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Job Details

(Senior) Process Validation Specialist - Biologics _ FRANCE

Company: SEC Recruitment
Location: France
Reference: BBBH106395
Closing Date: 24 Oct 16
Type: Permanent
Salary (£): 30,000 - 40,000
Benefits: Bonuses & Relocation Assistance

Job Summary:

Process Validation Specialist Biologics _ FRANCE? Big pharma company? Competitive salary package ? Relocation assistance? 5 years’ industrial GMP experience requested? English only mandatory language requirement as the line manager is himself a non-French speaker.NB: Biologics/vaccines profiles only will be considered for the role. ...


Process Validation Specialist Biologics _ FRANCE
? Big pharma company
? Competitive salary package
? Relocation assistance
? 5 years’ industrial GMP experience requested
? English only mandatory language requirement as the line manager is himself a non-French speaker.

NB: Biologics/vaccines profiles only will be considered for the role.

A top 10 big pharma developing Biologics & increasingly investing in their French centre is currently looking to on-board a talented Process Validation Specialist to join their Tech Ops teams & lead equipment validation as well as studies validation.

As an experienced professional in the field, you would lead the process validation initiatives in close collaboration with internal teams & external stakeholders.
Being a senior member of the organisation, you will represent the Process Validation department whilst audited/inspected.
In order to secure an interview at my client you would ideally come from an in house CDMO/pharmaceutical background having been working in a permanent position. Consultants keen on transitioning to a permanent stable role would also be considered by my client.
Master degree educated in life sciences, with an engineer or biotechnologist background, you would need to demonstrate at least 5 years of direct process validation experience in a GMP industrial setting.
Should an interview be set up, both your hands on experience at process validation & in authoring technical documentation would be challenged.
Excellent Project Management abilities are requested as you would evolved in a complex cross functional quality driven environment.
A solid understanding of quality & regulatory guidelines in the field is a mandatory requirement.

The successful candidate will not only be provided with excellent salary & benefit package but would also be given an opportunity to join a very stable & growing organisation planning on a 30% growth by the end of 2017. If you recognized yourself, please send your CV and cover letters at or call: +44 (0)20 7255 6665 for more information.

Do not hesitate to connect & follow me via LinkedIn so as to receive regular updates on openings I am recruiting for:

Caroline Mievre
Consultant - Pharmaceutical Division
(Bio)Pharmaceutical R&D

Tel: +44 (0)20 7255 6665
Fax: +44 (0)20 7255 6656
Mobile: +44 (0)7920 571953


3rd Floor 13 - 15 Moorgate London EC2R 6AD United Kingdom

+44 (0)20 7255 6600
+44 (0)1483 228 190
+33 (0)170807489
+33 (0)176753250

+49 (0)69 222 22 888
+41 (0)44 580 3717

Apply for this job: (Senior) Process Validation Specialist - Biologics _ FRANCE

Contact Information:

Address:  Head Office
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Tel:  00 44 (0) 207 255 6600
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