423 Medical Device Manufacturing jobs in the United States

Aseptic Manufacturing Associates (Level I, II, III) Grand Rapids, MI

Join the Grand River Aseptic Manufacturing team!

Grand River Aseptic Manufacturing (GRAM) is a leading contract development and manufacturing organization (CDMO) specializing in sterile injectable fill-and-finish services for liquid and lyophilized vials, syringes, and cartridges. We are committed to advancing patient care by providing our clients with the experience, technology, and quality record necessary for effective clinical trials and successful commercialization.

We are currently hiring Level I, II, and III Aseptic Manufacturing Associates!

Quality, Service, Collaboration, Courage. Do you exhibit these values and wish to be around others that do too? Are you interested in making a difference in your community and the world? Are you looking for a place where you can grow and learn in a diverse, community-minded culture? 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.

$23 to $29.44 per hour based on experience!

• 1st Shift: 6:00 am – 4:00 pm M-Th
• 2nd Shift: 2:00 pm – 12:00 am M-Th
• 3rd Shift: 10:00 pm – 8:00 am M-Th
• 4th Shift: 6:00 am – 6:00 pm F-Su

• Perform equipment preparation in a sterile environment, bulk drug formulation, and aseptic filling duties as needed.
• Accurately document data and complete batch records as needed.
• Perform cleaning and sanitization duties as instructed by the applicable procedure.
• Successfully complete facility’s aseptic gowning and manufacturing qualification program.
• Perform duties in ISO 5 (Grade A), and ISO 7 (Grade C) cleanrooms.

• Bachelor’s degree in Chemistry, Biology or related field is a +.
• Level I: HS Diploma or equivalent and 1+ years relevant work experience in a manufacturing, medical, and/or laboratory environment.
• Level II: HS Diploma or equivalent and 3+ years relevant experience, including sterile manufacturing.
• Level III: HS Diploma or equivalent and 4+ years relevant experience, including sterile manufacturing.
• The ability to become qualified for use of a full-face respirator is required when working with hazardous chemicals.
• Use of a Powered Air Purifying Respirator (PAPR) is required during chemical dispense and other activities.

• Medical, dental, vision, life insurance, and disability benefits available for you and your family on your first day of work.
• 401(k) program.
• Full-time employees accrue up to 13 days of time off per calendar year.
• 10 paid holidays per calendar year with immediate eligibility.
• Wellness time off: Earn 1 hour of time off for every 30 hours worked.
• Paid volunteerism from day 1: 16 hours of paid volunteer time per year!

Grand River Aseptic Manufacturing is an Equal Opportunity Employer. We embrace and encourage everyone’s differences in race, color, ancestry, national origin, gender, sexual orientation, marital status, height, weight, religion, age, disability, gender identity, genetic identity, military status, citizenship, or any other class legally protected by local, state, or federal law. We value the differences that make each and every one of you unique.

Grand River Aseptic Manufacturing only accepts employment applications through our Careers webpage. Please be mindful of fraudulent recruiting practices and job offers, and only discuss employment directly with Grand River Aseptic Manufacturing.

Aseptic Manufacturing Associates - GRAM Aseptic Manufacturing Associates (Level I, II, III) Grand Rapids, MI Join the Grand River Aseptic Manufacturing team! Grand River Aseptic Manufacturing (GRAM) is a leading contract development and manufacturing organization (CDMO) specializing in sterile injectable fill-and-finish services for liquid and lyophilized vials, syringes, and cartridges. We are committed to advancing patient care by providing our clients with the experience, technology, and quality record necessary for effective clinical trials and successful commercialization. We are currently hiring Level I, II, and III Aseptic Manufacturing Associates! Quality, Service, Collaboration, Courage. Do you exhibit these values and wish to be around others that do too? Are you interested in making a difference in your community and the world? Are you looking for a place where you can grow and learn in a diverse, community-minded culture? 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. Pay $23 to $29.44 per hour based on experience! Available Shifts 1st Shift: 6:00 am - 4:00 pm M-Th 2nd Shift: 2:00 pm - 12:00 am M-Th 3rd Shift: 10:00 pm - 8:00 am M-Th 4th Shift: 6:00 am - 6:00 pm F-Su What will you do in this role? Perform equipment preparation in a sterile environment, bulk drug formulation, and aseptic filling duties as needed. Accurately document data and complete batch records as needed. Perform cleaning and sanitization duties as instructed by the applicable procedure. Successfully complete facility's aseptic gowning and manufacturing qualification program. Perform duties in ISO 5 (Grade A), and ISO 7 (Grade C) cleanrooms. What does it take to be successful in this role? Bachelor's degree in Chemistry, Biology or related field is a +. Level I: HS Diploma or equivalent and 1+ years relevant work experience in a manufacturing, medical, and/or laboratory environment. Level II: HS Diploma or equivalent and 3+ years relevant experience, including sterile manufacturing. Level III: HS Diploma or equivalent and 4+ years relevant experience, including sterile manufacturing. The ability to become qualified for use of a full-face respirator is required when working with hazardous chemicals. Use of a Powered Air Purifying Respirator (PAPR) is required during chemical dispense and other activities. What's in it for you? Medical, dental, vision, life insurance, and disability benefits available for you and your family on your first day of work. 401(k) program. Full-time employees accrue up to 13 days of time off per calendar year. 10 paid holidays per calendar year with immediate eligibility. Wellness time off: Earn 1 hour of time off for every 30 hours worked. Paid volunteerism from day 1: 16 hours of paid volunteer time per year! Grand River Aseptic Manufacturing is an Equal Opportunity Employer. We embrace and encourage everyone's differences in race, color, ancestry, national origin, gender, sexual orientation, marital status, height, weight, religion, age, disability, gender identity, genetic identity, military status, citizenship, or any other class legally protected by local, state, or federal law. We value the differences that make each and every one of you unique. Grand River Aseptic Manufacturing only accepts employment applications through our Careers webpage. Please be mindful of fraudulent recruiting practices and job offers, and only discuss employment directly with Grand River Aseptic Manufacturing.

