103 Manufacturing jobs in Belding

Description

Agility, Impact, Methodology. Do you exhibit these values and wish to be around others that do too? Do you thrive in fast-paced environments where agility, adaptability, and high standards go hand in hand? Are you driven to make a meaningful impact, whether through your work, your support of others, or your commitment to your community? Are you motivated by a disciplined, science-based approach that ensures consistent excellence, safety, and integrity in everything you do? If these statements resonate with you, Grand River Aseptic Manufacturing (GRAM) welcomes you to apply to join our community of dedicated individuals improving lives every day!

Overview of this Position:

The Manufacturing Technician is responsible for performing various routine and unplanned sanitization, support, and preparation tasks following established procedures and cGMP regulations under guidance of a production supervisor and/or senior management.

This position is for the Butterworth manufacturing facility. Shifts include:

(A) Weekdays: Mon - Wed (and every other Thursday) 6:00 am to 6:00 pm

(B) Weeknights: Mon - Wed (and every other Thursday) 6:00 pm to 6:00 am

(C) Weekend days: Fri - Sun (and every other Thursday) 6:00 am to 6:00 pm

(D) Weekend nights: Fri - Sun (and every other Thursday) 6:00 pm to 6:00 am

Non-Negotiable Requirements:

• High school diploma or equivalent is required.

Preferred Requirements:

• Experience in the pharmaceutical industry is preferred.

Responsibilities Include (but are not limited to ):

• Follow production and manufacturing procedures.
• Perform equipment preparation, sterilization, and assist with filling operations.
• Accurately document data and complete batch records as needed.
• Perform cleaning and sanitization duties as instructed by the applicable procedure.
• Train on and adhere to strict operations procedures, protocols, and batch records.
• Train in various manufacturing tasks including, but not limited to: sanitization, component preparation and sterilization activities, and basic operation of equipment.
• Operate production equipment.
• Perform duties in Grade C cleanrooms and associated support areas including GMP warehouse.
• Qualification for use of a full-face respirator is required when working with hazardous chemicals.

Full job description available during formal interview process.

What Sets GRAM Apart from Other Employers:

MEDICAL BENEFITS starting day 1: Blue Cross Blue Shield medical and dental, vision, life insurance, and disability benefits are available to you and your family on your first day of work, with the company paying for 75% of the cost! Once eligible for the 401(k) program, all your contributions are immediately 100% vested, and you are immediately vested in GRAM contributions as well. We also offer generous off-shift premiums!

Paid VOLUNTEERISM starting day 1: GRAM encourages giving back to our community by offering 16 hours of paid volunteer time per calendar year!

PTO: Full-time employees accrue up to 13 days of time off per calendar year. You choose how to use this time for your vacation, sick, or mental health needs!

WELLNESS TIME OFF: Employees earn 1 hour of time off for every 30 hours worked to use how you choose.

PAID HOLIDAYS: We offer 10 paid holidays per calendar year with immediate eligibility!

PAY: Depends on Experience and is discussed during the interview process.

If you meet the required criteria listed above, GRAM welcomes you to apply today!

Our client is seeking a skilled Manufacturing Engineer to join their dynamic team. This hybrid role requires a blend of on-site presence for hands-on process improvement and remote work for analysis and design. You will be instrumental in optimizing manufacturing processes, improving efficiency, and ensuring the quality of production output. The ideal candidate has a strong background in manufacturing operations, process design, and problem-solving. Responsibilities include analyzing production data, identifying bottlenecks, and implementing solutions to enhance throughput and reduce waste. You will work closely with production staff, quality control, and engineering teams to drive continuous improvement initiatives. Experience with Lean Manufacturing principles, Six Sigma methodologies, and process automation is highly desirable. The ability to develop and implement new manufacturing procedures, equipment upgrades, and quality control measures is key. This role demands excellent analytical skills, a hands-on approach, and the ability to communicate effectively with diverse teams. Join us to make a tangible impact on our manufacturing operations and contribute to our commitment to excellence.

Responsibilities:

• Analyze manufacturing processes to identify areas for improvement in efficiency, quality, and cost reduction.
• Develop and implement process improvements using Lean Manufacturing and Six Sigma methodologies.
• Design, install, and test new manufacturing equipment and production lines.
• Create and maintain Standard Operating Procedures (SOPs) for manufacturing processes.
• Troubleshoot production issues and implement corrective actions.
• Collaborate with cross-functional teams, including production, quality, and R&D.
• Develop and manage project timelines and budgets for manufacturing initiatives.
• Ensure compliance with safety regulations and industry standards.
• Train production staff on new processes and equipment.
• Monitor key performance indicators (KPIs) and report on manufacturing performance.

