Manufacturing Services Associate
VIVOS Professional Services, LLC, Portsmouth, NH, United States
Job Title:
Manufacturing Services Associate I
Location:
Portsmouth, NH (Onsite)
Pay Rate:
$23.25/hr on W2
Position Summary
The Manufacturing Services Associate I supports cGMP manufacturing operations by ensuring production suites are properly stocked, maintained, and operational. This role assists production teams through material preparation, equipment upkeep, and cleaning activities while adhering to strict compliance standards. The associate will work under close supervision to develop a foundational understanding of cGMP requirements, aseptic techniques, and contamination control practices.
Key Responsibilities
Support daily operations of manufacturing suites by maintaining 6S standards, stocking materials, and cleaning soiled equipment and parts
Prepare, assemble, and autoclave components required for manufacturing processes; ensure timely delivery to production areas
Perform routine (daily/weekly) maintenance on analytical equipment to ensure operational readiness
Execute scheduled cleaning activities, including weekly and monthly cleaning of inoculum rooms and other controlled environments
Manage material movement, including preparation, transport, and delivery across production areas in compliance with GMP guidelines
Maintain facility cleanliness and equipment sanitation through routine cleaning procedures
Accurately document all activities in accordance with
Good Manufacturing Practices (GMP)
and
Good Documentation Practices (GDP) ; review documentation as required
Participate in training programs and maintain qualification status for all assigned tasks
Support administrative activities such as shift handovers, team meetings, email communication, and project participation
Demonstrate awareness of aseptic techniques and cross-contamination prevention while handling materials and products
Perform additional duties as assigned
Qualifications
Basic understanding of cGMP regulations (or willingness to learn in a regulated environment)
Strong attention to detail and adherence to documentation standards
Ability to follow standard operating procedures (SOPs) and work under supervision
Good organizational and communication skills
Ability to work in a team-oriented, fast-paced manufacturing environment
cGMP-regulated manufacturing setting
Requires adherence to strict safety, cleanliness, and compliance standards
May involve working in cleanroom environments and handling biological or pharmaceutical materials
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Manufacturing Services Associate I
Location:
Portsmouth, NH (Onsite)
Pay Rate:
$23.25/hr on W2
Position Summary
The Manufacturing Services Associate I supports cGMP manufacturing operations by ensuring production suites are properly stocked, maintained, and operational. This role assists production teams through material preparation, equipment upkeep, and cleaning activities while adhering to strict compliance standards. The associate will work under close supervision to develop a foundational understanding of cGMP requirements, aseptic techniques, and contamination control practices.
Key Responsibilities
Support daily operations of manufacturing suites by maintaining 6S standards, stocking materials, and cleaning soiled equipment and parts
Prepare, assemble, and autoclave components required for manufacturing processes; ensure timely delivery to production areas
Perform routine (daily/weekly) maintenance on analytical equipment to ensure operational readiness
Execute scheduled cleaning activities, including weekly and monthly cleaning of inoculum rooms and other controlled environments
Manage material movement, including preparation, transport, and delivery across production areas in compliance with GMP guidelines
Maintain facility cleanliness and equipment sanitation through routine cleaning procedures
Accurately document all activities in accordance with
Good Manufacturing Practices (GMP)
and
Good Documentation Practices (GDP) ; review documentation as required
Participate in training programs and maintain qualification status for all assigned tasks
Support administrative activities such as shift handovers, team meetings, email communication, and project participation
Demonstrate awareness of aseptic techniques and cross-contamination prevention while handling materials and products
Perform additional duties as assigned
Qualifications
Basic understanding of cGMP regulations (or willingness to learn in a regulated environment)
Strong attention to detail and adherence to documentation standards
Ability to follow standard operating procedures (SOPs) and work under supervision
Good organizational and communication skills
Ability to work in a team-oriented, fast-paced manufacturing environment
cGMP-regulated manufacturing setting
Requires adherence to strict safety, cleanliness, and compliance standards
May involve working in cleanroom environments and handling biological or pharmaceutical materials
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