Pharmaceutical Manufacturing Technician

EurofinsGroton, CT
$18 - $30Onsite

About The Position

Generate, assist and execute documentation associated with manufacture, Batch Documents, Log Books, Labels, check sheets , protocols, Change control, QTS etc Complete complex bulk product manufacturing activities to convert incoming raw materials into intermediate product Complete complex processing of intermediate bulk to convert this to a final patient ready final presentation Set up complex manufacturing equipment, manage and check documentation generated. Complete activities associated with the operation and maintenance of a classified manufacturing space Complete activities identified as operator care tasks associated with the maintenance and operation of complex manufacture equipment. Generate, manage and report operational performance associated data Identify, own and lead continuous improvement based projects

Requirements

  • High school diploma
  • Must hold a valid driver’s license
  • The role requires a Groton site presence. The job requires the operation of manufacturing equipment in the Groton manufacturing area. Standing, bending, climbing, reaching, and lifting upward of 55 pounds may be required. Personal Protective Equipment, such as gloves, a full Tyvek suit, breathable air, and/or a filtering face piece, is often required.
  • Must be able to wear appropriate PPE (i.e,. daily uniform, safety glasses, respirator,s and full protective suits) when necessary
  • Strong computer, scientific, and organizational skills
  • Excellent communication (oral and written) and attention to detail
  • Ability to perform heavy lifting (up to 55lbs)
  • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
  • Strong computer, scientific, and organizational skills
  • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude

Nice To Haves

  • Pharmaceutical manufacturing experience is a plus

Responsibilities

  • Generate, assist and execute documentation associated with manufacture, Batch Documents, Log Books, Labels, check sheets , protocols, Change control, QTS etc
  • Complete complex bulk product manufacturing activities to convert incoming raw materials into intermediate product
  • Complete complex processing of intermediate bulk to convert this to a final patient ready final presentation
  • Set up complex manufacturing equipment, manage and check documentation generated.
  • Complete activities associated with the operation and maintenance of a classified manufacturing space
  • Complete activities identified as operator care tasks associated with the maintenance and operation of complex manufacture equipment.
  • Generate, manage and report operational performance associated data
  • Identify, own and lead continuous improvement based projects

Benefits

  • Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
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