BioProcess Development Associate I

Posted 03 May 2021
SalaryUp to £50000.00 per annum
LocationUnited States of America
Job type Permanent
DisciplineLife Science and Pharmaceuticals
Reference19770
Contact NameDeLisa Chambers

Job description


BioProcess Development Associate I
Claremont Consulting has an immediate opening for a BioProcess Development Associate I. Direct Hire opportunity located in the Athens, GA area. Excellent benefits package provided.
Responsibilities:

  • Set up, execute, and monitor experiments related to downstream process development.

  • Monitor software or equipment malfunction as well as experiment errors.

  • Participate in root-cause analyses to determine the source of error.

  • Perform characterization assays measuring critical quality product attributes.

  • Monitor multiple projects simultaneously with minimal supervision.

  • Perform bioprocess workflows that include downstream biologics processes.

  • Assist in bioprocess workflows that include mammalian cell culture.

  • Follow established standard operating procedures and complete required documentation in a clear, concise, format according to proper GDPs, using GMP batch records and corporate forms and protocols.

  • Skillfully and accurately operate laboratory equipment such as pipettors, balances, biosafety cabinets, incubators, autoclaves, microscopes, and centrifuges.

  • Safe handling, storage, and maintenance of chemicals according to Environmental Safety Division and OSHA regulations.

  • Assist in daily operation and maintenance of the manufacturing facility.

  • Maintain detailed records that are legible, accurate, and readily understood.

  • Participate in occasional weekend work.

  • Interact with senior laboratory personnel to review progress and present results.

  • Perform other appropriate duties as assigned by Management.


Qualifications:

  • Experience in executing downstream processes from bench to pilot-scale; with preferably some experience working in cGMP manufacturing or regulated environment and/or a good understanding of regulatory/quality requirements.

  • Work experience in an industry that complies with cGMP is highly preferred.

  • Strict attention to detail.

  • Excellent written and oral communication skills.

  • Exceptional organizational and documentation skills.

  • Demonstrated ability to work productively in a team environment is a must.

  • Proven ability to multi-task and meet multiple high priority deadlines.

  • Demonstrated ability to work independently with limited supervision.

  • Proficient in data entry including programs/software such as Outlook, Microsoft Word, PowerPoint, and Excel.


Requirements:

  • Minimum of a bachelor's degree in biochemistry, protein chemistry, or related field and a minimum of 0-1 years of experience in a related position at a biotech or pharmaceutical company.

    • Candidates with a bachelor's degree in biochemistry or protein chemistry and a minimum of 2-4 years of experience in a related position in an academic laboratory may be considered.