Quality Engineer - Deviation Management (Biotech / Biomedical)

JOB DESCRIPTION :

• Primary responsibilities include day-to-day technical support to manufacturing operations, including resolution and reduction of process deviations, development and implementation of corrective / preventative actions, and leading manufacturing and laboratory investigations
• This individual will be responsible for providing scientific support for manufacturing areas within
• 's Manufacturing Division (MMD)
• This Individual will also develop working relationships with counterparts in other areas supporting aseptic manufacturing, testing, planning, and release and is required to utilize sound scientific and engineering principles to investigate process deviations
• Troubleshooting and root cause analysis of laboratory test failures and manufacturing atypical events, development of corrective / preventative actions is required
• Analysis of complex problems through critical analytical thinking and the design / execution of laboratory / pilot scale experiments is required
• Off-shift work may be required

Qualifications :

Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.

Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.