Engineering - Bio Process Associate - 1st Shift
Posted on :
14-03-2024
Employer Active
1 Vacancy
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Monthly Salary
Not Disclosed
Salary Not Disclosed
Vacancy
1 Vacancy
Posted on :
14-03-2024
Job Description
Req ID : 2625473
Job Description: Bio Process Associate
1st Shifthours are 7AM 3PM Monday Friday.
Onsite DevensLocal candidates Only
**Note there are 3 openings on this req**
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. SOPs 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 Sills:
1st Shifthours are 7AM 3PM Monday Friday.
Onsite DevensLocal candidates Only
**Note there are 3 openings on this req**
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. SOPs 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 Sills:
Employment Type
Full Time
Key Skills
- Internship
- Coaching
- Information Technology Sales
- Administration Support
- Financial Planning
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