Associate Scientist, QC PDM
Company: Gilead Sciences, Inc.
Location: Oceanside
Posted on: January 12, 2021
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Job Description:
Associate Scientist, QC PDM United States - California -
Oceanside Gilead Sciences, Inc. is a research-based
bio-pharmaceutical company that discovers, develops and
commercializes innovative medicines in areas of unmet medical need.
With each new discovery and investigational drug candidate, we seek
to improve the care of patients living with life-threatening
diseases around the world. Gilead---s therapeutic areas of focus
include HIV/AIDS, liver diseases, cancer and inflammation, and
serious respiratory and cardiovascular conditions. Making an impact
on a global scale Inclusion is one of the company---s five core
values. That---s because we know that we are stronger and more
innovative at Gilead when we are informed by a diverse set of
backgrounds, experiences and points of view. Gilead Sciences is a
biopharmaceutical company that discovers, develops and
commercializes innovative therapeutics in areas of unmet medical
need. The company's mission is to advance the care of patients
suffering from life-threatening diseases worldwide. When you join
Gilead, you join our mission to change the world by enabling people
to live healthier and more fulfilling lives. Come join a
mission-driven bio-pharmaceutical organization that values
inclusion and diversity, has a strong portfolio of products, and is
constantly CreatingPossible Associate Scientist, QC PDM Gilead
Sciences, Inc. is a research-based biopharmaceutical company
founded in 1987. Together we deliver life-saving therapies to
patients in need. With the commitment and drive you bring to the
workplace every day, you will be part of a team that is changing
the world and helping millions of people live healthier, more
fulfilling lives. Our worldwide staff is a close community where
you can see the tangible results of your contributions, where every
individual matters, and everyone has a chance to enhance their
skills through ongoing development. Our scientific focus has
resulted in marketed products that are benefiting hundreds of
thousands of people, a pipeline of late-stage drug candidates, and
unmatched patient access programs to ensure medications are
available to those who could otherwise not afford them. By joining
Gilead, you will further our mission to address unmet medical needs
and improve life by advancing the care of patients with
life-threatening diseases. Specific Responsibilities: Support
Quality Control functions for in-process, release, and stability
sample processing for testing/retain/reserve storage and shipping
support QC Program Owner for Reference Standards and execute the
role of Reference Standard Administrator for all primary and
working reference standards Responsible for sample plan
creation/modification for internally and externally manufactured
product and Quality System Database (GPLM) management for Contract
Lab establishment and maintenance Responsible for ongoing
management and support Laboratory information system templating and
program maintenance Support Laboratory Operational Management for
instruments and equipment through Change Management ownership,
protocol and report generation and approval Conducts data review
for release, stability and in-process testing Support the Quality
Systems for creation/ ownership of change management, CAPA,
trending, and other required metrics reporting Writing
investigations related to CAPA systems, particularly in relation to
Microbiology (Environmental/Clean Utility/In-Process Bioburden
Monitoring excursions). Ability to review data in LIMS, test
records, and laboratory notebooks Essential Functions: Conducts
routine analyses based on written procedures Reviews data and
results of testing to ensure compliance to appropriate
specifications and protocols. Possess and implements strong project
management skills Performs maintenance and calibration of
analytical instrumentation. Applies knowledge of current Good
Manufacturing Practices (cGMPs) and Good Laboratory Practices
(GLPs) daily. Participates in group meetings. May present data or
prepare information for others to present. Conduct non-routine
analysis of raw materials, intermediates, and finished product
samples, as required. Troubleshoot instrumentation and test
methods, as required. Assists in the training of QC staff, as
needed. Working knowledge and proficiency with Microsoft Office
software. Writes and executes protocols and reports. Evaluates
equipment for purchase and performs installations and
qualifications of the new instruments, as required. Troubleshoot
instrumentation/test methods. Lead/coordinate QC and
cross-functional projects with limited direction. Independently
plans and executes assigned experiments that support routine
development activities and project goals Writes and revises
methods, specifications, and SOP's as needed. Knowledge,
experience, and skills: 10 years of experience with AA degree 8
years of experience with BS degree in a relevant scientific
discipline. 6 years of experience with MS degree in a relevant
scientific discipline. Degree in Microbiology, Chemistry, Biology,
or equivalent scientific discipline or equivalent work experience
Intermediate skills with Microsoft Office software Basic to
intermediate computer skills Basic knowledge of aseptic handling
procedures Basic knowledge of safe handling of laboratory chemicals
and reagents Hands on laboratory skills related to Microbiology and
Chemistry testing 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 careersgilead.com for
assistance. For more information about equal employment opportunity
protections, please view the ---EEO is the Law' 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 log onto your
Internal Career Site to apply for this job.
Keywords: Gilead Sciences, Inc., Oceanside , Associate Scientist, QC PDM, Other , Oceanside, California
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