Job Information
Cole-Parmer Sr. Manager, Quality and Regulatory in Franklin, Massachusetts
Job Title: Sr. Manager, Quality and Regulatory Assurance
Reports To: VP, Quality
Position Location: Franklin, MA
FLSA Status (Exempt/Non-Exempt): FLSA Status: Exempt
Position Summary:
The Senior Manager, Quality and Regulatory Assurance position is responsible for the implementation and execution of the Quality program for all products, raw materials, processes and services. This position will work closely with all areas of the company; primarily Channel Management, Purchasing, Receiving, Manufacturing, Shipping, Sales and Customer Support. In addition, this position works closely on the front line with our customers to ensure that our outstanding quality standards and costing initiatives are upheld.
The role will handle quality issues either directly with our customers or through our channel management team. The role is responsible for overall tracking and interpreting statistical data relating to quality; recommends changes in standards, processes, equipment and materials to facilitate work and maintain quality. The role also interacts with supervisors to determine and resolve quality related issues.
Key Responsibilities:
Provide strategic leadership for the Quality Control Program to ensure all products, raw materials, processes and services meet the Company’s exceptionally high-quality standards
Ensure company compliance with accredited quality systems: 21 CFR part 820, ISO 13485, and applicable EU, UK, and Australian requirements
Continue to strategically evolve company quality system as well as transition system with revisions of standards
Acts as Management Representative and performs all duties and tasks associated with that designation. Acts a PRRC for European compliance.
Lead company audits either by accreditation bodies or by customers
Work with the appropriate teams to ensure proper action is taken and that the steps are initiated to avoid repeat errors.
Maintain documentation and revision level of quality documentation for all products or services
Maintain and communicate all quality data to department managers for problem identification, resolution, loss reporting
Report company quality data including complaints, nonconforming product, and corrective/preventive action activities
Review non-conformities (NCRs) for determining root cause, creating corrective actions, providing customer follow up and close NCRs within an acceptable timeframe
Perform problem-solving tests to develop corrective actions for quality issues and to initiate continuous improvement
Report Quality metrics and trends routinely to the company
Conduct routine quality checks of product on the productions floor and report errors and process improvement recommendations
Coordinate returns to vendors and ensure corrective actions are in place to prevent future defects
Performs other duties as assigned.
Minimum Requirements/Qualifications:
Bachelor’s degree from an accredited higher learning institution, preferably in a Quality or Engineering related field.
Experience in high volume manufacturing environment, preferably in medical devices or in-vitro diagnostics
Experience with European IVDD and IVDR compliance and regulations\
Experience with FDA 21 CFR Part 820 regulations
Minimum of 10 years’ experience related to quality assurance, lean manufacturing, regulatory compliance, and/or Six Sigma manufacturing
Holds Quality certifications in one or more of the following: ASQ/CQE, CMQ/OE, Six Sigma (Green or Black Belt)
Hands-on approach to troubleshoot and resolve quality related issues
Detail and Quality focused with strong organization, persuasion and negotiation skills
Ability to present information and respond to questions from various levels within the organization
Proficient in the use of MS Office
Thrives in a fast-paced, collaborative environment, efficiently works under pressures, within deadlines or other time essential constraints.
Excellent communication skills, both written and verbal, to clearly and concisely communicate to all levels of the organization.
Strong work ethic and an ability to excel within a rapidly changing and growing organization.
This position has not been approved for Relocation Assistance.
The above statements are intended to describe the general nature and level of the work being performed by people assigned to this job. They are not an exhaustive list of all of the duties and responsibilities associated with it.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status.