Upstream Manufacturing Associate III - 12hr. Rotation Shift (Days)

Thermo Fisher Scientific•Plainville, MA

9d•$23 - $35•Onsite

About The Position

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Location/Division Specific Information: Thermo Fisher Scientific Viral Vector Services (VVS), is a rapidly growing, dynamic gene therapy contract development and manufacturing organization. Our employees are committed to making a difference in our organization, for our client partners and the patients we serve. We are looking for top talent with proven competencies and strong character to join our team and help lead our organization into the future. Shift Hours: Day Shift 12 hrs. rotation (7a-7p) Plainville, MA - 5 Commerce Boulevard Summary: The Manufacturing Associate III, Upstream will report to a shift supervisor and work with peers to conduct manufacturing operations in Upstream per cGMP in a viral vector production environment. In addition, the associate will be cross trained to be able to perform functions across multiple manufacturing departments. The successful candidate will ensure to maintain proper training and compliance to cGMP standards as well as abide by Thermo Fisher Scientific corporate standards. A typical work week will be a rotating 12 hours shift structure for support of GMP manufacturing operations. The Associate in this role will be part of a cohesive team responsible for the execution of bioprocessing activities. The Associate will be required to follow procedures to ensure compliant execution of manufacturing activities The Manufacturing Associate may also be needed to support equipment documentation investigations and improvement initiatives within the manufacturing operations The Associate works under the supervision and direction of Lead Associate and Manufacturing Supervisor

Requirements

High School Diploma/GED/Equivalent Education is required.
1+ years' experience in a cGMP environment, warehouse, or related experience.
Ability to function in a fast-paced, dynamic environment with multiple priorities simultaneously.
Demonstrate strong attention to detail.
Able to read and follow procedures.
Ability to maintain aseptic qualification.
Ability to maintain qualification to work in a cleanroom environment.
Ability to work closely and effectively in a team environment.
Demonstrate initiative and drive to accomplish the job timely accurately and safely the first time is required.
Ability to apply knowledge of Good Manufacturing processes.
Ability to apply knowledge and skills in pharmaceutical processes equipment, instrumentation and procedures.
Adhere to all Personal Protective Equipment (PPE) requirements used within cGMP manufacturing.
Gown aseptically and/or sterile gown as needed
Write, read/review written documentation for extended periods of time
Specific vision requirements for this job include close vision, distance vision color vision peripheral vision depth perception and ability to adjust focus
Regularly required to talk and hear
Able to lift push or pull up to 50lbs (as needed)
Required to sit and stand for extended periods
Occasionally required to lift stand walk use hands to finger handle or feel reach with hands and arms, and stoop kneel or crouch
Must have the ability to work 7am-7pm on rotating days in a 24/7 operation to include weekends and holidays.

Responsibilities

Demonstrates safe work habits and adheres to safety procedures and guidelines
Participate in Tier 1 meetings
Supports team preparedness and room preparation activities
Supports maintenance of GMP Kanban in support of manufacturing operations
Support continuous improvement m process operations and systems.
Support tech transfer activities.
Seeks and welcomes feedback and responds to coaching
Expected to spend at least 80 - 90% of the time on the manufacturing floor
Working closely with related functional areas to achieve production goals and timelines.
Find opportunities and implement efficiency improvements.
Manage inventory supplies.