Vapi, Umbergaon
Qualification & Experience :-
i) B.Tech / B.E. / M.Sc. / B. Pharm in Mechanical Engineering, Biotechnology, Pharmacy, or related field.
ii) Experience: Minimum 5-6 years in a pharmaceutical equipment manufacturing company.
iii) Strong knowledge of GMP, ISO 9001, 13485, and regulatory guidelines.
Experience in QA, QC, and documentation control processes.
iv) Proficiency in MS Office, ERP software, and document control systems.
Excellent communication, analytical, and problem-solving skills.
Gender:- Male
key Responsibilities:-
i) Prepare, review, and update quality documents such as SOPs, protocols, batch records, validation reports, and manuals.
ii) Ensure proper documentation in compliance with regulatory requirements.
iii) Maintain document control systems, track revisions, and ensure accessibility.
iv) Assist in preparing reports for regulatory authorities and audits.
Experience | 5 - 6 Years |
Salary | 80 Thousand To 90 Thousand P.A. |
Industry | Legal / Law Services / Judiciary |
Qualification | B.E, B.Tech |
Key Skills | Documentation |
(50)Manufacturing / Production / Q...
(15)Supply Chain / Purchase / Proc...
(10)Accounting / Auditing / Taxati...
(6)Engineering / Engineering Desi...
(3)Front Office / Reception / Com...
(2)Sales & Marketing / Business D...
(2)HR / Recruitment / Administrat...
(1)IT Software - Application Prog...
(1)IT Software - Ecommerce / Inte...
(1)Cargo / Freight / Transportati...
(1)Corporate Planning & Strategy ...
(1)Legal / Law Services / Judicia...
(1)Health Care / Pharmaceuticals ...
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