Manufacturing supervisor

Baxter
Round Lake, IL Full Time
POSTED ON 6/20/2024

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

This is where my hands make life-sustaining products

You are driven by the knowledge that the products you help make saves and sustain lives. You can move quickly, address questions, and encourage teammates, all while getting quality products out on time.

You are calm, positive, and a key part of a fast-paced environment that emphasizes camaraderie and teamwork. As a Manufacturing Supervisor, you are happiest when you are moving, and we will not disappoint!

Baxter is known for its speed and high-quality product. Our manufacturing operations are around-the-clock to meet the needs of our customers.

Our high-caliber talent works through the challenges at hand while pushing toward meeting client order needs. Different shift assignments allow for flexibility and safety.

Your team

Baxter is focused on saving and sustaining lives by manufacturing high-quality products. We strive to create quality products for our customers each day.

Delivering life-saving products is about getting them right, and attention to detail is how we make sure we meet that challenge.

We are a team that supports each other throughout each shift. Working together in a supportive and open culture makes our processes evolve for the better and engages our workforce.

What You'll Be Doing

  • 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 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.

What You'll Bring

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.

  • 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 CEPHALOSPORINS.

LI-BB1

Last updated : 2024-04-28

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