Quality Assurance Consultant

2 weken geleden

Oegstgeest, Zuid-Holland, Nederland Unique Voltijd
Wat ga je precies doen

As a quality assurance consultant, you will contribute to safeguarding the integrity of our pharmaceutical products and processes. You'll tackle the challenge of maintaining the highest standards of quality control, working closely with cross-functional teams to ensure compliance and excellence. Your expertise in GMP environments, coupled with a proactive approach, will be pivotal in upholding our commitment to delivering safe and effective treatments. We value your problem-solving skills, attention to detail, and ability to thrive in a dynamic setting.

Responsibilities:

  • Oversight: maintain strict control over incoming goods, materials, and equipment, ensuring alignment with our quality standards.
  • Collaboration: work alongside QC and manufacturing teams to manage the equipment lifecycle and material quality.
  • Quality systems: review and approve QMS records and documents, playing a key role in upholding our quality assurance framework.
  • Point of contact: serve as the go-to quality assurance consultant for system implementations within the QC Cell Tech Operation.
  • Vendor relations: engage in supply chain management, including material and vendor qualifications, to ensure the integrity of our products.
Wat bieden we jou

Embark on a journey where your professional aspirations are nurtured and your well-being is paramount. We offer a suite of benefits tailored to enhance your life both inside and outside of work.

  • Temporary contract with potential for extension
  • Full-time position, 40 hours per week
  • Engagement in diverse, growth-oriented projects
  • Collaborative culture with a focus on contribution
  • Comprehensive support in the pharmaceutical field
Functie-eisen

Seeking a dedicated Quality Assurance Consultant with a robust scientific background and a proactive approach to quality management.

  • Master's in life science or related field
  • Minimum 3 years in GMP regulated environment
  • Proficient in QMS documentation and processes
  • Experience in cell therapy
  • Good stakeholder management
  • Strong problem-solving and critical thinking
  • An eye for detail and work accurately
  • Has a supportive quality mindset and drive knowledge sharing
  • Result-driven and a pro-active, can-do mindset
  • Fluent in English, Dutch proficiency beneficial
Over het bedrijf

Welcome to a pioneering biotechnology company with a presence across Europe and the U.S. Our mission is to innovate and develop groundbreaking medicines that significantly improve lives and the quality of life. At the company, we are dedicated to addressing unmet medical needs through a combination of cutting-edge science, advanced technology, and a spirit of collaboration. Our diverse portfolio includes novel small molecules, CAR-T therapies, and biologics, primarily focusing on oncology and immunology. With a full spectrum of capabilities extending from the laboratory to the patient, and a unique decentralized CAR-T manufacturing network, we are not just part of the industry; we are at the forefront of reshaping it. Join us in our quest to deliver substantial outcomes for patients, our team, and our shareholders, all while working in an accessible location that supports your professional journey.

The Team

Step into a team where diversity is not just embraced but celebrated. Our collaborative culture is the bedrock of our success, bringing together a wealth of expertise and experience. Here, every team member is valued for their unique contributions. We foster an environment of mentorship and professional growth, ensuring that you have the support to excel and the opportunity to lead. Our team is a testament to what can be achieved when passion meets purpose, and we are looking for someone who is ready to contribute to our collective success.

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