SonicJobs Logo
Left arrow iconBack to search

ARx Quality Control Manager

Adhesives Research Inc.
Posted 2 months ago, valid for 17 days
Location

Glen Rock, PA, US

Salary

Competitive

Contract type

Full Time

By applying, a Sonicjobs account will be created for you. Sonicjobs's Privacy Policy and Terms & Conditions will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.

Sonic Summary

info
  • The Quality Control (QC) Manager oversees the daily operations of the QC Laboratory, ensuring efficient testing of materials and compliance with regulations.
  • This position requires a Bachelor's degree in Chemistry or a related field, with a minimum of 10 years of relevant experience, including 5 years in leadership roles.
  • Key responsibilities include managing laboratory schedules, maintaining equipment, and ensuring inspection readiness, as well as leading internal audits and investigations.
  • The role emphasizes continuous improvement, operational excellence, and effective communication while fostering a culture of accountability among QC staff.
  • The salary for this position is competitive and commensurate with experience, reflecting the importance of leadership in maintaining quality standards.

FLSA Status:      Exempt     Grade Level:  S10

Department:      ARx Quality    Reports To:    ARx Director of Quality

Direct Reports: Principal Scientist, Quality Analyst, QC Chemist 1, II and III    


Job Summary:


The Quality Control (QC) Manager leads the daily operations of the QC Laboratory, ensuring timely, compliant, and efficient testing of raw materials, in-process materials, finished products, and stability samples. This role oversees laboratory compliance, inspection readiness, investigations, and continuous improvement initiatives while providing leadership to QC staff and driving operational excellence, continuous improvement, cost efficiency, and performance results.


Essential Functions:

•    Manage daily operations of the Quality Control Laboratory.

•    Ensure timely execution and completion of testing activities for raw materials, bulk products, finished products, and stability programs.

•    Develop and manage laboratory schedules, workload balancing, and resource allocation to meet business and production requirements.

•    Ensure laboratory equipment is properly maintained, calibrated, qualified, and available for use.

•    Maintain laboratory compliance with applicable regulatory requirements, company policies, and quality standards.

•    Ensure the laboratory remains in a constant state of inspection readiness.

•    Review, approve, and maintain laboratory documentation including test results, specifications, procedures, protocols, investigations, and reports.

•    Lead and support internal audits, customer audits, regulatory inspections, and third-party assessments.

•    Ensure adherence to data integrity requirements and Good Manufacturing Practices (GMP).

•    Monitor laboratory quality metrics (KPIs)  and implement corrective actions as needed.


Additional Responsibilities:

•    Lead, coach, mentor, and develop QC Laboratory personnel.

•    Conduct performance evaluations and support employee career development plans.

•    Foster a culture of accountability, continuous learning, and operational excellence.

•    Ensure adequate staffing, training, and competency assessments for laboratory personnel.

•    Oversee laboratory investigations including Out-of-Specification (OOS), Out-of-Trend (OOT), deviations, and laboratory errors.

•    Ensure timely and thorough root cause investigations and implementation of effective corrective and preventive actions (CAPA).

•    Monitor recurring issues and drive sustainable improvements to prevent recurrence.


Job Specifications:

•    Bachelor's degree in Chemistry or related scientific discipline required; advanced degree preferred with a minimum of 10 years related experience.

•    5+ years of leadership or management experience.

•    Experience managing laboratory investigations, audits, inspections, and quality systems.

•    Strong knowledge of GMP, GLP, data integrity requirements, and applicable regulatory standards. 

•    Strong leadership and people management skills.

•    Excellent problem-solving and root cause analysis abilities.

•    Effective communication and cross-functional collaboration skills.

•    Experience with laboratory systems, testing methodologies, and equipment qualification.

•    Strong organizational and project management skills.

•    Ability to drive continuous improvement and operational excellence initiatives.

•    Proficiency in data analysis, metrics management, and performance reporting.








Learn more about this Employer on their Career Site

Apply now in a few quick clicks

By applying, a Sonicjobs account will be created for you. Sonicjobs's Privacy Policy and Terms & Conditions will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.