Audit Documentation: Role Purpose: To manage and control all quality-related documentation in the pharmaceutical manufacturing unit, ensuring full compliance with CDSCO (Central) and State Government regulations. The Senior Quality Analyst will keep the site audit-ready by maintaining accurate, complete, and compliant records. Key Responsibilities: Prepare and organize all documentation required for CDSCO and State FDA inspections. Maintain audit-ready files, records, and logs at all times. Ensure timely and accurate responses to audit document requests. SOP & Master Documents: Draft, review, update, and control Standard Operating Procedures (SOPs). Manage issuance and control of master documents (BMR, BPR, specifications, test methods). Ensure Good Documentation Practices (GDP) across all departments. Batch Records & Logs: Review batch manufacturing and packaging records for completeness and correctness. Verify logbooks, forms, and data entries before final approval. Job Type: Full-time Pay: From ₹70,000.00 per month Work Location: In person Speak with the employer +91 9990928598
FDA-Approved Quality Chemist (QC) – WHO-GMP Pharmaceutical Plant Location: Ramnagar, Uttarakhand Company: Corbett Industries – WHO-GMP Certified Powder Manufacturing Unit About Us We are a newly established WHO-GMP certified pharmaceutical powder manufacturing company based in Ramnagar, Uttarakhand. We are in the process of applying for a drug manufacturing license and seek to build a strong Quality Control (QC) team to meet statutory and regulatory compliance requirements. Position: FDA-Approved Quality Chemist (QC) Job Type: Full-Time Industry: Pharmaceuticals Key Responsibilities Oversee and manage Quality Control activities as per Schedule M of the Drugs & Cosmetics Act. Ensure compliance with CDSCO and state FDA licensing requirements. Conduct and supervise testing of raw materials, in-process samples, and finished pharmaceutical products (Powders). Maintain accurate records, documentation, and test reports as per regulatory standards. Prepare and face audits from CDSCO , State Drug Authorities , and other regulatory bodies. Coordinate with production, QA, and regulatory teams for licensing and audit readiness. Qualifications & Requirements FDA Approved Quality Chemist with valid State FDA/Drug License (mandatory for CDSCO audit). Must possess at least one of the following licenses: Microbiology Instrumentation Chemical Analyst Candidates with two or all three licenses will be given preference. B.Pharm / M.Pharm / M.Sc. in Chemistry, Microbiology, or related field. Prior experience in QC in a WHO-GMP certified plant will be an added advantage. Strong knowledge of pharmaceutical regulatory requirements and Schedule M compliance . What We Offer Competitive salary package (negotiable for qualified candidates). Opportunity to work in a state-of-the-art WHO-GMP facility . Professional growth and involvement in licensing & audit processes from the ground up. How to Apply Interested candidates may send their updated CV, copies of their approval certificates, and state license details to [email protected] or contact at 9990928598. Job Types: Full-time, Permanent Pay: ₹35,000.00 - ₹65,000.00 per month Application Question(s): Applicant must have a state approved FDA License for Quality chemist role Work Location: In person
FDA-Approved Quality Chemist (QC) – WHO-GMP Pharmaceutical Plant Location: Ramnagar, Uttarakhand Company: Corbett Industries – WHO-GMP Certified Powder Manufacturing Unit About Us We are a newly established WHO-GMP certified pharmaceutical powder manufacturing company based in Ramnagar, Uttarakhand. We are in the process of applying for a drug manufacturing license and seek to build a strong Quality Control (QC) team to meet statutory and regulatory compliance requirements. Position: FDA-Approved Quality Chemist (QC) Job Type: Full-Time Industry: Pharmaceuticals Key Responsibilities Oversee and manage Quality Control activities as per Schedule M of the Drugs & Cosmetics Act. Ensure compliance with CDSCO and state FDA licensing requirements. Conduct and supervise testing of raw materials, in-process samples, and finished pharmaceutical products (Powders). Maintain accurate records, documentation, and test reports as per regulatory standards. Prepare and face audits from CDSCO , State Drug Authorities , and other regulatory bodies. Coordinate with production, QA, and regulatory teams for licensing and audit readiness. Qualifications & Requirements FDA Approved Quality Chemist with valid State FDA/Drug License (mandatory for CDSCO audit). Must possess at least one of the following licenses: Microbiology Instrumentation Chemical Analyst Candidates with two or all three licenses will be given preference. B.Pharm / M.Pharm / M.Sc. in Chemistry, Microbiology, or related field. Prior experience in QC in a WHO-GMP certified plant will be an added advantage. Strong knowledge of pharmaceutical regulatory requirements and Schedule M compliance . What We Offer Competitive salary package (negotiable for qualified candidates). Opportunity to work in a state-of-the-art WHO-GMP facility . Professional growth and involvement in licensing & audit processes from the ground up. How to Apply Interested candidates may send their updated CV, copies of their approval certificates, and state license details to sales@northernlifescience.com or contact at 9990928598. Job Types: Full-time, Permanent Pay: ₹35,000.00 - ₹65,000.00 per month Application Question(s): Applicant must have a state approved FDA License for Quality chemist role Work Location: In person