487 Supervisor jobs in Woburn
Production Supervisor
Posted 5 days ago
Job Viewed
Job Description
Responsibilities:
- Supervise and coordinate the activities of production staff, ensuring adherence to schedules and quality standards.
- Monitor production processes, identify bottlenecks, and implement solutions to improve efficiency and reduce waste.
- Train, mentor, and evaluate production team members, fostering a culture of performance and continuous learning.
- Ensure compliance with all safety regulations, company policies, and operational procedures.
- Manage inventory levels and material flow to support production demands.
- Collaborate with other departments, such as quality control, maintenance, and logistics, to ensure smooth operations.
- Implement and oversee lean manufacturing principles and other continuous improvement methodologies.
- Maintain production records, analyze performance data, and prepare reports for management.
- Troubleshoot production issues and implement corrective actions promptly.
- Foster a positive and motivating work environment for the production team.
Qualifications:
- Bachelor's degree in Manufacturing, Engineering, Business Administration, or a related field, or equivalent experience.
- Minimum of 3-5 years of experience in a manufacturing or production environment, with at least 1-2 years in a supervisory role.
- Proven leadership and team management skills.
- Strong understanding of manufacturing processes, quality control, and lean principles.
- Excellent problem-solving, analytical, and decision-making abilities.
- Proficiency in using production management software and standard office applications.
- Effective communication and interpersonal skills.
- Ability to work under pressure and meet deadlines.
- Knowledge of safety regulations and best practices in a manufacturing setting.
- Commitment to continuous improvement and operational excellence.
This role is based in Boston, Massachusetts , with a hybrid work schedule that blends on-site leadership with opportunities for remote work. Our client is dedicated to fostering a collaborative and innovative manufacturing environment. If you are a proactive leader with a passion for operational excellence, we encourage you to apply.
Production Supervisor
Posted 7 days ago
Job Viewed
Job Description
- Supervising and coordinating daily production activities to meet output targets.
- Managing, training, and motivating a team of production workers.
- Ensuring adherence to all safety protocols and manufacturing standards.
- Monitoring production processes and implementing corrective actions to resolve issues.
- Optimizing workflow and resource allocation for maximum efficiency.
- Conducting performance reviews and providing feedback to team members.
- Maintaining accurate production records and reports.
- Collaborating with quality control to ensure product standards are met.
- Participating in continuous improvement initiatives and lean manufacturing programs.
- Troubleshooting equipment malfunctions and coordinating maintenance as needed.
- High school diploma or GED required; Associate's or Bachelor's degree in a related field is a plus.
- Minimum of 3-5 years of experience in a manufacturing or production environment, with at least 1-2 years in a supervisory role.
- Proven leadership and team management skills.
- Strong understanding of manufacturing processes, quality control, and safety regulations.
- Excellent problem-solving and decision-making abilities.
- Good communication and interpersonal skills.
- Ability to work flexible hours and shifts as needed.
- Experience with lean manufacturing principles or Six Sigma is advantageous.
- Proficiency in basic computer applications (MS Office).
GMP Production Supervisor
Posted today
Job Viewed
Job Description
The actual location of this job is in Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
Join a global team of over 18,000 people making a meaningful difference from day one. As a GMP Manufacturing Supervisor at our Portsmouth site you will coordinate and support production activities for Cell and Gene processes.
Find out more about what a life at Lonza in Portsmouth, NH could look like for you by watching this short video.
What you’ll get:An agile career and dynamic working culture.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
Medical, dental and vision insurance.
The full list of our global benefits can be also found on .
What you’ll do:Coordinate and support the execution of Cell and Gene production activities, ensuring compliance with ET and site quality systems.
Lead and develop the manufacturing team to meet business needs and career goals.
Support the timely and complete delivery of clinical and commercial materials.
Coordinate various strategies, including EHS, Training, Gowning, Material, Visual Inspection, APS, Cleaning, Scheduling, Financial Management and EM.
Maintain manufacturing areas to the highest cleanliness and 6S standards.
Support technology transfer activities and ensure timely goal achievement.
Establish methods and procedures for attaining specific goals.
BS degree preferred significant experience may be considered in lieu of degree.
Minimum 5 years related experience with a degree or 8 years without.
Proven experience in biological GMP manufacturing operations.
Strong leadership and team development skills.
