What are the responsibilities and job description for the Biopharmaceutical Process Associate position at R&D Partners?
Role Overview
The Manufacturing Associate will play a crucial role in ensuring the smooth operation of our biopharmaceutical production processes. This includes understanding process theory and equipment operation, as well as being able to learn biopharmaceutical manufacturing processes.
Main Responsibilities
- Process Knowledge: Understand process theory and equipment operation, and be able to learn biopharmaceutical manufacturing processes.
- Technical Documentation: Provide feedback and/or suggested changes to operational procedures, assist in the incorporation of new technologies, practices and standards into procedures, and capable of writing and reviewing process documents.
- Quality and Compliance: Understand cGMPs as related to Commercial Operations, and ability to utilize Quality systems (Deviations, CAPAs, Change Requests, Action/Alert Reports, etc.).
- Business: Ability to participate on projects and contribute to outcomes, capability to learn and support new business systems (Track wise, ERP, etc.), and support trending of defined department metrics.
Qualifications
- Bachelor's degree in science related area or engineering, or Associate's degree in science related area or Biotech certificate with 2 years of experience in a biotech manufacturing environment or other regulated industry.
Benefits
- Medical insurance – PPO, HMO & HSA, Dental & Vision insurance, 401k plan, Employee Assistance Program, Long-term disability, Weekly payroll, Expense reimbursement, Online timecard approval.
