Production Documentation Executive at Covalent Laboratories
Covalent Laboratories is currently hiring for the position of Production Documentation Executive in the Production Documentation department within the Pharmaceutical industry.
Roles & Responsibilities
Production Documentation Executive Job in Gandla, Sangareddy – Covalent Laboratories
Covalent Laboratories is hiring Production Documentation Executives for its manufacturing facility in Gandla, Sangareddy, Telangana. This pharmaceutical industry position is ideal for candidates with 2 to 5 years of experience in production documentation, batch record management, SOP preparation, and compliance activities. Candidates with a B.Sc qualification can apply for this full-time opportunity.
Location
Gandla, Sangareddy, Telangana, India
Employment Type
Full-time
Experience Required
2 to 5 Years
Educational Qualification
B.Sc.
Key Responsibilities
- Prepare and review production documentation.
- Maintain batch manufacturing records.
- Ensure documentation compliance with SOPs.
- Support GMP compliance activities.
- Coordinate document control processes.
- Review production logbooks.
- Track documentation deviations.
- Assist during audits and inspections.
- Archive manufacturing records.
- Support continuous improvement initiatives.
Required Skills & Competencies
- Knowledge of GMP documentation.
- Batch record management skills.
- Documentation review expertise.
- Attention to detail.
- Compliance awareness.
- Computer proficiency.
- Communication skills.
- Time management abilities.
- Organizational skills.
- Problem-solving mindset.
Why Join Covalent Laboratories?
- Opportunity to work in a reputed pharmaceutical company.
- Exposure to regulated manufacturing operations.
- Professional growth opportunities.
- Supportive work environment.
- Long-term career development.
How to Apply
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