Manager, Quality Operations - Immucor, Inc.
Warren, NJ
About the Job
Werfen
Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.
The Manager of Quality Operations leads a team of quality specialists and ensures that product is produced that meets design specifications, quality system requirements, and regulatory requirements. This is a hands-on manager role that is directly involved with day-to-day operations required to produce medical device products. If you’ve got the necessary skills and experience to excel in this position, we want to hear from you. Apply today!
This position is not eligible for sponsorship for work authorization. Therefore, if you will require sponsorship from us for work authorization now or in the future, we cannot consider your application at this time.
Manager, Quality Operations - (Quality Assurance/Document Control/ Quality Operations)
Responsibilities:
Key Accountabilities:
- Maintain quality system compliance with ISO 13485, QSR, IVDR, CMDR, MDSAP, and any other applicable global regulations. Remaining up-to-date on current and upcoming regulations and guidances.
- Support manufacturing via review and approval of Root Cause Investigations, deviations and nonconformances.
- Provide on-going feedback to all functional groups to improve product quality and compliance throughout the design and manufacturing of products.
- Oversight and coordination of the Change Control and CAPA (deviation, NCMR, OOS, CAPA) programs. Provide guidance to area owners on completion of action items. Interact with site management as necessary to accomplish project goals and objectives.
- Participate in the development, planning and implementation of reagents, assays, software and hardware life cycle management for automated instrumentation and qualification of new/revised test methods, equipment and product/process validation initiatives related to manufacturing.
- Overall responsibility for Quality Operations approval of Design Transfer activities from R&D to Manufacturing, inclusive of production and manufacturing process qualifications.
- Assist the Quality Management Representative in escorting and providing information to Regulatory officials during external audits. Support supplier and internal audits, as needed.
- Manage the new hire and ongoing training programs for quality-related subjects. Manage personnel attendance and perform employee appraisals and competency evaluations as required.
- Manage the QA review and approval of incoming material, labeling, line opening/closing, in-process and finished device history records, including BASIS release and ERP transactions
- Support the QA review and approval of product, process, facility and equipment validation protocols and reports following current quality management system requirements
- Manage the QA storage locations for all quarantine and retains in accordance with associated procedures
- Manage the trending of metrics related to the Quality Management System and share with site management.
Manager, Quality Operations - (Quality Assurance/Document Control/ Quality Operations)
Qualifications:
Minimum Knowledge & Experience required for the position:
- Bachelors degree in a science related field (biology, chemistry, biomedical, etc)
- A minimum of five (5) years experience in medical device, IVD (in-vitro diagnostics), and/or pharmaceutical experience required
- Two(2) or more years experience in a quality management role, managing a team of 3 or more team members.
- Experience working in a manufacturing environment
- Extensive knowledge of Quality System Regulations (QSR). Working knowledge of 21 CFR 820, ISO 13485, EU IVDR, CMDR
- Proficiency in MS Office
- Experience with an eQMS is preferred (i.e. TrackWise or MasterControl)
- Strong consultative and interpersonal skills
- Ability to prioritize and multi-task
- Strong attention to detail and ability to summarize and communicate at all levels of the organization
- Team player (displays enthusiasm, confidence & commitment)
- Exceptional communication ability (verbal & written)
- Strong presentation skills. Facilitation and Leadership skills
- Ability to take initiatives and work independently
- Strong problem solving and analytical skills
Manager, Quality Operations - (Quality Assurance/Document Control/ Quality Operations)
Werfen appreciates and values diversity. We are an Equal Opportunity/Affirmative Action Employer M/F/D/V
We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 5,000 employees around the world comprise our Werfen team.