QA Officer at Eurofins

Leiden, South Holland, Netherlands -

Full Time

Start Date

Immediate

Expiry Date

17 Feb, 26

Salary

0.0

Posted On

19 Nov, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Assurance, GMP, ISO, Documentation Control, Audits, Training, Compliance, Change Control, Deviation Management, OOS Management, CAPA, Biopharmaceuticals, Biotechnology, Chemical Testing, Physical Testing, Regulatory Requirements

Industry

Medical and Diagnostic Laboratories

Description

Company Description Eurofins PROXY is part of the internationally operating Eurofins Scientific. We are the largest Dutch GMP Quality Control laboratory for the pharmaceutical industry. Eurofins PROXY specializes in chemical and physical testing for (bio)pharmaceutical raw materials, intermediates and final products, and offers a very diverse package of analytical testing methods for national and international clients within the (bio)pharmaceutical industry. Are you a quality-driven professional with an eye for detail and a passion for pharmaceutical processes? Then we are looking for you! For our location in Leiden, we are seeking a motivated QA Officer to strengthen our quality team. Job Description As a QA Officer, you are responsible for ensuring quality within our laboratory and operational processes. You will work according to GxP, ISO, and internal quality standards and play a key role in documentation control, audits, training, and compliance. Your responsibilities include: Manage and assess deviations, changes, complaints, OOS, and CAPA in accordance with GMP guidelines. Maintain and monitor the change control and deviation systems. Perform routine quality assurance tasks according to SOPs and quality standards. Contribute to the assurance of the quality system based on regulatory requirements (and implementation of regulatory changes). Participate in QA system initiatives and improvement projects. Train personnel on GMP and quality procedures. Conduct (internal) audits and support external inspections (e.g., by regulatory authorities). Execute, report, and follow up on self-inspections. Create and revise QA procedures and work instructions. Maintain the GMP documentation system and archive, including electronic systems. Support the creation, review, or updating of QA agreements. Manage documentation and compliance related to opiates and precursors. Oversee the implementation of new equipment from a QA perspective. Ensure compliance in equipment metrology, including documentation. Review pest control reports and other facility-related quality documents. Qualifications Bachelor’s degree or above in (bio) Chemistry, Biotechnology, (bio) Pharmacy, (molecular) Biology or related field -OR- a MBO degree with at least 3 years of experience. Minimum of 1 year of experience in the (bio)pharmaceutical industry. Minimum of 1 year of experience in a quality oriented environment (GMP / GLP / ISO). Organized, structured and accurate. High quality awareness. Proactive and customer orientated team-player. Fluency in Dutch or English; knowledge of both is preferred. Knowledge of GMP quality system and regulatory requirements (Eudralex, ICH). Knowledge of biological process development and manufacturing is preferred. Located in the Netherlands within reasonable distance of our site in Leiden. Additional Information PROXY and Eurofins: A world of possibilities This position is based at Eurofins PROXY on the Bio Science Park in Leiden. We have a close-knit team where collegiality and collaboration come first. We offer a responsible and challenging position within the team with room for your own ideas and input. Eurofins PROXY also offers: A competitive salary; Flexible working hours; 25 days of vacation with the option to purchase 7 additional days (based on a fulltime contract); Travel allowance of 23 cents net per kilometer. Are you traveling by public transport? Then your travel expenses will be fully reimbursed via NS Business Card; Participation in a pension scheme with 50% contribution by Eurofins; Each month, you accumulate a choice budget balance of 8.5% of your gross salary. This includes, among other things, holiday pay and a year-end bonus. You can choose to have this amount paid out, or you can use it to buy extra days off, for example. You choose what suits you best; Discount on additional health insurance; Tax benefit via FiscFree when purchasing various products and services via your gross salary, such as a bicycle, sports contribution, fitness, mobile telephony, computers & tablets or a weekend away; Professional training and opportunities for training and development; Training options via the online learning platform Good Habitz. Working at Eurofins PROXY offers you the flexibility and personal touch of working in a medium sized and dynamic company, whilst also allowing you to benefit from having Eurofins as a parent company. Our ambitious growth plans provide ample opportunities for our employees: Diverse developmental opportunities within the organization; A large client portfolio ensures a lot of diversity in your work. More about Eurofins Scientific Eurofins Scientific is an international life sciences company, which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the leading global emerging players in specialty clinical diagnostic testing. Eurofins employs approximately 63,000 people worldwide, spread across 950 state-of-the-art laboratories, and is active in 60 countries with a pro-forma turnover of €6,951 million in 2024. Eurofins has strong growth ambitions (CAGR 24%) with, in addition to very strong autonomous growth through its own start-ups, a large number of acquisitions every year. Would you like to know more? For questions regarding the position, please follow the link below ‘I’m interested’ in order to contact the hiring manager. Acquisition for this vacancy is not appreciated.

Responsibilities

As a QA Officer, you will ensure quality within laboratory and operational processes, working according to GxP, ISO, and internal quality standards. Your role includes managing deviations, conducting audits, and training personnel on GMP and quality procedures.