Bio Process Associate - 1st Shift
Listed on 2026-06-13
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Manufacturing / Production
Manufacturing Engineer, Manufacturing Production, Quality Engineering, Operations Engineer
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.
Key Skills- Experience in Bio Tech industry (single use facility)
- Motivated to learn / Team player
- Familiar with Microsoft Office Suite
- 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.
- Weigh and check raw materials. Assemble, clean and autoclave process components. Assist in maintaining material and component inventory levels.
- Work on routine manufacturing assignments per written procedures that are moderately complex with minimal instructions. Assist in revising and creating process documents, e.g. SOPs and Batch Records, and assist with process related investigations.
- 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 associate's 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 cleanroom or highly regulated environment desired.
Job Requirements
- Position handles hazardous materials
Work location:
Devens, MA
100% onsite role
Shift Time:
Tue - Fri 7:00am to 5:00pm
The starting hourly compensation for this assignment is the following range ($26- $30.67/hr). The final, individual compensation and any available benefits will be determined by your employer of record.
Equal Opportunity EmployerASK Consulting is an equal opportunity employer and does not discriminate against employees or applicants based on race, religion, color, sex, national origin, age, sexual orientation, gender identity, genetic information, disability, veteran status, or any other classification protected by federal, state, or local laws.
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