MS&T Specialist
Apply NowCareer Opportunities: MS&T Specialist (68261)
Requisition ID 68261 - Posted - Bulgaria
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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
At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community. When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way.
Already Working @Teva?
Make sure to apply through our internal career site on Twist—your one-stop shop for career development
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.
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