Supervisor Molding (3rd shift)

Responsibilities

• Supervise employees and manufacturing activities pertaining to the production of products and/or manufacturing processes in - and with manufacturing/technical knowledge of - 1 or more production areas, depending on the complexity of the areas, in addition to conducting performance reviews, including resolving performance issues.
• Oversee the scheduling of work orders and team performance metrics.
• Ensure appropriate staffing for all positions.
• Accountable to ensure staff are appropriately trained to perform assigned work.
• Accountable for productivity and quality metrics of staff and provide regular progress reports and manufacturing metrics to management and cross-functional stakeholders.
• Partner with engineering on investigations and/or corrective actions, perform non-conformance investigations for review with engineering, assures documentation content is valid, may participate in improvement projects.
• Other duties as assigned by leadership.

Education and Experience:

• Bachelor's Degree
• 3 years of experience in related manufacturing, quality and/or product development engineering role with people supervision responsibilities required.
• Knowledge, Skills, and Abilities (KSAs):
• Experience working in multi-cultural teams with cultural sensitivity
• Proven expertise in Microsoft Office Suite with working knowledge of Enterprise Resource Planning (ERP) system, preferably SAP
• Experience working in a medical device industry, preferred
• Excellent communication and interpersonal relationship skills; possessing strong collaboration skills in partnering with cross functional stakeholders to achieve objectives
• Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control
• Ensure proper handling, storage and disposal of all waste generated in the facility according to applicable laws within the waste management program (RCRA)
• Prepare regulatory and/or internal reports, complete waste determinations, sign waste manifests and coordinate proper training sessions for affected personnel
• Why Join Us?
• To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive.
• We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.
• To learn more about BD visit https://bd.com/careers.
• Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.
• .
• Primary Work Location
• USA PR - Anasco
• Additional Locations
• Work Shift
• PR 1000pm-630am M-F (United States of America)

Why Join Us?

Primary Work Location

Work Shift

Preferred Qualifications

• Experience working in a medical device industry, preferred
• Optional Skills