159 days ago on jobs.jnj.com

Regulatory Affairs Manager (m/f)

Cilag AG

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Regulatory Affairs Manager (m/f)

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Regulatory Affairs Manager (m/f)

Standorte:Schaffhausen, Schweiz
Regulatory Affairs
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Requisition ID: 000014ZN

" Caring for the world… one person at a time” inspires and unites the people of Johnson & Johnson. This culture of caring is the focus of our corporate philosophy, that are anchored in the internationally applicable Credo.


Cilag AGin Schaffhausen belongs to the group of Johnson & Johnson pharmaceutical companies operating under the “ Janssen Pharmaceutical Companies of Johnson & Johnson” trademark and manufactures high quality pharmaceutical products, active pharmaceutical ingredients (APIs) and medical devices.  Today Cilag AG is one of the largest pharmaceutical manufacturers in Switzerland supplying all the major global markets. The Schaffhausen facility is a Johnson & Johnson strategic launch and growth site for parenteral products and we have an impressive pipeline of new and innovative products.


Reporting into the Quality Assurance API and Solids Departmentwe are looking to hire an experienced


Regulatory Affairs Manager (m/f)





In this regulatory function located in Schaffhausen you will perform and support the following activities to ensure regulatory filing compliance as a basis to support the business for APIs manufactured at Cilag/Janssen in Schaffhausen:

  • Active Substance Master File, Drug Master File, Certificate of Suitability (CEP) Submissions: Coordination and preparation for new submissions, regular updates, variations, renewals
  • Customer communication (prior and after submission of regulatory filings and/or filing updates filing)
  • Collaboration with customers to develop and align regulatory filing strategies and implementation plans
  • Sunrise project: Regulatory actions, e.g. customer communication, filing renewals, filing transfers, filing withdrawals
  • Coordination and preparation of responses to deficiency letters or authority requests
  • Coordination and preparation of responses of customer requests related to filings and or other regulatory/technical questions or questionnaires
  • Preparation and submission of Open Parts, Letter of Access, TSE Statement, Kosher/Halal Statement, Allergens Statement, Melamin free Statement, Latex free Statement, etc.)
  • Regulatory assessments of Change Requests and development of regulatory implementation plan
  • Regulatory assessment of major Non Conformances
  • Regulatory consultation for Quality Assurance, Production, Quality Control, Sales, Purchasing
  • Preparation of FDA-GDUFA (Generic Drug User Fee Amendments) applications
  • Regulatory support for inspections and audits
  • Ensure regulatory filing compliance and continued lifecycle management
  • Partner with Global Regulatory groups to coordinate and ensure submission of filings for US and/or other countries and/or regulatory activities for Janssen Supply Chain (JSC) products manufactured in Schaffhausen
  • Partner with Production, Chemical and Analytical Development, Quality Control, Quality Assurance and other departments as needed



  • A minimum of a Bachelor's degree with a minimum of 6+ years of relevant experience in a highly regulated environment (preferably pharmaceutical industry) or an advanced degree (MS, PhD, etc.) with a minimum of 4+ years of experience is required.
  • Regulatory CMC or CMC experience is preferred. 
  • Good knowledge of English.
  • Basic knowledge of regulatory requirements is preferred. 
  • Drug development experience is preferred. 
  • A working knowledge of global HA laws, regulations, and guidance is required.
  • Experience developing regulatory strategies and an understanding of product development is preferred. 
  • Solid understanding of chemistry relevant is preferred. 
  • A demonstrated ability to communicate regulatory requirements is required. 
  • Excellent interpersonal, teamwork and verbal/written communication skills will be needed. 
  • Good organizational skills and an ability to manage multiple tasks/projects/priorities and complex systems simultaneously will be needed. 
  • Communicates cross-functionally and cross-company as well and presents and defends regulatory strategy and opinion to project teams. 
  • Ability to demonstrate model behavior that understands what the priorities are and encourages others to drive for results will be needed.


We are offering you a multifaceted challenge in a dynamic, international environment with attractive terms and an excellent infrastructure.

If you feel attractedby this challenge and want to be part of a successful and growing organization, then please send us your online application (CV, Motivation Letter, Working References etc.)

Primärer Standort
Cilag AG (8562)
Regulatory Affairs