- 2-5 Years of Experience working in manufacturing.
- Hands-on cGMP manufacture including both upstream virus production and downstream purification
- Prepare manufacturing support materials such as media and buffers
- Prepare manufacturing equipment such as packing of chromatography columns for the manufacture of clinical and commercial vectors
- Participate in investigations of process deviations by conducting data gathering, trending and data presentation as required
- Review manufacturing documents and procedures (such as SOPs and batch records) for virus production and purification
- Perform routine calculations and maintain appropriate records
- Maintain manufacturing equipment and records
- Maintain safety procedures and compliance records
- Contribute to the manufacturing process monitoring for products transfer from research to manufacturing, as needed
Education: Bachelors minimum
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.
