Sinclair is Hiring! Join Our Team as a Quality Control Specialist
We are currently recruiting for Quality Control Specialist at our Almere office in the Netherlands. The Quality Control Specialist is responsible for performing quality control testing on intermediate and final products in accordance with Standard Operating Procedures (SOPs), with in-depth technical knowledge across chemical, physical, and microbiological test methods. The Specialist supports method development and validation activities, coordinates weekly planning for the QC department in the absence of the Supervisor, and provides technical input into Corrective and Preventive Actions (CAPAs), including root cause investigations.
The ideal candidate will have MBO diploma in relevant field (Chemistry, Biology, Life Sciences) and is proficient in English and Dutch.
Location: De Strubbenweg 17, 1327 GB, Almere
About Sinclair
Founded in 1971, Sinclair is a global medical aesthetics organisation, that delivers an extensive product range. With an in-house commercial infrastructure, including manufacturing and a network of distributors in leading global markets, our products are sold in 55 countries worldwide.
This is a great time to join Sinclair as we continue to increase our product range and expand into new markets and territories.
Act with Integrity Consistently doing the right thing even when it’s the hard choice; 100% Compliance with all rules, standard operating procedures and guidelines
Results-Driven Make a business impact in all you do, whether sales, efficiency, operational excellence; it should make a meaningful impact
Innovation-Centered Redefining Aesthetics, we must be pioneering in how we do business; this can be in products, in service models, or strategy
One Company, One Goal Working towards unified mission, we are all Sinclair and be seen by customers as one company in every way
Own It! Be Accountable for your decisions, actions and consequences; Be Reliable to your customers and colleagues
[List the key responsibilities from the job description]
Testing & Technical Execution
Perform QC testing (chemical, physical, microbiological) in full accordance with SOPs
Maintain deep technical knowledge of measurement methods and the theoretical background of assigned analyses
Perform sampling and intake of raw materials/incoming goods, and release them in the ERP system
Troubleshoot and resolve technical issues related to QC equipment or testing procedures
Method Development & Quality Support
Assist in method development, verification/validation, and related QC projects
Assist in CAPA and change investigations, including closing root cause/impact assessment sections of non-conformity records
Report non-conformities to the QC Supervisor
Planning & Team Support
Capable of coordinating weekly QC department planning when acting as backup to the QC Supervisor
Train and mentor colleagues on complex QC test methods
Able to act as Supervisor backup on a rotating/as-needed basis, ensuring continuity of QC operations in the Supervisor's absence
Documentation
Keep relevant work instructions up to date
Essential:
MBO diploma in a relevant field (Chemistry, Biology, Life Sciences), or equivalent through relevant work experience;
Proven experience testing in a production/manufacturing environment;
Proficient in English (reading, writing, speaking);
Strong affinity for documentation and record-keeping activities;
Ability to work both independently and as part of a team;
Excellent time management skills, with ability to prioritize workload effectively;
Strong understanding of and adherence to laboratory safety protocols;
Solid theoretical understanding of QC equipment and underlying measurement;
Strong problem-solving skills.
Desirable:
Experience working in a GMP, ISO 13485, or equivalent regulated environment;
Dutch speaking and writing;
Experience with equipment qualification (IQ/OQ/PQ);
Willingness to be trained/certified as BHV (company emergency responder).
Role competencies:
Accuracy and attention to detail, particularly given the technical complexity of the tests performed at this level
Strong administrative and documentation skills, including SOP maintenance and technical report writing
Advanced Excel/Word skills, including data trending, statistical analysis, and structured technical documentation
Strong problem-solving and troubleshooting skills, applied to equipment malfunctions, out-of-trend results, and complex test discrepancies
Excellent planning skills, with the ability to independently coordinate the QC department's weekly planning when acting as Supervisor backup
Deep technical knowledge of QC equipment and test methodology, including theoretical background of assigned analyses
Analytical/root cause investigation skills, relevant to CAPA and non-conformity support
General Competencies
Team player, with the ability to mentor and support colleagues technically
Strong communication skills, both written (CAPA input, technical reports) and verbal (cross-functional coordination)
Resilience under pressure, especially given release-timeline dependencies and equipment troubleshooting under time constraints
Ownership and initiative, appropriate for someone capable of stepping into Supervisor responsibilities when needed
Positive, solutions-oriented attitude
Competitive Salary
Career Growth & Learning Opportunities
13th month bonus
25 vacation days
8% holiday pay
Travel allowance based on €0,23 per kilometre
Retirement savings plan
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.
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.
Please note if we receive a high volume of applications, we may close the role before the closing date noted.
By making this application you give consent for personal information to be used in automated decision-making processes relating to key job requirements which are stated in this ad.
Sinclair does not accept speculative or unsolicited CVs from Recruitment Agencies. Any unsolicited CVs received will be treated as property of Sinclair and Terms & Conditions associated with the use of such CVs will be considered null and void
