Quality Control Senior Associate
Aequor JD ·www.aequor.com
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100% Onsite - Rhode Island
Urgent backfill of AMAGJP00015468 (scrubbed resume attached)
Urgent role shortlisting EOD Tuesday 7/28
Standard 8-5 local hours
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
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
Urgent backfill of AMAGJP00015468 (scrubbed resume attached)
Urgent role shortlisting EOD Tuesday 7/28
Standard 8-5 local hours
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
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
Frequently asked questions
Who is hiring for the Quality Control Senior Associate role?
Aequor JD is hiring for the Quality Control Senior Associate position, a Shazamme client. Apply directly on the employer's career site.
Where is the Quality Control Senior Associate job located?
The Quality Control Senior Associate role with Aequor JD is based in West Greenwich, RI, US.
Is the Quality Control Senior Associate role full-time or contract?
This is a full time position at Aequor JD.
What experience level is the Quality Control Senior Associate role?
The Quality Control Senior Associate position is aimed at senior-level candidates.
How do I apply for the Quality Control Senior Associate role at Aequor JD?
Apply directly on Aequor JD's career page via the Apply button on this listing. ZammeJobs links straight through to the employer's ATS — no third-party form, no resume database.