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Form of workJob Description: Bio-Process Associate
1st Shift--- 7AM - 5PM EST Mon - Thurs OR Tues - Fri--this will be a set schedule based on needs of the Business
First Month for training will work Mon - Fri 7AM - 3PM EST. Once training complete will transition to their shift.
Onsite role--Devens
Local Candidates Only
The Bioprocess Associate uses current Good Manufacturing Practices (cGMPs) in the execution of commercial manufacturing processes for the manufacture of therapeutic proteins used in medicines that are revolutionizing the treatment of serious disease.
Job Responsibilities:
Operate production equipment within an assigned functional area adhering to Good Manufacturing Practices and
standard operating procedures.
Revise and create process documents and assist with process related investigations.
Train for proficiency in process automation and supporting business systems and in the operation of primary
production equipment within the assigned functional area.
Lead in maintaining material and components inventory level. Weigh and check raw materials.
Support a safe work environment and contribute to area specific initiatives associated with work safety.
Weighs and checks raw materials. Assembles, cleans and autoclaves process components. Assists in maintaining
material and component inventory levels.
Works on routine manufacturing assignments per written procedures that are moderately complex with minimal
instructions. Assists in revising and creating process documents, i.e. SOP's and Batch Records, and assists with
process related investigations.
Qualifications
Minimum 1 year experience in a Pharma environment
High school diploma is required.
Knowledge of science generally attained through completion of a certificate program or Associates Degree in
Biotechnology or a related field is desired.
Prior experience successfully participating on work teams where personal accountability, attention to detail,
collaboration, and results were expected.
Demonstrated proficiency in common computer tools and web based applications.
Prior experience with Good Manufacturing Practices (GMP) regulations and/or prior work experience in a clean
room or highly regulated environment desired.
Additional Job Requirements:
Position Handles Hazardous Materials
