Lab Manager, Genomics

CellCarta

Visualizza: 120

Giorno di aggiornamento: 07-11-2025

Località: Antwerp City Antwerp

Categoria: R & D IT - Software

Industria: Internet Publishing

Posizione: Mid-Senior level

Tipo di lavoro: Full-time

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Contenuto del lavoro

Lab Manager - Genomics

Are you a seasoned laboratory professional with a strong background in scientific experimentation and team leadership? We are seeking a Lab Manager to join our Wilrijk, Antwerp team and play a pivotal role in managing our laboratory operations.

In this position, you will oversee laboratory activities, including quality and regulations, day-to-day laboratory functions, and assay transfers. Your responsibilities will extend to people management, as you’ll lead and mentor a team of laboratory technologists. Your expertise will contribute to the optimization of operational efficiency, quality assurance, and safety protocols. If you’re a highly organized, results-driven, and collaborative laboratory professional, we invite you to join our team and make a significant impact on the future of patient therapy.

Main Responsibilities

Laboratory management

  • Have insight in the main objectives of protocols and experiments and make recommendations for technical improvements and follow up of assays.
  • Support the transfer of assays to the starLIMS workflow in close collaboration with data management, starLIMS team and project management.
  • Provide assistance in transferring protocols to other CellCarta sites.
  • Assist in optimizing operational efficiency, use of resources and project lead times.
  • Organize and participate in customer visits and audits.
  • Assists with the organization and prioritization of workload in order to meet project goals.
  • Maintain a strong collaboration with other departments to harmonize processes and work flows.
  • Coordinate, plan, prepare, perform and report complex scientific experiments.

People management

  • Technical management and coaching of a team of 15 laboratory technologists.
  • Conducting competence evaluations and perform performance and evaluation interviews.
  • Organize and documenting internal and external training courses.

Quality and safety

  • Develop SOPs and other applicable guidelines in accordance with the QMS
  • Monitoring of the quality system in collaboration with the quality and regulatory department
  • Provide (technical) support for laboratory equipment, stock management and order tracking

Qualifications And Skills

  • Bachelor or Masters with extensive experience in a highly regulated lab.
  • Excellent people management skills with proven experience in a coordinating/people management role.
  • Thorough understanding of relevant technology and technical/scientific field.
  • Work very independently.
  • Great communication and organizational skills.
  • Result oriented, creative and analytical thinker with a problem-solving mindset.
  • Scientific integrity and eager to learn/assimilate novel concepts.
  • Excellent documentation skills.
  • Dynamic personality, a true team player with good interpersonal skills.
  • Able to work under pressure.
  • Language skills: Advanced knowledge, orally and in writing of English, and knowledge of Dutch.
  • PC skills: in depth knowledge of MS Office, LIMS system(s), relevant software tools for data analysis, equipment operations, etc.

What can we offer

  • A dynamic and rapidly changing global environment allowing personal growth
  • A company that is fit for the future
  • A competitive salary and benefits
  • A great team you can work with

About CellCarta

CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 1000 employees in its 11 facilities located in Canada, USA, Belgium, Australia, and China.

Join us as we make an impact on the future of patient therapy!

The information collected to review your application will be processed by the human resources services of CellCarta Biosciences Inc. and its affiliates (collectively, “CellCarta”). The legal basis for this processing is the legitimate interest of CellCarta to evaluate the suitability of candidates for the roles available at CellCarta.

CellCarta will only process that information which is necessary to evaluate your application. This information includes identifying information such as your name, address, email address and phone number, as well as information about your education and professional experience, including previous positions and your CV. Such information is required for us to complete your applicant file, assess your suitability for the role and comply with applicable laws. CellCarta may obtain personal information from other sources, such as during reference, background, or employment checks, with your permission, and from third party sources such as recruitment and assessment sites or professional social media sites, in each case only if such information is relevant to reviewing your application. Your personal information will be retained only for so long as reasonably necessary and in accordance with applicable laws. This information will be processed confidentially and only accessed by those who have a need for the recruitment process. Please note that the information comprising your applicant file may be processed in a country that is not where you are located (for example, you might be in the European Economic Area or Québec, Canada, whereas your applicant file may be reviewed by CellCarta in the United States). If you are offered and accept employment with CellCarta Biosciences Inc. or one of its affiliates, the information collected will become part of your employment record. If you do not want us to retain your information, or want us to update it, please contact

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Scadenza: 22-12-2025

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