60558MKP - QA Scientist for Batch Release (KYMOS)

This job posting is part of the Talent Biohealth Job Marketplace, which will take place in person at CONNECTION DAY'26 on May 6 from 3:00 PM to 6:00 PM. The event is organized by Barcelona Activa in collaboration with Clúster Catalonia.Health at the World Trade Center building.

KYMOS is seeking to fill 1 position for the following role: .

Only candidates who meet the company’s requirements will be contacted. Attendance and details will be confirmed via email.

ROLES and RESPONSABILITIES

Due to our business expansion and facility growth, we are looking for a QA Scientist for Batch release to join our dynamic team.

Key responsibilities:

• Be involved in the revision of manufacturing batch records and packaging batch records and other batch review documents of pharmaceutical products to be released.
• Participate in the evaluation of deviations, OOS/OOT, complaints, CAPA and Change Controls of pharmaceutical products to be released ensuring the application of GMPs and according to the marketing authorisation or clinical trial authorisation.
• Participate in the certification process of batches susceptible to be released to the market or for clinical trials.
• Review of Quality/Technical Agreements between the company and manufacturers and marketing authorisation holders, especially with regard to batch certification activities.
• Review and approve the documentation involved in the activity of the company: CoA, Site Master File, SOPs, product specifications.
• Collaborate and participate in the revision of audit reports carried out by third-parties to the manufacturers of pharmaceutical products to be released.
• Collaborate in audits carried out by our clients and give support in the Inspections of regulatory authorities.
• Participate in the implementation and improvement of the quality system of the company

OFFER

Contract type: Permanent

Hours per week: 40

Working hours: 9am to 6pm

Gross annual salary: €27,000–€39,000