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Job Details

GMP Cell Therapy Expert

Company: i-Pharm Consulting
Location: Netherlands
Reference: CM-QA-Cell
Closing Date: 03 Jul 18
Type: Permanent
Salary (£): Negotiable

Job Summary:

Our multinational client is looking for a R&D Cell Therapy Expert to work in their expanding department. ...


Our multinational client is looking for a R&D Cell Therapy Expert to work in their expanding department. You would be responsible for ensuring scientific and technological consistency of technology improvement, implementation and integration projects according to GLP/GMP requirements

Job Title: R&D Cell Therapy Expert
Location: Netherlands

Benefits: Above market rate salary + fantastic benefits package
Permanent contract

• Guarantee process/assay consistency investigating equipment, material and procedure equivalency during technology transfer
• Lead non-GMP phase of non-compendial assay transfer during technology transfer
• Evaluate validation data packages and design validation studies for processes and assays according to GMP requirements
• Represent TD&I department in internal and external project specific meetings
• Provide scientific and technical content in both gap analysis and risk assessments
• Ensure adherence of project specific activities with planned timelines and targets
• Generate and review laboratory, technical and quality documentation relevant to or resulting from TD activities and report or present it

• MSc or PhD in biotechnology, biosciences, bioengineering.
• Relevant experience in the field of cell and gene therapy (ideally with both viral and non-viral vectors)
• Strong knowledge of cell characterization techniques (e.g. FACS, qPCR, ELISA)
• Broad experience in QC assay validation within GMP environment ideally in an international setting
• Ideally significant experience with Technology Transfer in a GMP environment (Focus on non-compendial Assays).
• Experience with bioprocess development (traditional and automated platforms) would be a plus.
• Good understanding of GMP and ATMP regulatory framework
• Planning and organizing skills, result driven, flexible, ability to manage independently multiple projects, team player.
• Able to manage priorities, under stress and at short notice
• Excellent communication skills in English (verbally and written)

About i-Pharm Consulting:
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.

To apply:
If you would like to discuss this vacancy further, please call Charlotte Miles on +44 (0)203 142 7819, or email If this role is not suitable, Charlotte is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

TD&I / Technology Development and Integration / GLP / GMP / QA / Quality Assurance / cell therapy / gene therapy / validation / QC / Netherlands / Central Europe / Eindhoven / Maastricht / Tilberg / Nederlands

Apply for this job: GMP Cell Therapy Expert

Contact Information:

Address:  Head Office
212 New King’s Road London
Reasons to work for i-Pharm Consulting
Tel:  +44 (0) 20 3189 2299
Website:  Visit Our Web Site

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