Quality Assurance Specialist III - Packaging

Gilead SciencesFoster City, CA
294d$117,895 - $152,570

About The Position

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference. Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfill their aspirations. Join Gilead and help create possible, together.

Requirements

  • 5+ years of relevant experience in a GMP environment or related field and BA/BS degree OR 3+ years of relevant experience in a GMP environment or related field and MA/MBA/MS degree.
  • Prior experience in pharmaceutical industry.

Nice To Haves

  • Demonstrates working knowledge of current Good Manufacturing Practices (GMPs).
  • Demonstrates working knowledge of Quality systems and processes.
  • Demonstrates knowledge of FDA / EMEA standards and guidelines.
  • Demonstrates basic knowledge of six sigma, LEAN and/or root cause analysis tools used for identifying and correcting deficiencies.
  • Demonstrates investigation skills and technical writing skills.
  • Demonstrates effective verbal, written, and interpersonal communication skills.
  • Demonstrates working proficiency in Microsoft Office applications.

Responsibilities

  • Reviews and approves CMO (Contract Manufacturing Organization) master batch records.
  • Performs review of primary and secondary packaging lot packets.
  • Performs review/approval of various GMP packaging documents related to CMO operations.
  • Executes QA release of packaged products for further processing or distribution.
  • Interfaces with CXOs to provide QA oversight of routine manufacturing/packaging activities.
  • Performs a variety of activities to ensure compliance with applicable regulatory requirements.
  • Adds to programs and processes to ensure high quality products and compliance with current Good Manufacturing Practices (GMPs).
  • Reviews manufacturing/packaging control data for in process and finished products with guidance from senior colleagues.
  • Authors applicable sections of annual product reviews related to manufacturing/packaging of product and reviews applicable CMO annual product review reports.
  • Supports CXO investigations and may lead Gilead investigations to ensure robust root cause assessment and identification of corrective and preventive action (CAPA).
  • Works with cross-functional teams during new product start-ups and product launch, with guidance from senior QA colleagues.

Benefits

  • Company-sponsored medical, dental, vision, and life insurance plans.
  • Discretionary annual bonus.
  • Discretionary stock-based long-term incentives (eligibility may vary based on role).
  • Paid time off.

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What This Job Offers

Job Type

Full-time

Career Level

Mid Level

Industry

Chemical Manufacturing

Education Level

Bachelor's degree

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