Amneal Hiring QC Technical Writer
- Company Overview
- Job Role & Responsibilities
- QC Technical Writer – Oral Solid Dosage (OSD)
- Eligibility / Qualifications
- Relevant Courses
- Location & Salary
- Application Process
- FAQs
- What is the minimum experience required?
- Is hands-on QC testing experience mandatory?
- Is pharmacopoeia knowledge essential?
- Does this role involve cross-functional coordination?
- Is this role specific to OSD documentation?
- Summary Table
B.Pharm, M.Sc QC Technical Writer Opening | Rajoda
Amneal hiring B.Sc, M.Sc, B.Pharm, M.Pharm candidates with 4–8 years QC documentation experience for Technical Writer role in Rajoda.
Amneal Pharmaceuticals is hiring experienced Technical Writers for its Quality Control (OSD) operations at Rajoda. The role suits professionals who have strong expertise in QC documentation, regulatory writing, and compliance-driven workflows. This is a focused position ideal for candidates who enjoy working with structured documentation, analytical content, and cross-functional collaboration.
Company Overview
Amneal Pharmaceuticals is a global pharmaceutical manufacturer with a diverse portfolio of high‑quality generic and specialty medicines. The company operates advanced manufacturing and quality systems supported by strict regulatory standards. Its QC teams play a pivotal role in ensuring data integrity, documentation accuracy, and regulatory readiness across all projects.
Job Role & Responsibilities
QC Technical Writer – Oral Solid Dosage (OSD)
- Prepare, review, and update QC documents including SOPs, test procedures, protocols, and analytical reports
- Ensure documentation accuracy, consistency, and alignment with regulatory guidelines
- Maintain document version control and support audit readiness activities
- Interpret pharmacopoeial requirements (USP, EP, IP) and incorporate changes into QC documentation
- Collaborate with QC, QA, ADL, and regulatory teams for timely updates and compliance support
- Participate in investigations, CAPA documentation, and data integrity improvements
- Use document management systems and MS Office tools for controlled documentation
Eligibility / Qualifications
- B.Sc, M.Sc (Chemistry/Life Sciences)
- B.Pharm / M.Pharm
- 4–8 years of experience in pharma technical writing or QC documentation
- Strong understanding of:
- Pharmacopoeia (USP, EP, IP)
- Regulatory expectations for QC data
- cGMP and GLP documentation practices
Relevant Courses
B.Pharm, M.Pharm Quality Assurance, M.Pharm Pharmaceutical Analysis, M.Sc Analytical Chemistry, PG Diploma in Regulatory Affairs, Certificate in Scientific Writing.
Location & Salary
- Location: Rajoda (Amneal Pharmaceuticals – OSD Facility)
- Salary: Based on experience and internal grade structure
Application Process
Interested and relevant candidates may share their profile at:
- Email: aartig@amneal.com
Include your updated CV, experience summary, current CTC, expected CTC, and notice period.
FAQs
What is the minimum experience required?
A minimum of 4 years in QC documentation or pharma technical writing.
Is hands-on QC testing experience mandatory?
Not mandatory, but familiarity with analytical workflows is preferred.
Is pharmacopoeia knowledge essential?
Yes. Understanding USP, EP, and IP requirements is critical.
Does this role involve cross-functional coordination?
Yes. Regular collaboration with QC, QA, regulatory, and analytical teams is required.
Is this role specific to OSD documentation?
Yes. Experience with OSD QC documentation is an advantage.
Summary Table
| Company | Amneal Pharmaceuticals |
|---|---|
| Vacancies | QC Technical Writer |
| Required Education | B.Sc, M.Sc, B.Pharm, M.Pharm |
| Experience | 4–8 years in QC documentation / technical writing |
To apply for this job email your details to aartig@amneal.com
