Biopharmaceutical Manufacturing Associate

Highly Competitive Salary
  1. Contract
  2. Good Manufacturing Practice (GMP)
  3. United States
Cambridge, USA
Posting date: 15 May 2024
QA.JC.60393

Biopharmaceutical Manufacturing Associate - Contract - Cambridge, MA

Proclinical is seeking a Biopharmaceutical Manufacturing Associate for our client. This is a contract position located in Cambridge, MA.

Primary Responsibilities:

The successful candidate will be responsible for various manufacturing tasks, including setting up processes, ensuring room readiness, and completing necessary paperwork. This role offers the opportunity to lead key activities and progress your career in a dynamic and inclusive environment.

Skills & Requirements:

  • Bachelor's degree in a biological, chemical science, engineering or equivalent professional experience.
  • High School Diploma with manufacturing production, cGMP experience.
  • Previous manufacturing or laboratory experience requiring aseptic or sterile technique.
  • Mechanical aptitude to operate pumps, scales, and PH meters.
  • Ability to maintain attention to detail and quality, and a high level of integrity and confidentiality.
  • Ability to read, understand, follow and comply with technical and written documents (SOPs.)
  • Ability to work around acids, bases, oxidizers and cleaning solvents while wearing appropriate PPE.
  • Ability to perform calculations using simple mathematical formulas.
  • Basic computer skills.

The Biopharmaceutical Manufacturing Associate will:

  • Operate processing equipment in accordance with SOPs in all classified areas.
  • Use proper aseptic technique while performing tasks in the ISO 7 and ISO 8 areas.
  • Troubleshoot process equipment and interact with maintenance personnel.
  • Load and unload materials, label according to SOPs, assemble valves, connectors.
  • Report deviations or potential issues immediately to the management team.
  • Comply with applicable EHS/GMP regulations, guidelines, policies, and standard operating & safety procedures.
  • Complete and document daily manufacturing tasks per standard operating procedures, batch document instructions, and logbooks.
  • Maintain a high level of competency with current and emerging digital platforms (SAP, EBR, AR/VR, etc).

If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at (+1) 267-846-2026 or j.cerchio@proclinical.com.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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