Production Supervisor - C Shift

MilliporeSigma; Jaffrey (NH); On-site; USD 60,000 - 95,000; Full time

Job summary

An established industry player is seeking a dynamic Production Supervisor for their C Shift operations. In this pivotal role, you will lead a dedicated team overseeing the production of life science filtration membranes. Your responsibilities will include ensuring quality and safety standards, driving process improvements, and fostering a collaborative environment. With a focus on leadership and communication, you will play a crucial role in meeting production targets while maintaining compliance with industry standards. If you are passionate about innovation and teamwork in a diverse setting, this opportunity is perfect for you.

Qualifications

• 3+ years in an FDA-regulated industry or manufacturing environment.
• 2+ years in a leadership role with increasing responsibilities.

Responsibilities

• Oversee manufacturing operations for life science filtration membranes.
• Manage a team, ensuring production targets and quality standards.
• Drive continuous improvement using lean tools.

Skills

Leadership

Communication

Problem-solving

Continuous Improvement

Team Management

Education

High School diploma or GED

Bachelor's Degree in Manufacturing or Engineering

Tools

Lean Tools

QMS

ISO Standards

cGMP Compliance

Job description

Join to apply for the Production Supervisor - C Shift role at MilliporeSigma

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. We are passionate about caring for our diverse community of people, customers, patients, and the planet. We seek curious minds eager to imagine the unimaginable with us.

Your Role

The Production Supervisor - C Shift (8:40 PM - 6:40 AM) oversees manufacturing operations for life science filtration membranes or devices. Responsibilities include managing a team, ensuring production targets, maintaining quality and safety standards, and fostering a safe, clean, and organized work environment. The role involves implementing manufacturing methods, monitoring workflow, troubleshooting issues, driving process improvements, training staff, ensuring cGMP compliance, and collaborating cross-functionally. Success depends on strong leadership, communication, and problem-solving skills, with a focus on safety, quality, and delivery performance.

Duties Include

1. Drive continuous improvement using lean tools and operator engagement.
2. Communicate expectations, plan, monitor, appraise, coach, and enforce policies.
3. Ensure KPIs are met (e.g., MPS, back order).
4. Maintain product integrity and traceability.
5. Manage employee performance through coaching and appraisals.
6. Collaborate with other departments to support teamwork.
7. Inform management of production issues impacting schedules.
8. Lead risk assessments, quality, and safety audits.

Who You Are

Minimum Qualifications:

• 3+ years in an FDA-regulated industry or manufacturing environment.
• 2+ years in a leadership role with increasing responsibilities.
• High School diploma or GED.

Preferred Qualifications:

• Bachelor's Degree in Manufacturing, Engineering, or related field.
• Knowledge of QMS, ISO, and cGMP.
• Strong leadership, communication, and troubleshooting skills.
• Ability to motivate and build high-performing teams.
• Proactive in driving change and process improvements.

What We Offer

We celebrate diversity and are committed to inclusion and growth. Join us to work in a culture that empowers everyone to make a difference and innovate in science and technology.

Apply now and become part of our diverse team! For more on our diversity, equity, and inclusion initiatives, visit our webpage.