Principal Scientist Quality Control Biologics Clinical Analytical Operations
Principal Scientist Quality Control Biologics Clinical Analytical Operations
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$ 182070 - 235620
1 Vacancy
Job Description
At Gilead were creating a healthier world for all people. For more than 35 years weve tackled diseases such as HIV viral hepatitis COVID19 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 worlds biggest health challenges and our mission requires collaboration determination and a relentless drive to make a difference.
Every member of Gileads team plays a critical role in the discovery and development of lifechanging scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions and were 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
Gilead Sciences Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat lifethreatening diseases including HIV viral hepatitis and cancer. Gileadoperatesin more than 35 countries worldwide with headquarters in Foster City California.
Clinical Analytical Operations:
The Principal Scientist Clinical Analytical Operations is vital for the success of Clinical Biologics QC providing support for strategic leadership and oversight of daily operations. Responsibilities include managingthe release testing supporting Gileads Clinical biologics drug substances and drug will contribute to refining QC procedures across Gileads biologics manufacturing network ensuring compliance with global cGMP and Gileads Quality Management System.
Department:
Global Quality Control GQCBiologics
Job Responsibilities:
Experienceovera broad set of Quality Control subfunctions with extensive knowledge of industry best practices and trends.
Indepth understanding and application of GMP principles concepts practices and standards in the US and internationally.
Must be able to develop and improve complex concepts techniques and standards and new applications based on quality principles and theories.
Must be able to develop solutions to complex problems which require a high degree of ingenuity creativity and innovativeness.
Must be able to exercise judgment and independently determine and take appropriate action where precedent may not exist.
Proven ability to work with senior management to develop and ensure the implementation of Companywide longterm solutions.
Demonstrated an ability to develop a vision for Quality Control functions and have shaped the capabilities of the function to fulfill that vision.
Demonstrated the ability to influence process and outcomes across functions.
Willing to support future laboratory work.
Willing to support Commercial QC team.
Qualifications:
10 Years experience with BS OR
8 Years with MS OR
5 Years with PhD in Chemistry Biochemistry or related field.
2 year of relevant experience in a GMP Lab environment including knowledge of analytical testing familiarity with laboratory instrumentation.
Preferred experience in Biopharmaceutical or Pharmaceutical quality control. Stays ahead of shifting trends in industry and GMP systems/software e.g. LIMS QMS Empower).
Must think critically and creatively and be able to work independently to determine appropriate resources for resolution of problems.
Strong organizational and planning skills.
Shows excellent verbal and written communication skills and collaborative interpersonal skills.
For additional benefits information visit:
For jobs in the United States:
Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment and is dedicated to fostering an inclusive work environment comprised of diverse perspectives backgrounds and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race color religion national origin sex age sexual orientation physical or mental disabilitygenetic information or characteristic gender identity and expression veteran status or other nonjob 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 for assistance.
For more information about equal employment opportunity protections please view theKnow Your Rights poster.
NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT
PAY TRANSPARENCY NONDISCRIMINATION PROVISION
Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.
Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.
For Current Gilead Employees and Contractors:
Please apply via the Internal Career Opportunities portal in Workday.
Required Experience:
Staff IC
Employment Type
Full-Time
