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Manufacturing Associate

2 months ago


West Greenwich, United States Randstad Life Sciences US Full time

Job Title: Associate Manufacturing Process Technician-NS

Location: 1 Year Contract

Location: West Greenwich, RI

Max PR: $32.10/hr

Night Shift 6:45PM 6:45AM

C and D Rotation Swing Shift Week 1 is 5 working days Week 2 is 2 working days. Candidates must be available to work weekends.

Ideal candidate: Systems MS office suite, Good written communication, experience working in a team not direct manufacturing experience understands the principles of safety culture and working effectively on a team, lab exposure and worked in an environment where safety is top priority. Manager is open to candidates that don't necessarily have experience in Biotech cross lateral could be anything with batch chemicals or chemical processing.


Summary

  • The Associate of Manufacturing will work in a dynamic production environment at the Company Rhode Island Drug Substance plant supporting commercial, clinical, and launch activities. Under general supervision, employee will perform operations in the Manufacturing area. Operations will be performed according to Standard Operating Procedures (SOPs).


Responsibilities include:

  • Hands on operations: setup, 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


BASIC QUALIFICATIONS:

  • Manager is requesting bachelors OR High school with 3 years work experience in manufacturing.