Solutia Life Sciences (recruitment division of Solutia) specializes in technical and middle management profiles in the pharmaceutical, biotech, and medical device sectors.
We are currently selecting a QA Scientist for a scientific-technical services company serving businesses in the chemical-pharmaceutical and veterinary sectors, located in Cerdanyola del Vallés.
Responsibilities:
* Batch Review: Verify manufacturing and packaging records for pharmaceutical batch releases.
* Deviation & Complaint Management: Assess deviations, OOS/OOT, complaints, CAPA, and Change Controls to ensure GMP compliance.
* Batch Certification: Support certification of batches for market release or clinical trials.
* Quality Agreements: Review agreements with manufacturers and authorization holders, focusing on batch certification.
* Document Approval: Approve essential documents (e.g., CoA, Site Master File, SOPs, specifications).
* Audit Collaboration: Participate in audits and inspections by clients and regulatory bodies.
* Quality System Improvement: Contribute to the ongoing enhancement of the quality system.
Here's what they offer:
* Flexible Working Hours and intensive schedule on Friday.
* 23 vacation days per year plus 24th and 31st of December.
* Fully stocked canteen and rooftop space (coffee, fruits, snacks, and beverages).
* Access to the employee benefits flexibility platform.
* Professional development and collaborative environment and a culture of empowerment.
Requirements:
* Life Sciences Degree
* 2 years of experience in Quality Control or Manufacturing activities in Quality Assurance in the Pharmaceutical Industry.
* Experience on Biologicals will be highly valued.
* A high level of English, both written and spoken is required for this position.