Associate Quality Control

Company: TechTrueUp
Location: West Greenwich
Posted on: May 7, 2022

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