Manufacturing QA resource in United States at Jobgether

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

This role is designed to provide hands-on quality assurance support within a pharmaceutical manufacturing environment, focusing on maintaining compliance and ensuring the integrity of core manufacturing and quality systems. You will play a key role in supporting day-to-day QA activities across deviations, change control, batch record review, investigations, and protocol execution. Operating in a fast-paced and regulated setting, you will help ensure that manufacturing processes remain aligned with GMP standards and internal quality expectations. This position requires someone who can quickly step into ongoing workflows, provide technical oversight, and support critical decision-making. You will collaborate closely with manufacturing, laboratory, and quality teams to resolve issues and maintain operational continuity. This is a flexible contract opportunity suited for a detail-oriented QA professional who thrives in dynamic, short-term engagements.

• Provide quality assurance support across manufacturing operations, including deviations, change controls, batch record review, and investigations.
• Review and support execution of manufacturing and laboratory protocols to ensure compliance with GMP and internal standards.
• Assist in resolving manufacturing-related quality questions and providing technical QA oversight as needed.
• Participate in and support investigations, ensuring appropriate documentation, root cause analysis, and corrective actions.
• Ensure accuracy, completeness, and compliance of quality documentation and manufacturing records.
• Collaborate with cross-functional teams including Manufacturing, QC laboratories, and Quality Operations to maintain product and process integrity.
• Support short-term quality and manufacturing initiatives requiring immediate QA expertise.
• Contribute to maintaining regulatory compliance and operational readiness in a dynamic production environment.

• Experience in pharmaceutical or biotech manufacturing QA within a GMP-regulated environment.
• Strong knowledge of quality systems including deviations, change control, batch record review, and investigations.
• Ability to review and interpret technical documentation such as protocols, manufacturing records, and laboratory reports.
• Experience working collaboratively with manufacturing and QC teams in resolving quality issues.
• Strong understanding of regulatory expectations and compliance requirements in pharmaceutical operations.
• Detail-oriented with strong analytical and problem-solving skills.
• Ability to work independently in short-term or contract-based assignments.
• Strong communication skills and ability to provide clear technical guidance to cross-functional teams.
• Experience in supporting both manufacturing and laboratory quality activities is highly preferred.

• 6–12 month contract opportunity with flexibility depending on project needs.
• Fully remote work arrangement.
• Opportunity to contribute to high-impact pharmaceutical manufacturing and quality initiatives.
• Exposure to diverse quality systems, manufacturing processes, and cross-functional teams.
• Hands-on experience in GMP-regulated environments with meaningful operational responsibility.
• Flexible engagement suited for experienced QA professionals seeking project-based work.
• Opportunity to strengthen expertise across deviations, batch review, and manufacturing quality support.