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Overview
Quality Assurance Specialist I - Springfield, MO Join to apply for the Quality Assurance Specialist I - Springfield, MO role at VetJobs. Job Description available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. This role is On-Site at the location detailed in the job post. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies. Quality Assurance Specialist I in Springfield, MO. Build your future at Curia, where our work has the power to save lives.
Responsibilities
Maintain Quality databases including Archival and scanning of cGMP documents and records, Departures, media fill programs, and training files
Represent Curia Quality Assurance when managing issues that require immediate corrective action. Ensure such action taken is appropriate and correctly documented
Solicit feedback from various departments for operational improvement
Author, review, and/or approve Quality Management System documents, including, but not limited to, change controls, SOPs, deviations, CAPAs, etc.
Assist in performing investigations
Perform and/or assist with internal audits, weekly walkthroughs, and/or external audits
Perform QA visual inspection activities associated with clinical and commercial drug product
With supervision, may respond or manage responses to clients regarding manufacturing and/or documentation issues
Develop and/or maintain Quality System metrics for management review
Assist in tracking and follow-up on Deviations, Change Controls, Investigations, and CAPAs
Qualifications
Minimum Education Required: High School/GED
Additional Qualifications/Responsibilities: Bachelor’s degree in Life Science or related field. Directly related experience in a GMP environment may augment degree requirements.
Minimum 0-3 years’ experience in a cGMP and FDA-regulated industry
Prior Experience In a GMP Regulated Environment Preferred
Education, experience, location and tenure may be considered along with internal equity when job offers are extended.
Supervisory responsibilities: This position does not have supervisory responsibilities.
Details
City: Springfield
State: Missouri
Job Code: Manufacturing Manufacturing
Affiliate Sponsor: Curia
Benefits
Generous benefit options (eligible first day of employment)
Paid training, vacation and holidays (vacation accrual begins on first day of employment)
Career advancement opportunities
Education reimbursement
401K program with matching contributions
Learning platform
And more!
Other
Seniority level: Entry level
Employment type: Full-time
Job function: Quality Assurance
Note: Referrals increase your chances of interviewing at VetJobs. Sign in to set job alerts for “Quality Assurance Specialist” roles.
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Quality Assurance Specialist I - Springfield, MO Join to apply for the Quality Assurance Specialist I - Springfield, MO role at VetJobs. Job Description available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. This role is On-Site at the location detailed in the job post. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies. Quality Assurance Specialist I in Springfield, MO. Build your future at Curia, where our work has the power to save lives.
Responsibilities
Maintain Quality databases including Archival and scanning of cGMP documents and records, Departures, media fill programs, and training files
Represent Curia Quality Assurance when managing issues that require immediate corrective action. Ensure such action taken is appropriate and correctly documented
Solicit feedback from various departments for operational improvement
Author, review, and/or approve Quality Management System documents, including, but not limited to, change controls, SOPs, deviations, CAPAs, etc.
Assist in performing investigations
Perform and/or assist with internal audits, weekly walkthroughs, and/or external audits
Perform QA visual inspection activities associated with clinical and commercial drug product
With supervision, may respond or manage responses to clients regarding manufacturing and/or documentation issues
Develop and/or maintain Quality System metrics for management review
Assist in tracking and follow-up on Deviations, Change Controls, Investigations, and CAPAs
Qualifications
Minimum Education Required: High School/GED
Additional Qualifications/Responsibilities: Bachelor’s degree in Life Science or related field. Directly related experience in a GMP environment may augment degree requirements.
Minimum 0-3 years’ experience in a cGMP and FDA-regulated industry
Prior Experience In a GMP Regulated Environment Preferred
Education, experience, location and tenure may be considered along with internal equity when job offers are extended.
Supervisory responsibilities: This position does not have supervisory responsibilities.
Details
City: Springfield
State: Missouri
Job Code: Manufacturing Manufacturing
Affiliate Sponsor: Curia
Benefits
Generous benefit options (eligible first day of employment)
Paid training, vacation and holidays (vacation accrual begins on first day of employment)
Career advancement opportunities
Education reimbursement
401K program with matching contributions
Learning platform
And more!
Other
Seniority level: Entry level
Employment type: Full-time
Job function: Quality Assurance
Note: Referrals increase your chances of interviewing at VetJobs. Sign in to set job alerts for “Quality Assurance Specialist” roles.
#J-18808-Ljbffr