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Opella

Global OTC & VMS self-care manufacturer

Transfer & Portfolio Optimization Responsible

Bioprocess & BiomanufacturingUpdated on Nov 14
Full-timeBudapest, HungaryHUF11.7M - HUF15.6M

About the Job

Requirements

  • A university degree in natural sciences, pharmacy, engineering, or similar relevant education, with at least six years of expertise in the pharmaceutical industry.
  • Very advanced project management skills and transfer project management expertise.
  • Very strong knowledge and experience of pharmaceutical product manufacturing processes.
  • Very strong negotiation, communication, and conflict management skills.
  • Business acumen.
  • Cross-functional collaboration skills and the ability to work in an international environment.
  • Assertiveness in complex team structures, persistence, pragmatism, and a results-oriented approach.
  • Ability to work independently in a continuously changing environment, proactively identifying solutions and opportunities.
  • Full command of written and spoken English.
  • Willingness to travel abroad.

Responsibilities

  • Lead complex product transfers of medicinal products, medical devices, food supplements, and cosmetics to and from external contract manufacturers or internal manufacturing sites.
  • Independently steer international, interdisciplinary teams within internal and external matrix structures.
  • Ensure project delivery on time while addressing quality, Good Manufacturing Practice (GMP), regulatory, cost, and supply-chain effectiveness considerations.
  • Evaluate detailed technical and financial assessments of product-transfer ideas and develop transfer proposals.
  • Develop comprehensive project plans, including resource planning and budgeting.
  • Monitor and report project progress to management and stakeholders at all levels.
  • Protect Opella’s interests in contract negotiations with contract manufacturers and prepare and negotiate transfer agreements.
  • Provide technical expertise on final-product production processes across galenical forms for assigned projects, and act as a technical expert consultant to T&PO group members and other EM functions when needed.
  • Continuously improve EM CHC transfer processes in close cooperation with corporate functions.

Desired Qualifications

  • Knowledge of international GMP and regulatory requirements, drug acts, and medical-device guidelines and regulations.

About the Company

Opella

Global OTC & VMS self-care manufacturer

Opella makes a wide range of over-the-counter medicines, vitamins, minerals, and supplements for global consumers, covering about 100 brands and an 11,000-strong workforce. It develops, manufactures, and markets non-prescription health products that people can buy ready-made in stores for common needs such as pain relief, digestion, and allergy relief. The company differentiates itself with a large global manufacturing footprint (13 sites and 4 science and innovation centers) and its B Corp certification, signaling accountability to social and environmental standards. Its goal is to simplify self-care and put health in people’s hands for half a billion consumers worldwide.

Company size
5,001-10,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Neuilly-sur-Seine, France
Founded
2018

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