The Role

We are looking for a Quality Control Analyst for our Quality Control department in Almere.

The Quality Control Analyst will be part of a team focused on improving overall quality, efficiency and effectiveness of the Quality Control department and will perform QC testing in accordance with written procedures.

The Quality Control Analyst will also take part in batch record review. You will also support the departments Operations and QA by analyzing, reporting and trending data, relevant to production and projects were applicable.

About Sinclair

Sinclair is a global aesthetics company. Our differentiated product portfolio offers complementary technologies, and our products are experiencing significant growth as we target clinical demand for effective, high quality, longer duration, natural looking and minimally invasive treatments.

Headquartered in London, UK, we directly employ over 500 people worldwide, operating out of administration offices in Chester, Barcelona, and Paris, and with commercial operations based throughout Europe, Asia, and the Americas.

This is a great time to join Sinclair as we continue to increase our product range and expand into new markets and territories.

The Role

Responsibilities:

• As a Quality control analyst, you will play an important role within the company, so you’ll be responsible for many things Including:

• Performs analysis / techniques according to authorized SOP’s.
• Operates apparatus needed
• Prepares reagents / reference substances were applicable
• Reading out all environmental / bioburden results of cleaning steps and aseptic work
• Documents all data required and accumulated raw data in applicable batch records / forms / digital datasheets
• Perform batch record review
• Correct maintenance of QC equipment and environment
• The QC-laboratory (stock, cleanliness, etc)
• Keeping relevant SOP’s (e.g apparatus, Test procedures) up to date
• Keeping personal training file up to date
• Correct execution of described tasks
• Reports any non-conformity (Results, SOP’s, apparatus etc.) to QC manager.

Your Skills & Experience – Do You Have What it Takes?

A bit about you – do you fit this description?

• Can work accurately.
• Has a high quality awareness.
• Team player and can work independent

Good communication skills

Desirable experience:

• Finished MLO ( niveau 3 or 4)
• Experience in working in a Quality Control department desirable
• English and Dutch speaker and writer.
• Preferably experience in working with a Quality Management System (preferably in a medical device production environment).
• Preferably experience with batch record review

What we offer

We have a real focus on developing our people, and by fostering an entrepreneurial culture, we encourage flexibility, accountability and autonomy. The company is full of opportunity for those who wish to grasp it. Our people thrive on engagement, development and a varied workload. You will often be included in projects that require you to collaborate cross-functionally.

We also offer:

• A competitive salary
• A 13th month
• 25 vacation days
• 8% holiday pay
• Travel allowance based on €0,19 per kilometre
• Retirement savings plan

This is an exciting opportunity to join a successful company, with big ambitions for the future.

If this sounds like you and you meet the requirements, please apply, we would love to hear from you.

Soort dienstverband: Voltijds

Salaris: €2.500,00 - €3.200,00 per maand

Aanvullende vergoedingen:

• 13e maand
• Vakantiegeld

Arbeidsvoorwaarden:

• Pensioen

Werkschema:

• Dagdienst
• Elk weekend
• Enkel weekenden
• ma-vr
• Overwerk
• Ploegendienst
• Weekendbeschikbaarheid

Ervaring:

• Quality: 1 jaar (Gewenst)