Validation Engineer

United Pharma; Pennsylvania; On-site; USD 90,000 - 130,000; Full time

Job summary

United Pharma in Pennsylvania seeks a Senior Validation Engineer to support equipment and instrument qualification within a GMP environment. You will execute qualification activities, review protocols, and manage a backlog of instruments requiring qualification.

A strong GMP background, meticulous attention to detail, and solid technical writing skills are essential. You will collaborate with Quality and Engineering teams to ensure compliance and maintain robust validation documentation.

Qualifications

• GMP qualification and validation experience.
• Detail-oriented with ability to identify gaps in protocols/documentation.
• Strong technical writing and communication skills.
• Pharmaceutical/biotech/CDMO experience preferred.

Responsibilities

• Execute equipment/instrument qualification and validation activities.
• Review protocols and flag quality, technical, or procedural errors.
• Backlog management of instruments requiring qualification.
• Manage validation documentation and project deliverables.
• Collaborate with Quality and Engineering teams to ensure GMP compliance.

Skills

Qualification & Validation

GMP experience

Technical writing

Attention to detail

Tools

Documentation tools

Job description

A leading biopharmaceutical organization is seeking a Senior Validation Engineer to support equipment and instrument qualification within a GMP environment.

Key Responsibilities:

• Execute equipment/instrument qualification and validation activities.
• Review protocols and flag quality, technical, or procedural errors.
• Work through a backlog of instruments requiring qualification.
• Manage validation documentation and project deliverables.
• Partner with Quality and Engineering teams to ensure GMP compliance.

Qualifications:

• Strong qualification and validation experience within a GMP environment.
• Excellent attention to detail and ability to identify protocol/documentation gaps.
• Strong technical writing and communication skills.
• Pharmaceutical, biotech, or CDMO experience preferred.