Qualifications:

• Bachelor's degree in Manufacturing Engineering, Mechanical Engineering, Industrial Engineering, or a related field.
• 3+ years of experience in manufacturing engineering or process improvement.
• Proficiency in Lean Manufacturing, Six Sigma, and statistical process control (SPC).
• Experience with CAD software and automation technologies is a plus.
• Strong analytical, problem-solving, and project management skills.
• Excellent communication and interpersonal abilities.
• Ability to work effectively both independently and as part of a team.

This position is based in Grand Rapids, Michigan, US , and operates on a hybrid schedule.

Our client, a leading manufacturing firm, is looking for a meticulous and detail-oriented Quality Control Inspector to join their team in **Grand Rapids, Michigan, US**. This role is fundamental to ensuring that all manufactured products meet stringent quality standards and specifications before reaching customers. You will be responsible for performing comprehensive inspections of raw materials, in-process components, and finished goods. Key duties include utilizing various measuring instruments and testing equipment, identifying defects, documenting inspection results accurately, and collaborating with production teams to address quality issues promptly. You will also participate in the development and implementation of quality control procedures and assist in root cause analysis of quality problems. The ideal candidate will have a high school diploma or equivalent, with a strong understanding of quality control principles and manufacturing processes. Previous experience as a Quality Control Inspector or in a similar quality assurance role is required, preferably within a manufacturing environment. Proficiency with calipers, micrometers, and other precision measuring tools is essential. Strong analytical skills, a keen eye for detail, and the ability to read and interpret technical drawings and specifications are paramount. Excellent record-keeping and communication skills are also necessary to effectively report findings and collaborate with cross-functional teams. This position is based in **Grand Rapids, Michigan, US**, a hub for manufacturing and innovation. This role requires full-time, on-site presence to conduct physical inspections and work directly with production personnel.

Our client is looking for a meticulous and detail-oriented Quality Control Specialist to join their manufacturing team in Grand Rapids, Michigan, US . This role is vital in ensuring that all manufactured products meet stringent quality standards and specifications. You will be responsible for conducting inspections, performing tests, documenting results, and identifying any deviations from quality requirements. The ideal candidate will have a strong understanding of quality control principles within a manufacturing environment, excellent observational skills, and the ability to work efficiently and accurately. This position requires a commitment to maintaining high-quality output and contributing to a culture of continuous improvement.

Key responsibilities include inspecting raw materials, in-process components, and finished goods to verify compliance with quality standards. You will perform various testing procedures using calibrated equipment and document all inspection and test results accurately in the quality management system. Identifying non-conforming products and initiating the appropriate procedures for quarantine and disposition is a crucial part of this role. You will also participate in root cause analysis for quality issues and contribute to the development and implementation of corrective and preventive actions (CAPA). Collaborating with production and engineering teams to resolve quality-related concerns and ensure product consistency is essential. Maintaining detailed records, generating quality reports, and ensuring proper calibration of testing equipment are also key duties. This role may involve participating in internal audits and assisting with customer quality inquiries. Staying updated on industry quality standards and best practices is important for continuous improvement. The ability to interpret technical drawings, specifications, and quality standards is necessary.

Qualifications:

• High school diploma or equivalent; Associate's degree in a technical field is preferred.
• Minimum of 3 years of experience in quality control or quality assurance in a manufacturing setting.
• Solid understanding of quality control principles, methodologies, and tools.
• Experience with inspection techniques and proficiency in using measuring and testing equipment.
• Ability to read and interpret technical drawings, specifications, and blueprints.
• Strong attention to detail and accuracy in documentation.
• Familiarity with ISO 9001 or other relevant quality management systems is a plus.
• Good communication and teamwork skills.
• Basic computer proficiency, including experience with spreadsheets and databases.

