Validation Specialist - IQ/OQ/PQ & GMP Compliance

Accupac; Mainland (PA); On-site; USD 50,000 - 60,000; Full time

Benefits offered by this job

Competitive Pay

Salary Range: $50,000.00 - $60,000.00

Bonus: Exempt employees are eligible

Medical, Dental, and Vision insurance

Health Savings Account

Life Insurance with Optional PTO Plan

Pet Insurance

Short-Term Paid Disability

401(k) Retirement Plan with Vested M</

Paid Time Off (PTO)

10 Paid Holidays

Health Advocacy Programs

Job summary

Accupac in Mainland, PA is seeking a Validation Associate to oversee and document validation activities. You will write and execute protocols, perform IQ/OQ testing, and maintain validation reports while ensuring compliance with SOPs and GMP standards.

You will collaborate with Quality Systems, Project Management, and Operations to ensure products meet quality and regulatory requirements. This role offers competitive pay and comprehensive benefits.

Qualifications

• Bachelor’s degree preferred or 1–4 years of experience in a cGMP-regulated environment.
• Strong organizational and documentation skills.
• Experience with IQ/OQ/PQ validation protocols.
• Familiarity with manufacturing, packaging, and cleaning processes.
• Ability to read, write, and communicate effectively in English.
• Strong attention to detail and ability to work independently.
• Proficiency in Microsoft Word, Excel, and PowerPoint.

Responsibilities

• Review customer documentation to assess required validation activities
• Write and execute protocols, perform IQ/OQ testing, and maintain validation reports
• Collaborate with Quality Systems, Project Management, and Operations teams
• Manage validation documentation in compliance with SOPs and GMP standards
• Support calibration and preventative maintenance tracking
• Maintain the Calibration Management database and ensure timely PMs and calibrations
• Investigate and resolve validation deviations and errors with QA and departmental managers

Skills

IQ/OQ/PQ validation protocols

Documentation

English communication

Attention to detail

Independent work

Education

Bachelor’s degree

Tools

MS Word

MS Excel

MS PowerPoint

Job description

Accupac in Mainland, PA is seeking a Validation Associate to oversee and document validation activities. You will write and execute protocols, perform IQ/OQ testing, and maintain validation reports while ensuring compliance with SOPs and GMP standards.

You will collaborate with Quality Systems, Project Management, and Operations to ensure products meet quality and regulatory requirements. This role offers competitive pay and comprehensive benefits.