Quality Manager / Responsible Person in Bucuresti

The opportunity

We’re looking for an experienced and autonomous Responsible Person (RP) to join our Romanian operations at Teva Pharmaceuticals. This is a pivotal role, combining strategic leadership with operational responsibility in a highly regulated, impactful environment—where your actions directly influence patient safety and product quality. At Teva, you’ll find a culture where we care about each other, act as one team, and give meaning to our work through purpose-driven challenges.

How you’ll spend your day

  • Acting as the Responsible Person (RP), ensuring full compliance with GDP, national and EU pharmaceutical regulations, and narcotic distribution laws.
  • Independently overseeing market release, recalls, and complaints related to medicinal products.
  • Leading quality management processes, including audits, SOPs, CAPAs, change control, and documentation systems.
  • Communicating directly with national health authorities and hosting inspections with full readiness at all times.
  • Maintaining licenses and authorizations related to medicinal and narcotic products, including reporting to authorities.
  • Providing strategic quality guidance and partnering closely with the General Manager and cross-functional commercial teams.
  • Leading and executing risk management activities across the distribution chain.
  • Participating in European-level quality councils and ensuring implementation of regional initiatives locally.
  • Ensuring continuous GDP training, quality awareness, and inspection readiness.
  • Being the key local quality contact for both internal stakeholders and external regulatory bodies.
  • Your experience and qualifications

  • Master’s Degree in Pharmacy, Medicine, or Biology (Pharmacist license mandatory); advanced degrees are a plus.
  • Minimum 3 years of experience in a RP, QP, or QA Manager role in a pharmaceutical company, ideally in a large international organization.
  • Proven ability to work independently, with full ownership of RP and QA responsibilities.
  • Strong understanding of GDP, GMP, and Romanian/EU legislation including those related to narcotic substances.
  • Experience managing health authority inspections, quality systems, and regulatory submissions.
  • Excellent communication skills and ability to influence at all levels of the organization.
  • Track record of implementing quality systems, continuous improvement, and issue escalation.
  • Fluent in English; Romanian language proficiency is essential for regulatory communications.
  • Strong problem-solving, decision-making, and risk assessment capabilities.
  • Enjoy a more rewarding choice

  • Competitive compensation package aligned with experience.
  • Benefits package: meal vouchers, healthcare subscription to a private clinic.
  • Highly professional team and organizational culture with strong values.
  • Professional development within the company.
  • Make a difference with Teva Pharmaceuticals

    APPLY ONLINE NOW!

    Pre-employment verification

    All job offers at Teva Romania are preceded by pre-screening candidates. In the case of all candidates who have passed to the final stage of recruitment, verification of the data provided in the recruitment process will be carried out, if deemed necessary. More detailed information will be provided to candidates prior to the verification process.

    Contact

    Datele de contact vor fi vizibile dupa ce veti aplica!

    Anunţ expirat
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