Supervisor I, Manufacturing 3rd Shift

Round Lake, IL, United States

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\xe2\x80\x99ll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter\xe2\x80\x99s 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\xe2\x80\x94 where your purpose accelerates our mission.

Summary

The supervisor position is responsible for implementing and supervising daily activities in a specific production area to ensure manufacturing goals and project deadlines are met while maintaining compliance with current good manufacturing practices (GMPs), environmental health and safety (EHS) guidelines and any other regulations that could apply. May monitor and control labor.

Essential Job Duties and Responsibilities

  • The Production 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 \xe2\x80\x93 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.
  • 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.
  • 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.
Qualifications
  • Demonstrated 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.
  • A good understanding and/or hands-on familiarity with the principles of lean manufacturing.
  • Strong professional writing skills and ability to prepare technical reports.
  • Experienced understanding of cGMPs and other regulatory guidelines applicable to the medical/pharmaceutical industry.
  • Ability to respond to detailed inquiries, and present information to groups and senior management.
  • Ability to work weekends and overtime when necessary is required.
Candidate should not be allergic to PENICILLIN or the CEPHALOSPORINS.

Education and/or Experience
  • BS degree preferred in a scientific, engineering, or business discipline with 3 or more years of manufacturing experience, preferably in an FDA-controlled, aseptic, pharmaceutical environment. Plus 2 or more years related supervisory experience required.
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 our employees, and we strive to be more transparent with our pay practices. To that end, this position has a salary range of $52,800 to $132,000 and also includes an annual incentive bonus. The above range represents the expected salary range for this position. The actual salary may vary based upon several factors including, but not limited to, relevant skills/experience, time in the role, business line, and geographic/office location

#IND-USOPS

#LI-DM1

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.

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

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Job Detail

  • Job Id
    JD4258489
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    $52800 - 132000 per year
  • Employment Status
    Permanent
  • Job Location
    Round Lake, IL, United States
  • Education
    Not mentioned