QC Specialist Incoming Goods

Hobson Prior; Leiden; On-site; EUR 47,430 - 66,960; Part time

Job summary

A leading biotechnology company in Leiden is seeking a QC Specialist Incoming Goods on a contract basis for six months. In this role, you'll manage quality control activities including reviewing incoming goods and ensuring compliance with GMP. Candidates should have a background in life sciences and familiarity with GMP guidelines. Strong communication skills and proficiency in tools like SAP and Excel are essential.

Qualifications

• Must have a background in life sciences, biotechnology, or a related field.
• Experience under GMP guidelines in the pharmaceutical or biotech industry is crucial.
• Experience in raw material quality control required.

Responsibilities

• Review and approve quality of incoming goods and raw materials.
• Perform sampling of raw materials.
• Update and maintain master data in the ERP system.

Skills

Background in life sciences

Familiarity with GMP

Experience in raw material quality control

Knowledge of SAP

Strong communication skills

Proactive mindset

Tools

SAP

Excel

SharePoint

Job description

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Are you ready to make a groundbreaking impact in the world of biotechnology? Join a growing company that's shaping the future of healthcare and science.

Hobson Prior is seeking a QC Specialist Incoming Goods to join our team on a contract basis for six months. In this role, you will be part of the QC Sample and Incoming Goods management team, focusing on quality control activities such as reviewing and releasing incoming goods, maintaining accurate data in systems, and ensuring compliance with Good Manufacturing Practices (GMP). You will also contribute to process improvements and collaborate with various departments to support operational excellence.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Review and approve the quality of incoming goods and raw materials.
• Perform sampling of raw materials.
• Update and maintain master data in the ERP system.
• Revise material specification forms for raw materials.
• Ensure proper documentation practices are followed.
• Archive documentation according to internal processes.
• Collaborate daily with other departments to ensure smooth operations.
• Write procedures and support investigations, corrective actions, and change controls.
• Enforce GMP compliance across all activities.
• Support sample management tasks, including receiving, storing, documenting, and inventory tracking.

Key Skills and Requirements:

• Background in life sciences, biotechnology, or a related field.
• Familiarity with working under GMP guidelines in the pharmaceutical or biotech industry.
• Experience in raw material quality control, including sampling and documentation.
• Knowledge of SAP, Excel, and SharePoint is a plus.
• Strong communication and interpersonal skills.
• Ability to adapt to changing priorities while maintaining high-quality standards.
• A proactive, self-driven mindset with critical thinking abilities.

For more information, please contact Abigail Sivertsen.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.hobsonprior.com/privacy-policy.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Contract

Job function

• Job function

  Science

• Industries

  Professional Services

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