Summary:
As the Equipment and Controls Qualification Specialist you will support qualification activities in a cGMP environment in partnership with the client's facility and their Global Shared Services team. The client is a pharmaceutical manufacturing company committed to excellence and a customer focused attitude is everything. The client prioritizes the pursuit of excellence because their work has the power to improve patients' lives with the pharmaceuticals they develop and manufacture.
In this role, you will:
• Prepare, review, and lead execution of qualification protocols
• Conduct qualification tests of existing equipment or software in accordance with internal protocols or external standards
• Prepare and own change controls for qualification documentation.
• Drive continuous improvement efforts for the site qualification/validation program
• Exhibit safety awareness and safe work practices.
Qualifications Required:
• BS in an Engineering or Science field
• 1-3 years' experience in a food or pharma manufacturing environment
• Demonstrated interpersonal skills
• Functional working knowledge with standard MS Office Products
• Understanding of Allen Bradley Programmable Logic Controllers and associated systems Have an understanding of cGMPs and associated regulations.
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.
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As the Equipment and Controls Qualification Specialist you will support qualification activities in a cGMP environment in partnership with the client's facility and their Global Shared Services team. The client is a pharmaceutical manufacturing company committed to excellence and a customer focused attitude is everything. The client prioritizes the pursuit of excellence because their work has the power to improve patients' lives with the pharmaceuticals they develop and manufacture.
In this role, you will:
• Prepare, review, and lead execution of qualification protocols
• Conduct qualification tests of existing equipment or software in accordance with internal protocols or external standards
• Prepare and own change controls for qualification documentation.
• Drive continuous improvement efforts for the site qualification/validation program
• Exhibit safety awareness and safe work practices.
Qualifications Required:
• BS in an Engineering or Science field
• 1-3 years' experience in a food or pharma manufacturing environment
• Demonstrated interpersonal skills
• Functional working knowledge with standard MS Office Products
• Understanding of Allen Bradley Programmable Logic Controllers and associated systems Have an understanding of cGMPs and associated regulations.
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.