18 Quality Assurance Senior Associate Jobs in West Greenwich, RI
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Quality Assurance Senior Associate
$77k-97k (estimate)
Full Time
2 Months Ago
Sorry! This job is no longer available. Please explore similar jobs listed on the left.
Advanced Bio-Logic Solutions Corp is Hiring a Quality Assurance Senior Associate Near West Greenwich, RI
Description:
Note:
"This posting is for Contingent Worker, not an FTE"
Note:
- ONSITE - USRI - PLEASE NOTE SHIFT REQUIRMENT BELOW
- ***This position works a rotating shift schedule, Week 1: Monday, Tuesday, Friday, Saturday Week 2: Sunday, Wednesday, Thursday, ~12 hours per day 6:45 AM – 7:00 PM ***
- In this vital role, will be responsible for PQA On the Floor in support of Manufacturing activities. This position requires working directly with Manufacturing staff during bulk drug substance operations to facilitate real-time decision-making regarding quality requirements and deviations.
- Provide Quality oversight to ensure that operations products are manufactured, tested, stored, and distributed according to current applicable regulations.
- Ensure that facilities, equipment, materials, organization, processes, procedures and products follow cGMP practices and other applicable regulations.
- Performs review and approval of cGMP processes, procedures, documents and records. Review logbooks, batch records, attachments, work orders, and other GMP documentation.
- Ensure that deviations from established procedures are documented per procedures.
- Ensure that production records and testing results are complete, accurate, and documented according to written procedures and cGMP requirements.
- Alert management of quality, compliance, supply and safety risks.
- Complete required assigned training to permit execution of required tasks.
- Bachelor’s Degree & 4 year of Quality/Manufacturing experience
- cGMP Experience
- Excellent written and verbal communication skills.
- 4 years of experience required in Quality Assurance - Biotech preferred but not necessary.
- Batch Record Review
- Good Manufacturing Practices
- Review executed batch records
- Perform quality oversight of manufacturing
- Help with comments, good documentation practices
- Work within team environment of quality professionals.
"This posting is for Contingent Worker, not an FTE"
Job Summary
JOB TYPE
Full Time
SALARY
$77k-97k (estimate)
POST DATE
04/17/2024
EXPIRATION DATE
06/15/2024
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