Quality Intern

Description

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 quality department has a vacancy in its Delft offices, for the following internship:

Quality Intern

The Position

Looking for an internship where you’ll genuinely contribute—not just observe? At Centrient Pharmaceuticals, we offer a hands-on opportunity to gain real experience within our Quality department.

As a Quality Intern, you will support key quality processes that ensure compliance, accuracy, and operational excellence.

You’ll work closely with the team on essential documentation and quality systems, gaining practical experience in a regulated pharmaceutical environment. This internship offers real responsibility and valuable learning opportunities within Quality.

The main activities and responsibilities

• Batch Record Management: Printing batch records and labels for 7-ADCA and enzymes, archiving, and maintaining the database.
• Document Management: Handling documents in Master Control to ensure accurate record-keeping.
• Training Matrix Development: Establishing and maintaining a training matrix in Master Control to track compliance.

Who we’re looking for:

• Enrolled in a MBO or HBO program or a related discipline.
• Responsible, organized and ability to work independently and as a part of a team.
• Ability to work in an international environment.
• Curious and enthusiastic, with an interest in quality.
• Flexible with a can-do attitude and a willingness to learn.

Terms and reward

• The internship includes a 6-month contract and requires 40 hours per week.
• The internship allowance is €350 gross per month for MBO students and €500 gross per month for HBO students.
• We strive for the earliest possible start date for the internship.
• Presence in the office is mandatory 5 days per week

The Procedure

Please submit your application 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 HRNL@centrient.com. 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