Job Description

This medical device client is looking for a Validation Consultant for a 2 month engagement to carry out installation qualification of the following Agilent analytical instruments:

• Gas chromatography - mass spectrometry (GC-MS)
• Inductively Coupled Plasma - mass spectrometry (ICP-MS)
• Liquid Chromatogrphy - mass spectrometry, Quadruple Time of Flight (LC-MS / QTOF)

Qualifications

• Qualified candidates will possess a Bachelor’s degree in related field along with 6 plus years related industry experience.
• Candidates must have excellent verbal communication and technical writing skills.
• Experience in executing protocols including systems such as Process Validation, computer controlled systems validation, utilities, manufacturing equipment such as computer controlled filling systems, formulation systems and basic knowledge of laboratory validation (not required but preferred).
• Familiarity with many aspects of validation is expected.
• Experience with temperature mapping.
• Proficient in Microsoft Word, Excel, Power Point and Project.
• Must be willing to travel regionally and/or nationally throughout the US.

All candidates must be legally eligible to work in the United States.

We are an equal opportunity employer. M/F/D/V

ProPharma Group does not accept unsolicited resumes from recruiters/third parties.  Please, no phone calls or emails to anyone regarding this posting.