Quality Operations Specialist III jobs in United States
cer-icon
Apply on Employer Site
company-logo

Curia ยท 6 hours ago

Quality Operations Specialist III

Curia is a global contract development and manufacturing organization focused on providing life-saving treatments. The Quality Operations Specialist III is responsible for QA oversight, review, and quality approval of large-scale expansion project deliverables, ensuring compliance with cGMPs and regulatory expectations.

BiotechnologyHealth CareManufacturing
check
H1B Sponsor Likelynote

Responsibilities

Serve as a quality resource and approving authority in support of validation, change control, work orders, and other related documents as the quality approver. Support departmental strategic goals to assure the highest quality standards and regulatory compliance
Provide quality compliance direction for validation and manufacturing activities. Serve as the quality liaison by providing compliance requirements for new product opportunities, including new equipment and technology
Direct process improvements and goals for Curia using current regulations and demonstrated best practices. Serve as a quality liaison between the site and customers or regulatory agencies during facility audits/inspections
Support effective and efficient continuous quality and cost improvement efforts
Read/interpret SOPs to ensure compliance
Maintain up to date trainings
Other duties as assigned

Qualification

Validation activitiesRegulatory complianceQuality assuranceChange controlCAPAPharmaceutical industry experienceMentoringCollaborationAttention to detail

Required

Bachelor's degree (BS or BA) in a scientific or related field from a four-year accredited college or university
Minimum of five (5) years of progressively increasing responsibility in the pharmaceutical or biologics industry, with experience in validation activities, regulatory compliance, and/or quality. Must also have relevant experience in change control, deviations, and CAPA
Demonstrated understanding of laboratory, manufacturing, packaging, regulatory affairs, compliance, and quality assurance requirements for biological and aseptic drug product manufacturing
Experience working with third-party contract manufacturing in the pharmaceutical industry, strong preferred
Must pass a background check
Must pass a drug screen
May be required to pass Occupational Health Screening

Preferred

Experience working with third-party contract manufacturing in the pharmaceutical industry, strong preferred

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!

Company

Curia is a biotechnology company that offers discovery biology, synthetic, medicinal chemistry, and small-scale manufacturing services.

H1B Sponsorship

Curia has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (34)
2024 (17)
2023 (8)

Funding

Current Stage
Late Stage
Total Funding
unknown
2025-03-07Debt Financing
2017-08-31Private Equity

Leadership Team

leader-logo
Steve Lavezoli
Vice President, Biologics Division
linkedin
Company data provided by crunchbase