Werfen North America→
Intern, Laboratory Services at Werfen North America in Norcross, GA
InternshipOn-siteNorcross, GA
Skills
computer software implementationfda standardsiso standardssop complianceosha regulationscgmp regulations
Job Description
Summary: Werfen North America is a leading company in specialized diagnostics, focusing on innovation and quality in healthcare solutions. The Intern in Laboratory Services will perform project-related tasks associated with the qualification, validation, and implementation of software for Quality Laboratories, assisting in customizing solutions to fit the GMP environment.
Responsibilities:
- Follows applicable SOPs, OSHA regulations and cGMP regulations
- Technical writer for SOPs, Forms, attachments, and training and creation associated with applicable software
- Performs administrative tasks and duties, when applicable; including writing and reviewing case studies, writing and reviewing testing protocols, writing validation documents
- Understands FDA and ISO standards applicable to the software and consequences of Nonconformance
- Conducts themselves in a polite, helpful, and professional manner with all employees both inside and outside of the department
- Assists with special projects and other duties as assigned
- Maintains work area, equipment, department, and all storage areas in a clean, neat, and orderly manner
- Interacts cooperatively with coworkers, supervisors or managers of other departments and receives direction well from superiors
Required Qualifications:
- Currently enrolled in a Bachelor's degree ( BS/BA) program in Computer Science or a related field with a minimum of 3 years completed from an accredited four-year college or university
- Strong verbal and written communication, interpersonal skills
- Minimum of 3 years of previous college or university experience
Preferred Qualifications:
- Computer software implementation experience preferred
Required Skills: Computer software implementation, FDA standards, ISO standards, SOP compliance, OSHA regulations, cGMP regulations