We are actively looking for a Laboratory Specialist Biomedical Quality Control for a pharmaceutical laboratory.
LABORATORY SPECIALIST BIOMEDICAL QC - Temporary position
Start date : November, 2025
End of date : End of February, 2026
Location : Lengnau
* Perform analyses of finished products, samples in progress, raw materials, excipients, cleaning samples, validations and environmental monitoring according to established procedures.
* Ensure the maintenance and proper functioning of the BCQC laboratory equipment.
* Draft and review work instructions (WI) and other quality documents within the allotted time.
* Manage orders and the preparation of materials needed in the laboratory (standards, controls, chemicals, solutions and consumables).
* Collaborate in solving chemical and biochemical issues (quality deviations, regulatory requests, etc.).
* Document all laboratory activities, including errors and deviations, in accordance with GDP (Good Documentation Practices) guidelines.
* Provide technical support to colleagues during troubleshooting activities.
* Communicate effectively with the BCQC Manager regarding ongoing activities, gaps and identified issues.
* Ensure that colleagues, supervisor and clients have the necessary information in a timely manner.
* Comply with cGMP rules, quality policies, procedures and instructions defined by the Quality function.
* Participate in continuous improvement initiatives and track deviations.
* Apply the security rules and procedures implemented by the EHSS function.
* Contribute to safety initiatives and report near misses.
* Adhere to the company's values and standards of ethics and legal compliance.
* Take responsibility for one's presence, performance and productivity.
* Act with a customer-oriented mindset.
* Demonstrate intellectual curiosity and adopt practical process improvement (PPI).
Profile:
* Diploma of Laboratory Technician in the chemical, biochemical, pharmaceutical fields or equivalent.
* Minimum 2 years of experience in a chemical or biochemical laboratory.
* Experience in a GMP regulated environment
* Mastery of the Empower software (essential).
* Fluent English (written and spoken), with German being an asset.
Gi Life Sciences Contact :
CHAUVIN Kevin :
LIUZZO Jessica :
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