GMP Analytical Validation Engineer (Onsite)

ZP Group; Miami (FL, PA); On-site; USD 83,000 - 90,000; Full time

Benefits offered by this job

Medical, Dental, Vision

401(k)

PTO

Sick leave

Paid holidays

Job summary

Piper Companies is seeking an experienced Analytical Validation Engineer to support pharmaceutical laboratory operations in a GMP setting. The role focuses on instrument selection, installation, qualification, commissioning, and decommissioning, with hands-on validation and investigations.

The successful candidate will have strong GMP instrumentation experience, IQ/OQ/PQ expertise, and the ability to manage multiple priority projects while collaborating with quality, engineering, and laboratory

Qualifications

• Bachelor's degree in a related scientific discipline.
• 5+ years GMP pharmaceutical experience.
• Hands-on with validation activities (IQ/OQ/PQ) and investigations.

Responsibilities

• Support GMP laboratory commissioning and decommissioning.
• Assist instrument installation, qualification, commissioning, and decommissioning.
• Execute IQ/OQ/PQ activities for instruments and equipment.
• Provide technical support across the instrument lifecycle.
• Participate in laboratory investigations from initiation to completion.
• Lead/root-cause investigations and implement CAPAs.
• Document final investigation reports and findings.
• Collaborate with cross-functional teams to resolve issues.
• Maintain GMP compliance and follow procedures.

Skills

GMP environment experience

Analytical validation

Laboratory operations

Cross-functional collaboration

Education

Bachelor's in Chemistry/Biology/Biochemistry or related

Tools

HPLC (Waters)

AA

Autotitrators

NIR/ICP/FT-IR

Job description

Piper Companies is seeking an experienced Analytical Validation Engineer to support pharmaceutical laboratory operations in a GMP setting. The role focuses on instrument selection, installation, qualification, commissioning, and decommissioning, with hands-on validation and investigations.

The successful candidate will have strong GMP instrumentation experience, IQ/OQ/PQ expertise, and the ability to manage multiple priority projects while collaborating with quality, engineering, and laboratory