QA Validation Associate II

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a QA Validation Associate II in the United States.

We are seeking a detail-oriented and proactive QA Validation Associate II to support quality assurance processes for pharmaceutical products. In this role, you will review and validate manufacturing documentation, ensure compliance with cGMP and industry standards, and collaborate with cross-functional teams to facilitate timely batch releases. You will also participate in quality improvement initiatives and provide critical oversight to maintain high standards across documentation, testing, and product release. This position offers the opportunity to contribute to a culture of quality, continuous improvement, and operational excellence in a regulated environment.

Accountabilities:

• Review and validate manufacturing documentation, including batch records, master batch records, SOPs, method validation protocols, and test reports.
• Ensure completeness, accuracy, and compliance with cGMP and internal quality standards.
• Support evaluation and disposition of intermediates, bulk drug substances, and finished products.
• Track batch status, communicate escalations, and coordinate with cross-functional teams to meet QA deadlines.
• Contribute to process improvement initiatives to enhance batch review efficiency and quality outcomes.
• Participate in investigations, deviations, and CAPA activities as assigned.
• Collaborate with Manufacturing, Technical Support, Supply Chain, and Planning teams to resolve documentation discrepancies.
• Generate reports and communicate progress to management.

Requirements

• Bachelor’s degree in a relevant scientific or technical field.
• 3–5 years of experience in pharmaceutical QA, validation, or GMP-related roles.
• Knowledge of pharmaceutical manufacturing processes, laboratory systems, and equipment, preferably in solid or semisolid dosage forms.
• Familiarity with cGMP regulations, FDA requirements, and validation practices.
• Experience with documentation review, batch disposition, and QA processes.
• Strong attention to detail, critical thinking, and decision-making skills.
• Effective communication skills and ability to collaborate in cross-functional teams.
• SAP experience is preferred.

Benefits

• Competitive salary range: $72,000–$93,000 per year.
• Comprehensive health, dental, and vision benefits.
• Retirement savings plan (401k).
• Paid vacation and holidays.
• Opportunities for professional development and career growth.
• Supportive team environment with focus on quality and compliance.

Jobgether is a Talent Matching Platform that partners with companies worldwide to efficiently connect top talent with the right opportunities through AI-driven job matching.

When you apply, your profile goes through our AI-powered screening process designed to identify top talent efficiently and fairly.
🔍 Our AI evaluates your CV and LinkedIn profile thoroughly, analyzing your skills, experience, and achievements.
📊 It compares your profile to the job’s core requirements and past success factors to determine your match score.
🎯 Based on this analysis, we automatically shortlist the 3 candidates with the highest match to the role.
🧠 When necessary, our human team may perform an additional manual review to ensure no strong profile is missed.

The process is transparent, skills-based, and free of bias — focusing solely on your fit for the role. Once the shortlist is completed, we share it directly with the company that owns the job opening. The final decision and next steps (such as interviews or additional assessments) are then made by their internal hiring team.

Thank you for your interest!