What are the responsibilities and job description for the cGMP/Lab Biochemistry Analyst (On-Site) position at NetSource, Inc.?
Please note that this is a 12 month Contract and is On-Site.
JOB DESCRIPTION:
- Role is ONSITE 100% in Malvern, PA
- This role is more of a Laboratory Analyst
- Must have a Bachelor''''s degree
- Must have prior experience as Laboratory Analyst
- Previous experience as a Bench Scientist
- Will be executing experiments
- Will consider candidates with Bachelors degree and 2 years exp, OR a Masters degree and 1 year exp
- Must have Protein or Impurities assays experience
- Must have previous experience in a Laboratory
- Must have cGMP experience
Required Qualifications:
Bachelor’s degree or equivalent, in Chemistry, Biochemistry or related subject area, with a minimum of 2 or more years of related industry laboratory experience is required, or a Master’s degree with 1 or more years of related industry laboratory experience is required.
Strong technical writing and verbal communication skills are required. Demonstrates excellent interpersonal skills (written and oral) and the ability to work in a cross-functional customer-focused environment is required.
Experience with a minimum of two of the following techniques is required:
Plate-based biochemical assays (impurity, HCP), ELISA, FRET, Cell based potency assays.
Experience working in a cGMP environment is required. Perform experiments and data review according to SOPs and protocols.
Experience with electronic laboratory notebook is preferred.
Excellence in bioassay trouble shooting is preferred.
Ability to work with limited guidance to plan, execute, and follow through with studies is preferred.
Strong technical writing and verbal communication skills are required. Demonstrates excellent interpersonal skills (written and oral) and the ability to work in a cross-functional customer-focused environment is required.
Experience with a minimum of two of the following techniques is required:
Plate-based biochemical assays (impurity, HCP), ELISA, FRET, Cell based potency assays.
Experience working in a cGMP environment is required. Perform experiments and data review according to SOPs and protocols.
Experience with electronic laboratory notebook is preferred.
Excellence in bioassay trouble shooting is preferred.
Ability to work with limited guidance to plan, execute, and follow through with studies is preferred.
Applicants must provide their phone number. Reference job number A5373.