Senior Executive, Lab QA
About this role
This role is responsible for defining and specifying the activities, processes, and standards required to fulfill quality requirements for manufactured materials, components, and products within a global pharmaceutical environment. The position builds and maintains the infrastructure and systems necessary to consistently ensure the timely delivery of quality-compliant products. It supports the auditing, monitoring, and evaluation of laboratory quality activities against defined internal and regulatory standards. The role ensures efficient and effective workflows, procedures, policies, and laboratory inspection programs are in place and adhered to across quality laboratory operations. It manages in-process product quality in coordination with vendors and contract manufacturers. The position facilitates communication with customers and vendors to resolve quality-related issues in a timely and compliant manner. It reports and troubleshoots manufacturing process deviations and defects identified in finished goods. The role contributes to continuous improvement initiatives aimed at reducing defects, errors, and rework across laboratory and manufacturing operations. It also supports the identification and development of outsourcing vendors and suppliers according to organizational quality standards.
Essential Functions:
- Define and specify quality activities, processes, and standards for laboratory quality assurance programs in compliance with regulatory requirements
- Build and maintain quality infrastructure and systems to ensure timely delivery of compliant pharmaceutical products
- Conduct audits and monitoring of laboratory quality activities and outputs against internal and regulatory standards including 21 CFR Part 210 & 211 and GMP guidelines
- Ensure efficient workflow, procedures, policies, and laboratory inspection programs are implemented and maintained across quality laboratory operations
- Manage in-process product quality in coordination with vendors and contract manufacturers to meet defined quality specifications
- Communicate with customers and vendors to investigate and resolve quality and laboratory-related issues in a timely manner
- Report and troubleshoot manufacturing process deviations and defects identified in laboratory testing and finished goods
- Identify and implement process improvements to reduce costs, defects, errors, and rework in laboratory and manufacturing operations
- Support the identification and development of outsourcing vendors and suppliers according to organizational quality standards and policies
Additional Responsibilities:
Company at a glance
Amneal Pharmaceuticals, Inc. (NASDAQ: AMRX) is guided by a simple belief: essential medicines should be accessible to everyone. What began as a promise to deliver high-quality, affordable medicines has evolved into a diversified portfolio spanning complex generics and injectables, biosimilars, and specialty medicines, including more than 290 products, with scale and capabilities that help reach patients across the healthcare system while combining world-class precision with a deep sense of personal responsibility for every dose we deliver.
Content is for informational purposes only and 3rd party content does not reflect Amneal’s opinions.
Amneal has the right to remove comments that violate another’s copyright or intellectual property, mention an Amneal product, use profanity or are defamatory, promote and solicit for third-party sites, initiatives, or products, or are factually inaccurate or misleading or spam.
Amneal recommends that you consult with your healthcare provider regarding personal health matters. To report a product complaint or adverse event related to an Amneal product, contact Drug Safety at 877-835-5472, option 3 or [email protected]. If you are currently experiencing a life-threatening event, please immediately contact 911.
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