Manufacturing Supervisor II - 1st Shift

Baxter•Cleveland, OH

12d•Onsite

About The Position

In the role of Manufacturing Supervisor II, you will contribute significantly to producing high-quality healthcare products accurately and efficiently. This position allows you to lead and cultivate a motivated team in a dynamic environment, ensuring smooth operations that meet rigorous quality standards.

Requirements

Proven track record of interpersonal and leadership skills with the ability to lead, coach, motivate, and enforce company policy and standard operating systems.
Ability to interface well and collaborate with other departments while leading effectively in a team environment.
Comprehensive understanding of associated manufacturing machinery and procedures.
Ability to manage multiple priorities in a high-paced manufacturing plant setting.
Strong professional writing skills and capability to prepare technical reports.
Ability to clearly communicate information during regulatory/client inspections.
Understanding of GMPs and other applicable regulatory guidelines.
Strong assessment and troubleshooting skills.
Ability to respond to detailed inquiries and present information to groups and senior leaders.
Ability to supervise multiple groups/shifts, if applicable.
Skilled in Microsoft Office and capable of operating enterprise software.
Ability to collect, interpret, and analyze data to resolve paths for process improvement and potential root causes.
Demonstrated critical thinking and problem-solving skills.
Solid understanding of manufacturing business insight.
Bachelor’s degree or equivalent experience in technical, operations, business, or a related field is preferred, along with more than 3 years of advancing manufacturing leadership experience; OR Associate's degree accompanied by over 5 years of advancing leadership experience in manufacturing; OR High school diploma or equivalent experience, along with over 10 years of advancing leadership roles in manufacturing.
Proven background managing manufacturing teams in a high-speed production setting.
Applicants must be authorized to work for any employer in the U.S. We cannot sponsor or transfer sponsorship of an employment visa.

Nice To Haves

Injection molding or other types of plastic manufacturing background preferred.

Responsibilities

Communicate guidance, support, direction, and leadership through effective interactions with all personnel during daily operations.
Supervise day-to-day production, scheduling, staffing, material management, compliance, training, and auditing activities.
Identify, prioritize, and provide resources as appropriate.
Interview, hire, coach, motivate, develop, recognize, and manage the performance of direct reports.
Provide regular feedback to all direct reports.
Assist in setting performance objectives and development plans and supervise progress.
Review, approve, and lead documentation for batch and system records.
Assist in the release of products for distribution and meeting product release time goals.
Identify, initiate, and facilitate continuous improvements, lean manufacturing activities, and initiatives like 5S, visual management, and kaizens.
Identify and implement VIPs.
Ensure resources and raw materials are applied in the most efficient and productive manner possible.
Develop training content and facilitate and verify appropriate training assignment and completion for employees in the area.
Ensure compliance with all GMP rules, product documentation, specifications, SOPs, and FDA requirements as required.
Submit and/or maintain and distribute reports related to attendance, labor, efficiency, safety, scrap, and others as needed.
Perform/lead technical reviews, investigations, and process improvement projects.
Provide manufacturing insights for the integration and validation of new equipment and processes.
Resolve technical, material, and cGMP problems that may impact project deadlines.
Provide guidance and troubleshooting assistance as needed during a deviation in the process.
Represent the company during FDA inspections or provide information as necessary to FDA that establishes credibility and demonstrates compliance with cGMPs.
Monitor capital expenditures and assist in developing budgets.
Learn, understand, and apply rigorous quality standards, established guidelines, and current Good Manufacturing Practices (cGMP).
Notify the supervisor and take appropriate action if any safety, quality, mechanical, or discrepancy issues occur.
Sustain a clean and safe work area using 6S principles.

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