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Quality Assurance Technician – France (Occitaine) – Cohesive and Family-sized Company – Competitive Salary.

Annual-performance-bonusCity-locationSalary-above-industry-standard

The Company

Our client is a fast growing CDMO in the cell manufacturing industry. They are deeply committed to creating innovative cell therapies to address unmet medical needs.

Their goal is to provide cutting-edge, life-saving cell treatments to patients, giving them new hope. Their key strengths are their ability to respond swiftly to changing market conditions and provide our customers with great levels of personalisation.

You will be responsible for the entire administration of the pharmaceutical quality system while reporting to the Pharmacist in Charge (PR) in the Quality Assurance Department (documentation, quality events, audits, training).

The Role

  • Participate in pharmaceutical quality events such as deviations and CAPA, as well as the development of innovative cell therapies.

  • The work entails managing and developing quality documentation in accordance with the Good Manufacturing Practices (GMP) guidance, which includes updating, revising, disseminating, monitoring, and archiving current documentation.

  • Participate in the on-site inspection and revision of production and quality control documents for batch certifications.

  • Aid in the planning of client audits and Health Authority inspections.

You

  • You have a Bac + 3 in Quality, Health, Safety, and the Environment (QHSE) and experience in quality assurance or control in regulated industries such as pharmaceuticals and agri-food.

  • You have a 1st experience as a quality assurance technician or quality control technician;

  • You have worked in a certified organisation and are knowledgeable about Quality Management System standards such as ISO 9001, ISO 13485, and GMP guidelines.

  • You are proficient in Office software;

  • You are a team player and adaptable, you want to discover the diverse missions of Quality Assurance in an innovative biotech.

  • Someone who is keen to be part of a company with a cohesive and family feel ; a company with clear goals and accomplishments to be made.

What should you do next?

This QA Technician role is one not to be missed; it encompasses the opportunity to work with a promising CDMO. To discuss this role further or to find out about other roles I’m currently working on, please get in touch or hit apply to submit your current CV.

Unless otherwise stated, if applying for a job within the UK or European Union, you must ensure that you are already authorised to work there.

Carrot Recruitment acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.

We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, colour, sex, age, national origin, religion, sexual orientation, gender identity and/or expression.

If there are any arrangements or adjustments we can make to assist you at interview then please let us know and we'll be more than happy to assist.

 

Apply Now!

Job Consultant

Enzo Bagmanian

Regulatory, Quality & PV

Recruitment Consultant

+44 (0) 2393 874 292

enzo@carrotpharma.co.uk

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