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PROCESSING APPLICATION
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Job Requirements of Bio Process Associate - 1st Shift:
-
Employment Type:
Contractor
-
Location:
Devens, MA (Onsite)
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Bio Process Associate - 1st Shift
Careers Integrated Resources Inc
Devens, MA (Onsite)
Contractor
Job Description: Bio Process Associate
1st Shift--hours are 7AM - 3PM Monday - Friday.
Onsite, Devens--Local candidates Only
Description:
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:
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.
Shift: 7a - 3p Monday - Friday
Additional Job Requirements:
Position Handles Hazardous Materials
1st Shift--hours are 7AM - 3PM Monday - Friday.
Onsite, Devens--Local candidates Only
Description:
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:
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.
Shift: 7a - 3p Monday - Friday
Additional Job Requirements:
Position Handles Hazardous Materials
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