Netherlands Job Openings

Kite Pharma

QC Associate

Hoofddorp

FULL TIME

November 29, 2024

Job Description

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.

Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.

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 Gilead and help create possible, together.

Job Description

About Kite Pharma, A GILEAD Company
Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors.

Kite Europe is currently adding additional talent as it focuses on developing the European Region in support of providing maximum access to patients with unmet needs. We’re a state-of-the art manufacturing site in the Netherlands (Amsterdam-Hoofddorp).

We’re currently seeking to recruit highly motivated talents for different positions, to join us and be part of our exciting journey in the development of innovative cancer immunotherapies and their translation to the treatment of patients with cancer.

Department Description
As QC Analytical associate you’ll be joining a team in which people of all backgrounds and experiences are respected, and where working together focused on saving lives, by finding the cure for cancer, is a daily activity.

You’ll be reporting to the Team lead QC Analytical.

In this role, you will analyze all kinds of samples (raw material and final product samples). Due to the nature of the treatment this role requires high level of proficiency and ownership of the process, with a high skill level of aseptic techniques. For a more extensive understanding of the responsibilities please see below.

Your new role
  • Perform testing of raw material and final product samples
  • Review test results
  • Assist in conducting lab investigations regarding out of specifications (OOS) results deviations related to QC Analytical or Incoming goods procedures
  • Troubleshoot instrumentation
  • Participate in routine maintenance of lab equipment and lab spaces
  • Participate in waste management and perform other duties as required

About you
  • MBO/HBO degree in Analytical Chemistry/ Molecular Biology or equivalent.
  • Previous experience in QC environment in the Biotech and/or Pharmaceutical Industry is a plus.
  • Familiarity with Molecular Biology, Analytical and/or Biochemical testing techniques required in determining the quality and efficacy of parenteral products, preferably with reference to cell therapy products (e.g. ELISA/ q PCR/ dd PCR/ Cell culture / western blotting).
  • Working Knowledge of c GMP, GLPs, Pharmacopoeia, regulatory requirements for testing and validation pertaining to the Pharmaceutical Industry is a pre.
  • Strong interpersonal, verbal and written communication skills are essential in this collaborative work environment.
  • Ability to be flexible to work in shifts, flexible with your schedule, and work overtime as needed

For jobs in the United States:
As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact careers@gilead.com for assistance.
For more information about equal employment opportunity protections, please view the ‘Know Your Rights’ poster.
NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT
PAY TRANSPARENCY NONDISCRIMINATION PROVISION

Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.
Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.

For jobs in France:
Conformément à la Loi « Informatique et Libertés » (06/01/78), nous vous informons du fait que les données personnelles renseignées pourront faire l'objet d'un traitement informatique par Gilead et pourront être transmises aux Organismes Sociaux. Par ailleurs, vous disposez d'un droit d'accès, de rectification et de suppression des données vous concernant. Vous pouvez exercer ce droit en contactant: France Data Privacy@gilead.com

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