14 Senior Associate Quality Assurance - West Greenwich RI Jobs in West Greenwich, RI
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Senior Associate Quality Assurance - West Greenwich RI
$80k-98k (estimate)
Full Time
1 Week Ago
VetJobs is Hiring a Senior Associate Quality Assurance - West Greenwich RI Near West Greenwich, RI
Job DescriptionATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.
This position works a rotating day shift (A or B shift), with five days worked during one week (M, Tu, F, Sa, Su) and two days the following week (W, Th). Shift hours are 7am to 7pm.
LiveWhat You Will DoLet’s do this. Let’s change the world. In this vital role you will be responsible for Plant Quality Assurance (PQA) On the Floor in support of Manufacturing activities. This position provides the opportunity to work directly with Manufacturing staff during bulk drug substance operations to facilitate real-time decision-making regarding quality requirements. This is an outstanding opportunity to foster a positive relationship and learning environment between Manufacturing and Quality staff, and also to provide coaching, guidance and direction to Manufacturing, Quality Control, and Facilities/Engineering staff regarding compliance and quality systems. This position works a rotating day shift (A or B shift), with five days worked during one week (M, Tu, F, Sa, Su) and two days the following week (W, Th). Shift hours are 7am to 7pm.
Minimum Education RequiredHigh School/GED
Job_CategoryPharmaceutical
Additional Qualifications/ResponsibilitiesWe are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a self-starter with these qualifications.
Basic Qualifications
City*West Greenwich
State*Rhode Island
Job CodePharmaceutical Pharmaceutical
Affiliate SponsorAmgen
This position works a rotating day shift (A or B shift), with five days worked during one week (M, Tu, F, Sa, Su) and two days the following week (W, Th). Shift hours are 7am to 7pm.
LiveWhat You Will DoLet’s do this. Let’s change the world. In this vital role you will be responsible for Plant Quality Assurance (PQA) On the Floor in support of Manufacturing activities. This position provides the opportunity to work directly with Manufacturing staff during bulk drug substance operations to facilitate real-time decision-making regarding quality requirements. This is an outstanding opportunity to foster a positive relationship and learning environment between Manufacturing and Quality staff, and also to provide coaching, guidance and direction to Manufacturing, Quality Control, and Facilities/Engineering staff regarding compliance and quality systems. This position works a rotating day shift (A or B shift), with five days worked during one week (M, Tu, F, Sa, Su) and two days the following week (W, Th). Shift hours are 7am to 7pm.
- Provide Quality oversight to ensure that products are manufactured, tested, stored, and distributed according to current Good Manufacturing Practices (cGMP), Good Distribution Practices (GDP), and other applicable regulations.
- Provide Quality oversight during on-the-floor analytical testing.
- Ensure that facilities, equipment, materials, processes, and procedures follow cGMPs and other applicable regulations.
- Ensure that changes that could potentially impact product quality are assessed according to procedures.
- Ensure that deviations from established procedures are investigated and documented per procedures.
- Ensure that production records and testing results are complete, accurate, and documented according to written procedures and cGMP requirements.
- Perform review and approval of cGMP processes, procedures, and records, including but not limited to, Standard Operating Procedures (SOPs), batch records, deviations, and logbooks.
- Author, review, and approve quality documents such as risk assessments, training materials, engineering documents, automation documents, protocols, and reports.
- Alert senior management of potential quality, compliance, supply, or safety risks.
- Complete assigned training to permit execution of required tasks.
- Drive operational improvement initiatives, programs, and projects.
- Perform other tasks, as assigned, to assist in completion of activities associated with the attainment of group, departmental, and company goals.
Minimum Education RequiredHigh School/GED
Job_CategoryPharmaceutical
Additional Qualifications/ResponsibilitiesWe are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a self-starter with these qualifications.
Basic Qualifications
- High school/GED 4 years Quality/Manufacturing work experience OR
- Associate’s 2 years Quality/Manufacturing work experience OR
- Bachelor’s 6 months Quality/Manufacturing work experience OR
- Master's
- Bachelor’s degree and 2 years of Quality/Manufacturing work experience
- Experience working in a cGMP environment
- Experience with decision making
- Experience with analytical testing and/or general compendia testing
- Experience working with batch records and other GMP documentation
- Knowledge of data integrity requirements
- Proficient in Microsoft Office (e.g., Outlook, Word, Excel, PowerPoint, MS Teams)
- Experience collaborating within and across functional areas and demonstrated customer service focus
- Excellent written and verbal communication skills
- Ability to prioritize and navigate ambiguity, with minimal oversight, in a fast-paced environment
City*West Greenwich
State*Rhode Island
Job CodePharmaceutical Pharmaceutical
Affiliate SponsorAmgen
Job Summary
JOB TYPE
Full Time
SALARY
$80k-98k (estimate)
POST DATE
06/21/2024
EXPIRATION DATE
07/13/2024
WEBSITE
vetjobs.com
HEADQUARTERS
Lake Saint Louis, MO
SIZE
<25
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