Position: QC Trainee
Department: Quality Control (QC)
Location: Gozaria, Gujarat
About Celogen:
Celogen Pharma Pvt. Ltd. is a growing pharmaceutical manufacturing company engaged in the development and manufacturing of high-quality pharmaceutical formulations for domestic and international markets. The company operates three advanced manufacturing facilities, including a dedicated hormone manufacturing unit at Mehsana, Gujarat, Ponda, Goa and another manufacturing unit at Daman, Daman & Diu. With a strong focus on quality, compliance, hygiene, and operational excellence, Celogen Pharma is committed to delivering safe, effective, and affordable healthcare solutions while maintaining high standards across all its operations.
This job posting is in a hormone formulation manufacturing division of Celogen Pharma.
Job Summary:
The QC Trainee will assist the Quality Control team in performing routine analytical testing of raw materials, packaging materials, in-process samples, finished products, and stability samples. The trainee will gain practical exposure to laboratory operations, analytical instruments, Good Laboratory Practices (GLP), and pharmaceutical quality systems.
Key Responsibilities:
- Perform routine analysis of raw materials, in-process samples, finished products, and packaging materials as per approved specifications and test methods.
- Assist in sample receipt, labeling, storage, and laboratory documentation.
- Prepare reagents, standard solutions, volumetric solutions, and laboratory buffers as per approved procedures.
- Operate and maintain laboratory instruments under supervision.
- Record analytical observations accurately in accordance with Good Documentation Practices (GDP).
- Follow Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and Data Integrity principles during all laboratory activities.
- Ensure cleanliness and proper maintenance of laboratory equipment, instruments, and work areas.
- Report any Out of Specification (OOS), Out of Trend (OOT), deviations, or abnormal observations to the reporting manager.
- Support stability studies, method verification, and validation activities whenever assigned.
- Participate in laboratory investigations, CAPA implementation, and audit preparation.
Educational Qualifications & Experience:
- B.Sc / M.Sc (Chemistry, Analytical Chemistry, Pharmaceutical Chemistry, Organic Chemistry, Biotechnology, Microbiology, or other relevant Life Sciences)
- Freshers or candidates with up to 1 year of experience in Pharmaceutical Quality Control are encouraged to apply.
Required Skills:
- Basic understanding of pharmaceutical quality control principles and laboratory practices.
- Knowledge of GLP, GMP, GDP, and pharmaceutical regulatory requirements.
- Basic understanding of analytical techniques and laboratory instruments.
- Good analytical and problem-solving abilities.
- Strong attention to detail and documentation accuracy.
- Basic proficiency in MS Office applications.
- Good verbal and written communication skills.
- Willingness to work in shifts, if required.
Pay: ₹162,000.00 - ₹180,000.00 per year
Ability to commute/relocate:
- Mahesana, Gujarat: Reliably commute or planning to relocate before starting work (Required)
Education:
Work Location: In person
