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Senior Associate Scientist Jobs
Company | Kite Pharma |
Address | , Santa Monica, Ca |
Employment type | FULL_TIME |
Salary | $117,725 - $152,350 a year |
Expires | 2023-06-12 |
Posted at | 1 year ago |
At Gilead we believe every employee deserves a great leader. As a people leader now or in the future, we expect that you will model and create an environment of inclusion, be intentionally focused on the hiring, development, growth and retention of talent, and empower teams to align and achieve goals.
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!
Kite is seeking a highly motivated individual to join Kite as a Senior Associate Scientist to provide Quality Control oversight of Global Raw Materials and Reagents Center of Excellence.
Responsibilities include (but not limited to):
- Conduct investigations regarding out of specifications (OOS) results. Address and manage deviations related to analytical procedures.
- Monitor and trend data, complete routine record review of test data and related documents for raw materials release.
- Manage creation and revision of raw materials specifications.
- Work with internal and external resources to maintain lab in an optimal state.
- Develop and validate GMP test methods for raw materials. Author and review SOPs, qualification/validation protocols, and reports. Manage method development at contract labs.
- Work independently with minimal supervision and ability to identify, effectively communicate, and troubleshoot issues.
- Perform other duties, including QC inspections and routine testing of raw materials
- Maintain, calibrate and operate equipment and instruments supporting Raw Material Testing labs
- Provide updates at daily and weekly meetings.
- Represent the Global Raw Materials and Reagents Center of Excellence’s short and long term goals in cross functional task forces and collaborative efforts
Basic Qualifications:
- MA/MS in Chemistry or Biochemistry with 4+ years’ hands-on laboratory experience in a biotech/biopharmaceutical setting OR
- High School diploma with 10+ years’ hands-on laboratory experience in a biotech/biopharmaceutical setting
- BA/BS Chemistry or Biochemistry with 6+ years’ hands-on laboratory experience in a biotech/biopharmaceutical setting OR
Preferred Qualifications:
- Technical writing experience in quality records
- Experience leading method development, method validation, investigations, deviations, and CAPAs
- Exceptional oral and written communication skills
- Ability to work independently, prioritize projects, and thrive in a dynamic environment
- Excellent interpersonal, collaborative, and time management skills
- Experience operating in a GMP environment
- Experience with biochemical and biophysical analytical methods: pH, Osmolality, Conductivity, Visual Inspection, Protein assays, FT-IR, PCR, etc.
- Experience in managing cross-functional projects is a plus
- Experience with statistical sampling methods (WHO guidelines, ANSI, etc)
- Understanding of global compliance and guidance for GMP manufacturing and raw materials
- Experience in US and International compendial methods (Visual Inspection, pH, osmolality, conductivity, endotoxin, etc.), ELISA, Gel/Western Blot, FT-IR, HPLC, PCR for materials, buffers, and reagents
#QCQA123
#IND123
The salary range for this position is: $117,725.00 - $152,350.00. 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 [email protected] for assistance.
For more information about equal employment opportunity protections, please view the 'Know 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 jobs in France:
Conformément à la Loi « Informatique et Libertés » (06/01/78), nous vous informons du fait que les données personnelles renseignées pourront faire l'objet d'un traitement informatique par Gilead et pourront être transmises aux Organismes Sociaux. Par ailleurs, vous disposez d'un droit d'accès, de rectification et de suppression des données vous concernant. Vous pouvez exercer ce droit en contactant: [email protected]
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