Quality Control Senior Associate with Analytical Testing, HPLC and Laboratory

Aequor

West Greenwich (RI)

On-site

USD 65,000 - 90,000

Full time

3 hours ago
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Job summary

Aequor is seeking a Quality Control Senior Associate onsite in West Greenwich, Rhode Island. The role focuses on analytical testing using HPLC/UPLC and other lab methods under the Bioanalytics team.

You will generate documentation, ensure cGMP compliance, operate instrument, and participate in investigations; contract 12 months with extension, 8-5 local hours.

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

Responsibilities

  • 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
  • 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

Skills

HPLC
Quality Control
Laboratory chemistry experience

Job description

Quality Control Senior Associate with Analytical Testing, HPLC and Laboratory Experience (Onsite Job in West Greenwich, RI)
Terms: Contract W2 Only
Duration : 12 Months Contract (Will Get Extended for Long)
Description:

100% Onsite - Rhode Island

Standard 8-5 local hours

The role will be on-site based out of client 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.

Skill Sets:

HPLC, Quality Control, Laboratory chemistry experience

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
  • 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
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