specialist in rockville

posted
job type
contract
salary
US$ 32 per hour
apply now

job details

posted
location
rockville, maryland
job category
Manufacturing & Production
job type
contract
salary
US$ 32 per hour
reference number
141293
apply now

job description

Contract position: A leading pharmaceutical manufacturer is looking for a Biopharm Manufacturing Associate to prepare biopharmaceutical intermediates in Rockville, MD area. It is a 1-year CONTRACT position with no per diem. Candidates must be able to work a flexible schedule including weekends. Must be open to ALL shifts.

Responsibilities for the Specialist

  • Perform production operations including fermentation or cell culture operations, preparation of media and buffer solutions, chromatographic separation, filtration and concentration operation.
  • Complete daily manufacturing tasks per standard operating procedures and batch document instructions. Monitor critical process parameters. Document manufacturing activities clearly and accurately.
  • Ensure all processing equipment and materials necessary are adequate and available to set the team up for success. Ensure all production activities are completed in a safe and compliant manor.

Requirements for the Specialist

  • BS/BA (e.g. Engineering, Life Sciences, Chemistry) or Associates Degree with 2+ or more years of directly related experience.
  • Understanding of the basic FDA cGMP regulations.

Benefits

  • 401k
  • Healthcare

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

skills

manufacturing associate,associate,pharma,biopharma,bio-pharma,bio pharma

qualification

Associates Degree

responsibilities

Perform production operations including fermentation or cell culture operations, preparation of media and buffer solutions, chromatographic separation, filtration and concentration operation. Complete daily manufacturing tasks per standard operating procedures and batch document instructions. Monitor critical process parameters. Document manufacturing activities clearly and accurately. Ensure all processing equipment and materials necessary are adequate and available to set the team up for success. Ensure all production activities are completed in a safe and compliant manor.

educational requirements

Associate