Instagram
youtube
Facebook

(Senior) Quality Assurance Manager (M/F/D) And Deputy Rp 80%

7+ years
Not Disclosed
10 Jan. 31, 2025
Job Description
Job Type: Full Time Education: M.Sc./M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

📌 (Senior) Quality Assurance Manager (m/f/d) and Deputy RP | Basel, Switzerland
📍 Location: Basel, Switzerland
💼 Company: Teva Pharmaceuticals (Mepha Pharma AG)
🕒 Experience: 7+ years in pharmaceutical industry, 5+ years in QA/QC

About Teva in Switzerland

Teva’s Swiss operations consist of Mepha Pharma AG and Teva Pharma AG, both major players in the pharmaceutical industry. With a combined portfolio of 320+ products, the company leads in generics, over-the-counter medicines, biosimilars, and original medicines targeting critical diseases such as central nervous system disorders, respiratory diseases, and cancer.

Role Overview

Teva Switzerland is seeking a Senior Quality Assurance Manager to join the Commercial Quality Team. This role includes overseeing GMP/GDP compliance, managing product releases, quality incidents, complaints, and major product launches. As Deputy RP, the role involves ensuring regulatory adherence and contributing to audits, inspections, and continuous improvement processes.

Key Responsibilities

Swiss Market Releases: Perform product releases, manage deviation and change control.
Deputy RP: Act as Deputy Responsible Person (Stv. FvP) and ensure quality compliance.
Manage Quality Issues: Oversee incidents, complaints, recalls, and technical agreements.
Product Launches: Manage and support major product launches in Switzerland.
Documentation and SOPs: Create and maintain Standard Operating Procedures and Working Instructions.
Audit and Inspection Readiness: Contribute to inspection readiness, assist local authority inspections, and lead internal audits.
Cross-Functional Collaboration: Work with internal teams like Regulatory Affairs, Pharmacovigilance, and external suppliers.

Qualifications

🎓 Education:

  • Master’s Degree in Pharmacy, Medicines, Biology, or related field.

💼 Experience:

  • 7+ years working in a pharmaceutical company, including 5+ years in a QA/QC function.
  • Experience in Swiss market release and in-depth knowledge of GMP/GDP guidelines.
  • Proven leadership in matrix organizations and managing cross-functional teams.

Desired Skills

  • Fluent in German and English (both written and spoken).
  • Strong attention to detail and proactive approach to quality assurance.
  • Strong communication skills, team player, and adaptable to change.

Reports To

Head of Quality Assurance

What We Offer

  • A dynamic role in a growing organization with an international reach.
  • Opportunities for personal development and challenging tasks.
  • Benefits such as a lunch card, public transport allowance, and easy access to Basel SBB.

📩 Apply Now