Mangalam Drugs & Organics Limited, a well-established pharmaceutical and API manufacturing company, has announced multiple openings at its API Manufacturing Plant located in GIDC, Vapi. The company is seeking experienced professionals with relevant API industry exposure to join various departments, including ADL, Quality Assurance, Production, and EHS.
This recruitment drive presents an excellent opportunity for science graduates and postgraduates looking to advance their careers in the pharmaceutical manufacturing sector while working in a GMP-compliant environment.
About the Opportunity
The company is looking for qualified candidates with 2 to 5 years of experience in the API industry. Selected candidates will contribute to critical functions such as analytical method development, quality assurance review activities, production documentation, and environmental health & safety operations.
Open Positions
1. Analytical Development Laboratory (ADL)
Position: Chemist to Officer
Qualification: B.Sc. / M.Sc.
Vacancies: 2
Key Responsibilities:
Analytical method development
Method validation activities
Testing of raw materials
Laboratory documentation and compliance
2. Quality Assurance (QA)
Position: Chemist to Officer
Qualification: B.Sc. / M.Sc.
Experience: 2–5 Years
Sections Available:
BMR Review
Engineering & Services Review
Dispatch Review
AQA & CQA
Vacancies:
BMR Review – 4
Engineering & Services Review – 2
Dispatch Review – 2
AQA & CQA – 2
3. Production
Position: Chemist to Officer
Qualification: B.Sc. / M.Sc.
Vacancies: 3
Key Responsibilities:
Recovery operations
Production documentation
Batch manufacturing support
Process compliance monitoring
4. Environment, Health & Safety (EHS)
Position: Chemist
Qualification: B.Sc./M.Sc. + PDIS/ADIS
Vacancies: 1
Required Skills:
Knowledge of safety regulations and standards
Risk assessment techniques
Hazard identification and mitigation
Workplace safety management
Why Join Mangalam Drugs & Organics?
Opportunity to work in a reputed API manufacturing facility
Exposure to GMP-regulated pharmaceutical operations
Career growth across QA, Production, ADL, and EHS functions
Professional work environment with industry-standard practices
Hands-on experience with regulatory compliance and quality systems
Application Process
Interested candidates should share their updated CV along with:
Current CTC
Total Experience
Relevant API Industry Experience
Email: kpandey@mangalamdrugs.com
Candidates are advised to mention the department and position applied for in the email subject line to facilitate faster processing.
Technical FAQs
1. What is Analytical Method Validation in an API manufacturing facility?
Analytical Method Validation is the documented process of proving that an analytical method is suitable for its intended purpose. Parameters evaluated include accuracy, precision, specificity, linearity, robustness, and detection limits as per ICH guidelines.
2. What is the role of BMR Review in Quality Assurance?
Batch Manufacturing Record (BMR) Review ensures that every manufacturing step has been executed according to approved procedures. QA verifies documentation accuracy, process compliance, deviations, and batch traceability before product release.
3. Why is recovery operation important in API production?
Recovery operations help reclaim solvents and valuable process materials, reducing manufacturing costs, improving sustainability, and ensuring efficient resource utilization while maintaining product quality standards.
4. What is Hazard Identification and Risk Assessment (HIRA) in EHS?
HIRA is a systematic process used to identify workplace hazards, evaluate associated risks, and implement control measures to prevent accidents, injuries, environmental incidents, and regulatory non-compliance.
5. What are Current Good Manufacturing Practices (cGMP) in pharmaceutical manufacturing?
cGMP refers to regulations that ensure pharmaceutical products are consistently produced and controlled according to quality standards. It covers documentation, equipment qualification, personnel training, process validation, and quality management systems.
Conclusion:
Mangalam Drugs & Organics Limited’s latest recruitment initiative offers promising career opportunities for experienced pharmaceutical professionals. Candidates with API manufacturing expertise and strong technical knowledge in QA, ADL, Production, or EHS should consider applying to become part of a growing and quality-driven organization.

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