Job Details  
Advertiser: Quanta Consultancy Services Limited

Job Title: QA Validation Specialist
Rate:£0 Per Year
Description: Rate:         Hourly Rate (Euros)
Location:  Munster Province, Ireland.

Experienced QA Validation Engineer required to work for a Bio-pharmaceutical Organisation in Ireland. You will be working within the QA Validation team and reporting to the Project Manager.

Role Overview:

Complete Document Preparation and Field Execution activities for the initial Qualification and Validation of the Biotech facility. 

Experience with any of the following equipment is required:

- Clean Utilities
- Upstream
- Downstream
- CIP (may include Cleaning Validation)
- SIP (including Thermal/Temperature Mapping)
- QC Labs


Essential Duties and Responsibilities include, but are not limited to, the following:

- Drive User Requirement Spec (URS) and SIA (System Impact Assessment) approval.
- Generate Equipment Qualification Assessments (EQAs) and subsequent IQ, OQ and where necessary PQ, Cleaning Validation protocols; drive approval of same.
- Execute IQ, OQ and where necessary PQ protocols and drive post-approval of same.
- Interface with Commissioning and Process Sciences teams.
- Support CIP and SIP validation programs as necessary.
- Support Management in Project delivery.

 Job Requirements: Skills, and abilities required to perform the job.

Proven BioTech experience in the given area, as follows:

- Lead position: 5 years BioTech C&Q experience, of which 2 years as a working Lead.
- Team Member position: 5 years BioTech... Please go to to see the full advert text.
Skills Required: QA Validation Specialist
Job Type: Contract
Start Date: 25-07-2017
Contact: Nicolle Kniebe Contact E-mail: Click
Contact Tel: (0) 1442 860 521 Contact Fax:
Reference: 19499/NK Added: 24-08-2017
  IMPORTANT: For jobs based in the UK it is unlawful to employ a person who does not have permission to live and work in the UK. Please ensure you have this permission before applying, unless the advert states otherwise.
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