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Integrated Resources, Inc. is a staffing and recruitment agency that provides talent acquisition services to clients in sectors such as IT, healthcare, and life sciences.

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Integrated Resources INC
Posted 11y ago

Process Engineer, downstream purification

Integrated Resources INC
Lexington, MA, United States
OnsiteContract
Responsibilities
  • Designing studies
  • Executing experiments
  • Data analysis
Requirements
  • BS degree in Chemical Engineering
  • Biochemistry/Protein Chemistry or related disciplines with 0-3 years of relevant experience in a biotechnology/pharmaceutical environment
Technical tools mentioned
Column ChromatographyTFFNormal Flow Filtration

Job description

Company Description:

A Few Words About Us
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description:

As a member of the Manufacturing Science & Technology group in Process Development department, this individual will join a group of process scientist and engineers to support downstream processes of commercial productions and late stage clinical process development and productions. The scope of work will include designing studies under instruction, executing experiments and data analysis to support GMP investigations and manufacturing change controls and to reduce reoccurring deviations. The focus of the work will be downstream unit operations such as column chromatography, harvest clarification, TFF and normal flow filtration. This individual will interact with other PD groups and other departments including manufacturing, PTS, QC, QA and Engineering etc.


BS degree in Chemical Engineering, Biochemistry/Protein Chemistry or related disciplines with 0-3 years of relevant experience in a biotechnology/pharmaceutical environment is required.

Experience with column chromatography and TFF is required. Knowledge of the quality systems and other regulatory requirements necessary to manufacture biologics in a cGMP environment is preferred.

The successful candidate must:

•Have hands-on downstream process development experience

•Be able to learn to work independently and on cross-functional teams

•Have good written and verbal communication skills


Feel free to forward my email to your friends/colleagues who might be available



Additional Information:

Archana Melwani

Clinical Recruiter

Integrated Resources, Inc

IT REHAB CLINICAL NURSING

Inc. 5000 – 2007-2014 (8th Year)

Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70

Tel: 732-549-2030 x130

Direct: 732-429-1853

Fax: 732-549-5549





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