CAI is a 100% employee-owned company established in 1996, that has grown year over year to almost 500 people worldwide. We provide commissioning, qualification, validation, start-up, project management, design and other consulting services to FDA regulated and mission critical industries.
CAI will be at the Boston ISPE Product Show, Wednesday, September 18th @ Gillette Stadium in Foxborough, MA - please stop by and see us! We'll have Hiring Managers and Recruiting staff on hand at booth w74 and the career fair.
CAI is seeking motivated Aseptic Process Engineers and Aseptic Validation Engineers to support biotech and pharmaceutical projects across the country. These are full-time opportunities with competitive compensation and benefits which include: up to 15% retirement contribution, 24 days PTO and 5 sick days per year, health insurance at extremely low cost to employee, financial support for both internal and external professional education as well as 70% long term disability paid for by the company.
As consultants to numerous types of industry, our employee owners are driven by the challenge and constant diversity of assignments, while having the stability of a consistently growing company.
Travel is required to achieve full success for the agents and the clients we serve. Most travel occurs within the US, but international travel can be also be requested as interested. Please check CAI out on Glassdoor to get a better perspective on our culture and travel. We are extremely proud that our employee owners have given us so many 5 star ratings.
BS or MS in a relevant engineering or science field, or equivalent experience
Excellent oral and written communication skills in English
Able to travel domestically and internationally if required
Able to work (paid) overtime as needed
Able to work in the US without sponsorship now or any time in the future
Aseptic Process Engineering Experience:
Three (3) or more years of experience in designing, operating, installing, troubleshooting, commissioning and/or qualifying of:
cGMP manufacturing process activities within isolators or biosafety cabinets (e.g. Cell and Gene Therapy
Sterile Operations - Vial/prefilled syringe/cartridge filling lines
Automated visual inspection systems
Automated formulation systems
Other Desired Experience:
Commissioning and Qualification
Developing Validation / Verification Master Plans
Performing formal risk assessments / FMEA
Identifying Critical Attributes and Critical Process Parameters
Developing User Requirements
Writing qualification protocols, commissioning plans/test scripts, and summary reports
Developing trace-ability matrices
Project planning and estimating
Schedule development and execution
Issue tracking and resolution