Supervisor Molding (3rd shift)

BD; Añasco (PR); On-site; USD 65,000 - 90,000; Full time

Job summary

BD is seeking a Manufacturing Supervisor in Puerto Rico (Anasco) to lead production activities across multiple areas. The role requires supervising staff, ensuring staffing and training, and maintaining productivity and quality metrics in a regulated environment.

Strong collaboration with engineering and cross-functional teams is essential, with adherence to safety protocols and waste management regulations. Applicants should have a Bachelor's degree and 3 years of related supervision experience.

Qualifications

• Experience working in multi-cultural teams with cultural sensitivity.
• Excellent communication and interpersonal skills; able to collaborate with cross-functional stakeholders.
• Adhere to Environmental Health & Safety rules and waste management requirements.
• Experience in a medical device or regulated manufacturing environment preferred.

Responsibilities

• Supervise employees and manufacturing activities across production areas.
• Oversee work orders scheduling and track team performance metrics.
• Ensure staffing coverage and staff training for assigned work.
• Monitor productivity and quality metrics; report to management.
• Partner with engineering on investigations and corrective actions; review non-conformance findings.

Skills

Multicultural teamwork

Strong communication

Cross-functional collaboration

Safety and regulatory awareness

Education

Bachelor's Degree

Tools

SAP

Microsoft Office

Job description

We are the people who give possibilities purpose

BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

Job Description

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.

Required Skills

Optional Skills

Primary Work Location

USA PR - Anasco

Work Shift

PR 1000pm-630am M-F (United States of America)