Job Title: Quality Specialist

Duration: 12 months

Location: Wilson, NC

Qualifications:

Education: Must possess a B.A. /B.S. degree (preferably in Science or Engineering).

Required experience and skills:

• Possesses an advanced knowledge and ability to operate information systems (SAP and Veeva Systems preferred) required to complete job responsibilities with the ability to generate data and reports from these systems.

• Must possess a minimum of minimum of three (3) years' experience in a GMP pharmaceutical manufacturing facility with either direct involvement in Quality functions supporting release and compliance activities or indirect involvement in Quality functions through execution of activities such as: batch record/documentation reviews, investigations, corrective actions, complaints, quality system management, etc.

• Must possess highly developed written and oral communication and teamwork skills.

• Additionally must have strong attention to detail, problem solving skills, and proficient in time management.

• Identifies and solves a range of problems in straightforward situations and analyzes possible solutions and assesses each using standard procedures.

• Flexible, Multitasker, able to work under pressure and adheres to project timelines.

• Ability to independently respond to advances requests for data and trending of data and proactively utilizes trending of data to improve the operation or drive change.