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Job Details

Cell Therapy Expert

Company: i-Pharm Consulting
Location: Netherlands
Reference: CM-QA-Cell
Closing Date: 05 Mar 18
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

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

Requirements:

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

Responsibilities:
• 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

Requirements:
• 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.

www.i-pharmconsulting.com


To apply:
If you would like to discuss this vacancy further, please call Charlotte Miles on +44 (0)20 3189 7819, or email cmiles@i-pharmconsulting.com. 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.

Keywords:
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: Cell Therapy Expert

Contact Information:

Address:  Head Office
212 New King’s Road London
SW6 4NZ
England
Reasons to work for i-Pharm Consulting
Tel:  +44 (0) 20 3189 2299
Website:  Visit Our Web Site

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