 4.0 years

1 - 3 Lacs

ahmedabad

Work from Office

The candidate must have experience in OSD IPQA / DOC. / Validation Exp.- 0 to 04 (OSD Formulation) Key Responsibilities: In-Process Quality Assurance (IPQA): Perform line clearance, in-process checks, and monitoring during manufacturing and packaging. Ensure adherence to Standard Operating Procedures (SOPs), Good Documentation Practices (GDP), and cGMP guidelines. Monitor critical process parameters during production to ensure consistent product quality. Handle deviation, change control, incident reports, and CAPA documentation. Documentation (DOC.): Preparation, review, and control of SOPs, protocols, batch records, logbooks, and other quality-related documents. Ensure compliance with regul...

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ADL - Senior Officer / Executive / Asst. Manager Aneta Pharmaceuticals

3.0 - 8.0 years

3 - 8 Lacs

ahmedabad

Work from Office

We are looking for a skilled professional with 3 to 8 years of experience in OSD formulation to join our team as an ADL - Sr.Officer / Executive / Asst. Manager at Aneta Pharmaceuticals Pvt. Ltd. Roles and Responsibility Develop analytical methods for finished products, including oral solids and liquids. Collaborate with cross-functional teams to ensure timely product development. Conduct experiments and collect data to support method development. Analyze and interpret data to identify trends and areas for improvement. Implement quality control measures to ensure compliance with regulatory requirements. Provide technical support and guidance to junior team members. Job Requirements Strong kn...

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Technology Transfer Manager Evertogen Life Sciences

7.0 - 12.0 years

8 - 15 Lacs

Jadcherla

Work from Office

We are looking for a meticulous and experienced Technology Transfer Manager to spearhead the efficient transfer of technology for solid dosage forms at Evertogen Life Sciences . This pivotal role involves overseeing the seamless transition of OSD products from R&D or third-party development to our manufacturing plant, ensuring successful scale-up, unwavering regulatory compliance, and adherence to the highest quality standards. The ideal candidate will champion the preparation and review of critical technical documents, including technology transfer protocols, BMR/BPR, and process validation reports, while actively coordinating with cross-functional teams such as QA, QC, RA, and Production. ...

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