Chemox Pharma Hiring for Quality Assurance – Officer Position

Chemox Pharma Pvt. Ltd., a GMP & ISO certified company and reputed manufacturer & exporter of pharmaceutical APIs and intermediates, is actively hiring for the Quality Assurance – Officer position at its manufacturing unit located in Dahej, Bharuch, Gujarat. This is an exciting opportunity for B.Sc. or M.Sc. qualified candidates with 2–3 years of QA experience in the API or Intermediate industry to be part of a highly compliant and quality-focused environment.

About Chemox Pharma Pvt. Ltd.

Chemox Pharma is a transnational pharmaceutical company that has earned its reputation through a commitment to excellence in producing high-quality APIs and intermediates. The company emphasizes regulatory compliance, process safety, and continuous improvement—making it an ideal workplace for QA professionals seeking career stability and growth.

Job Details: QA Officer – API/Intermediate

Position: Quality Assurance Officer (API/Intermediate)

Location: Chemox Pharma Pvt. Ltd., D-3/143, Dahej Industrial Estate, Near Suva Chowkdi, Dahej-392130, Bharuch, Gujarat, India

Qualification: B.Sc. / M.Sc. in Chemistry or a related science discipline

Experience: 2–3 years of hands-on experience in Quality Assurance, preferably in API or Intermediate manufacturing. Note: This role is open to male candidates only.

Key Responsibilities:

• Implement QA policies and procedures in alignment with current GMP standards.
• Review and manage SOPs, Batch Manufacturing Records (BMRs), Batch Packing Records (BPRs), Equipment Cleaning Records (ECRs), and analytical raw data to support batch release activities.
• Handle deviations, out-of-specification (OOS) reports, and non-conformances with appropriate investigations and documentation.
• Conduct internal audits and participate in external audits, ensuring CAPA (Corrective and Preventive Actions) are implemented promptly.
• Oversee manufacturing floor inspections, verifying cleanliness, labelling, and compliance with quality standards.
• Manage the issuance and tracking of documents, raw materials, packaging materials, and finished goods.
• Support GMP training programs for cross-functional teams and contribute to quality culture.
• Coordinate with cross-departmental teams (QC, production, engineering) to drive quality improvements and ensure timely documentation.

How to Apply: 

Interested and eligible candidates are encouraged to send their updated resumes to:

Email: hr@chemoxpharma.com

Please mention your Total Experience, Current CTC, Expected CTC, and Notice Period in the email.