Role Summary
In this role, you will play an integral part in technology transfer, process validation, and lifecycle management of biotechnological drug product processes.
You will work in an environment that encourages ownership, accountability, and continuous learning, balancing independent technical responsibility with strong cross‑functional collaboration at site and global level.
Key Responsibilities
- Lead and support technology transfer and process validation activities for biopharmaceutical drug product manufacturing (sterile injectables)
- Design, execute, and evaluate technical, scale‑up, and validation studies
- Provide scientific and technical support to Manufacturing, including support during routine production, deviations, investigations, and change implementation
- Drive process optimization and continuous improvement initiatives
- Prepare and maintain technical, validation, and regulatory documentation in compliance with GMP and regulatory requirements
- Support regulatory submissions and participate in internal and external inspections
- Collaborate with cross‑functional partners and global Pfizer subject matter experts
- Includes work in lab scale and manufacturing scale facility (executing studies, supporting technical transfers batch manufacturing etc).
Qualifications
- University degree (VSS / 300 ECTS) in Pharmacy, Biotechnology, Chemical Engineering, Food Technology, Natural Sciences, or a related discipline
- 3 years of working experience in technical services, technology transfer, process validation, or process support within the pharmaceutical or biopharmaceutical industry
- Working knowledge of GMP and regulatory expectations
- Scientific understanding of process engineering, biochemical engineering, protein biochemistry, or purification processes
- Proficiency in English and Croatian
- Strong digital skills, including MS Office tools
What You Bring
- A strong sense of ownership and accountability
- Analytical thinking and a problem‑solving mindset
- Ability to manage multiple priorities in a dynamic manufacturing environment
- Clear and effective communication and collaboration skills
- Willingness to learn, adapt, and continuously develop technical expertise
- Ability to work both independently and as part of diverse, cross‑functional teams
Nice to Have
- Hands‑on experience with drug product technology transfer and/or process validation
- Experience using statistical tools or digital quality systems in a regulated environment
What You Get
- Organized transport to and from the site
- Work with modern automated systems
- Strong education program
- Christmas, Easter and holiday bonus
- Affordable meals in an on-site cafeteria
- Opportunities for career enhancement and development
- Yearly pay increase and bonus based on performance
- Further professional development in a supportive environment
- Free psychotherapy and coaching sessions for employees and people close to them
- Bravo employee recognition system
- Opportunity for working on projects with other Pfizer sites and locations
- Free fruit and hot beverages on the site
Why Pfizer
At Pfizer, you will find a culture grounded in integrity, quality, and respect for people. We empower colleagues to own their careers, grow their capabilities, and make a meaningful impact through their work.
As part of the Technical Services & Validation team, you will collaborate with passionate, knowledgeable colleagues locally and globally, contributing to innovative solutions that support reliable manufacturing and patient safety.
Work Location Assignment: Hybrid
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email [email protected]. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Engineering
Skills Required
- University degree in Pharmacy, Biotechnology, Chemical Engineering, or related discipline
- 3 years of experience in technical services, technology transfer, or process validation
- Knowledge of GMP and regulatory expectations
- Scientific understanding of process engineering or protein biochemistry
- Proficiency in English and Croatian
- Strong digital skills including MS Office
Pfizer Compensation & Benefits Highlights
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Healthcare Strength — Health coverage includes comprehensive medical with robust mental‑health networks, plus dental and vision options, and coverage for infertility/family‑building and transgender‑affirming care. Recent U.S. summaries name mental‑health partners and outline multiple plan choices.
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Retirement Support — The retirement program provides a 401(k) with company match plus an additional employer Retirement Savings Contribution, along with financial‑planning support and company‑paid life and disability insurance. These elements are highlighted as part of the core U.S. package.
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Parental & Family Support — Parental leave is described as up to 26 weeks in the U.S. when combining paid non‑medical parental leave with medical recovery where applicable, with exact pay and weeks dependent on circumstances and plan elections. Family‑building support includes egg preservation, adoption, and surrogacy coverage.
Pfizer Insights
What We Do
Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.
Why Work With Us
We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.
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Hybrid Workspace
Employees engage in a combination of remote and on-site work.









