Job Details
Posted 18 June, 2026
Job Id: 628679
Senior Quality Control Associate
Job Description
Target PR Range: 19-23/hr DOE
The role will be on-site based out of Rhode Island and will work under the mentorship of the front-line manager. The Bioanalytics team provides analytical expertise in testing the following: in-process, release and stability samples. The laboratory employs a variety of test methodologies that use sophisticated equipment including: HPLC/UPLC, capillary electrophoresis and general chemistry methodologies such as: Appearance, Color, Clarity, pH, Osmolality, Polysorbate, Protein Concentration, and Sub-Visible Particle testing.
Responsibilities include the following:
* Follow safety guidelines, cGMPs (Good Manufacturing Practices) and other applicable regulatory requirements
* Generate complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks
* Ensures that facilities, equipment, materials, organization, processes, procedures and products follow cGMP practices and other applicable regulations
* Operate laboratory equipment and instrumentation
* Performs review and approval of assays, documents and records
* Supports Continual Improvement initiatives
* Alerts management of quality, compliance, supply and safety risks
* Participate in laboratory investigations
* Perform general laboratory housekeeping activities
* Completes required assigned training to permit carry through of required tasks
* Performs additional duties as specified by management
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The experienced professional we seek thrives in a fast paced environment, and possesses these qualifications.
Basic Qualifications
* Master’s Degree
OR
* Bachelor’s Degree and 1-2 years of Quality experience
OR
* Associate’s degree and 6 years of Quality experience
OR
* High school diploma/GED and 8 years of Quality experience
Preferred Qualifications
* 1-2 years experience in HPLC/UPLC, capillary electrophoresis and general chemistry methodologies such as: Appearance, Color, Clarity, pH, Osmolality, Polysorbate, Protein Concentration, and Sub-Visible Particle testing
* Demonstrated experience in laboratory investigations, method validation, audits, QC processes
* Proven ability to interpret scientific data
* Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal direction
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.
