Jobs in Durham, NC

About the role

This role is responsible for all computerized system validation (CSV) and data integrity (DI) activities, working under the direction of the Validation Lead and alongside the CQV team.

What you'll bring

• Bachelor’s degree in engineering, computer science, or related field.
• Minimum 5 years of CSV experience in GMP pharmaceutical or biotech environments.
• Proven experience with equipment‑level PLC/HMI validation (OEM systems) and historian connectivity.
• Must be local in or around RTP, must be able to work on site 100%.
• For US geography, the salary range for this position is shown below.
• The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice.
• Therefore, in some circumstances, the actual salary could fall outside of this expected range.
• This salary range is subject to change and may be modified in the future.
• Hands‑on experience with PAT instrument integration (e.g., NIR, moisture analyzers) is a strong plus.

Benefits