Quality Control Manager - Kinston, United States - ACE Partners

Description

QC ManagerPharmaceuticalStart date:
ASAP$120,000-$125, % bonus

Kinston, NCIn this position, you will oversee and regulate the daily quality inspection tasks for incoming, in-process, final, and batch records.

Your responsibilities will include leading the Quality Control team to ensure inspections are conducted effectively and promptly, with a focus on adhering to procedures and fostering continuous improvement initiatives.

Essential Duties and Responsibilities:
Supervises staff directly, addressing personnel matters, conducting performance evaluations, and administering managerial discipline when required.
Oversees quality control supervisors as direct reports.
Guides and directs the Incoming Inspection, In-Process Inspection, and Batch Release teams with a positive and patient demeanour.

Cultivates and reinforces an "immediate audit readiness" approach to ensure records and actions are executed with accuracy, legibility, and prompt retrievability.

Ensures adherence to quality system documents, cGMPs, ISO standards, and FDA regulations.
Coordinates and prioritises quality inspection, testing, and batch record review and release to support Operations and product release.
Identifies and pursues opportunities for enhancing existing processes and procedures.

Assists in quality assurance enhancement efforts by evaluating products, processes, or materials to develop control or improvement strategies aimed at enhancing the customer experience.

Collaborates with technical staff in conducting root cause failure analysis and implementing corrective and preventive actions to prevent recurrence.

Oversees verbal communications and visual checks of work activities to ensure compliance with quality requirements, ensuring appropriate corrective actions, discrepancy reports, and follow-up activities are carried out.

Reviews documentation and records for accuracy, determining product impact, release eligibility, or need for Non-Conformance Reports.
Manages documentation and procedural development during the qualification of new equipment/inspection methods.
Establishes, implements, and enhances Quality Control Key Performance Indicators (KPIs) metrics.
Establishes goals and objectives for the Quality Control organization and training programs to foster team development.
Supports investigations related to Non-Conformances, Audit observations, Corrective and Preventive Actions (CAPAs), or Issue Reviews as necessary.

Education and Experience:
Bachelor's Degree in Chemistry OR Biology8+ or more years of experience in quality, with at least 3 years in a supervisory capacity

Knowledge, Skills, and Abilities:
Experience with Metrology Equipment.
Proficient in adhering to relevant Standard Operating Procedures (SOPs) in accordance with company policy.
Support and actively contribute to Lean Sigma programs and initiatives aimed at achieving set targets.

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