Piper Companies is looking for an Analytical Computer System Validation Specialist to support CSV activities for an analytical lab group at a major pharmaceutical company in the Rahway, NJ area.

Responsibilities for the Analytical Validation Engineer include :

• Experience in Pharmaceutical Laboratory Operations
• Must be familiar and have experience with laboratory instrument selection, installation (IQ / OQ) and qualification (PQ)
• Serves as technical lead for qualifications
• Experience supporting laboratory investigations from beginning to end, including root cause identification, implementation of CAPAs, and authoring the final investigation; writes protocols
• Hands-on experience with laboratory GMP instruments (i.e. AA, HPLC (waters), Autotitrators, NIR, ICP, FT-IR, particle counter, Gas analyzer)

Qualifications for the Laboratory Analytical Engineer include :

• Bachelor’s Degree in Chemistry, Biology, or Biochemistry with minimum of 5 years experience in a GMP environment.
• Familiarity with pH meters, conductivity testing, and balances
• Understanding of compendial testing for USP / EP / JP
• Strong written and verbal communication skills.

Compensation for the Analytical Validation Engineer include :

• Year-long consulting assignment
• Pay : $45-$55 / hour

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Last updated : 2024-07-01