Job Title: Entry-Level Pharmaceutical Operations
Job Description
We are seeking a Pharmaceutical Quality Technician to perform equipment preparation, bulk drug formulation, and aseptic filling duties. The role involves accurately documenting data and completing batch records, as well as performing cleaning and sanitization duties in compliance with applicable procedures. You will also need to successfully complete the facility's aseptic gowning and manufacturing qualification program and perform duties in ISO 5 (Grade A) and ISO 7 (Grade C) cleanrooms.
+ These positions are for off-shift roles.
+ Week 1 schedule: Thursday to Sunday from 6 PM to 6 AM.
+ Week 2 schedule: Friday to Sunday from 6 PM to 6 AM
+ Following a 48/36 hour rotation.
Responsibilities
+ Perform equipment preparation, bulk drug formulation, and aseptic filling duties.
+ Accurately document data and complete batch records.
+ Execute cleaning and sanitization duties as instructed by the applicable procedure.
+ Complete the facility's aseptic gowning and manufacturing qualification program.
+ Operate within ISO 5 (Grade A) and ISO 7 (Grade C) cleanrooms following cGMP regulations.
Essential Skills
+ Bachelor's degree in Science field (Biology, Chemistry, Health Sciences, Microbiology, etc.)
Pay and Benefits
The pay range for this position is $ - $ /yr.
MEDICAL BENEFITS starting day 1: Blue Cross Blue Shield medical and dental, vision, life insurance, and disability benefits are available to you and your family on your first day of work, with the company paying for 75% of the cost! Once eligible for the 401(k) program, all your contributions are immediately 100% vested, and you are immediately vested in GRAM contributions as well. We also offer generous off-shift premiums!
Paid VOLUNTEERISM starting day 1: GRAM encourages giving back to our community by offering 16 hours of paid volunteer time per calendar year!
PTO: Full-time employees accrue up to 13 days of time off per calendar year. You choose how to use this time for your vacation, sick, or mental health needs!
WELLNESS TIME OFF: Employees earn 1 hour of time off for every 30 hours worked to use how you choose.
PAID HOLIDAYS: We offer 10 paid holidays per calendar year with immediate eligibility!
Workplace Type
This is a fully onsite position in Grand Rapids,MI.
Application Deadline
This position is anticipated to close on Oct 22, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

Job Title: Aseptic Manufacturing AssociateJob Description
As an Aseptic Manufacturing Associate, you will play a crucial role in equipment preparation, bulk drug formulation, and aseptic filling. You will be responsible for accurately documenting data and completing batch records. Additionally, you will perform cleaning and sanitization duties as per the applicable procedures. Successful completion of the facility's aseptic gowning and manufacturing qualification program is required. Duties will be performed in ISO 5 (Grade A) and ISO 7 (Grade C) cleanrooms.
Responsibilities
+ Perform equipment preparation, bulk drug formulation, and aseptic filling.
+ Accurately document data and complete batch records.
+ Perform cleaning and sanitization duties as instructed by applicable procedures.
+ Complete the facility's aseptic gowning and manufacturing qualification program.
+ Work in ISO 5 (Grade A) and ISO 7 (Grade C) cleanrooms.
Essential Skills
+ Proficiency in GMP and cGMP regulations.
+ Experience with laboratory and aseptic techniques.
Additional Skills & Qualifications
+ Bachelor's degree OR a high school diploma and relevant work experience.
+ Level I: 2+ years in a manufacturing, medical, and/or laboratory environment.
+ Level II: 3+ years in a manufacturing, medical, and/or laboratory environment with sterile manufacturing experience.
+ Level III: 4+ years in a manufacturing, medical, and/or laboratory environment with sterile manufacturing experience.
Work Environment
This role involves off-shift hours at Butterworth. The schedule is as follows: 6 PM to 6 AM Thursday-Sunday on week one, and 6 PM to 6 AM Friday-Sunday on week two, alternating between 48 and 36-hour weeks. The company offers a comprehensive benefits package starting on day one, including medical, dental, vision, life insurance, and disability benefits, with the company covering 75% of the cost. A 401(k) program with immediate vesting in contributions is available, along with generous off-shift premiums. Employees receive 16 hours of paid volunteer time per calendar year, accrue up to 13 days of PTO for vacation, sick, or mental health needs, and earn one hour of wellness time off for every 30 hours worked. The company also provides 10 paid holidays per year with immediate eligibility.
Job Type & Location
This is a Permanent position based out of Grand Rapids, Michigan.
Pay and Benefits
The pay range for this position is $ - $ /yr.
MEDICAL BENEFITS starting day 1: Blue Cross Blue Shield medical and dental, vision, life insurance, and disability benefits are available to you and your family on your first day of work, with the company paying for 75% of the cost! Once eligible for the 401(k) program, all your contributions are immediately 100% vested, and you are immediately vested in GRAM contributions as well. We also offer generous off-shift premiums!
Paid VOLUNTEERISM starting day 1: GRAM encourages giving back to our community by offering 16 hours of paid volunteer time per calendar year!
PTO: Full-time employees accrue up to 13 days of time off per calendar year. You choose how to use this time for your vacation, sick, or mental health needs!
WELLNESS TIME OFF: Employees earn 1 hour of time off for every 30 hours worked to use how you choose.
PAID HOLIDAYS: We offer 10 paid holidays per calendar year with immediate eligibility!
Workplace Type
This is a fully onsite position in Grand Rapids,MI.
Application Deadline
This position is anticipated to close on Oct 18, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

