Skip to content
CV Rocket
Get started
How it worksThe enginePricingBlogContactSign in

Open nowPosted 60 days ago

Supervisor Quality Control

sinclair46 open roles

Where
Almere, Netherlands
Get the CV for this job

From $25 per CV, paid once. No subscription.

Your applicationOpen nowSupervisor Quality Controlsinclair · Almere, Netherlands

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on sinclair's own form.

The reply lands in your private mailbox

3×more interviews than doing it yourself with ChatGPT.

The clock on this job

Early applications get read.

7.8% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 1.7%1 day
  2. 3.5%3 days
  3. 7.8%7 days
  4. 14.6%14 days
  5. 34.1%30 days
This job: posted 60 days ago

The posting

Sinclair is Hiring! Join Our Team as a Supervisor Quality Control 🚀

We are currently recruiting for Supervisor Quality Control at our Almere office in the Netherlands. The Supervisor Quality Control is responsible for the day-to-day coordination and technical oversight of the QC team within a Class III medical device manufacturing environment. This role ensures that all chemical, physical, and microbiological testing is performed accurately and on time, supports the review of raw material intake and batch record testing data, and maintains equipment qualification and QC documentation in line with GMP/ISO 13485 requirements. The QC Supervisor leads, trains, and plans the daily work of QC Analysts, and acts as a key backup for QC-related operational and technical matters, ensuring continuity of QC operations at all times. This is a hands-on leadership role requiring both strong technical QC expertise and proven team supervision experience..

The ideal candidate will have HLO/Bachelor's degree and is fluent in English and Dutch with a minimum of 3 years experience leading a team.

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.

Sinclair Values:

✅ 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

What You'll Be Doing:

Team Leadership & Planning

  • Supervise, coach, and support QC Analysts in daily operations.
  • Create and manage daily/weekly QC team planning to ensure test turnaround times are met.
  • Train new QC Analysts and maintain team competency matrix.
  • Act as backup for the Quality Manager during absences.
  • Conduct performance conversations / input into appraisals.

Testing & Technical Execution

  • Perform and/or oversee chemical, physical, and microbiological QC testing per approved methods.
  • Ensure all QC testing is completed within required timelines to support batch disposition by Quality/QA.
  • Perform review and release of incoming raw materials in ERP/QMS (raw material release authority sits with QC).
  • Perform QC review of batch record test data (intermediate and finished product) for completeness and accuracy, and forward results to the Quality team for final batch disposition.

Equipment & Method Lifecycle

  • Own qualification (IQ/OQ/PQ) and calibration scheduling of QC equipment.
  • Support new QC projects, including specification and purchasing of new equipment.
  • Ensure method validation/verification status is current and documented.

Quality System & Compliance

  • Report non-conformities to the Quality team and initiate Out-of-Specification (OOS) investigations.
  • Provide QC data and technical input to Quality team for CAPA investigations.
  • Maintain work instructions/SOPs relevant to QC processes, ensuring version control.
  • Maintain personal training file and ensure team training records are current.
  • Support internal and external audits as QC subject matter expert.
  • Ensure GDP (Good Documentation Practice) compliance in all QC records.

Your skills and experience

Essential:

🔹HLO / Bachelor's degree in Laboratory Techniques (or equivalent through relevant work experience);

🔹Fluent in English, both spoken and written, to a professional level;

🔹Minimum 3 years of experience leading/supervising a team, ideally within a regulated (GMP/ISO 13485) laboratory or QC environment;

🔹Proven experience with daily/weekly planning of laboratory or QC testing activities, balancing workload against release deadlines and unplanned investigations;

🔹Hands-on laboratory experience in a regulated environment;

🔹Experience with QC test methods (chemical, physical, and/or microbiological).

Desirable: 🔹Dutch speaker and writer (fluent)

🔹Hands-on experience with QC equipment (operation, troubleshooting, and ideally qualification/calibration)

🔹Experience in a Class III / high-risk medical device environment specifically

What We're Looking For:

🔹Accuracy and attention to detail in test execution, data recording, and batch record review, with zero tolerance for transcription or calculation errors given GMP/GDP requirements.

🔹Strong technical/analytical competency across chemical, physical, and microbiological test methods, with the ability to troubleshoot atypical or out-of-trend results.

🔹Sound administrative and documentation skills, including SOP/work instruction authoring, training file management, and audit-ready recordkeeping.

🔹Proficiency in Excel and Word, including formulas, data trending/analysis in Excel (e.g., pivot tables, control charts) and structured technical writing in Word.

🔹Working knowledge of ERP/QMS systems for raw material release and documentation workflows.

🔹Risk-based decision making, able to judge when a result, deviation, or trend requires escalation versus routine handling.

🔹Planning and prioritization skills to balance daily QC workload against release timelines and other priorities.

Perks & Benefits:

💰 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

From $25, paid onceGet the CV for this job

What happens when you press

One press. We do the rest.

  1. A CV for this posting

    Written against sinclair's own wording, from every piece of relevant proof in your profile.

  2. 25 readers review it

    Recruiter, hiring manager, skeptic and more read every draft, round after round. You get the best round.

    The review screen in CV Rocket: how each CV was read, round by round.

  3. We apply on sinclair's form

    Our application engine gets through the hardest forms there are. Where a question needs you, AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

    An application in CV Rocket: every answer filled in on the employer's form.

  4. Every reply, sorted

    sinclair's answer lands in your private mailbox, and we classify it on arrival: interview, question, rejection.

    The CV Rocket inbox: each employer reply classified as an interview, an action or a rejection.

  5. Reply with AI

    AI helps you write the email, checks it and sends it. We show you whether the recruiter read it.

  6. The interview in your calendar

    Full integration with your calendar. The invitation goes straight in.

    An interview invitation in the CV Rocket inbox, added to the candidate's calendar.
Get the CV for this job

From $25 per CV, paid once. No subscription.

Why it works

3×

more interviews than doing it yourself with ChatGPT.

ChatGPT writes a CV and never learns what happened to it. We see every reply. For each CV we know:

  • How it was written, and how the review scored it
  • When we applied, and how long after the posting went up
  • Which posting, which company, which city
  • Who got the interview, and who heard nothing

That is how we know which CVs get called.

Get the CV for this job

From $25 per CV, paid once. No subscription.

The numbers game

More applications. More interviews.

Every application goes out with its own CV, written for that posting and paid once. Send enough of them and the law of large numbers finds you the job.

Get the CV for this job
By hand5–10
With CV Rocket100
applications a day

Nearby

Live postings like this one

Same employer first, then the same role elsewhere.

Before you press

Straight answers

Get the CV for this job

From $25 per CV, paid once. No subscription.

What if my background isn't good enough?

We make the most of the background you have. The CV uses every piece of relevant proof your profile holds, and one of the 25 readers reads your whole profile and flags what the CV left out.

Do you really apply for me?

Yes, on the employer's own form, the hardest ones included. Where a question needs you, you answer it right there and AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

Is it a subscription?

No. You pay once per CV, from $25. Every application goes out with its own CV, written for that posting.

One job. One CV.
Paid once.

Pick the posting you want. We write for it, apply for you and catch the reply.

Get the CV for this job

From $25 per CV, paid once. No subscription.