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Quality Assurance Senior Associate

Contract: West Greenwich, Rhode Island, US

Salary Range: 27.00 - 28.00 | Per Hour

Job Code: 371270

End Date: 2026-09-23

Days Left: 27 days, 7 hours left

Description:
Title:  Quality Assurance Senior Associate
Duration: 12 Months
Location: West Greenwich, RI 
 
Schedule: Rotating 12-hour shifts, 6:45 AM – 7:00 PM
Week 1: Monday, Tuesday, Friday, Saturday
Week 2: Sunday, Wednesday, Thursday
 
Job Summary:
  • The Plant Quality Assurance (PQA) Associate will provide on-the-floor Quality oversight in support of Manufacturing activities, including bulk drug substance operations.
  • This role will work closely with Manufacturing teams to ensure compliance with cGMP requirements and support real-time decision-making related to quality requirements and deviations.
Key Responsibilities:
  • Provide Quality oversight to ensure products are manufactured, tested, stored, and distributed in compliance with applicable regulations.
  • Ensure facilities, equipment, materials, processes, procedures, and products follow cGMP and other regulatory requirements.
  • Review and approve cGMP processes, procedures, documents, and records.
  • Review batch records, logbooks, work orders, attachments, and other GMP documentation.
  • Ensure deviations from established procedures are properly documented.
  • Verify production records and testing results are complete, accurate, and compliant with written procedures and cGMP requirements.
  • Identify and escalate quality, compliance, supply, and safety risks to management.
  • Collaborate with Manufacturing and the PQA shift team to ensure required activities are completed.
  • Complete all required training and maintain qualification for assigned tasks.
  • Spend the majority of the shift in a cleanroom environment, including gowning in and out of frocks and coveralls.
Required Skills & Qualifications:
  • GMP/cGMP experience is mandatory.
  • Experience in Quality Assurance and/or Manufacturing within a regulated environment.
  • Knowledge of batch records, logbooks, deviations, and GMP documentation.
  • Understanding data integrity requirements.
  • Strong decision-making and problem-solving skills.
  • Ability to work independently while effectively collaborating within a team.
  • Proficient in MS Office: Outlook, Word, Excel, PowerPoint, and Teams.
  • Excellent written and verbal communication skills.
  • Ability to prioritize tasks and work effectively in a fast-paced environment with minimal oversight.
  • Comfortable working in a cleanroom environment for the majority of the shift.
  • Preferred Qualifications
  • Bachelor’s degree with 2+ years of Quality or Manufacturing experience.
  • Experience working in a cGMP environment.
  • Experience with analytical testing and/or general compendial testing.
  • Experience reviewing and working with batch records and other GMP documentation.
  • Demonstrated ability to collaborate across functional teams with a strong customer-service focus.
Salary and Other Compensation:
The annual [salary/hourly rate] for this position is between $27.00 - 28.00 per hour. Factors which may affect pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate.
 
Benefits:
The Company offers the following benefits for this position, subject to applicable eligibility requirements:
[medical insurance], [dental insurance], [vision insurance], [401(k) retirement plan], [life insurance], [long-term disability insurance], [short-term disability insurance],
[paid parking/public transportation], [Paid time off], [Days/hours of paid sick and safe time], [Days/hours of paid vacation time], [Weeks of paid parental leave], [Paid holidays annually], [any additional benefits applicable].
Job Requirement
  • Plant Quality Assurance
Reach Out to a Recruiter
  • Recruiter
  • Email
  • Phone
  • sakshi malviya
  • sakshi.malviya@collabera.com
Apply Now
Apply Now
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