Ability to coordinate complex projects and ensure timely delivery.
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
GMP Production Supervisor
Posted today
Job Viewed
Job Description
The actual location of this job is in Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
Join a global team of over 18,000 people making a meaningful difference from day one. As a GMP Manufacturing Supervisor at our Portsmouth site you will coordinate and support production activities for Cell and Gene processes.
Find out more about what a life at Lonza in Portsmouth, NH could look like for you by watching this short video.
What you’ll get:An agile career and dynamic working culture.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
Medical, dental and vision insurance.
The full list of our global benefits can be also found on .
What you’ll do:Coordinate and support the execution of Cell and Gene production activities, ensuring compliance with ET and site quality systems.
Lead and develop the manufacturing team to meet business needs and career goals.
Support the timely and complete delivery of clinical and commercial materials.
Coordinate various strategies, including EHS, Training, Gowning, Material, Visual Inspection, APS, Cleaning, Scheduling, Financial Management and EM.
Maintain manufacturing areas to the highest cleanliness and 6S standards.
Support technology transfer activities and ensure timely goal achievement.
Establish methods and procedures for attaining specific goals.
BS degree preferred significant experience may be considered in lieu of degree.
Minimum 5 years related experience with a degree or 8 years without.
Proven experience in biological GMP manufacturing operations.
Strong leadership and team development skills.
Ability to coordinate complex projects and ensure timely delivery.
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
GMP Production Supervisor
Posted today
Job Viewed
Job Description
The actual location of this job is in Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
Join a global team of over 18,000 people making a meaningful difference from day one. As a GMP Manufacturing Supervisor at our Portsmouth site you will coordinate and support production activities for Cell and Gene processes.
Find out more about what a life at Lonza in Portsmouth, NH could look like for you by watching this short video.
What you’ll get:An agile career and dynamic working culture.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
Medical, dental and vision insurance.
The full list of our global benefits can be also found on careers/benefits .
What you’ll do:Coordinate and support the execution of Cell and Gene production activities, ensuring compliance with ET and site quality systems.
Lead and develop the manufacturing team to meet business needs and career goals.
Support the timely and complete delivery of clinical and commercial materials.
Coordinate various strategies, including EHS, Training, Gowning, Material, Visual Inspection, APS, Cleaning, Scheduling, Financial Management and EM.
Maintain manufacturing areas to the highest cleanliness and 6S standards.
Support technology transfer activities and ensure timely goal achievement.
Establish methods and procedures for attaining specific goals.
BS degree preferred significant experience may be considered in lieu of degree.
Minimum 5 years related experience with a degree or 8 years without.
Proven experience in biological GMP manufacturing operations.
Strong leadership and team development skills.
Ability to coordinate complex projects and ensure timely delivery.
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
GMP Production Supervisor
Posted today
Job Viewed
Job Description
The actual location of this job is in Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
Join a global team of over 18,000 people making a meaningful difference from day one. As a GMP Manufacturing Supervisor at our Portsmouth site you will coordinate and support production activities for Cell and Gene processes.
Find out more about what a life at Lonza in Portsmouth, NH could look like for you by watching this short video.
What you’ll get:An agile career and dynamic working culture.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
Medical, dental and vision insurance.
The full list of our global benefits can be also found on careers/benefits .
What you’ll do:Coordinate and support the execution of Cell and Gene production activities, ensuring compliance with ET and site quality systems.
Lead and develop the manufacturing team to meet business needs and career goals.
Support the timely and complete delivery of clinical and commercial materials.
Coordinate various strategies, including EHS, Training, Gowning, Material, Visual Inspection, APS, Cleaning, Scheduling, Financial Management and EM.
Maintain manufacturing areas to the highest cleanliness and 6S standards.
Support technology transfer activities and ensure timely goal achievement.
Establish methods and procedures for attaining specific goals.
BS degree preferred significant experience may be considered in lieu of degree.
Minimum 5 years related experience with a degree or 8 years without.
Proven experience in biological GMP manufacturing operations.
Strong leadership and team development skills.
Ability to coordinate complex projects and ensure timely delivery.
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
Production Floor Supervisor
Posted 7 days ago
Job Viewed
Job Description
Responsibilities:
- Supervise and coordinate the daily activities of the production floor staff, including assigning tasks, monitoring performance, and providing guidance.
