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Sr. Quality Control Associate
40 Technology Way West Greenwich, RI 02817 US
Job Description
*Depending on experience
Fully Onsite - 8-5 (Flexible)
Ideal Candidate: 1-2 years of experience in a GMP setting + a B.S. Please review the top 3 skillsets.
Job Details: Under general supervision, this position will perform routine procedures to support drug substance and drug product testing within Quality Control. Tasks may include but are not limited to performing sample collection, sample handling, testing equipment/laboratory support. This position will be responsible for one or more of the following activities: - Performing routine laboratory procedures - Documenting, computing, compiling, interpreting, and entering data into computerized systems- Maintaining and operating specialized equipment - Initiating and /or implementing changes in controlled documents. Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory notebooks.
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 Master's degree
OR
o Bachelor’s degree and 1-2 years of Quality or Analytical Laboratory experience
OR
o Associate's degree and 3-5 years of Quality or Analytical Laboratory experience
OR
o High school diploma/GED and?5 years of Quality or Analytical Laboratory experience
Preferred Qualifications
• Experience in GMP analytical laboratory
• Experience with HPLC/UPLC, general chemistry, capillary electrophoresis
• 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
Equal Opportunity Employer: We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.
Fraud Alert: Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it’s from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.
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