Production Director jobs at Teva in Romania, Bucharest

We are seeking an experienced and strategic EHS Lead (Associate Director) to oversee and continuously improve our Environment, Health, and Safety programs at the factory level. This is a key leadership role responsible for ensuring compliance with Romanian legislation and corporate policies, while fostering a culture of safety, sustainability, and operational excellence. You will also coordinate Business Continuity Management (BCM) and administrative functions, playing a vital role in protecting our people, assets, and the environment.

You bring over 5 years of hands-on experience in EHS, with at least 3 years in a leadership role.
You’ve successfully managed complex safety systems in a regulated environment and have a strong track record in implementing ISO standards, managing audits, and leading cross-functional teams.
Your ability to balance strategic oversight with operational execution makes you a trusted advisor and effective leader.

- University degree in a relevant field.
- Specialized certifications in occupational safety and environmental protection.
- In-depth knowledge of Romanian OHS and environmental legislation.
- Proven experience with ISO 14001 implementation and EHS audits.
- Strong leadership, communication, and team coordination skills.
- Experience managing budgets, KPIs, and performance metrics.
- Fluent in Romanian and English (written and spoken).
- Familiarity with GMP compliance and manufacturing best practices is a plus

Curs în domeniul securității și sănătății în muncă
Curs evaluator de risc SSM
Curs Cadru Tehnic PSI
Curs Inspector de mediu si Responsabil Gestionare deseuri

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

As anyou will conduct activities necessary for the determination of the safety profile and the characterization, monitoring, and mitigation of risk for the assigned products throughout the product lifecycle and provide comprehensive safety information to patients, prescribers, and regulators.

• Be accountable for medical evaluation/interpretation of aggregate safety data of assigned products and non-assigned products, as required, including, but not limited to, signal detection and evaluation, dose escalation evaluations, regulatory safety reports (PSUR, PADER, DSUR), and ad-hoc safety review/assessments (such as Health Hazard Assessments, abbreviated safety evaluations, and Health Authority requests).
• Review complex Health Hazard Assessments and Health Authority requests.
• Perform signal management activities such as signal validation QC, authoring of complex signal evaluations, and signal evaluation review. Act as medical reviewer to assess causality, consolidate safety information from different sources to determine whether a signal qualifies as a risk.
• Support risk management activities for assigned products globally and contribute to the preparation of Risk Management Plans (RMPs), REMS, design of additional risk minimization measures as well as management of these plans throughout the product’s lifecycle. The Safety Physician is responsible to define the important identified risks, important potential risks, and the missing information.
• Represent PV in cross-functional Product Label Working Group. Conduct evaluation and determination of safety related sections of the product label, both initial and throughout the product lifecycle; key member for safety related label negotiations with regulatory agencies as well as in the development and maintenance of CCSI.
• Provide PV support and safety contributions to Health Authority submissions and responses. Represent safety during due diligence of products.
• Collaborate with different functional internal (Medical Affairs, Clinical Development, Quality, etc.) and external stakeholers (KOLs, CROs, etc.) effectively representing PV position on any safety concerns as well as the overall safety profile of assigned products. Collaborate with other cross-functional teams to ensure execution of the safety strategy.

•
• Clinical practice experience and/or epidemiological degree/training
• Experience working in pharmacovigilance and drug safety, as a safety physician –
• Proven ability to handle safety surveillance tasks and chair safety committee meetings
• Ability to serve as a subject matter expert
• Outstanding communication skills with an ability to collaborate with different departments and partner with and influence others without direct authority
• Ability to work cross-functionally within a matrix / international team across multiple time-zones
• Oral and written
fluency in English

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

• Oversee end-to-end production operations, including manufacturing, planning, and storage, in compliance with GMP and internal quality systems.
• Approve and implement production plans and ensure execution meets targets for quality, timelines, and efficiency.
• Champion compliance by ensuring procedures, production orders, and documentation align with quality and regulatory standards.
• Lead investigations into deviations and non-conformities, identifying root causes and implementing corrective actions.
• Optimize manufacturing processes and technology, continuously seeking improvements in cost, quality, and throughput.
• Manage production budgets and monitor key economic and technical indicators to ensure performance within targets.
• Direct and develop a skilled production team, fostering a culture of safety, accountability, and operational excellence.
• Collaborate cross-functionally with QA, R&D, Validation, IT, and Supply Chain to ensure seamless flow of operations.

• University degree in Pharmacy, Chemical Engineering, Industrial Engineering, or a related scientific field.
• Minimum 5 years of experience in pharmaceutical or GMP-regulated production environments, including 3+ years in a leadership role.
• Proven operational excellence, expertise in GMP compliance, quality systems, and manufacturing best practices.
• Strong understanding of production planning, documentation standards, change control, and technical process optimization.
• Experience managing budgets, KPIs, and performance metrics in a regulated setting.
• Exceptional leadership and communication skills with a demonstrated ability to lead cross-functional teams.
• Comfortable working in a fast-paced, matrixed organization, balancing strategic thinking with hands-on execution.
• Fluent in English (written and spoken); Romanian language fluent.

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

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.