Production Supervisor

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 7000 strong.

Our success comes from a specific focus in these rapidly evolving diagnostic areas our commitment to customers and our dedication to innovation and quality. Were passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care.

Position Summary:

The Cuvettes Production Supervisor is responsible for daily production and inventory management ensuring goals are met quality production efficiency and timely delivery of existing and new/modified products to stock. The Cuvettes Supervisor is also responsible for leading department staff in support of manufacturing activities.

This role will oversee our 2nd shift. Hours: Monday-Friday 2:00pm-10:30pm.

The annual base salary rangefor this role is currently$80000 to $90000. This is a bonus-eligible employee compensation will ultimately depend on factors including education relevant experience skillset knowledge and particular business needs.

Key Accountabilities

Essential Functions:

• Execute assigned weekly production plan as per weekly schedule.
• Ensure all department work is done in accordance with Good Manufacturing Practices (GMP) and all related standard operating procedures (SOPs).
• Continually work to achieve assigned production goals; meet unscheduled peaks in workload as necessary to ensure timely release of product and to avoid back orders.
• Manage inventory to insure quality production and efficiency.
• Maintain adequate staffing needs in support of business objectives; work to avoid overtime hours achieve assigned production goals meet unscheduled peaks in workload ensure timely release of product and to avoid back orders. Coordinate qualification and validation trials.
• In accordance with company policy process and approve staff work hours in companys time-clock system; approve time off requests ensuring business needs are continually met.
• Maintain effective manufacturing and control of products in compliance with all established manufacturing specifications and control procedures.
• Identify department training needs and implement appropriate training measures; mentor and train staff to enhance both individual and department performance.
• Oversee maintenance of department training records.
• Identify and address staffing needs with management.
• Continually evaluate performance of direct reports; take appropriate disciplinary action in accordance with company policy as necessary.
• Ensure safe working conditions throughout the department at all times ensuring adherence to all safety policies and procedures; work with management to identify and address safety matters and concerns.
• Ensure support for the transfer of technology (product) to routine manufacturing; evaluate new technologies and the pilot work that is required to assure minimum problems with initial and subsequent manufacturing.
• Manage special projects as assigned by management.
• Ensure accurate records and documentation in accordance with Good Documentation Practices (GDP) and all related SOPs.
• Identify production and manufacturing issues and work to implement corrective action.
• Work cross-functionally to coordinate corrective action for technical problems related to raw materials finished products; minimize rejects and field complaints.
• Ensure and maintain compliance with the Companys quality system requirements through training and adherence to policies procedures and processes.
• Other duties as assigned.

Minimum Knowledge & Experience Required for the Position:

• High school diploma or equivalent; additional training/education a plus.
• Minimum of five (5) years previous related manufacturing experience within a regulated medical device manufacturing or pharmaceutical environment.
• Previous lead or supervisory experience including experience with staffing and time management.
• Knowledge of lean manufacturing principles preferred.
• Demonstrated ability to support business goals and objectives related to cost and manufacturing processes.
• Understanding of coagulation-based manufacturing processes and company products.
• Good understanding of GDP GMP Good Laboratory Practices (GLP) FDA and ISO.
• Working knowledge of Microsoft Office and experience with large Enterprise Resources Planning (ERP) system.
• Good written and verbal communication.
• Ability to work as part of a team.
• Ability to identify and correct problems.
• Good leadership abilities.

If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV.

Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination harassment or retaliation based upon an individuals race color religion gender sexual orientation gender identity/expression national origin/ancestry age mental/physical disability medical condition marital status veteran status or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process please contact for assistance.

We operate directly in over 30 countries and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7000 employees around the world comprise our Werfen team.