Posted 6d ago

Quality Assurance Manager

@ Atalys
Santo Domingo, N/A, Dominican Republic
$0/bi-wkOnsiteFull Time
Responsibilities:Oversee quality management, Lead audits, Maintain QMS effectiveness
Requirements Summary:7+ years in Quality Management in medical device/pharma; ISO 9000/13485; FDA QSR/cGMP; lead QMS, CAPA, audits; strong leadership.
Technical Tools Mentioned:QMS, CAPA, ERP, IQ/OQ/PQ
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Job Description

Position Summary:



The Quality Manager is responsible for the planning, coordination, and implementation of Quality Management



System (QMS) processes to ensure quality in production and shipping of products, to meet ISO and regulatory



requirements and standards, and to support business requirements.



Essential Duties and Responsibilities:



· Accountable for effective integration and execution of company and customer, quality assurance and



quality control (QA/QC) requirements in new product development, process validation/verification,



production, storage and distribution of product



· Approves product quality plans, in collaboration with the customer, when applicable.



· Leads production risk analysis and mitigation program, including but not limited to PFMEA.



· Coordinate quality department resource assignment to optimize and assure product quality throughout



the project timelines and lifecycle.



· Identify and recommend metrology equipment and personnel needed to fulfill new and existing



product/project requirements.



· Manage metrology/inspection team.



· Ensures that team members are meeting inter-departmental goals and timelines, as well as, working with



Production team in meeting quality goals.



· Conducts management and employee meetings regarding quality related customer issues, production



issues and procedures related to quality that directly relate to customer requirements.



· Ensures staff and employees have a clear understanding of all customer quality requirements.



· Reviews technical problems and procedures of all departments and recommends solutions to problems or



changes in procedures.



· Accountable for customer interface with quality aspects of: product qualification, quality planning and



specification compliance related matters. Assigns Quality Engineering staff as appropriate.



· Collaborates with all department managers and senior staff to ensure the quality program is running



efficiently and effectively.



· Responsible for the Quality Management System (QMS) maintenance and development. Lead, support



and delegate quality system improvement programs and initiatives. Maintain QMS certifications. Ensure



the promotion and awareness of regulatory and customer requirements throughout the organization.



· Quality Management System Management Representative. Manage internal and external quality system



audits and communicate results to team. Lead and coordinate observation corrective action.



· Primary interface with regulatory auditors



· Maintain trend analysis on key quality system effectiveness metrics. Inform plant leadership team of



trends, propose and coordinate action to prevent adverse trends development and improve performance.



· Schedule and conduct site Management Review Meetings.



· Owner of corrective and preventive action (CAPA) system. Track CAPAs for timeliness of completion,



implementation and effectiveness.



· Work with plant leadership team to establish operational objectives and goals. Monitor progress to ensure goals are achieved. · Owner of complaint management system. Track, assure resolution, and respond to customer complaints or customer satisfaction issues. · Owner of ERP quality modules, responsible for content and content maintenance. · Owner of Document Control/Management System, including: specifications, engineering changes, quality records, QMS documents, etc. · Owner of equipment calibration and maintenance. · Accountable for procedural compliance with facility and manufacturing pest controls, environmental controls and microbiological analysis and control. · Lead and manage quality management system team project meetings, delegate tasks, prioritize activities and manage resources. · Lead and manage direct reports while fostering personnel development. · Adheres to the Quality Policy and Core Values of the organization. · Other duties as assigned by Plant Manager and Director of Quality. This job description indicates the general nature and level of work, duties and responsibilities expected of the incumbent. The incumbent may be asked to perform other duties as required. The job description may be changed if needed as determined by the Company. Required Competencies, Skills and Experience · Personal knowledge and experience with regulatory compliance, Audits, CAPA Submissions and IQ, OQ, PQ submittals. · Excellent problem solving & root cause analysis skills are required. · Interpersonal communication and project management skills a must. · Strong leadership skills that inspire team confidence and respect while motivating team members in a creative and effective manner. · Must have a desire for achieving excellence in customer satisfaction, process and product quality and reliability. · Strong understanding of ISO 9000, ISO 13485 and FDA QSR/cGMP quality standards. · Must be extremely detail-oriented with respect to documentation and communication. Education and Job Experience Requirements · Minimum 7 years of proven experience in a Quality Management role, responsible for overall Quality Systems in the Medical Device and or Pharmaceutical Delivery industries. · Plastics experience preferred · Understanding of statistics required · Six Sigma certification preferred · BS degree in engineering or related discipline desirable but not required · MS Degree a plus.



Compensation:




  • Salary is DOP$177,000, bi-weekly basis

  • Fuel/car allocation 10,000 per month

  • 85% private health insurance cost subsidy(complementary)

  • Company pay lunch up to RD1,500 per week

  • Company Incentive Bonus Program