Quality Control Analyst

Raleigh, North Carolina  /  South Atlantic  /  Full Time

CAI is seeking motivated Quality Control Analyst to support biotech and pharmaceutical projects in Raleigh, Durham, Sanford, Wilson, Rocky Mount, and Greenville, North Carolina. Relocation assistance is available. These are full-time opportunities with competitive compensation and benefits which include: Long Term Disability and Life Insurance provided by the company. Health insurance at very low cost to employee, 15% retirement contribution, 24 days PTO, 5 sick days per year, and support for continued professional education.
CAI is a 100% employee-owned company providing CQV, start-up, project management and consulting services to FDA regulated and mission critical industries.  CAI was established in 1996 and has steadily grown to be an industry leader with 500 employees worldwide.
A potential candidate should be able to practice proper analytical techniques. The candidate should be able to adhere to all GMP requirements, FDA/EMEA regulations, and have effective interactions/communication with Quality management. The QC Analyst may also support the identification and implementation of corrective and preventive actions. He/she should be able to work effectively within the group, within Quality, and across the site.
*Perform routine QC testing using the following analytical methods:
*Physical testing (pH, appearance, osmolality, conductivity, sub-visible particulates)
*Participate in method troubleshooting, qualification and validation if needed.
*Write and revise documents such as SOPs, specifications and technical reports.
*Support investigations to determine root cause of deviations and non-conforming results and implement appropriate corrective and preventative actions in a timely manner.
*Liaise with other departments including Analytical Development, Quality Assurance, and Manufacturing to address compliance issues and to implement corrective actions and to improve programs.

Requirements include: 
BA or BS in chemistry or equivalent discipline
0-2 years of related experience in a GMP quality control laboratory or equivalent experience.
Excellent oral and written communication skills in English 
Able to travel domestically and internationally if required 
Able to work (paid) overtime 
Able to work in the US without sponsorship now or any time in the future. 



  • 100% Employee Owned
  • 24 Days PTO/5 Sick days per year
  • Medical / Dental / Vision
  • Professional Development
    (Approximately $5,000 paid career-related, continuing education)
  • ESOP/401k – 15% Company Contribution
  • Company Paid Long-Term Disability
  • Company Paid Life Insurance
  • No Layoffs in Company History