PURPOSE
- Lead cross-functional project teams and be full accountable for driving and ensuring timely and on-budget delivery of projects such as New Product Development, Product Transfers, and Technical Improvement.
- Drive product and process improvement initiatives related to the assigned portfolio (Pain, Alergy, Digestive Health and Pharma)
- Single Point of Contact in Cimanggis Site (for External Stakeholders)
KEY TASKS
- Lead portfolio governance and performance of Projects, Regulations and Product Lifecycle Management (launches, technical transfers, technical changes, and roll-outs).
- Manage end-to-end processes related to projects and portfolio maintenance, strengthening and balancing resources in the project team.
- Execute performance critical analysis, develop and drive improvement initiatives for the portfolio.
- Responsible for timely and effective execution of projects, product and technical changes and roll-outs; meeting the project success criteria by implementing quality by design concept including manufacturing and analytical documentation.
- Provide experience-based support to ensure best input and guidance into Feasibility Stage of NPDs and Transfers led by Regional Portfolio Manager and Procurement.
- Lead project team by motivating members to meet project goals, committing to their responsibilities and project milestones
- Work creatively and analytically to develop scenario and risk-based approach on project planning in order to meet the market needs. Manage the project budgets including all internal and external cost and resources.
- Lead the training program for all staff, provide coaching and development personnel. Responsible to hire, dismiss and develop with the budgeted resource plan according to Bayer Plant Cimanggis procedure and legal requirement.
Skills And Qualifications
- Pharmacist or Science Graduate with experience in GMP aspect and exposed in all manufacturing aspects with emphasize in formulation development,technology and production, regulatory and quality requirements is preferred
- Have professional experience in pharmaceutical manufacturing, development, manufacturing, quality and assessment of products
- Have a very good overview of product portfolio, regulatory affairs and regulations, a network to other companies would be of advantage.
- Familiar with GMP and regulatory principles; occupational safety and health, and environmental control and all relevant Government regulations in quality control operations (knowledge of drug regulations and guidance documents on drug development, registration, variations and line extensions)
- Main competencies for the job (Core, Leaders, Technical competencies)
- Ability to influence, to build relationships with associations and stakeholders, and to successfully negotiate is required. (Experienced with project teams, Excellent communication & leadership skills)
Bayer Indonesia is committed to building a diverse, equitable, and inclusive workforce. We believe that diversity in all its forms enriches our company culture, expands our perspectives, and drives innovation. We welcome and encourage applicants of all backgrounds, divisions, experiences, and identities to apply for the positions
Application Period: 11/13/2024 - 11/23/2024
Reference Code: 833736
Division: Consumer Health
Location: Indonesia : West Java : Cimanggis
Functional Area: Supply Chain Management
Position Grade: VS 1.2
Employment Type: Regular
Work Time: Standard working hours
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