Analytical Chemist Jobs at SAIN Medicaments | Chemistry Graduates Apply Now
Analytical Chemist Jobs are now available for professionals seeking Quality Assurance Jobs in the pharmaceutical sector. This opportunity is ideal for candidates with experience in analytical QA, compliance, and data review. If you are looking to grow in Chemistry Jobs, this role offers strong exposure to GMP environments, regulatory standards, and analytical operations in a fast-growing pharma company.
- Job Title: Executive / Sr. Executive – Analytical Quality Assurance (AQA)
- Industry: Pharmaceuticals (Formulation)
- Department: Quality Assurance
About the Company:
SAIN Medicaments Pvt. Ltd is a growing pharmaceutical company focused on quality-driven manufacturing and compliance excellence. The company offers strong career growth in Analytical Chemist Jobs and Quality Assurance Jobs. With a focus on regulatory standards and analytical excellence, it provides a platform for professionals to build expertise in Chemistry Jobs within a GMP-regulated environment.
Job Overview:
This role in Analytical Chemist Jobs focuses on Quality Assurance Jobs within a pharmaceutical formulation setup. The position involves reviewing analytical data, ensuring compliance with regulatory standards, and maintaining data integrity. It is ideal for candidates aiming to advance in Chemistry Jobs with hands-on experience in QA systems, documentation, and analytical oversight.
Key Responsibilities:
- Review and approve analytical data, test reports, and certificates of analysis (CoA)
- Ensure compliance of QC laboratory activities with GMP, GLP, and regulatory guidelines
- Review of analytical method validation, method transfer, and verification documents
- Oversight of stability studies, protocols, and reports
- Review of calibration and qualification records of analytical instruments (HPLC, GC, UV, etc.)
- Ensure data integrity compliance (ALCOA+ principles) in all analytical records
- Review and approval of SOPs, specifications, protocols, and reports
- Handle deviations, OOS (Out of Specification), OOT (Out of Trend), CAPA, and change controls
- Participate in internal, external, and regulatory audits and ensure audit readiness
- Coordinate with QC, Production, and Regulatory teams for compliance and quality improvements
GMP & Compliance Responsibilities:
- Ensure adherence to GMP, GLP, and regulatory requirements (USFDA, WHO, MHRA, etc.)
- Maintain proper documentation and traceability of all analytical activities
- Support regulatory inspections and client audits
- Ensure implementation of quality systems and continuous improvement
Key Skills:
- Analytical QA Review
- GMP / GLP Compliance
- Data Integrity (ALCOA+)
- OOS / OOT Investigation
- Method Validation & Transfer
- Audit Handling
- Documentation & Compliance
Eligibility Criteria:
- Qualification: M.Sc / B.Sc (Chemistry / Analytical Chemistry)
- Experience: 2–6 years in Analytical QA / QC with QA exposure in the pharma industry
Preferred Candidate Profile:
- Strong experience in data review and documentation
- Exposure to regulatory audits (USFDA, WHO, EU, etc.)
- Good understanding of analytical instruments and laboratory practices
- Strong attention to detail and compliance mindset
This opportunity in Analytical Chemist Jobs offers a strong platform for professionals aiming to grow in Quality Assurance Jobs within the pharmaceutical industry. It provides hands-on experience in compliance, analytical review, and regulatory processes. Candidates looking to build a stable and rewarding career in Chemistry Jobs will benefit from the exposure and learning this role offers.
