Qualification & Experience :-
i) / . / . / 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, , 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
No. of Openings
1
Education
B.E, B.Tech
Role
Documentation Assistant
Industry Type
Legal / Law / Judiciary
Gender
Male
Job Country
India
Type of Job
Full Time
Work Location Type
Work from Office
Face interview location
Umbergaon, Gujarat