VIVOS Professional Services, LLC
Manufacturing Associate I – Biotech
VIVOS Professional Services, LLC, Walkersville, Maryland, United States, 21793
VIVOS Professional Services, LLC provided pay range
This range is provided by VIVOS Professional Services, LLC. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $23.00/hr - $28.00/hr
Direct message the job poster from VIVOS Professional Services, LLC
Shift:
3rd Shift – Sunday to Wednesday, 10:00 PM – 8:30 AM
Role Purpose The Manufacturing Associate I is responsible for supporting the manufacture of therapeutic proteins (API) under cGMP conditions. This role focuses on executing established manufacturing processes, following SOPs, monitoring equipment, and performing basic laboratory and facility support tasks. Associates will develop a foundational understanding of cGMP compliance while working under close supervision and demonstrating proper aseptic techniques.
Key Responsibilities
Manufacturing Operations (40%)
Set up, operate, and monitor manufacturing equipment and production processes
Perform Clean-in-Place (CIP) and Steam-in-Place (SIP) operations
Accurately document production activities in written and electronic systems in compliance with GMP and GDP requirements
Review documentation as required
Training & Qualification (20%)
Attain qualification for all assigned tasks
Maintain individual training plans and compliance records
Laboratory Support (10%)
Perform basic laboratory testing including pH, conductivity, and sample testing
Perform material movements and transfer raw materials and chemicals within production areas
Facility & Equipment Maintenance (10%)
Conduct routine cleaning and sanitization of equipment and facility areas
Support 6S and continuous improvement initiatives
Administrative & Team Support (10%)
Participate in shift handoffs, meetings, and project activities
Perform administrative tasks including email communication and documentation
Complete other duties as assigned
Qualifications Education
High School Diploma or equivalent (required)
Associate’s or Bachelor’s degree preferred
Preferred field of study: Science-related discipline
Experience
0–3 years of experience
Prior manufacturing experience preferred (biotech, pharmaceutical, or regulated environment a plus)
Basic understanding or willingness to learn cGMP principles
Strong attention to detail and documentation accuracy
Proven logical reasoning, critical thinking, and decision-making skills
Ability to follow written procedures and work effectively in a team environment
Seniority level Entry level
Employment type Contract
Job function Manufacturing
Industries Pharmaceutical Manufacturing
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Base pay range $23.00/hr - $28.00/hr
Direct message the job poster from VIVOS Professional Services, LLC
Shift:
3rd Shift – Sunday to Wednesday, 10:00 PM – 8:30 AM
Role Purpose The Manufacturing Associate I is responsible for supporting the manufacture of therapeutic proteins (API) under cGMP conditions. This role focuses on executing established manufacturing processes, following SOPs, monitoring equipment, and performing basic laboratory and facility support tasks. Associates will develop a foundational understanding of cGMP compliance while working under close supervision and demonstrating proper aseptic techniques.
Key Responsibilities
Manufacturing Operations (40%)
Set up, operate, and monitor manufacturing equipment and production processes
Perform Clean-in-Place (CIP) and Steam-in-Place (SIP) operations
Accurately document production activities in written and electronic systems in compliance with GMP and GDP requirements
Review documentation as required
Training & Qualification (20%)
Attain qualification for all assigned tasks
Maintain individual training plans and compliance records
Laboratory Support (10%)
Perform basic laboratory testing including pH, conductivity, and sample testing
Perform material movements and transfer raw materials and chemicals within production areas
Facility & Equipment Maintenance (10%)
Conduct routine cleaning and sanitization of equipment and facility areas
Support 6S and continuous improvement initiatives
Administrative & Team Support (10%)
Participate in shift handoffs, meetings, and project activities
Perform administrative tasks including email communication and documentation
Complete other duties as assigned
Qualifications Education
High School Diploma or equivalent (required)
Associate’s or Bachelor’s degree preferred
Preferred field of study: Science-related discipline
Experience
0–3 years of experience
Prior manufacturing experience preferred (biotech, pharmaceutical, or regulated environment a plus)
Basic understanding or willingness to learn cGMP principles
Strong attention to detail and documentation accuracy
Proven logical reasoning, critical thinking, and decision-making skills
Ability to follow written procedures and work effectively in a team environment
Seniority level Entry level
Employment type Contract
Job function Manufacturing
Industries Pharmaceutical Manufacturing
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