Analytical Validation Engineer at Piper Companies
Titusville, NJ 08560, USA -
Full Time


Start Date

Immediate

Expiry Date

12 Oct, 25

Salary

60.0

Posted On

13 Jul, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Chemistry, Interpersonal Skills, Collaboration, Thinking Skills, Biochemistry, Biology

Industry

Pharmaceuticals

Description

Piper Companies is looking for an Analytical Validation Engineer to support commissioning and decommissioning activities for a major pharmaceutical company in the Titusville, 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)
  • Experience supporting laboratory investigations from beginning to end, including root cause identification, implementation of CAPAs, and authoring the final investigation
  • 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.
  • Proven ability to manage multiple projects/tasks simultaneously and independently.
  • Demonstrated interpersonal skills including flexibility, collaboration and inclusion skills and ability to work in a team environment.
  • Demonstrated self-starter with capability to develop innovative solutions to challenges.
  • Proven analytical aptitude, critical thinking skills and ability to apply key concepts.

Compensation for the Analytical Validation Engineer include:

  • Salary Range: $55 - $60/hr
  • Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays
Responsibilities
  • Experience in Pharmaceutical Laboratory Operations
  • Must be familiar and have experience with laboratory instrument selection, installation (IQ/OQ) and qualification (PQ)
  • Experience supporting laboratory investigations from beginning to end, including root cause identification, implementation of CAPAs, and authoring the final investigation
  • Hands-on experience with laboratory GMP instruments (i.e. AA, HPLC (waters), Autotitrators, NIR, ICP, FT-IR, particle counter, Gas analyzer
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