Associate Scientist

job
  • Randstad Life Sciences US
Job Summary
Location
King of Prussia ,PA
Job Type
Contract
Visa
Any Valid Visa
Salary
PayRate
Qualification
BCA
Experience
2Years - 10Years
Posted
18 Dec 2024
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Job Description

Upstream Associate Scientist - First Shift

1 Year (potential for extension)

King of Prussia, PA

Max PR: $27.79/hr? (please ensure the team is aware this is nonnegotiable)


Shift: 1st shift standard day shift (i.e. Mon-Fri; 40 hrs/wk; 8 hrs/day; 7:30 AM – 4:00 PM) with early morning/evening and weekend work required occasionally, as needed. - 100% ONSITE


  • Key items the HM is looking for on the resume:
  • Bachelor of Science degree in Chemical Engineering, Biology, Chemistry, or other engineering or scientific field
  • 1+ years of cGMP experience o Knowledge of cGMP guidelines and standards.
  • Knowledgeable of : upstream equipment (aka unit operations) and process overview (media prep, small scale, large scale), Analytical equipment (VI-Cell, NOVA, Centrifuge, tubing welder), PLC / DCS / HMI

Required:

• Bachelor of Science degree in Chemical Engineering, Biology, Chemistry, or other engineering or scientific field.

• Familiarity with protein purification process operations and Good Manufacturing Practices (GMP) regulations.

Top Request-

  • Bachelor of Science degree in Chemical Engineering, Biology, Chemistry, or other engineering or scientific field
  • 1+ years of cGMP experience o Knowledge of cGMP guidelines and standards.
  • Knowledgeable of : upstream equipment (aka unit operations) and process overview (media prep, small scale, large scale), Analytical equipment (VI-Cell, NOVA, Centrifuge, tubing welder), PLC / DCS / HMI


o Proficiency in executing standard procedures required in addition to some non-routine work.

Interview Process:

  • Pending Information

Job Responsibilities

• Preparation of buffer solutions, chromatographic separation, filtration and concentration operation, etc.

• Completing daily manufacturing tasks per standard operating procedures and batch document instructions.

• Documenting all manufacturing activities clearly and accurately.

• Ensures all production activities are completed in a safe and compliant manor. Maintain and prepare high quality documentation. Dispense large and small amounts of raw materials Perform CIP and SIP of product tanks

• Work with hazardous materials under the appropriate safety procedures

• Performs other functions as necessary or as assigned.

Education & Qualifications

Basic Qualifications:

• Bachelor of Science degree in Chemical Engineering, Biology, Chemistry, or other engineering or scientific field.

• Familiarity with Good Manufacturing Practices (GMP) regulations.


Preferred Qualifications:

• Bachelor of Science degree in Chemical Engineering, Biology, Chemistry, or other engineering or scientific field

• 1+ years of cGMP experience o Knowledge of cGMP guidelines and standards.

• Knowledgeable of : upstream equipment (aka unit operations) and process overview (media prep, small scale, large scale), Analytical equipment (VI-Cell, NOVA, Centrifuge, tubing welder), PLC / DCS / HMI

• Proficiency in executing standard procedures required in addition to some non-routine work.


Top Skills for Candidate:

• Ability to work in highly matrixed organization.

• Ability to multi-task within a multi-functional team environment.

• Able to troubleshoot.

• Capable of following written instructions and have clear written communication skills as well as computer literacy.

• Familiar with basic scientific principles and have experience in routine bench work and/or instrumental analysis.

• Ability to author, revise and/or support SOP's, change controls, deviations.

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