qa officer

Capijob; Bretagne; Sur place; EUR 45 000 - 60 000; Plein temps

Résumé du poste

A leading global provider in biopharma seeks a Quality Assurance Operator to join their team in Bretagne. You will ensure compliance with quality standards and manage QA activities in a chemical manufacturing context. The ideal candidate has a background in applied sciences or engineering and proficiency in quality management systems like GMP and ISO. A competitive salary and benefits including insurance and bonuses are offered.

Prestations

Competitive salary package

Hospital and group insurance

Luncheon vouchers

Bonus scheme

Flexible time system

Holiday plan

Qualifications

• Experience in quality assurance within biopharma or chemical industries.
• Strong understanding of regulatory compliance in GMP and ISO standards.

Responsabilités

• Implement quality assurance standards compliant with GMP and ISO.
• Plan and supervise testing and inspection of materials and products.
• Develop and supervise corrective and preventive actions.

Connaissances

Knowledge about ISO Quality Management standards and/or GMP

Chemical background

Proficient in English and Dutch

Ability to nurture partnership and teamwork

Formation

Master or Bachelor in applied sciences or engineering

Outils

MS Office suite (Excel, Word, PowerPoint, Access)

SAP

Description du poste

Overview

Société : VWR International GmbH, part of Avantor

We set science in motion to create a better world and have done so for over 100 years. Through our diverse and passionate global workforce of 14,000+ professionals – we've become a trusted provider of mission-critical products and services to customers in the biopharma, healthcare, education & government, and advanced technologies & applied materials industries. If you want to help us solve the world's most complex challenges and join an inclusive community that supports your career development – you belong here, with us. Apply now and help us forge new paths to create a better world.

Position Overview: Avantor, a leading global provider of products and services to customers in the biopharma, healthcare, education & government, and advanced technologies industries, is looking for a Quality Assurance Operator Private Label Chemicals to join the team in Leuven! Reporting to the Manager Quality Assurance Chemical Manufacturing in Belgium and together with your colleagues, you will be responsible for QA activities within the VWR Chemicals area of VWR International, part of Avantor and this linked to laboratory activities.

Responsibilities

• Interpret and implement quality assurance standards to assure compliance with GMP, ISO 9001, (ISO 13485) and ISO 17025/34 and industry regulatory requirements.
• Draft quality assurance policies, procedures, work instructions and supporting documentation in accordance with the VWR International policy, Legal Environmental & Safety regulation, ISO14001 and OHSAS18001.
• Interact with company management, internal departments, and other sites to successfully implement and maintain Quality Systems and the accompanying document management systems.
• Evaluate adequacy of QA standards, review the implementation and efficiency of quality and set up inspection systems.
• Plan, conduct and supervise testing and inspection of materials and products to ensure finished product quality.
• Devise sampling procedures and directions for recording and reporting quality data.
• Collect, compile and analyze statistical quality data to identify areas for improvement in the quality system.
• Prepare reports to communicate outcomes of quality activities.
• Investigate customer complaints and/or non-conformance issues.
• Develop, recommend and supervise corrective and preventive actions.
• Evaluate and/or approve changes to product/equipment specifications and processes.
• Identify training needs and coordinate training interventions to meet quality standards.
• Perform and document internal audits and other quality assurance activities.
• Coordinate and/or support on-site audits conducted by third parties and regulatory agency inspections.
• Evaluate audit/inspection findings and implement appropriate corrective actions.
• Implement and supervise risk management activities.
• Ensure up to date batch records, review and approve completed batch record, analysis forms and other related production records, and complete the release of non-GMP products, support release of GMP licensed products by the Qualified Person.
• Ensure the calibration of premises and equipment.
• Regularly connect with the production team, QA, QC and Supply Chain responsible to find opportunities for quality and efficiency improvement.

Qualifications

• Experience Required: Master or Bachelor in applied sciences or engineering.
• Knowledge about ISO Quality Management standards and/or GMP.
• You have a chemical background.
• Ability to nurture partnership and teamwork across internal functions.
• Proficient in English and Dutch both written and spoken; French on an equivalent level would be helpful.
• Proficient in MS Office software, Excel, Word, PowerPoint, Access and SAP.

Further Information

We offer the opportunity to work in a multifaceted environment where collaboration is key. Next to a competitive salary package in line with your qualifications and experience we offer hospital and group insurance, luncheon vouchers and a bonus scheme. Avantor's flexible time system and holiday plan allows for a phenomenal work-life balance.

Avantor Sciences is an Equal Opportunity Employer. The collective talents and perspectives of our associates drive the good we create in the world – and why we are focused on building a diverse, equitable and inclusive culture. Ensuring every associate is empowered to grow, succeed and shape our evolving culture.

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