Top 9 Quality specialist Jobs in Paris, Ky

Manufacturing Quality Assurance Specialist II - 2nd Shift
Kindeva Drug Delivery Careers —Lexington, KY
- Full-time
- Mid-level
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Quality Improvement Specialist Sr/UKHC
University of Kentucky —Lexington, KY
- $62,400 - $111,634 a year
- Weekends as needed
- Background check
- Pass drug screening
- Office
2d
EXPANSION Validation Specialist
Piramal Pharma Solutions Inc. —Lexington, KY
- Mid-level
- 2 years
- Communication skills

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Quality Improvement Specialist Sr/UKHC
University of Kentucky —Lexington, KY
A Master’s degree in industrial or systems engineering or a related field, as well as an extensive background in performance and quality improvement,…
$62,400 - $111,634 a year
2d

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Quality Specialist
Engineered Profiles LLC —Columbus, OH
Assist in training floor associates on procedures & quality gauges / tools. 401k Retirement Plan- Company matching. Assist in tracking trends or quality issues.
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Quality Specialist
US AMR-Jones Lang LaSalle Americas, Inc. —New Albany, OH
Bachelor’s degree in a scientific, engineering, or technical field. This position is highly visible and requires strong documentation discipline, technical…
$67,000 - $97,000 a year
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Manufacturing Quality Assurance Specialist II - 2nd Shift

Kindeva Drug Delivery Careers -
Lexington, KY

Quick Apply

Job Details

Full-time

Qualifications

Raw material quality management
Performance improvement leadership
Document review (document control)
Quality records maintenance
Defect resolution root cause analysis
Laboratory document review
Preventive action implementation
Drug regulation
Production deviation management
Compliance audits & assessments
Quality control preventive actions
Corrective and preventive actions (CAPA)
GMP
Mid-level
Internal investigations
Quality control audit
Quality reports
Audit Reporting
Change management
Manufacturing process inspections
Production validation processes
Quality assurance experience within pharmaceutical industry
Compliance documentation
Internal compliance assessments
Regulatory/legal compliance standards in production
Quality control experience within pharmaceutical industry
Operational excellence initiatives
Quality audits
Production batch record review
Root cause analysis

Full Job Description

Our Work Matters
At Kindeva, we make products that save lives, ensuring better health and well-being for patients around the world.

The Impact You Will Make: Responsible for on-shift support of manufacturing operations, providing quality involvement and oversight during all stages of pharmaceutical development, manufacturing, and testing. Also responsible for review of controlled Current Good Manufacturing Practices (cGMP) documentation and manufacturing records, including any deviations or Out-of-Specification (OOS) results that may have occurred during lot production. Participates in the release of raw materials, intermediates, and final products. Performs internal and external audits of facilities and products, observes critical operations and procedures as they occur, audits documentation, records activities, and keeps management informed on quality issues.

Responsibilities:

Supports on-shift manufacturing operations and activities, including but not limited to real-time auditing of production batch records, samplin,g and Acceptable Quality Levels (AQLs), and line clearances.
Supports the development and maintenance of Quality Systems as appropriate.
Leads continuous improvement objectives to assure compliance with Drug Enforcement Administration (DEA) and Food and Drug Administration (FDA) regulations.
Advises senior management on findings and recommendations related to internal and external auditing.
Manages deviation, Out-of-Specification (OOS), Corrective and Preventive Action (CAPA), and Change Control Systems.
Evaluates proposed changes to processes, equipment, materials, or documentation to ensure compliance with regulatory and quality standards. Participates in investigations and root cause analyses for deviations, OOS results, and audit findings.
Ensures timely implementation and effectiveness checks of CAPAs to prevent recurrence of quality issues.
Reviews and approves cGMP documentation, including but not limited to procedures, batch records, validation protocols, development reports, specifications, raw data, executed batch records, material and batch disposition, and other related documents.
Develops and maintains metrics and trending reports for Compliance-related activities.Job Details

California residents should review our Notice for California Employees and Applicants before applying.

Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees—regardless of format—without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.

Equal Opportunity Employer:

Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.

Do you see yourself as part of the Kindeva mission? Click Apply Now Today!

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Refine Your Search

quality specialist jobs in paris, ky

Manufacturing Quality Assurance Specialist II - 2nd Shift

Quality Improvement Specialist Sr/UKHC

EXPANSION Validation Specialist

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I want to receive the latest job alert for quality specialist in paris, ky

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