Job Title: Aseptic Manufacturing AssociateJob Description
As an Aseptic Manufacturing Associate, you will play a crucial role in equipment preparation, bulk drug formulation, and aseptic filling. You will be responsible for accurately documenting data and completing batch records. Additionally, you will perform cleaning and sanitization duties as per the applicable procedures. Successful completion of the facility's aseptic gowning and manufacturing qualification program is required. Duties will be performed in ISO 5 (Grade A) and ISO 7 (Grade C) cleanrooms.
Responsibilities
+ Perform equipment preparation, bulk drug formulation, and aseptic filling.
+ Accurately document data and complete batch records.
+ Perform cleaning and sanitization duties as instructed by applicable procedures.
+ Complete the facility's aseptic gowning and manufacturing qualification program.
+ Work in ISO 5 (Grade A) and ISO 7 (Grade C) cleanrooms.
Essential Skills
+ Proficiency in GMP and cGMP regulations.
+ Experience with laboratory and aseptic techniques.
Additional Skills & Qualifications
+ Bachelor's degree OR a high school diploma and relevant work experience.
+ Level I: 2+ years in a manufacturing, medical, and/or laboratory environment.
+ Level II: 3+ years in a manufacturing, medical, and/or laboratory environment with sterile manufacturing experience.
+ Level III: 4+ years in a manufacturing, medical, and/or laboratory environment with sterile manufacturing experience.
Work Environment
This role involves off-shift hours at Butterworth. The schedule is as follows: 6 PM to 6 AM Thursday-Sunday on week one, and 6 PM to 6 AM Friday-Sunday on week two, alternating between 48 and 36-hour weeks. The company offers a comprehensive benefits package starting on day one, including medical, dental, vision, life insurance, and disability benefits, with the company covering 75% of the cost. A 401(k) program with immediate vesting in contributions is available, along with generous off-shift premiums. Employees receive 16 hours of paid volunteer time per calendar year, accrue up to 13 days of PTO for vacation, sick, or mental health needs, and earn one hour of wellness time off for every 30 hours worked. The company also provides 10 paid holidays per year with immediate eligibility.
Job Type & Location
This is a Permanent position based out of Grand Rapids, Michigan.
Pay and Benefits
The pay range for this position is $ - $ /yr.
MEDICAL BENEFITS starting day 1: Blue Cross Blue Shield medical and dental, vision, life insurance, and disability benefits are available to you and your family on your first day of work, with the company paying for 75% of the cost! Once eligible for the 401(k) program, all your contributions are immediately 100% vested, and you are immediately vested in GRAM contributions as well. We also offer generous off-shift premiums!
Paid VOLUNTEERISM starting day 1: GRAM encourages giving back to our community by offering 16 hours of paid volunteer time per calendar year!
PTO: Full-time employees accrue up to 13 days of time off per calendar year. You choose how to use this time for your vacation, sick, or mental health needs!
WELLNESS TIME OFF: Employees earn 1 hour of time off for every 30 hours worked to use how you choose.
PAID HOLIDAYS: We offer 10 paid holidays per calendar year with immediate eligibility!
Workplace Type
This is a fully onsite position in Grand Rapids,MI.
Application Deadline
This position is anticipated to close on Oct 17, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

