Manufacturing Group Lead - 3rd Shift

Technical Needs; Manchester (NH); On-site; USD 75,000 - 110,000; Full time

Job summary

Technical Needs is seeking a Production Cleanroom Team Lead for Manchester, NH to supervise the night shift in a sterile, regulated environment. You will oversee assembly, testing and documentation of mechanical and electrical devices while upholding quality and safety standards.

The role requires hands-on manufacturing experience, strong leadership, and familiarity with cGMP, GDP, ISO, QSR and FDA regulations.

Qualifications

• Minimum of 3 years hands-on manufacturing experience, with at least 1 year in a leadership role
• Experience with assembly, testing, and documentation of mechanical and electrical devices
• Knowledge of production practices in a cGMP & GDP environment
• Strong interpersonal, communication, and leadership skills
• Medical device manufacturing experience preferred
• Working knowledge of Microsoft Office and basic computer skills

Responsibilities

• Oversee night shift production activities ensuring quality and safety
• Lead assembly, testing, and documentation of devices
• Maintain cleanroom integrity and regulatory compliance
• Foster communication between workers and management
• Monitor team performance and motivate staff

Skills

Leadership

Communication

Team leadership

GMP knowledge

Regulatory compliance

Tools

Microsoft Office

Job description

Our client is looking for a Production Cleanroom Team Lead in the manufacturing industry, working in a sterile, controlled environment. In this role, you will be responsible for overseeing production activities during the night shift, ensuring product quality and safety standards are met, and maintaining cleanroom integrity. You’ll lead assembly, testing, and documentation of mechanical and electrical devices while monitoring team performance and fostering effective communication between workers and management. This position requires strong leadership skills, hands‑on experience in manufacturing, and familiarity with cGMP, GDP, ISO, QSR, and FDA regulations. You should be comfortable working in a fast‑paced, regulated environment and have excellent attention to detail, along with the ability to motivate and guide your team to meet production goals and quality standards.

Required Skills, Education and Experience

• Minimum of 3 years hands‑on experience in a manufacturing environment, with at least 1 year in a leadership role
• Experience with assembly, testing, and documentation of mechanical and electrical devices
• Knowledge of production practices in a cGMP & GDP environment
• Strong interpersonal, communication, and leadership skills
• Medical device manufacturing experience preferred
• Working knowledge of Microsoft Office and basic computer skills

Work Schedule

Monday–Friday, 11:00 PM–7:00 AM, starting Sunday night at 11 PM