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Open nowPosted 7 hours ago

QC Analyst

Centrient Pharmaceuticals Netherlands

Where
Delft, South Holland, Netherlands
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Your applicationOpen nowQC AnalystCentrient Pharmaceuticals Netherlands · Delft, South Holland, Netherlands

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  4. CV RocketApplied on Centrient Pharmaceuticals Netherlands's own form.

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13.5% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
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  4. 21.8%14 days
  5. 36.6%30 days
  6. 58.9%60 days
This job: posted 7 hours ago

The posting

Centrient Pharmaceuticals is the leading manufacturer of beta-lactam antibiotics, and a provider of next generation statins and anti-fungals. We produce and sell intermediates, active pharmaceutical ingredients and finished dosage forms.

We are a pharmaceutical company with a clear Purpose: to improve lives throughinnovative and sustainable manufacturing of medicines.

With our commitment to Quality, Reliability and Sustainability at the heart of everything we do, our over 1800 employees work continuously to meet our customers’ needs. We work towards a sustainable future by actively participating in the fight against antimicrobial resistance.

Founded 150 years ago as the ‘Nederlandse Gist- en Spiritusfabriek’, our company was known as Gist Brocades. Headquartered in Rotterdam (Netherlands), we have production facilities and sales offices in China, India, the Netherlands, Spain, the United States and Mexico. Centrient Pharmaceuticals is wholly owned by Bain Capital Private Equity, a leading global private investment firm.

The QA department has a vacancy in its Delft offices, for the following position:

QC Analyst

The Position

Analyse according to GMP standards raw material, intermediate and Enzymes samples, to guarantee the quality of Centrient products.

The main activities and responsibilities

  • Analysis of raw materials, in-process control (IPC), 7-ADCA and Enzymes samples according the described methodology and ensuring the proper documentation management.
  • Reporting of analytical results.
  • Investigate any deviation detected during the analysis.
  • Manage and archive the department’s documentation.
  • Determine the final status of the product after analysis.
  • Prepare standards and buffer solutions.
  • Keep the laboratory equipment clean and verified, documenting the operations performed in the correspondent logbooks.
  • Manage the documentation related to the laboratory, including FRM, WI and SOPs, among others.
  • Analysis review: register the data and operations performed in the correspondent logbooks,
  • Ensure that all the testing is performed according to methods and protocols approved.

The Ideal Candidate

  • MLO or HLO diploma;
  • At least 1 year of experience in a similar position;
  • Ability to work independently and accurately;
  • Ability to work well together;
  • Problem analysis/solution-oriented;
  • Ability to withstand high work pressure;
  • Have discipline and perseverance;
  • Show decisiveness;
  • Drive and involvement;
  • Initiative-rich;
  • Result-oriented.

Terms and reward

  • A work environment where your personality, knowledge and competences are the key to success;
  • 34,5 holidays;
  • Thirteenth month of 10%;
  • 12 weeks of gender neutral parental leave;
  • Laptop & cell phone;
  • Performance bonus
  • Competitive pension plan.

The Procedure

Please submit your application before 19 November 2026 via the 'apply' button and upload your CV & cover letter in English. We also ask you to include information on your current remuneration. Only applications with CV and Cover Letter will be considered.

For more detailed information about the role feel and about the Recruitment & Selection process you can contact us via [email protected]. We invite you to visit our website www.centrient.com for information about our company.

Reference check procedures are part of the Centrient Recruitment & Selection Process. You will be contacted when a reference check is required.

Acquisition in regard to this vacancy is not appreciated

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