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Job Description

    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 companys 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 Bachelors degree in Pharmacy, Chemistry, Biotechnology, or a related field. Masters 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. Job Type: Full-time Schedule: Morning shift Experience: total work: 2 years (Preferred) Work Location: In person,

Employement Category:

Employement Type: Full time
Industry: Manufacturing
Role Category: Not Specified
Functional Area: Not Specified
Role/Responsibilies: Third party contract manufacturing Job in

Contact Details:

Company: Florencia Healthcare
Location(s): All India

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Keyskills:   GMP Regulatory Requirements Quality Standards Negotiation Vendor Management Project Management Analytical Skills MS Office ProblemSolving

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