Third Party Contract Manufacturing

1 week ago

Noida Sector Noida Uttar Pradesh, India Florencia Healthcare Full time

Third-Party Contract Manufacturing Job Description for a Pharma Company

**Position**: Third-Party Contract Manufacturing Manager (Pharma)

**Job Summary**

The Third-Party Contract Manufacturing Manager is responsible for overseeing the end-to-end management of contract manufacturing operations for the pharmaceutical company. This includes identifying, onboarding, and managing third-party manufacturers, ensuring compliance with regulatory requirements, quality standards, and production timelines while optimizing costs and maintaining strong vendor relationships.

**Key Responsibilities1. Vendor Management**
- Identify, evaluate, and onboard contract manufacturing organizations (CMOs) that align with the company’s quality and cost requirements.
- Negotiate contracts, terms, and conditions with CMOs to achieve favorable outcomes.
- Build and maintain strong relationships with third-party manufacturers to ensure seamless operations.

**2. Operations Management**
- Coordinate with internal teams (e.g., R&D, procurement, quality assurance, and supply chain) to ensure the timely transfer of technology, raw materials, and production schedules to CMOs.
- Monitor and oversee production activities to ensure adherence to timelines and budgets.
- Resolve operational bottlenecks and escalate critical issues to leadership when necessary.

**4. Cost and Performance Optimization**
- Analyze production costs and identify opportunities for cost savings without compromising on quality.
- Develop and track performance metrics (KPIs) for third-party manufacturers, ensuring continuous improvement in operations.

**5. Documentation and Reporting**
- Maintain comprehensive records of contracts, agreements, and manufacturing operations.
- Prepare regular reports on CMO performance, production status, and any challenges encountered.
- Ensure timely submission of regulatory filings and required documentation in collaboration with the regulatory affairs team.

**Qualifications Education**
- Bachelor’s degree in Pharmacy, Chemistry, Biotechnology, or a related field.
- Master’s degree or MBA is a plus.

**Experience**
- 2+ years of experience in pharmaceutical manufacturing, contract manufacturing, or supply chain management.
- Proven experience in managing third-party manufacturing partnerships.

**Skills and Competencies**
- Strong knowledge of GMP, regulatory requirements, and quality standards in the pharmaceutical industry.
- Excellent negotiation and vendor management skills.
- Ability to manage multiple projects and prioritize tasks effectively.
- Strong analytical and problem-solving skills.
- Proficient in MS Office Suite and ERP systems.

Pay: ₹15,000.00 - ₹30,000.00 per month

Schedule:

- Morning shift

**Experience**:

- total work: 2 years (preferred)

Work Location: In person

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