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Overview
Quality Control is searching is for an analyst to support routine testing of Raw Materials in the Wet Chemistry laboratory.
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 (IDs, LODs, 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
Top 3 Must-Have Skill Sets
Daily Responsibilities
Daily responsibilities will be focused on executing analytical testing of raw materials in a GMP laboratory.
Full Time
$76k-99k (estimate)
06/24/2024
07/07/2024
infotreeglobal.com
Plymouth, MI
<25
The following is the career advancement route for Quality Control Associate positions, which can be used as a reference in future career path planning. As a Quality Control Associate, it can be promoted into senior positions as a Construction Inspection Services Manager that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Quality Control Associate. You can explore the career advancement for a Quality Control Associate below and select your interested title to get hiring information.
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