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10.0 - 15.0 years
0 Lacs
maharashtra
On-site
You will be responsible for overseeing the Quality Assurance department of the Pharmaceutical formulation unit. Your key responsibilities will include: - Demonstrating a minimum of 10 to 15 years of experience in QA within the Pharmaceutical industry - Possessing knowledge of Regulatory requirements and documentation such as water validation, process validation, etc. - Conducting training sessions for junior staff on incident management, change control, CAPA, and other relevant topics - Demonstrating expertise in WHO GMP / cGMP standards Your qualifications should include: - M.Pharm / B.Pharm / M.Sc. degree - Minimum of 10 to 15 years of experience in QA within the Pharmaceutical formulation...
Posted 1 week ago
3.0 - 7.0 years
0 Lacs
maharashtra
On-site
You will be responsible for ensuring the quality of pharmaceutical formulations in the QA department. Your key responsibilities will include: - Minimum 3 to 5 years of experience in QA department of pharmaceutical formulation - Knowledge of In-Process Quality Assurance (IPQA) is required - Familiarity with Good Manufacturing Practices (GMP) - Preferable to have experience in Regulatory work No additional details of the company are mentioned in the job description.,
Posted 1 month ago
10.0 - 15.0 years
0 Lacs
maharashtra
On-site
You should have a minimum of 10 to 15 years of experience in the QA department of Pharmaceutical formulation. Your responsibilities will include having knowledge of regulatory requirements and documentation such as water validation, process validation, incident management, change control, CAPA, etc. It is essential for you to be capable of providing training to junior staff. Familiarity with WHO GMP/cGMP is a requirement. The ideal candidate will hold an M.Pharm/B.Pharm/M.Sc. degree.,
Posted 2 months ago
5.0 - 10.0 years
4 - 6 Lacs
Mumbai
Work from Office
Urgent job opening for Senior Quality Assurance Executive at Dombivli. Qualification : B.Sc., M.Sc. Experience : 6 to 8 years Description of Job Responsibilities 1) Responsible for Preparation and review of master documents of QA department and review of all master documents and formats of respective departments other than QA. 2) Responsible for review of technical documents such as Technology Transfer, MPCR, BPCR, Specification and Standard test procedure, stability data, etc. 3) Responsible for preparation of training schedule and provide training on QA-related topics, guidelines, regulatory and cGMP requirements to all concerned employees. 4) To evaluate Quality and stability of finished ...
Posted 5 months ago
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