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4 Job openings at Nootan Pharmaceuticals (Baddi)
Plant Manager

Hyderabad, Telangana

10 years

INR Not disclosed

On-site

Full Time

Job Title: Plant Manager – Pharma Manufacturing Location: Baddi Experience: 10+ years in pharma manufacturing; 3+ years in leadership Qualification: B.Pharm / M.Pharm / B.Sc / B.Tech (Chemical/Pharma) Role Summary: Responsible for overseeing all plant operations including production, quality, maintenance, and compliance. Ensures timely, cost-effective, and GMP-compliant manufacturing. Key Responsibilities: Manage day-to-day manufacturing activities as per production plan. Ensure compliance with cGMP, WHO-GMP, and regulatory norms. Coordinate with QA/QC for quality assurance and batch release. Monitor efficiency, minimize downtime, and implement process improvements. Handle audits, documentation, and regulatory inspections. Lead and motivate plant staff, ensuring training and performance. Ensure adherence to safety and environmental standards. Job Types: Full-time, Permanent Pay: Up to ₹120,000.00 per month Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Ability to commute/relocate: Hyderabad, Telangana: Reliably commute or planning to relocate before starting work (Required) Work Location: In person

QA Executive

Baddi, Himachal Pradesh

0 years

INR 2.0 - 3.0 Lacs P.A.

On-site

Full Time

Documentation, QMS, Validation & Related Activities Job Types: Full-time, Permanent Pay: ₹200,000.00 - ₹300,000.00 per year Schedule: Day shift Work Location: In person

QA Executive

Baddi

0 years

INR 2.0 - 3.0 Lacs P.A.

On-site

Full Time

Documentation, QMS, Validation & Related Activities Job Types: Full-time, Permanent Pay: ₹200,000.00 - ₹300,000.00 per year Schedule: Day shift Work Location: In person

QC Manager

Baddi

0 years

INR 3.3702 - 12.0 Lacs P.A.

On-site

Full Time

QC Manager – Key Responsibilities Oversee testing of raw materials, packing materials, finished products, and stability samples as per pharmacopeial standards. Ensure compliance with cGMP, GLP, Schedule M, and WHO guidelines. Manage QC documentation, review COAs, STPs, SOPs, and ensure timely release of batches. Handle OOS, OOT, deviations, and implement CAPA effectively. Supervise calibration, maintenance, and qualification of lab instruments. Coordinate with the microbiology team for environmental monitoring and water testing. Lead stability studies and ensure regulatory compliance as per ICH. Train and supervise QC staff; ensure audit readiness at all times. Ensure data integrity and proper record-keeping (ALCOA+ compliance). Job Types: Full-time, Permanent Pay: ₹28,085.45 - ₹100,000.00 per month Schedule: Day shift Supplemental Pay: Performance bonus Work Location: In person

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