64 Engineering - Bio Process Associate Jobs in Devens, MA
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Engineering - Bio Process Associate
$88k-107k (estimate)
Full Time
0 Months Ago
On Board Companies is Hiring an Engineering - Bio Process Associate Near Devens, MA
On-Board Scientific is hiring a Bio Process Associate in Devens, MA!For immediate consideration please send your resume to resumes@onboardusa.com
Subject Line: Position, Title, and State you are Located
About Us:On-Board Services, Incorporated is an on-site contract service provider for a local manufacturing entity providing full time positions to our employees. We offer benefits as well as 401k.
Position Details:Job title: Bio Process AssociatePosition Type: Full Time /12 month contractJob location: Devens, MA 100% On siteShift: 1st shift 7am - 5p - Mon-Thurs (10hrs) or Tues - Fri (Four 10hr days) First Month for training will work Mon - Fri 7AM - 3PM EST. Once training complete will transition to their shift.Compensation: $29-31.40 hourly (Based on Experience)
Summary: 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.
Responsibilities:• Operate production equipment within an assigned functional area adhering to Good Manufacturing Practices andstandard 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 primaryproduction 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 maintainingmaterial and component inventory levels.• Works on routine manufacturing assignments per written procedures that are moderately complex with minimalinstructions. Assists in revising and creating process documents, i.e. SOP’s and Batch Records, and assists withprocess 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. Apply Today!www.onboardusa.com
On-Board was founded in 1976 by Robert L. Wilson to provide Engineering and Design services to the chemical manufacturing industry. Today, On-Board is a thriving privately held family of companies with services including Consulting, Professional Engineering, Industrial Maintenance and Facility Management, Contracted Manufacturing and Production Services, as well as Temporary Staffing and Recruiting throughout North America.
The On-Board Family of Companies conducts operations through its Corporate Headquarters located in East Windsor, NJ along with Regional Offices in New Castle, DE and Wake Forest, NC. On-Board’s Mission is to provide “Flexible Service by applying the talents of our people, work processes and technology to meet our clients’ expectations in a Safe, Responsible and Dependable manner.”
On-Board Companies provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, religion, sex, national origin, age, disability, or genetics.JD# 24-00487
Subject Line: Position, Title, and State you are Located
About Us:On-Board Services, Incorporated is an on-site contract service provider for a local manufacturing entity providing full time positions to our employees. We offer benefits as well as 401k.
Position Details:Job title: Bio Process AssociatePosition Type: Full Time /12 month contractJob location: Devens, MA 100% On siteShift: 1st shift 7am - 5p - Mon-Thurs (10hrs) or Tues - Fri (Four 10hr days) First Month for training will work Mon - Fri 7AM - 3PM EST. Once training complete will transition to their shift.Compensation: $29-31.40 hourly (Based on Experience)
Summary: 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.
Responsibilities:• Operate production equipment within an assigned functional area adhering to Good Manufacturing Practices andstandard 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 primaryproduction 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 maintainingmaterial and component inventory levels.• Works on routine manufacturing assignments per written procedures that are moderately complex with minimalinstructions. Assists in revising and creating process documents, i.e. SOP’s and Batch Records, and assists withprocess 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. Apply Today!www.onboardusa.com
On-Board was founded in 1976 by Robert L. Wilson to provide Engineering and Design services to the chemical manufacturing industry. Today, On-Board is a thriving privately held family of companies with services including Consulting, Professional Engineering, Industrial Maintenance and Facility Management, Contracted Manufacturing and Production Services, as well as Temporary Staffing and Recruiting throughout North America.
The On-Board Family of Companies conducts operations through its Corporate Headquarters located in East Windsor, NJ along with Regional Offices in New Castle, DE and Wake Forest, NC. On-Board’s Mission is to provide “Flexible Service by applying the talents of our people, work processes and technology to meet our clients’ expectations in a Safe, Responsible and Dependable manner.”
On-Board Companies provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, religion, sex, national origin, age, disability, or genetics.JD# 24-00487
Job Summary
JOB TYPE
Full Time
SALARY
$88k-107k (estimate)
POST DATE
07/14/2023
EXPIRATION DATE
08/31/2024
WEBSITE
on-boardcompanies.com
HEADQUARTERS
New York City, NY
SIZE
<25
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