Supervisor Manufacturing - Shift C (10:00pm - 6:00am)

Baxter•Aibonito, PR

3d•Onsite

About The Position

This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job—you will find purpose and pride.

Requirements

BA OR BS in Engineering/ or related field with 1-3 years of manufacturing experience.
One-year previous supervisor in a manufacturing FDA regulated environment preferred.
Bilingual (English and Spanish).
Excellent interpersonal relations skills.
Must be knowledgeable of Baxter specifications and procedures.
Strong knowledge of Baxter manufacturing process.
Knowledge on GMP-QSR’S, OSHA, BHEST, SPEC, SOP and HR policies.
Work closely with other departments administrative and managers.
Keeps good communication upward and downward the administrative chain of command.

Responsibilities

Supervise all assembly operation including the packing area assuring compliance of manufacturing and quality regulations, and production standards.
Customer satisfaction through high quality, service and low cost.
Supervise assembly and packing operations within a manufacturing cell.
Deals with associates, materials and equipment problems (opportunities)
Maintains absenteeism to a minimum level according to Baxter policies.
Trains and evaluates new employees.
Plan cross training for regular associates.
Maintain a motivated work force.
Coordinates and supervise code changes.
Keep process monitoring on quality and performance targets.
Promotes a world class environment through working team and suggestions.
Develop and establish process improvement.
Evaluates complaints data.
Must be knowledgeable of specifications and procedures.
Knowledge of specifications and procedures.
Knowledge of manufacturing processes and line capacity.
May affect P/L positively by the implementation of scrap and cost reduction programs and with the optimization of resources and capacity.
Manually document (ex: checker chart) and/or electronically (ex: POMs) the required information to comply applicable procedures and specifications. This information includes but is not limited tp process parameters, lots, amount of production, and others.
Promote a zero-harm work place, and assure that required EHS resources are available and that all applicable EHS practices and rules are being followed by supervised employees.

Benefits

medical and dental coverage that start on day one
insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts
educational assistance programs
paid holidays
paid time off ranging from 20 to 35 days based on length of service
family and medical leaves of absence
paid parental leave
commuting benefits
Employee Discount Program
Employee Assistance Program (EAP)
childcare benefits