Pharmaceutical Manufacturing Technician

Eurofins USA PSS Insourcing Solutions•Groton, CT

6h•Onsite

About The Position

Eurofins Scientific is an international life sciences company providing a unique range of analytical testing services. This role involves generating, assisting, and executing documentation associated with manufacturing processes, including Batch Documents, Log Books, Labels, check sheets, protocols, and Change Control. The technician will complete complex bulk product manufacturing activities to convert incoming raw materials into intermediate product, and then process these intermediates into a final patient-ready presentation. Responsibilities also include setting up complex manufacturing equipment, managing and checking documentation, and completing activities related to the operation and maintenance of a classified manufacturing space. Additionally, the role involves operator care tasks for complex manufacturing equipment, generating and reporting operational performance data, and identifying, owning, and leading continuous improvement projects.

Requirements

High school diploma
Must hold a valid driver’s license
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
Authorization to work in the United States indefinitely without restriction or sponsorship
The job requires the operation of manufacturing equipment in the Groton manufacturing area.
Must be able to wear appropriate PPE (i.e,. daily uniform, safety glasses, respirator,s and full protective suits) when necessary

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