- Ensure all production processes are carried out safely, efficiently, and in accordance with quality standards and company policies.
- Monitor production output and quality metrics, identifying areas for improvement and implementing corrective actions.
- Manage workflow and scheduling to meet production targets and delivery deadlines.
- Train and mentor new and existing employees on production procedures, safety protocols, and equipment operation.
- Conduct regular safety inspections and enforce safety regulations to maintain a safe working environment.
- Maintain accurate production records, including output, waste, and downtime, and report on key performance indicators (KPIs).
- Collaborate with quality control, maintenance, and engineering departments to resolve production issues and implement process improvements.
- Ensure the proper maintenance and functioning of production machinery and equipment.
- Implement lean manufacturing principles and best practices to reduce waste and increase efficiency.
- Manage inventory of raw materials and finished goods on the production floor.
- Promote a positive and productive work culture among the production team.
- Conduct performance reviews and provide feedback to team members.
- Assist in the development and implementation of new production techniques and technologies.
- Ensure compliance with all environmental and safety regulations.
- High school diploma or equivalent; Associate's or Bachelor's degree in a related field is a plus.
- Minimum of 5 years of experience in a manufacturing or production environment, with at least 2 years in a supervisory or lead role.
- Proven leadership and team management skills.
- Strong understanding of manufacturing processes, quality control, and safety procedures.
- Experience with lean manufacturing principles and continuous improvement methodologies.
- Excellent problem-solving and decision-making abilities.
- Proficiency in using manufacturing equipment and relevant software.
- Strong communication and interpersonal skills.
- Ability to work effectively under pressure and meet demanding production targets.
- Familiarity with OSHA regulations and safety best practices.
- Experience with inventory management and production planning.
- Ability to read and interpret technical drawings and specifications.
Be The First To Know
About the latest Supervisor Jobs in Woburn !
LPN - Shift Supervisor
Posted today
Job Viewed
Job Description
We are helping people overcome. Join us.
The LPN Shift Supervisor works as part of a multi-disciplinary team providing excellent medical care by overseeing the medical needs of the residents while monitoring the operation of the med room by the medical assisting team. As an LPN at Hope Network you will model and teach exemplary care to floor staff and coordinate care needs with external medical entities.
Here are just some of the ways Hope Network invests in you for all that you do:
• Pay starting from$25/ hour (commensurate with experience)
• Medical, Dental, and Vision Benefits Eligible on Day One
• Retirement Plan with Employer Match
• Generous Paid Time Off
• Educational Reimbursement
• Learning & Development Opportunities
• Supportive Work Environment
• Employee Assistance Program
Job Responsibilities:
Treatment
• Assist nursing team with dispensing, monitoring, procurement, and evaluating efficacy of client medications, including intermuscular injections.
• Assist nursing team with monitoring and treating chronic and acute medical conditions within the scope of practice
Leadership
• Pass medications and facilitate supervision of medication passes, when needed
• Provide training and hands-on assistance in residents' activities of daily living and self-care tasks.
• Coordinate and implement infection control and other quality assurance procedures
• Be a super-user with the electronic medication administration record (eMAR) to facilitate quality monitoring, as needed
Coordination of Care
• Act as liaison with psychiatrist, external medical providers, guardians, residents, and staff
• Collaborate with pharmacies and staff regarding medication orders.
• Participate in the development and implementation of individual treatment plans for residents.
• Assist with medical appointments as necessary
• Close work with the nursing team and interdisciplinary team to think outside of the box to find solutions to meet residents where they are; to provide truly patient centered care.
Job Requirements:
• You appreciate a high level of autonomy in leading medical care.
• You seek evidence-based decision making within your scope of practice
• You value positive work culture, team cohesion, and building up of co-workers
• Advocacy and empathy are pillars of your nursing practice
• You demonstrate positivity and professionalism in communication.
• You thrive both when working independently and with a multidisciplinary team.
Licensing Requirements
• Active State of Michigan Practical Nurse Licensure (LPN).
• Prior experience in a residential setting preferred
• Experience working with electronic medical records.
• Valid driver's license with acceptable driving record.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
LPN - Shift Supervisor
Posted today
Job Viewed
Job Description
We are helping people overcome. Join us.
