JT 996 Manufacturing Process Technician

Rhode Island, RI
Temporary
Pharmaceutical
Mid Level

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

  • Hands-on operations: set-up, cleaning, and sanitization of various manufacturing equipment
  • Weighing out buffers/media per defined manufacturing procedures (MPs) and standard operating procedures (SOPs)
  • Following GMP documents (SOPs, MPs) with strict adherence to safety and compliance
  • Performing and monitoring critical processes with the ability to perform basic troubleshooting
  • Performing in-process sampling of equipment and operating analytical equipment
  • Performing parts washing and sterilization activities
  • Maintaining an organized and clean workspace
  • Working in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves when performing all work
  • Initiating and being involved quality deviation reports, as required
  • Drafting and revising documents (SOPs, MPs)
  • Identifying, recommending, and implementing improvements related to routine functions
  • Assisting in the review of documentation for assigned functions (equipment logs, batch records)
  • Working around high-pressure systems, occasionally work around/moving heavy equipment with powered industrial vehicles
  • Available to work various shifts (day/nights) as dictated by the production schedule Able to work in teams to complete operational tasks
  • Ability to take direction well, follow documents and policies at all times Ability to take initiative
  • Champion Lean Transformation and OE initiatives; facilitate the drive towards continuous improvement in all Manufacturing areas.
  • Develop relationships and connections within the Manufacturing department and with key site stakeholders
  • Support DI&B initiatives to increase inclusion, connectivity, and engagement within the team
  • Create a positive work environment through interactions with team members Able to regularly lift up to 35lbs, push and pull objects that require up to 50lbs of force, and work on your feet for long durations Able to perform the list of physical movements that may be necessary to perform daily functions on the production floor: bending, reaching above the head, climbing, kneeling, squatting, stooping, walking upstairs, and standing on portable stairs or ladders up to 6 feet off of the ground

Qualifications:

  • High school/GED and 1 year of work or military experience OR​ Associates degree​
  • Experience in a technical field
  • Experience with advance computer systems
  • Demonstrated ability to follow procedures
  • Ideal candidate: life science / biology background. This is an upstream position so experience with cell culture is also a bonus

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

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