# Production Manager

**Company:** [Experts Plus Recruitment Services](https://jobs.workable.com/companies/4gYviqrYksJarKRgzBj92E.md)
**Location:** Delhi, India
**Workplace:** on site
**Employment type:** Full-time
**Department:** Healthcare

[Apply for this job](https://jobs.workable.com/view/eb322080-563d-453a-87cf-242aa3330b80)

## Description

Title: **PRODUCTION MANAGER**(Pharmaceuticals)

**Location:** Lagos, Nigeria (travel to site/regulators as required)  
**Reports to:** Plant Director / Country Director

### **Key responsibilities**

●     Convert MPS into daily production plans; execute batch records right-first time.

●     Enforce cGMP on the floor: ALCOA+ data integrity, line clearance, reconciliation.

●     Drive deviation/OOS/OOT investigations, CAPA, change control with QA.

●     Own qualification/validation: URS/IQ/OQ/PQ, process & cleaning validation.

●     Keep critical utilities/environments in control (HVAC/HEPA, DP, PW/WFI, clean steam).

●     Coach supervisors/operators; 5S, visual management, tiered daily meetings.

●     Coordinate maintenance/spares for granulators, blenders, tablet presses, coating, caps/lines, autoclaves (if sterile).

●     Support audits (NAFDAC/WHO-GMP/customer), tech transfers, and NPIs.

●     Improve yields, cycle times, safety, and schedule adherence.

## Requirements

### **Must-have qualifications & experience**

●     B.Pharm/BSc Pharmacy, Chemical/Pharma Engineering, or related.

●     7–12 years in GMP pharma production; ≥3 years in a supervisory/manager role.

●     Hands-on with batch docs, validations, cleaning verification, and regulatory inspections.

### **Skills**

●     Deep GMP/ICH (Q7–Q10); investigation writing; risk tools (FMEA/FTA).

●     Cross-functional leadership (QA/Eng/SCM/RA); Excel/ERP competence.

### **Nice-to-have**

●     Start-up/greenfield builds; WHO/EU/FDA audit exposure; Lean/Six Sigma.