GMP Analytical Validation Engineer — Onsite

Zachary Piper Solutions; Miami (FL, PA); On-site; USD 125,000 - 135,000; Full time

Benefits offered by this job

Medical, Dental, and Vision coverage

401(k)

PTO

Sick leave as required by law

Paid holidays

Job summary

Piper Companies is seeking an Analytical Validation Engineer to support commissioning and decommissioning activities for a major pharmaceutical organization in Titusville, NJ. The role focuses on GMP laboratory operations and instrument qualification throughout the lifecycle.

The ideal candidate has 5+ years in GMP pharmaceutical settings, hands-on instrument qualification experience (IQ/OQ/PQ), and the ability to manage multiple projects with cross-functional teams.

Qualifications

• Bachelor's degree in Chemistry, Biology, Biochemistry, or a related scientific discipline
• 5+ years of GMP pharmaceutical experience
• Hands-on experience with GMP laboratory operations and instrument lifecycle
• Experience with IQ/OQ/PQ activities and investigations
• Ability to manage multiple projects independently in a regulated environment
• Strong analytical and problem-solving skills with cross-functional collaboration

Responsibilities

• Support laboratory commissioning and decommissioning in a GMP setting
• Oversee instrument selection, installation, qualification, commissioning, and decommissioning
• Execute IQ/OQ/PQ activities for instruments and equipment
• Provide technical support throughout instrument lifecycles
• Lead investigations and implement CAPAs and final reports
• Collaborate with lab, quality, and engineering teams to resolve issues
• Maintain GMP compliance and established procedures

Skills

Analytical thinking

Problem-solving

Communication

Team collaboration

Education

Bachelor's in Chemistry/Biology/Biochemistry or related

Tools

GMP laboratory instruments

IQ/OQ/PQ execution

Laboratory instrument installation/qualification

HPLC (Waters)

AA

Autotitrators

NIR

ICP

FT-IR

Particle counters

Gas analyzers

Job description

Piper Companies is seeking an Analytical Validation Engineer to support commissioning and decommissioning activities for a major pharmaceutical organization in Titusville, NJ. The role focuses on GMP laboratory operations and instrument qualification throughout the lifecycle.

The ideal candidate has 5+ years in GMP pharmaceutical settings, hands-on instrument qualification experience (IQ/OQ/PQ), and the ability to manage multiple projects with cross-functional teams.