to manage and supervise pharmaceutical production activities. The ideal candidate will ensure all manufacturing processes comply with
GMP standards
, production targets, and quality requirements.
Key Responsibilities:
Supervise daily manufacturing operations for tablets, capsules, or liquid formulations.
Ensure all production activities are carried out as per
batch manufacturing records (BMR)
and
standard operating procedures (SOPs)
.
Maintain
GMP, safety, and documentation standards
throughout the manufacturing process.
Monitor process parameters, yield, and equipment performance during production.
Coordinate with QA/QC, packing, and maintenance teams for smooth plant operations.
Ensure line clearance, proper material usage, and timely completion of production schedules.
Review and sign BMRs, logbooks, and process documents.
Train and guide operators and assistants on process handling and compliance requirements.
Handle deviations, incidents, and change controls in coordination with QA.
Ensure proper housekeeping and adherence to
EHS (Environment, Health & Safety)
guidelines.
Required Qualifications & Skills:
B.Pharm / M.Pharm / B.Sc. / M.Sc. (Chemistry)
or equivalent qualification.
2-6 years
of experience in
pharmaceutical formulation manufacturing.
Strong understanding of
GMP, GDP, and regulatory guidelines (WHO, USFDA, MHRA, etc.).
Ability to handle equipment like RMG, FBD, compression, coating, and mixing machines.
Good knowledge of in-process checks and documentation practices.
Excellent coordination, leadership, and problem-solving skills.
Preferred Skills:
Experience in
tablet, capsule, or liquid manufacturing
units.
Familiarity with
process validation, yield improvement, and compliance audits.
Exposure to
SAP or digital documentation systems
will be an added advantage.
Salary:
As per industry standards (commensurate with experience and skills).
Job Types: Full-time, Permanent
Pay: ₹9,746.12 - ₹33,847.98 per month
Benefits:
Health insurance
Provident Fund
Work Location: In person
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