Assistant Manager – Production Documentation | Emnar Pharma Private Limited | Visakhapatnam, Andhra Pradesh, India
Emnar Pharma Private Limited is seeking an experienced Assistant Manager – Production Documentation for its pharmaceutical manufacturing facility located in Parawada, Visakhapatnam, Andhra Pradesh. This position is suitable for professionals with 15–18 years of experience in pharmaceutical documentation, manufacturing records management, and regulatory compliance. The selected candidate will oversee production documentation processes, ensure adherence to GMP and regulatory guidelines, and coordinate with production, quality assurance, and regulatory teams. This role requires strong expertise in batch record review, document control systems, and audit readiness. Emnar Pharma offers a structured environment for experienced professionals to contribute to quality-driven manufacturing processes while ensuring operational transparency and compliance with pharmaceutical industry standards.Location
Parawada, Visakhapatnam, Andhra Pradesh, IndiaEmployment Type
Full-timeExperience Required
15–18 YearsCompensation & Benefits
Salary: Not DisclosedAbout Emnar Pharma Private Limited
Emnar Pharma Private Limited is engaged in pharmaceutical manufacturing with a strong focus on quality systems, regulatory compliance, and operational excellence across production and documentation processes.Position Overview
The Assistant Manager – Production Documentation will manage and supervise production documentation systems to ensure regulatory compliance and data accuracy in pharmaceutical manufacturing operations.Key Responsibilities
- Review and manage batch manufacturing records and production documentation.
- Ensure documentation compliance with GMP and regulatory guidelines.
- Maintain document control systems and SOP updates.
- Coordinate with QA and production teams for documentation accuracy.
- Prepare documentation for internal and external audits.
- Track deviations, CAPA documentation, and compliance records.
- Ensure proper archiving and retrieval of production documents.
- Monitor documentation workflow and approval systems.
- Train production teams on documentation practices.
- Ensure data integrity across documentation processes.
Required Skills & Competencies
- Extensive knowledge of GMP documentation practices.
- Experience in pharmaceutical manufacturing documentation systems.
- Strong understanding of regulatory audit requirements.
- Excellent document review and quality control skills.
- Ability to coordinate with cross-functional teams.
- Strong analytical and compliance monitoring skills.
- Knowledge of batch record management systems.
- Leadership and team management capabilities.
- Strong communication and organizational skills.
- Commitment to regulatory compliance and documentation accuracy.
Educational Qualification
B.ScAbout the Project & Industry
The pharmaceutical industry requires strong documentation systems to maintain regulatory compliance, traceability, and product quality assurance across manufacturing operations.Why Join Emnar Pharma Private Limited?
- Leadership role in pharmaceutical documentation management.
- Opportunity to work in a regulated manufacturing environment.
- Exposure to regulatory inspections and quality systems.
- Long-term career growth in pharmaceutical operations.
How to Apply
Interested candidates can apply by sending their updated resume to: hrunit2@emnar.com Check our website — www.ackjobs.com — regularly for the latest updates in the job market. Join our WhatsApp and social media groups from the website.