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(Sr) Process Engineer - MSAT

Geplaatst 1 apr. 2025
Delen:
Werkervaring
5 tot 10 jaar
Full-time / part-time
Full-time
Functie
Soort opleiding
Taalvereiste
Engels (Vloeiend)

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Join Kite in the Fight Against Cancer

We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet.

Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows.

Job Description

We are looking for a motivated (Sr) Process Engineer to join our Life Cycle Engineering (LCE) team within the Manufacturing Science and Technology (MSAT) department.

In this role, you will provide technical expertise for pharmaceutical products, supporting cross-functional projects focused on continuous improvement and technology transfer.

This position requires a strong background in pharmaceutical manufacturing and offers the chance to collaborate with global teams to drive process optimization and ensure product quality in a fast-paced, evolving environment.

Responsibilities:

  • Lead and support the evaluation and implementation of continuous improvement projects, innovative technologies, and process automation, ensuring seamless implementation of new products and technologies in manufacturing.
  • Advanced understanding of process development, validation, and lifecycle management to support comparability studies, process validation, and licensure changes.
  • Act as primary contact on behalf of pillar for global organizations and site manufacturing, assisting in maintaining alignment and fostering operational excellence.
  • Design and oversee development studies, author and review protocols, reports and technical documentation for process characterization and validation studies. Including, executing process development studies for continuous improvement projects, deviation root cause analysis and new pipeline introductions.
  • Provide process development support as a representative of MSAT for the manufacturing site.
  • Collaborate with technical and operational stakeholders to draft, review, and finalize compliance and GMP documentation with a focus on advanced technical writing.
  • Author impact assessments and root cause analysis for complex deviations to maintain routine manufacturing operations and determine appropriate CAPA for manufacturing.
  • Represent the site MSAT function in global change management initiatives.
  • Facilitate risk assessments and implement remediation measures to support manufacturing improvements.
  • Act as a Subject Matter Expert (SME) for defined stages of lifecycle management, ensuring product and process quality as well as compliance, and providing support during regulatory inspections.
  • Deliver technical and scientific training.
  • Contribute to MSAT's strategic objectives and provide mentorship to junior engineers, fostering their growth and development.
  • Serve as delegate for the manager during periods of absence, ensuring continuity in leadership and operations.

Requirements:

  • Education: Bachelor’s degree in Biochemical Engineering, Chemical Engineering, Biotechnology, or a related field. A Master's in a relevant discipline is a plus.
  • Experience: Minimum of 5+ years of experience in a pharmaceutical operations or GMP environment with proven expertise in cell culture, cell therapy, and aseptic processing.
  • Technical Expertise: Strong knowledge of cGMP compliance, root-cause analysis, process development, and life cycle management. Experience with molecular biology, immunology, and virology is highly desirable.

Skills:

  • Advanced problem-solving skills with the ability to manage and develop solutions to complex technical challenges.
  • Advanced communication and interpersonal skills, with the ability to work cross-functionally.
  • Advanced skill in project management, quality systems, and risk management.
  • Ability to work independently and manage multiple priorities in a fast-paced environment.
  • Able to put lean principles and continuous improvement methodologies into practice.
  • General knowledge in digitalization and data automation tools.

Join us in this impactful role and be a driving force in the development and optimization of cutting-edge pharmaceutical products. If you're passionate about innovation, quality, and improving patient outcomes, we want to hear from you!

About Us

Change The World With Us

Everyone at Kite is grounded by one common goal – curing cancer. Every day, we aim to establish a direct line between that purpose and our day-to-day work.

We are creating Kite together, with the recognition that the best teams are built by the best people. We maintain an attitude of curiosity, and creativity with each challenge as we develop a new market for cancer therapies. We appreciate and respect one another, and most importantly, we don’t take success for granted.

While we’ve come a long way to make what others viewed as impossible, possible, we know one thing is certain. Today is just the beginning.

Equal Employment Opportunity (EEO)

It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual’s gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.

For the past three decades, members of our team have been at the forefront of cancer immunotherapy. Today, we are a leader in engineered T cell therapy, changing the paradigm of cancer treatment with what is potentially the biggest breakthrough since the introduction of combination chemotherapy more than 60 years ago.

Farmaceutisch
Hoofddorp
2.000 medewerkers