Associate Quality Control
Company: TechTrueUp
Location: West Greenwich
Posted on: May 7, 2022
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Job Description:
Job DescriptionDescription:***100% onsite***
"Our Client requires all staff, staff augmentation external
workers, and certain other external workers, in the United States
and Puerto Rico to be vaccinated from COVID 19 as a condition of
assignment at Our Client. In accordance with applicable law, Our
Client will provide reasonable accommodations to staff augmentation
external workers who qualify on the basis of a medical reason or a
sincerely held religious belief, practice, or observance. Such
accommodation may not pose an undue hardship to Our Client, its
operations, or its staff."
Experience with LIMS would be a great preference - analytical data
reporting system Compendia experience is a plus but not required
Lab experience is a must (pro or academia)
Overview: Quality Control is searching is for an analyst to support
routine testing of Raw Materials. This person will be responsible
for working in the Quality analytical laboratory, using GMPs and
GDPs to execute analytical testing.
The ideal candidate enjoys tackling challenges and excels at time
management with attention to detail.
Responsibilities will include, but are not limited to: Performing
analytical testing for general chemistry (pH, osmolality,
appearance, etc.), Interacting cross-functionally with a wide
variety of people and teams; Troubleshoot, solve problems and
communicate with stakeholders. Participate in initiatives and
projects that may be departmental or organizational in scope.
Evaluate lab practices for compliance and operational excellence on
a continuous basis.
What we are looking for: Experience with analytical laboratory
testing with the ability to plan and perform routine tasks with
efficiency and accuracy. Demonstrated ability to work independently
and deliver right first time results Excellent communication skills
(written and verbal) Must have focus on data integrity Qualified to
work in the U.S. without employer sponsorship Commitment of a
40-hour work week in West Greenwich, RI Experience: Bachelor's
degree OR Associate's degree and 1-2 years of Quality or Analytical
Laboratory experience OR High school diploma/GED and 3 years of
Quality or Analytical Laboratory experience
Preferred Qualifications: 1-3 years of experience in GMP analytical
laboratory Experience with bench chemistry Experience with
Compendial testing Self-motivated, strong organizational skills and
ability to manage multiple tasks at one time with minimal
supervision Strong communication skills (both written and oral),
facilitation and presentation skills Understanding and application
of principles, concepts, theories and standards of GMP QC
analytical laboratories. Understanding of biopharmaceuticals
process and related unit operations Strong analytical skills with
the ability to collect, organize, analyze, and disseminate
significant amounts of information with attention to detail and
accuracy Independent, self-motivated, organized, able to multi-task
in time-sensitive environments. Demonstrated experience in
investigations and QC processes
Keywords: TechTrueUp, Warwick , Associate Quality Control, Other , West Greenwich, Rhode Island
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