Associate Quality Control (QC)
40 Technology Way West Greenwich, RI 02817 US
Job Description
*Depending on experience
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:
o Bachelor’s degree OR
o Associate's degree and 1-2 years of Quality or Analytical Laboratory experience OR
o 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
Internal Use Only General and Administrative
? Experience with Compendial testing
? Self-motivated, strong organizational skills and ability to manage multiple tasks at onev 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
• Strong Analytical Skills – Ideal candidate will have at least 4 years of experience
performing analytical testing
• Attention to Detail – Ideal candidate will be thorough and deliver polished work product.
• Can Do Attitude – Ideal Candidate will have a positive attitude and be willing to
participate in lean initiatives on site.
Daily Responsibilities
Daily responsibilities will be focused on executing analytical testing of raw materials in a GMP
laboratory.
Interview Process
Phone screening of possible candidates. Possible second phone screen and/or in-person interview for those who pass the initial phone screening. We can start interviewing immediately and will be available as needed.
Red Flags: Candidates with no lab experienceÂ
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