Manufacturing Operator I - Tailored Management
Portsmouth, NH 03801
About the Job
Manufacturing Services Associate I
Location: 101 International Drive, Portsmouth, NH, United States
Schedule: 40 hours/week with some weekends required on a rotating basis.
Pay Rate: $23.25per hour (weekly pay schedule)
Contract Length: 1 year, opportunity for extension or conversion dependent on performance, attendance, and business need
Benefits: Medical, dental, and vision benefits are available
Our client is one of the world's largest healthcare manufacturing organizations, helping pharmaceutical, biotech, and nutrition companies to bring their treatments to market. United by their vision to bring any therapy to life, they support their customers with a combination of technological insight, world-class manufacturing, scientific expertise, process excellence, and innovation. Their work enables our customers to develop and commercialize their therapeutic discoveries, allowing their patients to benefit from life-saving and life-enhancing treatments. Join their team and enable a healthier world by supporting their healthcare customers on the path to commercialization!
Description:
This role is on the manufacturing shift which is "days " 7 AM - 7 PM with a 12 hour day every other weekend.
The Manufacturing Services Associate I is responsible for supporting all cGMP manufacturing production suites. They support the production groups by ensuring the suites are appropriately stocked with raw materials and consumables, assemble and autoclave assemblies for use, clean soiled parts, perform daily/weekly maintenance on analytical equipment, and complete scheduled cleaning requirements that are not fulfilled by the company's contracted cleaning staff. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique and cross contamination awareness in handling of products and materials.
Duties & Responsibilities:
• Perform 6S and stock each suite daily, clean soiled parts daily.
• Determine production needs for autoclaved assembles and deliver to suites.
• Perform daily and weekly maintenance activities on analytical equipment.
• Perform weekly and monthly cleans of inoculum rooms.
• Report all activities in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate.
• Attain qualification for all assigned tasks and maintain individual training plan
• Prepare materials for transport and delivery to manufacturing suites. Perform material movements into, out of, and across the production areas.
• Maintain facility and equipment through routine cleaning and sanitization.
• Administrative tasks – attending suite shift exchange, meetings, sending/receiving emails, participating in projects, perform other duties as assigned.
• Perform other duties as assigned.
Qualifications:
• 1+ year of relevant experience
• High School Diploma or GED
Upon acceptance of offer, candidates will be required to submit to a 7-year background check and will undergo a urine 5-panel drug screening.
Location: 101 International Drive, Portsmouth, NH, United States
Schedule: 40 hours/week with some weekends required on a rotating basis.
Pay Rate: $23.25per hour (weekly pay schedule)
Contract Length: 1 year, opportunity for extension or conversion dependent on performance, attendance, and business need
Benefits: Medical, dental, and vision benefits are available
Our client is one of the world's largest healthcare manufacturing organizations, helping pharmaceutical, biotech, and nutrition companies to bring their treatments to market. United by their vision to bring any therapy to life, they support their customers with a combination of technological insight, world-class manufacturing, scientific expertise, process excellence, and innovation. Their work enables our customers to develop and commercialize their therapeutic discoveries, allowing their patients to benefit from life-saving and life-enhancing treatments. Join their team and enable a healthier world by supporting their healthcare customers on the path to commercialization!
Description:
This role is on the manufacturing shift which is "days " 7 AM - 7 PM with a 12 hour day every other weekend.
The Manufacturing Services Associate I is responsible for supporting all cGMP manufacturing production suites. They support the production groups by ensuring the suites are appropriately stocked with raw materials and consumables, assemble and autoclave assemblies for use, clean soiled parts, perform daily/weekly maintenance on analytical equipment, and complete scheduled cleaning requirements that are not fulfilled by the company's contracted cleaning staff. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique and cross contamination awareness in handling of products and materials.
Duties & Responsibilities:
• Perform 6S and stock each suite daily, clean soiled parts daily.
• Determine production needs for autoclaved assembles and deliver to suites.
• Perform daily and weekly maintenance activities on analytical equipment.
• Perform weekly and monthly cleans of inoculum rooms.
• Report all activities in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate.
• Attain qualification for all assigned tasks and maintain individual training plan
• Prepare materials for transport and delivery to manufacturing suites. Perform material movements into, out of, and across the production areas.
• Maintain facility and equipment through routine cleaning and sanitization.
• Administrative tasks – attending suite shift exchange, meetings, sending/receiving emails, participating in projects, perform other duties as assigned.
• Perform other duties as assigned.
Qualifications:
• 1+ year of relevant experience
• High School Diploma or GED
Upon acceptance of offer, candidates will be required to submit to a 7-year background check and will undergo a urine 5-panel drug screening.
Source : Tailored Management