PfizerTechnical Services & Validation Specialist (m/f)
This is a maternal leave replacement position in Savski Marof.
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.
Engineering