Technical Writer GMP

3 weken geleden

Geleen, Limburg, Nederland Oxford Global Resources Voltijd

Do you have experience in quality assurance under GMP and a strong background in technical writing? Are you looking for a dynamic role in an international and inspiring environment?

Job Description
As a Technical Writer, you will be responsible for investigating deviations, conducting root cause analyses, and implementing CAPAs (Corrective and Preventive Actions) within a cGMP environment. You will collaborate with various departments, including QA, Manufacturing, Supply Chain, and QC.
The primary focus of this role is writing SOPs and addressing comments to ensure compliance and efficiency in procedures.

Responsibilities:

  • Monitor timelines for deviations and events while ensuring effective communication between departments.
  • Conduct in-depth investigations to identify root causes and propose corrective actions.
  • Drive process and procedural improvements.
  • Support the team with the submission of change controls, investigations, and CAPAs.
  • Review and create SOPs to maintain compliance with regulatory standards.

Requirements:

  • Bachelor's degree in Science, Pharma, or Logistics.
  • 2-5 years of experience.
  • Experience in quality assurance under GMP regulations.
  • Strong organizational and problem-solving skills.
  • Ability to work in a fast-paced environment and manage multiple priorities.
  • Excellent written and verbal communication skills.

Benefits:

  • A diverse, challenging role with various QA responsibilities.
  • Interaction with multiple departments within a large organization.
  • Salary range: €2500 - €3500 per month.
  • Long-term assignment.
  • Location: Sittard.
  • Employment type: Temporary role; until the end of March.
  • Language: English.

Would you like to contribute to process improvements in a regulated environment? Apply today

  • Technical Writer

    2 weken geleden

    Geleen, Limburg, Nederland Panda International Voltijd

    Are you an experienced investigator passionate about quality and compliance in a cGMP environment? We seek a Technical Writer – Deviation Investigator to join our leading CMO. In this role, you will be responsible for initiating and leading investigations into process deviations, identifying root causes, and implementing corrective actions to prevent...

  • Technical Writer

    2 weken geleden

    Geleen, Limburg, Nederland Panda International Voltijd

    Are you an experienced investigator passionate about quality and compliance in a cGMP environment? We seek a Technical Writer – Deviation Investigator to join our leading CMO. In this role, you will be responsible for initiating and leading investigations into process deviations, identifying root causes, and implementing corrective actions to prevent...

  • Sr. Technical Expert QC

    4 dagen geleden

    Geleen, Limburg, Nederland Lonza Voltijd

    Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small,...

  • MSAT Bioprocess Engineer mRNA

    7 dagen geleden

    Geleen, Limburg, Nederland Lonza Voltijd

    Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there is no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small,...

  • Biotech Associate

    1 week geleden

    Geleen, Limburg, Nederland Lonza Voltijd

    Biotech AssociateLocation: GeleenAre you a fresh graduate with a Technical/Vocational degree (MBO4/HBO) in Biotechnology, Biology, or a related field? Do you want to work in an innovative environment where you contribute to the production of cell therapy products?As a Biotech Associate at Lonza, you will be responsible for the execution of cell therapy...

  • Biotech Associate

    7 dagen geleden

    Geleen, Limburg, Nederland Lonza Voltijd

    Posted Job Advert Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big...

  • CSV Specialist

    6 dagen geleden

    Geleen, Limburg, Nederland Lonza Voltijd

    CSV Specialist Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big...

  • Technical Writer GMP regio Geleen

    3 weken geleden

    Geleen, Nederland Oxford Global Resources Voltijd

    Do you have experience in quality assurance under GMP and a strong background in technical writing? Are you looking for a dynamic role in an international and inspiring environment? Job Description As a Technical Writer, you will be responsible for investigating deviations, conducting root cause analyses, and implementing CAPAs (Corrective and Preventive...

  • Technical Writer

    4 weken geleden

    Geleen, Nederland Panda International Voltijd

    Are you an experienced investigator passionate about quality and compliance in a cGMP environment? We seek a Technical Writer – Deviation Investigator to join our leading CMO. In this role, you will be responsible for initiating and leading investigations into process deviations, identifying root causes, and implementing corrective actions to prevent...

  • Technical Writer

    4 weken geleden

    Geleen, Nederland Panda International Voltijd

    Are you an experienced investigator passionate about quality and compliance in a cGMP environment? We seek a Technical Writer – Deviation Investigator to join our leading CMO. In this role, you will be responsible for initiating and leading investigations into process deviations, identifying root causes, and implementing corrective actions to prevent...

  • Technical Writer

    3 weken geleden

    Geleen, Nederland Panda International Voltijd

    Are you an experienced investigator passionate about quality and compliance in a cGMP environment? We seek a Technical Writer – Deviation Investigator to join our leading CMO. In this role, you will be responsible for initiating and leading investigations into process deviations, identifying root causes, and implementing corrective actions to prevent...

  • Logistic Associate, Production Support

    3 dagen geleden

    Geleen, Nederland public.client.lonza.display.name Voltijd

    Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small,...

  • Production Associate

    4 weken geleden

    Sittard-Geleen, Nederland Panda International Voltijd

    We are looking for a Production Support Associate for our major pharmaceutical client in Geleen. They are responsible for executing activities in and around the cleanroom, ensuring process/run preparation, inventory management, and maintenance of the cleanroom for the manufacturing of cell and gene therapy products.This role supports a GMP-compliant...

  • Production Associate

    4 weken geleden

    Sittard-Geleen, Nederland Panda International Voltijd

    We are looking for a Production Support Associate for our major pharmaceutical client in Geleen. They are responsible for executing activities in and around the cleanroom, ensuring process/run preparation, inventory management, and maintenance of the cleanroom for the manufacturing of cell and gene therapy products. This role supports a GMP-compliant...

  • Production Associate

    3 weken geleden

    Sittard-Geleen, Nederland Panda International Voltijd

    We are looking for a Production Support Associate for our major pharmaceutical client in Geleen. They are responsible for executing activities in and around the cleanroom, ensuring process/run preparation, inventory management, and maintenance of the cleanroom for the manufacturing of cell and gene therapy products.This role supports a GMP-compliant...