Sr Supv, Manufacturing
Hayward, CA 
Share
Posted 17 days ago
Job Description

This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives- where your purpose accelerates our mission.

Your Role at Baxter

The Supervisor II, Manufacturing position is responsible for implementing and supervising all activities in the production area to ensure manufacturing goals and project deadlines are met while maintaining compliance with current good manufacturing practices (cGMPs), environmental health and safety (EHS) guidelines and any other regulations that could apply. Focus is on optimization for the use of raw materials, equipment and personnel in producing quality products. Monitor and ensure efficiency and effectiveness in various areas. May include managing capital expenditure and developing budgets. Recommends manufacturing policies, procedures and programs. May supervise more than one area

What you'll be doing

  • Supervisor is expected to provide guidance, support, direction and leadership through positive interactions with all personnel during daily operations.

  • Responsible for supervising the day-to-day production, scheduling, staffing, material management, compliance, training and auditing activities - to meet customer requirements including deadlines and quality standards.

  • Interview, hire, coach, motivate, develop and discipline staff. Conduct annual performance reviews for all direct reports. Assist in setting performance objectives and development plans. Monitor progress.

  • Review, approve, and manage documentation for batch and system records. Assist in release of product for distribution. Assist in meeting product release time goals.

  • Emphasize training programs designed to enable staff to consistently execute all manufacturing processes with strict compliance to cGMPs and EHS regulations.

  • Develop and implement performance measurement and internal auditing programs in order to routinely evaluate operation efficiency and quality. Implement changes as needed based on assessments.

  • Perform/lead technical reviews, investigations and process improvement projects.

  • Provide manufacturing input into integration and validation of new equipment and processes.

  • Resolves 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. Provide information as necessary to FDA that establishes credibility and demonstrates compliance with cGMPs.

  • Provide a positive and equitable working environment emphasizing the Baxter Shared Values: Respect /Responsiveness / Results.

  • Identifies, initiates and facilitates continuous improvements, lean manufacturing activities and initiatives, such as 5S, visual management, kaizens.

  • This role is also be responsible for identifying and implementing Manufacturing savings projects.

  • Learn, understand and apply rigorous quality standards, Standard Operating Procedures (SOPs) and Current Good Manufacturing Practices (cGMP)

  • Submits and/or maintains and distributes reports related to attendance, labor, efficiency, safety, scrap and others as needed.

  • Work weekends and daily overtime and work inside cleanroom to monitor, coach, and lead team.

What you'll bring

  • Bachelor's degree required.

  • 3-5 years manufacturing experience

  • 2+ years of supervisory experience

  • To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. List knowledge, skills, and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.

  • Proven track record of interpersonal and leadership skills with ability to interface well with other departments, and lead effectively and efficiently in a team environment.

  • In-depth process knowledge of related manufacturing equipment and processes.

  • Ability to manage multiple priorities in a manufacturing plant setting.

  • Ability to analyze and interpret scientific and statistical data.

  • Strong professional writing skills and ability to prepare technical reports. Ability to clearly articulate information during regulatory/client inspections.

  • Ability to understand 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.

  • Computer proficiency in Microsoft Office and ability to use enterprise software.

  • Ability to collect and analyze data and information to determine paths for process improvement and potential root cause

  • Demonstrated critical thinking and problem-solving skills.

  • Working knowledge of manufacturing business acumen.

We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $76,000 - $104,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.

#LI-KV1

The successful candidate for this job may be required to verify that he or she has been vaccinated against COVID-19, subject to reasonable accommodations for individuals with medical conditions or religious beliefs that prevent vaccination, and in accordance with applicable law.

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

EEO is the Law
EEO is the law - Poster Supplement
Pay Transparency Policy

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our .

133332

 

Job Summary
Company
Start Date
As soon as possible
Employment Term and Type
Regular, Full Time
Required Education
Bachelor's Degree
Required Experience
3 to 5 years
Email this Job to Yourself or a Friend
Indicates required fields