• Development of engineering Bill of Materials (BOM) in ERP management software.
• Identifying and quoting manufacturing methods and new materials with suppliers.
• Monitoring ordering and receipt of materials, ensuring compliance and documentation.
• Coordinating engineering and production builds, including drafting manufacturing work instructions.
• Managing trade compliance activities and supporting design verification builds with the manufacturing team.

• A bachelor's degree in mechanical, electrical, or biomedical engineering.
• 3 years with medical device experience
• Experience with MS Office suite.
• Engineering experience in a engineering manufacturing environment or new product development experience
• Experience with writing technical documentation, protocols, and reports.

• Opportunity to work on cutting-edge medical device projects.
• Collaborative work environment with a focus on innovation.
• Professional development and growth opportunities.
• Engagement in meaningful work that impacts healthcare.
• Quarterly reviews to monitor progress and support your career path.

• Development of engineering Bill of Materials (BOM) in ERP management software.
• Identifying and quoting manufacturing methods and new materials with suppliers.
• Monitoring ordering and receipt of materials, ensuring compliance and documentation.
• Coordinating engineering and production builds, including drafting manufacturing work instructions.
• Managing trade compliance activities and supporting design verification builds with the manufacturing team.

• A bachelor's degree in mechanical, electrical, or biomedical engineering.
• 3 years with medical device experience
• Experience with MS Office suite.
• Engineering experience in a engineering manufacturing environment or new product development experience
• Experience with writing technical documentation, protocols, and reports.

• Opportunity to work on cutting-edge medical device projects.
• Collaborative work environment with a focus on innovation.
• Professional development and growth opportunities.
• Engagement in meaningful work that impacts healthcare.
• Quarterly reviews to monitor progress and support your career path.

• Development of engineering Bill of Materials (BOM) in ERP management software.
• Identifying and quoting manufacturing methods and new materials with suppliers.
• Monitoring ordering and receipt of materials, ensuring compliance and documentation.
• Coordinating engineering and production builds, including drafting manufacturing work instructions.
• Managing trade compliance activities and supporting design verification builds with the manufacturing team.

• A bachelor's degree in mechanical, electrical, or biomedical engineering.
• 3 years with medical device experience
• Experience with MS Office suite.
• Engineering experience in a engineering manufacturing environment or new product development experience
• Experience with writing technical documentation, protocols, and reports.

• Opportunity to work on cutting-edge medical device projects.
• Collaborative work environment with a focus on innovation.
• Professional development and growth opportunities.
• Engagement in meaningful work that impacts healthcare.
• Quarterly reviews to monitor progress and support your career path.

• Development of engineering Bill of Materials (BOM) in ERP management software.
• Identifying and quoting manufacturing methods and new materials with suppliers.
• Monitoring ordering and receipt of materials, ensuring compliance and documentation.
• Coordinating engineering and production builds, including drafting manufacturing work instructions.
• Managing trade compliance activities and supporting design verification builds with the manufacturing team.

• A bachelor's degree in mechanical, electrical, or biomedical engineering.
• 3 years with medical device experience
• Experience with MS Office suite.
• Engineering experience in a engineering manufacturing environment or new product development experience
• Experience with writing technical documentation, protocols, and reports.

• Opportunity to work on cutting-edge medical device projects.
• Collaborative work environment with a focus on innovation.
• Professional development and growth opportunities.
• Engagement in meaningful work that impacts healthcare.
• Quarterly reviews to monitor progress and support your career path.

• Develop engineering Bill of Materials (BOM) in ERP management software.
• Identify and quote manufacturing methods and new materials with suppliers.
• Monitor ordering and receipt of materials, coordinating shipping of engineering parts.
• Manage trade compliance activities and coordinate engineering and production builds.
• Draft manufacturing work instructions and develop protocols with manufacturing facilities.

• A bachelor's degree in mechanical, electrical, or biomedical engineering.
• Experience with MS Office suite.
• Engineering experience in a manufacturing environment.
• 3 years Experience in regulated industry, preferably medical devices.
• Ability to travel up to 20% to San Antonio office or international manufacturing facilities.

• Opportunity to work on cutting-edge medical technology projects.
• Gain valuable experience in a fast-paced manufacturing environment.
• Collaborate with a diverse team of professionals in the healthcare field.
• Potential for contract extension based on performance.
• Engage in quarterly reviews to monitor your progress and career growth.

• Medical and Prescription Drug Plans
• Dental Plan
• Vision Plan
• Health Savings Account
• Health Flexible Spending Account
• Dependent Care Flexible Spending Account
• Supplemental Life Insurance
• Short Term and Long Term Disability Insurance
• Business Travel Insurance
• 401(k), Plus Match
• Weekly Pay