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Validation Analyst - Cleaning and Process Validation – Co. Down

Recruitment Plus

  • Antrim / Armagh / Down
  • Negotiable
  • Permanent full-time
  • Updated 11/11/2017
  • Zuzana Foley
this job is expired
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Description

Validation Analyst - Cleaning and Process Validation - Co. Down - D004865 Please hit the apply now button above and Zuzana who is based in our Dundalk office will be in contact if you are suitable.

 

Validation Analyst - Cleaning and Process Validation - Co. Down - D004865

Recruitment Plus is currently recruiting for an experienced Validation Analyst in Co. Down who will primarily be based within our clients Down facility.  The successful candidate will be based within the Validation Department, and will be involved in carrying out chemical analysis of in-process / finished product samples, collection and analysis of cleaning validation samples and completion of all associated documentation in accordance with the relevant validation protocols and standard operating procedures (SOPs).

Location: Co. Down commutable from Co. Monaghan, Louth, Cavan, Fermanagh and Meath.

Salary: NEG DOE

Duration: Full-Time, Permanent

Essential Criteria:

  • Third level qualification in a chemistry related discipline with a strong analytical background or a minimum of 12 months relevant industry experience in an analytical laboratory setting and A-level(s) in a science related subject.
  • Laboratory experience as part of studies.
  • Good communication skills, written and oral.
  • Good organisation skills.

Desirable Criteria:

  • Experience in Wet Chemistry Techniques. Working knowledge of HPLC / UPLC

The role will involve use of the following standard techniques:

  • Wet chemistry
  • UV/Vis Spectrometry,
  • Potentiometric analysis,
  • Karl Fischer, moisture determinations,
  • High Performance Liquid Chromatography / Ultra Performance Liquid Chromatography (HPLC & UPLC)
  • Dissolution
  • Gas Chromatography (GC)
  • Other duties will include preparation of Validation Protocols, Validation Reports, Validation Master Plan and SOPs, product and equipment sampling, analytical method development and subsequent analytical method validation.
  • Applicants should be able to demonstrate good working knowledge of current Good Manufacturing Practices (cGMP) and current Good Laboratory Practices (cGLP).

 

Please hit the apply now button above and Zuzana who is based in our Dundalk office will be in contact if you are suitable.

Unfortunately, Recruitment Plus is not in a position to respond to each individual application due to the high volume of submissions. We will only contact those candidates whose CV matches the criteria for the vacancy. Thank you for your patience.

At RecruitmentPlus, we respect your privacy. Your CV is sent to us in complete confidence and will never be forwarded to a third party without your consent.

Ref: D004865
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