MS&T Specialist

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

Our Team, Your Impact

BALKANPHARMA TROYAN is looking for MS&T Specialist based in Troyan

About the role:

The role is responsible for supporting pharmaceutical product development, technology transfer, and process validation activities to ensure robust, compliant, and efficient manufacturing processes. The position also prepares and maintains technical documentation, analyzes manufacturing and experimental data, and contributes to continuous improvement, quality, and GMP compliance initiatives

How You’ll Spend Your Day

• Transfer, Support Development and optimize pharmaceutical products, including preparation of technical documentation and manufacturing instructions.

• Support the production of experimental, registration, and validation batches, ensuring accurate documentation and data integrity.

• Prepare and review pharmaceutical development reports, validation protocols, reports, and CTD Module 3 documentation.

• Participate in process validation, technology transfer, scale-up activities, and maintenance of validated manufacturing processes.

• Investigate manufacturing deviations, out-of-specification results, and technical issues, implementing corrective and preventive actions where required.

• Perform statistical analysis of experimental and production data to support process improvements and quality enhancement initiatives.

• Ensure compliance with GMP, quality systems, environmental, health and safety requirements, and applicable company procedures.

Your Skills and Experience

• University degree in Pharmacy, Chemistry, Biology, Pharmaceutical Technology, or a related scientific discipline.

• Minimum 1 year of experience in pharmaceutical manufacturing, pharmaceutical development, or a related GMP-regulated environment.

• Knowledge of pharmaceutical manufacturing processes, technology transfer, process validation, and quality systems.

• Proficiency in MS Office and experience working with computerized systems such as SAP, Change Control, CAPA, or Deviation Management is an advantage.

• Good command of English, both written and spoken.

• Ability to perform data analysis and apply statistical methods to support scientific and manufacturing activities.

• Strong problem-solving, collaboration, communication, change management, and continuous learning mindset.

How We’ll Take Care of You

• Dynamic and challenging work environment in the leading pharmaceutical company in the world and the biggest pharmaceutical company in Bulgaria

• Competitive remuneration with bound performance

• Opportunity for development

• Job specific training

• Food allowance

• Organized transport Lovech-Troyan-Lovech

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Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.