Technical Writer

Amneal Pharmaceuticals LLC; Ahmedabad District; On-site; INR 700,000 - 900,000; Full time

Job summary

Amneal Pharmaceuticals LLC invites qualified professionals to join our USFDA/MHRA approved manufacturing plant in Ahmedabad. The opening is in Quality Control (OSD) with designation Officer/Sr. Officer/Executive, for GLP/Technical Writer/Documentation profiles.

Candidates should have B.Pharm/M.Pharm/M.Sc. and 4–7 years of experience in pharma technical writing or QC documentation, with strong analytical, writing and communication skills, and a solid grasp of pharmacopeial and regulatory

Qualifications

• 5+ years’ experience in pharma technical writing or QC documentation.
• Excellent analytical, writing & communication skills.
• Strong understanding of pharmacopeial & regulatory standards.

Responsibilities

• Prepare, review & update QC documents (SOPs, reports, protocols).
• Work with cross-functional teams to ensure compliance & accuracy.

Skills

Pharma technical writing

QC documentation

Analytical skills

Communication skills

Regulatory standards

Education

B Pharm/M Pharm/ M Sc.

Job description

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Amneal is a high-quality producer of solid and Injectable generic products and one of the fastest-growing global generics producers. We believe that the world is our family’ and we are committed for consistently producing high quality affordable medicines. Amneal is expanding its operations in India and invites people who share its value of relentless pursuit of quality, integrity, treating each other with respect and encouraging the very best in everyone to join the Amneal family. To know more about us and what we stand for, please visit our website (www.amneal.com)

We have an opportunity for competent, dynamic and motivated candidates to join our USFDA/MHRA approved manufacturing plants in Ahmedabad for following is brief details of venue, timing and positions:

Please find the details of openings for our various departments:

Department: Quality Control (OSD)

Qualification: B Pharm/M Pharm/ M Sc.

Designation: Officer/ Sr. Officer/ Executive

Profile specific: GLP/ Technical Writer/ Documentation

Experience: 4- 7 Years

Job Location: Rajoda, Ahmedabad

Desired Profile:

• 5+ years’ experience in pharma technical writing or QC documentation.
• Excellent analytical, writing & communication skills.
• Strong understanding of pharmacopeial & regulatory standards.
• Prepare, review & update QC documents (SOPs, reports, protocols).
• Work with cross-functional teams to ensure compliance & accuracy.

Please do not apply if you are from API and other than Pharma background

Note: Candidate should have relevant experience in USFDA regulatory approved pharmaceuticals (Preferred 21 CFR compliance) organization.