JAMP India Pharmaceuticals has announced a hiring opportunity for professionals in the Corporate Quality Assurance (CQA) department. The company is looking for qualified candidates for the position of Senior Executive / Assistant Manager.
This role is ideal for professionals with experience in nitrosamine risk assessment, regulatory compliance, analytical method development, and quality investigations. Candidates who have strong knowledge of pharmaceutical quality systems and regulatory expectations will have an advantage.
Interested and eligible candidates can send their updated CV to the email mentioned below.
Job Overview
Position: Senior Executive / Assistant Manager
Department: Corporate Quality Assurance
Company: JAMP India Pharmaceuticals
Job Location: India
Employment Type: Full-time
Key Roles and Responsibilities
Risk Assessment and Reporting
- Conduct comprehensive nitrosamine and elemental impurity risk assessments for new products, technology transfers, and lifecycle changes.
- Prepare scientifically sound assessment reports aligned with regulatory expectations and internal quality systems.
Cross-Functional Collaboration
- Collaborate with internal teams and external stakeholders to compile, review, and finalize risk assessment reports.
- Act as a technical contact for queries related to nitrosamine and elemental impurity evaluations.
Analytical Method Development and Testing Oversight
- Coordinate with external laboratories and partners on analytical method development, validation, and confirmatory testing.
- Review AMV protocols, reports, CoAs, and analytical test results.
Regulatory and Data Support
- Collect and interpret impurity data to support mitigation strategies and global regulatory submissions.
- Provide technical input for regulatory submissions and responses to agency queries.
Investigations
- Lead OOS investigations, AI-related investigations, and deviation investigations related to nitrosamine impurities.
- Conduct root cause analysis and develop CAPA actions.
Change Impact Assessments
- Evaluate manufacturing process changes, supplier changes, and material modifications.
- Assess the impact on nitrosamine and elemental impurity risk profiles.
Quality and Compliance
- Represent the Corporate Quality Assurance function in internal and external meetings.
- Drive continuous improvement initiatives related to impurity control strategies.
- Ensure strong adherence to GMP and quality agreements.
Required Qualifications
Candidates applying for this role should have:
- Bachelorโs or Masterโs degree in Pharmacy, Chemistry, or related life science field
- Experience in pharmaceutical quality assurance or regulatory compliance
- Knowledge of nitrosamine risk assessment and impurity control strategies
- Understanding of GMP, regulatory guidelines, and analytical validation
- Strong analytical and documentation skills
- Ability to collaborate with cross-functional teams
Salary and Benefits
The expected salary range for this position is:
โน6,00,000 โ โน12,00,000 per year
Benefits may include:
- Competitive compensation package
- Career growth opportunities
- Exposure to global regulatory projects
- Work with experienced pharmaceutical quality professionals
How to Apply
Interested and eligible candidates should send their updated CV to the email address below.
Email: dkothari@jamppharma.com
Applicants are advised to mention the position name in the subject line while applying.
