Job Description

- QC Documentation Officer Company: Systacare Remedies - A WHO-GMP Certified Company Location:Amritsar Experience Required: 1-2 years Qualification: B.Pharm / M.Sc Gender:Male / Female Key Responsibilities: Prepare and maintain SOPs, STPs, and STSs as per regulatory requirements. Ensure accurate documentation in line with WHO-GMP and other regulatory standards. Maintain records related to QC processes, validation, and compliance. Support the preparation and review of quality-related reports. Possess and apply basic knowledge of QC instruments and Good Laboratory Practices (GLP). Utilize strong computer skills for drafting, editing, and maintaining documentation. Desired Skills: Good understanding of pharmaceutical documentation processes. Familiarity with GLP and QC operations. Strong attention to detail and organizational skills. Proficiency in MS Office and other documentation tools. Why Join Us? At Systacare Remedies, a WHO-GMP certified company, we prioritize quality and regulatory compliance. Join our team to grow your career in a professional environment where your expertise contributes directly to pharmaceutical excellence.

Job Type: Full-time

Pay: ?14,789.09 - ?25,207.76 per month

Benefits:

Health insurance
Work Location: In person