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BeOne

Senior Pharmaceutical Affairs Manager

RemoteGermany only
Published
Experience
Senior
Employment
Full-time
€103.2k–€129k/yr
Check eligibility

Open to DE only. Set where you work from to check your eligibility.

No BS summary

Senior Pharmaceutical Affairs Manager with 7+ years of GxP/Regulatory experience, fluent in German and English. Must have experience in affiliate settings and be willing to travel up to 10%.

Required skills

M/S OfficeVeeva VaultSAP

Required languages

German FluentEnglish Fluent

What you'll do

  • Acts as local contact person or deputy local contact person for competent authorities in DE
  • Acts as deputy Information Officer
  • Acts as deputy GDP Responsible Person according section 52a German drug law
  • Supports in local internal and external audits as well as regulatory inspections incl. CAPA.
  • Creates and reviews GxP relevant local governance documents within the RA and QA area, supports other functions (e.g. PV, Medical) in relation to creation and review of GxP relevant governance documents
  • Reviews and approves promotional and non-promotional material
  • Maintains the local quality manual
  • Maintains and develops local GxP training oversight for DE/AT staff and develops specific GxP trainings e.g. for sales representatives
  • Supports in product recalls/mock recalls
  • Processes product complaints
  • Owns and processes change controls
  • Owns and processes deviations
  • Coordinates local distribution activities at the interface to EU distribution and local distributors.
  • Contributes to EU regulatory activities and enquiries such as HA requests, RA intelligence, etc in relation to Regulatory Life Cycle Management of marketed products as well as in relation to development products
  • Oversees EU E2E labelling process
  • Coordinates local activities in relation to EU labelling change procedures and other regulatory life cycle management activities, provides labelling source documentation and acts of owner of local label is owner of the LCM tracking database
  • Performs local commercial artwork proofreading and provides commercial artwork request and approval
  • Manages publication of SmPC (Fachinfo Service) and other publications ( e.g. Rote Liste)
  • Supports BeOne functions and departments (Market Access, Customer Engagement, Medical) in relation to GxP relevant enquiries and document requests and selected projects
  • Acts as BeOne representative in professional societies

What they require

  • 7+ years experience within the GxP/Regulatory field, preferably in affiliate settings
  • Fluent German & English
  • Travel : approx. 10%

Benefits

  • We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals focused on fighting cancer.

BiotechEnterprisebeone.es/

What people say about this company

3.0/ 5

€103.2k–€129k/yr