Technical Services and Validation Associate (m/f)

<div><div>This is a maternal leave replacement position in Savski Marof.</div><div><div><div><div><div><div><div><div></div></div></div></div></div></div></div></div></div><p></p><p><b>Role Summary</b></p><p>In this role, you will play an integral part in technology transfer, process validation, and lifecycle management of biotechnological drug product processes.</p><p>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.</p><p></p><p><b>Key Responsibilities</b></p><ul><li><p>Support <b>technology transfer and process validation activities</b> for biopharmaceutical drug product manufacturing (sterile injectables)</p></li><li><p>Design, execute, and evaluate <b>technical, scale‑up, and validation studies</b></p></li><li><p>Provide <b>scientific and technical support</b> to Manufacturing, including support during routine production, deviations, investigations, and change implementation</p></li><li><p>Drive <b>process optimization and continuous improvement</b> initiatives</p></li><li><p>Prepare and maintain <b>technical, validation, and regulatory documentation</b> in compliance with GMP and regulatory requirements</p></li><li><p>Support <b>regulatory submissions</b> and participate in internal and external inspections</p></li><li><p>Collaborate with cross‑functional partners and global Pfizer subject matter experts</p></li><li><p>Includes work in lab scale and manufacturing scale facility (executing studies, supporting technical transfers batch manufacturing etc).</p></li></ul><p></p><p><b>Qualifications</b></p><ul><li><p>University degree (VSS / 300 ECTS) in <b>Pharmacy, Biotechnology, Chemical Engineering, Food Technology, Natural Sciences, </b>or a related discipline</p></li><li><p>Experience in <b>technical services, technology transfer, process validation, or process support</b> within the pharmaceutical or biopharmaceutical industry</p></li><li><p>Working knowledge of <b>GMP and regulatory expectations</b></p></li><li><p>Scientific understanding of process engineering, biochemical engineering, protein biochemistry, or purification processes</p></li><li><p>Proficiency in <b>English and Croatian</b></p></li><li><p>Strong digital skills, including <b>MS Office</b> tools</p></li></ul><p></p><p><b>What You Bring</b></p><ul><li><p>A strong sense of <b>ownership and accountability</b></p></li><li><p>Analytical thinking and a <b>problem‑solving mindset</b></p></li><li><p>Ability to manage multiple priorities in a <b>dynamic manufacturing environment</b></p></li><li><p>Clear and effective <b>communication and collaboration skills</b></p></li><li><p>Willingness to learn, adapt, and continuously develop technical expertise</p></li><li><p>Ability to work both <b>independently and as part of diverse, cross‑functional teams</b></p></li></ul><p></p><p><b>Nice to Have</b></p><ul><li><p>Hands‑on experience with <b>drug product technology transfer and/or process validation</b></p></li><li><p>Experience using <b>statistical tools or digital quality systems</b> in a regulated environment</p></li></ul><p></p><div><p><b><span>What You Get</span></b><span> </span></p></div><ul><li><p><span><span><b>Organized transport</b> to and from the site</span></span><span> </span></p></li><li><p><span><span>Work with<span> </span><b>modern automated systems </b></span></span><b><span> </span></b></p></li><li><p><b><span><span><span>Strong education</span><span> </span>program </span></span><span> </span></b></p></li><li><p><span><span><span>Christmas, Easter</span><span> </span>and holiday<span> </span><b>bonus</b> </span></span><span> </span></p></li><li><p><span><span>Affordable meals in an<span> </span><b><span>on-site cafeteria </span></b></span></span><b><span> </span></b></p></li><li><p><span><span>Opportunities for<span> </span><b><span>career enhancement</span><span> </span>and development</b> </span></span><span> </span></p></li><li><p><span><span>Yearly<span> </span><b>pay increase</b><span> </span>and<span> </span><b>bonus</b> based on performance</span></span><span> </span></p></li><li><p><span><span>Further professional development in a<span> </span><b><span>supportive environment </span></b></span></span><b><span> </span></b></p></li><li><p><span><span><b>Free psychotherapy and coaching</b><span> </span>sessions for employees and people close to them</span></span><span> </span></p></li><li><p><span><span>Bravo<span> </span><b>employee recognition</b><span> </span>system </span></span><span> </span></p></li><li><p><span><span>Opportunity<span> </span><span>for working on</span><span> </span>projects with other<span> </span><b>Pfizer sites and locations </b></span></span><b><span> </span></b></p></li><li><p><span><span><b>Free fruit and hot beverages<span> </span></b>on the site</span></span><span> </span></p></li></ul><p></p><p><b>Why Pfizer</b></p><p>At Pfizer, you will find a culture grounded in <b>integrity, quality, and respect for people</b>. We empower colleagues to <b>own their careers</b>, grow their capabilities, and make a meaningful impact through their work.</p><p>As part of the Technical Services &amp; Validation team, you will collaborate with <b>passionate, knowledgeable colleagues</b> locally and globally, contributing to innovative solutions that support reliable manufacturing and patient safety.</p><p>  <br />Work Location Assignment: Hybrid</p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Engineering<p></p><p></p>