Documentation Assistant (Full Time)

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

  Graduate (B.Tech/B.E)

• 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