QC Documentation Officer

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