Job Title: Aseptic Manufacturing AssociateJob Description
As an Aseptic Manufacturing Associate, you will play a crucial role in equipment preparation, bulk drug formulation, and aseptic filling. You will be responsible for accurately documenting data and completing batch records. Additionally, you will perform cleaning and sanitization duties as per the applicable procedures. Successful completion of the facility's aseptic gowning and manufacturing qualification program is required. Duties will be performed in ISO 5 (Grade A) and ISO 7 (Grade C) cleanrooms.
Responsibilities
+ Perform equipment preparation, bulk drug formulation, and aseptic filling.
+ Accurately document data and complete batch records.
+ Perform cleaning and sanitization duties as instructed by applicable procedures.
+ Complete the facility's aseptic gowning and manufacturing qualification program.
+ Work in ISO 5 (Grade A) and ISO 7 (Grade C) cleanrooms.
Essential Skills
+ Proficiency in GMP and cGMP regulations.
+ Experience with laboratory and aseptic techniques.
Additional Skills & Qualifications
+ Bachelor's degree OR a high school diploma and relevant work experience.
+ Level I: 2+ years in a manufacturing, medical, and/or laboratory environment.
+ Level II: 3+ years in a manufacturing, medical, and/or laboratory environment with sterile manufacturing experience.
+ Level III: 4+ years in a manufacturing, medical, and/or laboratory environment with sterile manufacturing experience.
Work Environment
This role involves off-shift hours at Butterworth. The schedule is as follows: 6 PM to 6 AM Thursday-Sunday on week one, and 6 PM to 6 AM Friday-Sunday on week two, alternating between 48 and 36-hour weeks. The company offers a comprehensive benefits package starting on day one, including medical, dental, vision, life insurance, and disability benefits, with the company covering 75% of the cost. A 401(k) program with immediate vesting in contributions is available, along with generous off-shift premiums. Employees receive 16 hours of paid volunteer time per calendar year, accrue up to 13 days of PTO for vacation, sick, or mental health needs, and earn one hour of wellness time off for every 30 hours worked. The company also provides 10 paid holidays per year with immediate eligibility.
Job Type & Location
This is a Permanent position based out of Grand Rapids, Michigan.
Pay and Benefits
The pay range for this position is $ - $ /yr.
MEDICAL BENEFITS starting day 1: Blue Cross Blue Shield medical and dental, vision, life insurance, and disability benefits are available to you and your family on your first day of work, with the company paying for 75% of the cost! Once eligible for the 401(k) program, all your contributions are immediately 100% vested, and you are immediately vested in GRAM contributions as well. We also offer generous off-shift premiums!
Paid VOLUNTEERISM starting day 1: GRAM encourages giving back to our community by offering 16 hours of paid volunteer time per calendar year!
PTO: Full-time employees accrue up to 13 days of time off per calendar year. You choose how to use this time for your vacation, sick, or mental health needs!
WELLNESS TIME OFF: Employees earn 1 hour of time off for every 30 hours worked to use how you choose.
PAID HOLIDAYS: We offer 10 paid holidays per calendar year with immediate eligibility!
Workplace Type
This is a fully onsite position in Grand Rapids,MI.
Application Deadline
This position is anticipated to close on Oct 16, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

Our client is a leading manufacturing firm seeking a motivated and experienced Manufacturing Operations Supervisor to join their facility in Grand Rapids, Michigan, US . This role is pivotal in overseeing daily production activities, ensuring efficiency, quality, and safety standards are met. The ideal candidate will have a strong background in manufacturing processes, excellent leadership skills, and a commitment to continuous improvement. You will be responsible for managing a team of production associates, optimizing workflow, and troubleshooting production challenges to meet output targets.

Key Responsibilities:

• Supervise and coordinate the activities of production personnel to ensure efficient operation of the manufacturing floor.
• Monitor production processes, identify areas for improvement, and implement solutions to enhance productivity and reduce waste.
• Ensure all production activities comply with safety regulations, quality standards, and company policies.
• Train and develop production staff, providing guidance and performance feedback.
• Manage daily production schedules and ensure timely completion of orders.
• Maintain equipment and ensure it is properly serviced and operational.
• Conduct regular inspections of the production area to ensure cleanliness and orderliness.
• Collaborate with other departments, such as planning, quality control, and maintenance, to ensure smooth operations.
• Troubleshoot production issues and implement corrective actions promptly.
• Maintain accurate production records and reports.

Qualifications:

• High school diploma or equivalent; Associate's or Bachelor's degree in a related field is a plus.
• Minimum of 4 years of experience in a manufacturing environment, with at least 2 years in a supervisory or leadership role.
• Proven understanding of manufacturing processes, production planning, and quality control principles.
• Strong leadership, communication, and team-building skills.
• Experience with Lean Manufacturing or Six Sigma methodologies is desirable.
• Ability to interpret production schedules and work orders.
• Proficiency in using manufacturing software and tools.
• Strong problem-solving and decision-making capabilities.
• Commitment to safety and quality in the workplace.