Process Engineer II

The Opportunity

We are looking for a Process Engineer II, working in the Pharmaceuticals & Medical Products industry in Framingham, Massachusetts, United States.

Job description:

  • Executes concurrent projects of moderate scope and complexity, with minimal supervision.
  • Interprets and executes policies and procedures. 
  • Recommends modifications to operating policies.
  • Functions as a technical expert on equipment or systems (RSE); leads troubleshooting of operations, develops preventative maintenance procedures, and maintains engineering documentation.
  • Leads efforts with manufacturing, process development, facilities, quality assurance and other departments in developing requirements and recommendations for system modifications.
  • Executes tasks, under the direction of project managers, to complete design, engineering, construction, commissioning, and qualification for projects within schedule and budget constraints.
  • Coordinates the work of consultants and engineering firms on development of standard design documents.
  • Develops project scopes, schedules and budgets.
  • Obtains and critiques quotes for system/facility modifications and work with vendors to execute.
Details

The pay range we are offering is 40 to 50 per hour. This position may present an opportunity to go permanent.

Our Client

Our client is an award-winning clinical development company.  Improving lives globally with 20+ years experience in clinical research and strategic resourcing.  Elevating results with proven strategies, comprehensive solutions, and customized delivery models.

Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.

Strong relationships provide you connections and access to great opportunities.  Industry expertise sets you up for success with helpful insights, career coaching, and professional training.  Grow and learn while you put your skills to work.  

Experience Required for Your Success
Requirements:
  • BS in Mechanical or Chemical Engineering
  • 3-6 years experience in pharmaceutical/biopharmaceutical industry or related industry/cGMP environment
Skills:
  • General understanding of Quality Systems
  • General understanding and wide application of technical principle, theories, and concepts in the Biotech/Pharmaceutical field
  • General knowledge of other related disciplines
Demonstrated skills in the following areas: 
  • Problem solving and applied engineering 
  • Basic technical report writing 
  • Working knowledge of pharmaceutical/biotech process 
  • Experience in Bio-Pharmaceuticals 
  • Direct experience with regulated environments (i.e. cGMP, OSHA, EPA)
  • Working knowledge of specialized equipment/processes
  • General knowledge of Commissioning and Qualification
  • Effectively interact with a variety of communication and working styles
  • Ability to independently determine when additional internal/external resources are required to solve problems
What Do You Think?

Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.

Not exactly? Join Our Talent Community, and we'll let you know of additional opportunities.

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