Lead Hand, Mixing

7 months ago

New Tecumseth, Canada Baxter Full time

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.

07Job Description

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 Lead Hand 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. We are currently looking for an energetic, hard-working Lead Hand to work full-time on our Midnight shift (Monday to Friday 23:00-07:00) at our Alliston facility. We offer an Employee Stock Purchasing Plan, Defined contribution pension plan and medical/dental benefits on your first day 

In this role, you will:

Identify improvements opportunities within the Viaflex Mixing Department.

Drive department performance transformation through process improvement initiatives.

Lead 6S initiatives within the department to reach the department goals.

Work with cross functional teams to drive projects to completion.

Manage and schedule TPM’s with in the department and coordinate with contractors to complete.

Generate Critical Work Requests for tasks required.

Support in coordinating Validation activities as required.

GENERAL EXPECTATIONS

The top two priorities for all Baxter Alliston employees are Safety and Quality:

Safety : Support our goal to achieve a “Zero Harm Environment”, by ensuring the safety of yourself and your co-workers by:

 Following all safety procedures

 Understanding potential hazards in your area

 Wearing appropriate PPE

 Reporting all incidents / near-misses / concerns

 Embracing 6s

Quality : Ensure the quality of our products to ensure patient safety and achieve our mission of “Saving and Sustaining Lives”. This can be achieved by:

+++Following Good Manufacturing Practices (GMP) +++

Adhering to all quality procedures

Completing training on-time

Doing it Right the First Time, and

Reporting any quality concerns immediately.

As part of the plant’s Enterprise Management System (EMS ), all employees must embrace a culture of Continuous Improvement by:

Participating in improvement activities

Identifying and implementing continuous improvement ideas

Participating in Tier meetings

Recognizing your peers, and

Embracing 6s.

What you'll be doing:

Identifies, designs, and implements improvements that provide fast, sustainable, and low-risk/high-reward benefits for the assigned areas.

Identifies improvements to cycle times, production sequences, material flow, etc. to ensure that the assigned area has the capacity to maintain the supply chain and/or introduce new products.

Coaches’ area members on process ownership, standard ways of working and to have a sustainable process for improvement.

Evaluates, recommends, and provides technical support in the selection, installation, and qualification of processing equipment.

Supports areas initiatives to ensure compliance with internal and external regulatory requirements (GMP, OSHA, SHE, etc.).

Monitor activities of team members and machines to ensure efficient production of quality product.

Hands-on equipment and process troubleshooting, repair, and improvement. Support Mixing Operations and Special projects on a regular basis / as assigned, according to Current Good Manufacturing Practices (cGMPs).

Promotes a continuous improvement mentality and problem-solving methodology through addressing daily Mixing needs and improvements, along with coordinating and owning NCRs/CAPAs as required.

What you'll bring:

Successful completion of High School diploma or GED (Mechanical, Electrical, Industrial, Chemical, Electronics)

Manufacturing/Quality/Continuous Improvement experience in a GMP environment

Required: 3 – 6 years

Communicates well, minimally comfortable at the interpersonal and small group levels.

Strong ability to balance multiple priorities with excellent time management skills.

Able to organize own work and prioritize work for others.

Strong problem-solving skills and ability to identify root cause.

Effectively leads and develops staff.

Able to make decisions given sufficient input and support.

Able to explain technical issues using verbal or written form clearly and logically.

Preferred:

Strong communication skills, above average interpersonal, small group and large audience skills.

Able to bring structure to a team/process so that efforts are concerted and organized.

Able to make key decisions in the face of ambiguity, balances accuracy and timeliness.

Excels at simplification allowing non-technical team members to understand the issues. Produces correct, concise documents detailing technical content

Nice to have:

University degree, Bachelor of Engineering, Green Belt Six Sigma (Mechanical, Electrical, Industrial, Sciences, Project Management)

Significant project engineering/management in healthcare manufacturing

Preferred: 6+ years

#LI-AR1

#IND-CA

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