Technical Specialist Jobs

• Minimum of 3-5 years’ experience of Quality Assurance experience in the Pharmaceutical/Biotech Industry.

• Experience in the use of validated computer systems for management of regulated documents and training, including electronic records and electronic signatures.

• Experience with Veeva Vault required.

• Experience with ComplianceWire, required.

• Experience in maintaining cGMP compliance, preferred.

• Excellent organizational skills and the ability to handle multiple priorities and projects.

• Excellent communication skills with the ability to interact with all levels throughout the organization.

• Strong written and verbal communication skills as well as attention to detail