The LPN Shift Supervisor works as part of a multi-disciplinary team providing excellent medical care by overseeing the medical needs of the residents while monitoring the operation of the med room by the medical assisting team. As an LPN at Hope Network you will model and teach exemplary care to floor staff and coordinate care needs with external medical entities.
Here are just some of the ways Hope Network invests in you for all that you do:
• Pay starting from$25/ hour (commensurate with experience)
• Medical, Dental, and Vision Benefits Eligible on Day One
• Retirement Plan with Employer Match
• Generous Paid Time Off
• Educational Reimbursement
• Learning & Development Opportunities
• Supportive Work Environment
• Employee Assistance Program
Job Responsibilities:
Treatment
• Assist nursing team with dispensing, monitoring, procurement, and evaluating efficacy of client medications, including intermuscular injections.
• Assist nursing team with monitoring and treating chronic and acute medical conditions within the scope of practice
Leadership
• Pass medications and facilitate supervision of medication passes, when needed
• Provide training and hands-on assistance in residents' activities of daily living and self-care tasks.
• Coordinate and implement infection control and other quality assurance procedures
• Be a super-user with the electronic medication administration record (eMAR) to facilitate quality monitoring, as needed
Coordination of Care
• Act as liaison with psychiatrist, external medical providers, guardians, residents, and staff
• Collaborate with pharmacies and staff regarding medication orders.
• Participate in the development and implementation of individual treatment plans for residents.
• Assist with medical appointments as necessary
• Close work with the nursing team and interdisciplinary team to think outside of the box to find solutions to meet residents where they are; to provide truly patient centered care.
Job Requirements:
• You appreciate a high level of autonomy in leading medical care.
• You seek evidence-based decision making within your scope of practice
• You value positive work culture, team cohesion, and building up of co-workers
• Advocacy and empathy are pillars of your nursing practice
• You demonstrate positivity and professionalism in communication.
• You thrive both when working independently and with a multidisciplinary team.
Licensing Requirements
• Active State of Michigan Practical Nurse Licensure (LPN).
• Prior experience in a residential setting preferred
• Experience working with electronic medical records.
• Valid driver's license with acceptable driving record.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
LPN - Shift Supervisor
Posted today
Job Viewed
Job Description
We are helping people overcome. Join us.
The LPN Shift Supervisor works as part of a multi-disciplinary team providing excellent medical care by overseeing the medical needs of the residents while monitoring the operation of the med room by the medical assisting team. As an LPN at Hope Network you will model and teach exemplary care to floor staff and coordinate care needs with external medical entities.
Here are just some of the ways Hope Network invests in you for all that you do:
• Pay starting from$25/ hour (commensurate with experience)
• Medical, Dental, and Vision Benefits Eligible on Day One
• Retirement Plan with Employer Match
• Generous Paid Time Off
• Educational Reimbursement
• Learning & Development Opportunities
• Supportive Work Environment
• Employee Assistance Program
Job Responsibilities:
Treatment
• Assist nursing team with dispensing, monitoring, procurement, and evaluating efficacy of client medications, including intermuscular injections.
• Assist nursing team with monitoring and treating chronic and acute medical conditions within the scope of practice
Leadership
• Pass medications and facilitate supervision of medication passes, when needed
• Provide training and hands-on assistance in residents' activities of daily living and self-care tasks.
• Coordinate and implement infection control and other quality assurance procedures
• Be a super-user with the electronic medication administration record (eMAR) to facilitate quality monitoring, as needed
Coordination of Care
• Act as liaison with psychiatrist, external medical providers, guardians, residents, and staff
• Collaborate with pharmacies and staff regarding medication orders.
• Participate in the development and implementation of individual treatment plans for residents.
• Assist with medical appointments as necessary
• Close work with the nursing team and interdisciplinary team to think outside of the box to find solutions to meet residents where they are; to provide truly patient centered care.
Job Requirements:
• You appreciate a high level of autonomy in leading medical care.
• You seek evidence-based decision making within your scope of practice
• You value positive work culture, team cohesion, and building up of co-workers
• Advocacy and empathy are pillars of your nursing practice
• You demonstrate positivity and professionalism in communication.
• You thrive both when working independently and with a multidisciplinary team.
Licensing Requirements
• Active State of Michigan Practical Nurse Licensure (LPN).
• Prior experience in a residential setting preferred
• Experience working with electronic medical records.
• Valid driver's license with acceptable driving record.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.