Analytical Validation Engineer

Piper Companies; Titusville (NJ); On-site; USD 80,000 - 100,000; Full time

Job summary

Piper Companies is seeking an Analytical Validation Engineer to support key pharmaceutical operations in Titusville, NJ. The role involves enhancing laboratory operations, instrument qualifications, and managing investigations. Candidates should have a degree in relevant fields and substantial GMP experience. Comprehensive benefits and competitive hourly compensation are offered.

Benefits

Medical

Dental

Vision

401K

PTO

Sick Leave

Qualifications

• Minimum of 5 years experience in a GMP environment.
• Proven ability to manage multiple projects/tasks independently.
• Hands-on experience with laboratory GMP instruments.

Responsibilities

• Support commissioning and decommissioning activities.
• Experience in laboratory investigations, including CAPA implementation.
• Familiar with laboratory instrument selection, installation and qualification.

Skills

Pharmaceutical Laboratory Operations

Root Cause Identification

Analytical Aptitude

Critical Thinking

Collaboration Skills

Education

Bachelor’s Degree in Chemistry, Biology, or Biochemistry

Tools

HPLC

AA

NIR

FT-IR

Job description

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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
  
  

This job opens for applications on 02/12/2025. Applications for this job will be accepted for at least 30 days from the posting date.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Business Consulting and Services

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