Scientist — Quality Control Biologics (Analytical Lifecycle Management) position at Gilead Sciences.| United States Of America

Gilead Sciences Scientist — Quality Control Biologics (Analytical Lifecycle Management)

Experience: Highly Experienced

Pattern: full-time

Country:

Copy Link Report

Associate

United States ..........United States Of America

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 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 life-threatening diseases, including HIV, viral hepatitis, and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.    Key Responsibilities:    Commercial Analytical Lifecycle Management:   The Scientist, Analytical Lifecycle Management is vital for the success of C ommer cial Biologics QC, providing support for strategic leadership and oversight of daily operations. Responsibilities include supporting Commercial specification strategies, reference standard s , raw materials, and critical reagents programs, analytical method validations and transfers, and the compendial review program.   The   role will contribute to monitoring QC test method execution and   leading the analytical lifecycle management of C ommercial biologics drug substances and drug products.     Department     Global Quality Control – GQC-Biologics       Job Responsibilities      Experience   over   a   broad set of Quality Control sub-functions with extensive knowledge of industry best practices and trends.  In-depth 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 Company-wide long-term solutions.  Demonstrated the ability to motivate and engage individuals.  Demonstrated the ability to influence process and outcomes across functions.  Willing to support future laboratory work.  Willing to support Commercial QC team.    Basic Qualifications:   PhD in Chemistry, Biochemistry or related field OR  Master's Degree in Chemistry , Biochemistry or related field and 4+ years of relevant experience OR  Bachelor's Degree in Chemistry , Biochemistry or related field and 6+ years of relevant experience OR  Associate’s Degree in Chemistry , Biochemistry or related field and 8+ years of relevant experience OR  High School Degree and 10+ years of relevant experience     Preferred Qualification: Experience developing and/or leading reference standard and critical reagent programs for commercial or late-stage biologics drug substances and drug products products . Experience authoring validation protocols and reports for commercial or late-stage products. Experience leading or participating in the development of product specification setting for commercial or late-stage products. 1+ year of relevant QC experience in a GMP Lab environment, including knowledge of analytical testing, familiarity with laboratory instrumentation and GMP systems/software ( e.g. LIMS, QMS, Empower) for biologics drug substances and drug products.  Experience in Biopharmaceutical or Pharmaceutical quality control. Stays ahead of shifting trends in industry.  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.  The salary range for this position is: $136,340.00 - $176,440.00. 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: 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 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. 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.

Other Ai Matches

Sr Manager, Technical Services Applicants are expected to have a solid experience in handling Technical Services related tasks

Intern - Corporate Affairs & Legal - US Legal Business Partner Applicants are expected to have a solid experience in handling Job related tasks

Intern - Quality - PDM Applicants are expected to have a solid experience in handling Job related tasks

Director, US HIV Prevention (PrEP) Forecasting Applicants are expected to have a solid experience in handling US HIV Prevention (PrEP) Forecasting related tasks

Intern - Finance - MBA Leadership Development Program Applicants are expected to have a solid experience in handling Job related tasks

Intern - Clinical Operations - Early Phase Virology Applicants are expected to have a solid experience in handling Job related tasks

Director, R&D Finance - FP&A Applicants are expected to have a solid experience in handling R&D Finance - FP&A related tasks

Director, RWE Virology Safety Epidemiology Applicants are expected to have a solid experience in handling RWE Virology Safety Epidemiology related tasks

Medical Science Liaison- Upper Manhattan, Bronx, Brooklyn, Queens, Long Island, Westchester Applicants are expected to have a solid experience in handling Bronx, Brooklyn, Queens, Long Island, Westchester related tasks

Site Quality Head Applicants are expected to have a solid experience in handling Job related tasks

Public Affairs Manager Applicants are expected to have a solid experience in handling Job related tasks

Associate Director, PDM Business Process & Operational Excellence - Foster City Applicants are expected to have a solid experience in handling PDM Business Process & Operational Excellence - Foster City related tasks

Associate Director, Clinical Development Applicants are expected to have a solid experience in handling Clinical Development related tasks

Sr IT Business Analysis Specialist (Tech Dev Biologics Clinical Manufacturing) Applicants are expected to have a solid experience in handling Job related tasks

Scientist, Translational Inflammation Applicants are expected to have a solid experience in handling Translational Inflammation related tasks

Sr People Technology Product Manager (Talent Management) Applicants are expected to have a solid experience in handling Job related tasks

Building Automation Systems Engineer, Manager Applicants are expected to have a solid experience in handling Manager related tasks

Senior Accountant I, STS - GFS APAC Applicants are expected to have a solid experience in handling STS - GFS APAC related tasks

Sr Medical Scientist - Tampa FL Applicants are expected to have a solid experience in handling Job related tasks

(Associate) Director Market Access (m/f/d) – LIVE Portfolio Applicants are expected to have a solid experience in handling Job related tasks

Sr Device Engineer I Applicants are expected to have a solid experience in handling Job related tasks

Senior Director Commercial Operations (m/f/d) German Affiliate Applicants are expected to have a solid experience in handling Job related tasks

Cell Therapy Account Manager (CTAM) Region: Dresden / Leipzig / Magdeburg Applicants are expected to have a solid experience in handling Job related tasks

Scientist — Quality Control Biologics (Analytical Lifecycle Management) job opportunity at Gilead Sciences.

Saved Jobs

No Job Saved

Other Ai Matches