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Quality Control, Lab Operations Technician II

United States - Maryland - FrederickQualityRegular

Descrizione del lavoro

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 fulfil their aspirations. Join Gilead and help create possible, together.

Job Description

Everyone at Kite is grounded by one common goal – curing cancer. Every single day, we seek to establish a direct line between that purpose and our day-to-day work. Join us in our mission!

We are seeking a highly motivated individual to join us as a Lab Ops Tech II of Quality Control Analytical team in our commercial cell therapy production center located in Frederick, MD. In this role, you will work within the Quality Control Department in supporting our efforts in this exciting new area of cancer immunotherapy. You will be responsible for maintaining the QC laboratory manage QC samples from manufacturing for QC testing, to maintain lab equipment operation and to support for business operations.

** Shift is M-F 8am-4:30pm **

Responsibilities (include but are not limited to):

  • Maintain, calibrate and operate equipment and instruments supporting cell bioassays, Flow Cytometry, ELISA and PCR assays
  • Work with internal resources to maintain lab in an optimal state by maintaining a clean, tidy and, above all, safe work environment.
  • Perform general laboratory duties such as aliquoting, media preparation, equipment maintenance,
  • Track and test products according to test methods and protocols. Testing can include cell counts, pH, osmolality, and others as assigned
  • Troubleshoot fairly standard issues and identify when a deviation from standard process occurs
  • Gather metric information for use in continuous improvement of areas of responsibility
  • Data entry and review
  • Monitor and trend data, complete routine record review of test data and related documents for in-process testing, drug substance and drug product release
  • Monitor the GMP systems currently in place to ensure compliance with documented policies
  • Additional duties as assigned

Basic Qualifications:

  • AA Degree and 1+ years’ experience in regulated pharmaceutical/Biotech environments or similar role OR
  • High School Degree and 2+ years’ experience in in regulated pharmaceutical/Biotech environments or similar role

Preferred Qualifications:

  • Experience in Quality Control.
  • Experience in aseptic techniques and clean room operations
  • Strong knowledge of GMP, GDP, SOPs and quality control processes
  • Maintain data integrity and ensure compliance with company policy, SOPs, WIs and specifications
  • Excellent interpersonal, verbal and written communication skills in this collaborative work environment.
  • Comfortable in a fast-paced Biopharmaceutical environment with minimal direction and able to adjust workload based upon changing priorities
  • Experience with sample chain of custody, general lab procedures such as operating centrifuges, working in a Biological Safety Cabinet and experience with inventory and laboratory management systems such as LabVantage (LIMS) or similar.
  • Proficient in MS Word, Excel, Power Point and other applications.
  • Job requires some overtime, weekend or holiday work as needed.

Does this sound like you? If so, apply today!

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The salary range for this position is: $54,655.00 - $70,730.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.


For additional benefits information, visit:

https://www.gilead.com/careers/compensation-benefits-and-wellbeing

* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.


For jobs in the United States:

As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations@gilead.com for assistance.

For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster.

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