You will join a biopharma/ATMP manufacturing environment, supporting MSAT, PAD, and QC activities with senior-level analytical and validation expertise. The role exists to ensure robust qualification and validation strategies, compliant GMP...
Interested? Send your CV to Miguel Gomes at m.gomes@panda-int.com or call +31 (0)20 2044 502 / +41 (0)44 5514 407 to discuss the...
Titelman (o.titelman@panda-int.com) or Luke Piercy (l.piercy@panda-int.com) call +31 (0)20 2044 502 today to secure your spot...
We are seeking an experienced QA Qualification Specialist to support a Quality Assurance Engineering department in a regulated manufacturing environment. You will ensure that qualification activities meet regulatory and procedural requirem...
confidentially? Maurits van Sloun ? m.vansloun@panda-int.com ? Phone: +32 460 25 75 29 Are you an experienced freelance QA...
Demonstrated knowledge of domestic and international GCP regulations Experience managing audit findings and CAPAs Experience... in regulatory inspection support and CAPA oversight Exposure to international clinical development programs and global GCP...
. Required scientific/technical knowledge of GAMP5 and international Data Integrity guidelines. Preferred Requirements Experience...? Interviews and offers can move quickly. Send your CV to Oluali Titelman at o.titelman@panda-int.com or call +31 (0)20 2044 502...
A global MedTech organisation operating in the diagnostics and women's health space is looking for a Senior Regulatory Affairs Specialist (IVD) to support its growing Regulatory Affairs function across the EMEA region. This 6-month contra...
interview process is moving quickly. Submit your CV to m.vansloun@panda-int.com or call +32 460 25 75 29 to secure your place....
The Quality Control Analyst operates within the OPEX team in a pharmaceutical manufacturing environment. The role focuses on executing, optimizing, verifying, and validating analytical methods for raw materials used in medicinal products. T...