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Quality Technical Agreements Specialist

1+ years
Not Disclosed
10 Nov. 30, 2024
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/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

Job Title: Quality Technical Agreements Specialist

Location: Prague, Czech Republic (Hybrid - 3 office days per week)
Company: Teva Pharmaceuticals


Who We Are

Teva Pharmaceuticals is a global leader in the pharmaceutical industry, dedicated to making healthcare more affordable and accessible. With operations in nearly 60 countries, we produce life-changing medicines used by over 200 million people daily. We invite passionate individuals to join us in our mission to make a difference worldwide.


The Opportunity

We are seeking a Quality Technical Agreements Specialist to join our Global Quality Technical Agreements (QTA) team in Prague or Brno. This hybrid position involves the preparation, maintenance, and management of Quality Agreements with suppliers, contractors, and clients, ensuring compliance and efficiency across operations.


Key Responsibilities

  • Quality Agreements Management

    • Draft and prepare new Quality Technical Agreements (QTAs).

    • Review, maintain, and update existing QTAs to meet organizational and regulatory standards.

    • Facilitate agreement negotiations and maintain clear communication with internal and external stakeholders.

  • Administrative and Strategic Tasks

    • Manage and update Teva's global QTA database.

    • Administer corporate QTA templates and contribute to process improvements.

    • Participate in developing departmental procedures for enhanced operational efficiency.

  • Training and Development

    • Assist in training new team members and providing guidance on QTA processes.


Qualifications and Experience

  • Education:

    • University degree in pharmacy, chemistry, biology, biotechnology, or a related field (other disciplines will be considered).

  • Experience:

    • Pharma industry experience and knowledge of GMP regulations are advantageous.

  • Skills:

    • Proficiency in English (written and spoken).

    • Strong document review and editing skills.

    • Excellent computer and project management abilities.

    • Highly organized, detail-oriented, and capable of meeting deadlines.

    • Effective negotiation and communication skills.


Employee Benefits

  • Competitive salary with annual performance bonuses.

  • Career growth opportunities within a leading global pharmaceutical company.

  • Flexible working hours and hybrid work environment.

  • 5 weeks of holiday, 3 sick days, and home office options.

  • Meal vouchers (120 CZK/day).

  • Access to a benefit cafeteria system.

  • Life and pension insurance coverage.

  • Company-provided mobile phone and laptop.


Application Process

If this opportunity aligns with your career goals, please send your CV in English. Only shortlisted candidates will be contacted. All personal information will be treated confidentially.


Teva’s Commitment to Diversity

Teva Pharmaceuticals is an equal opportunity employer. We embrace diversity and ensure equal treatment for all candidates regardless of race, gender, age, religion, or other protected characteristics. Should you require accommodations during the application process, please let us know.

Make an impact with Teva Pharmaceuticals – apply today!