Quality Analyst - (Manufacturing) at Nesco Resource, LLC
Salt Lake City, UT 84108
About the Job
Shift Schedule: Monday - Friday 8:00am - 5:00pm
The job requirements include the following essential areas of responsibilities:
• Performing QA review/approval of investigation reports, change controls, Standard Operating Procedures, investigation documentation, and process/facility change control documents.
• Manage and track tasks for assigned Quality projects, CAPAs, and/or Audit Response commitments, and other initiatives to assure on time completion.
• Responsible for collaborating with appropriate departments to resolve both technical and compliance issues by providing Quality Assurance oversight.
Education/Certification/Experience:
• Bachelor's Degree, preferably in a scientific discipline (biology, chemistry or closely related field) or equivalent education/experience with a minimum of 10 years relevant progressive experience in the pharmaceutical industry.
• Requires a minimum of 3 years of experience in Quality Assurance, Quality Engineering, or Compliance role within pharmaceutical industry.
Skills/Knowledge/Abilities:
• Computer proficiency with comprehensive working knowledge of MS Office products, Learning Management Systems (LMS), EDMS and ERP systems, as well as Quality systems such as Trackwise.
• Self-directed with ability to organize and prioritize work
• Ability to communicate effectively with excellent written and oral communication skills
• Ability to interact positively and collaborate with co-workers and management
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.
#EDS014
The job requirements include the following essential areas of responsibilities:
• Performing QA review/approval of investigation reports, change controls, Standard Operating Procedures, investigation documentation, and process/facility change control documents.
• Manage and track tasks for assigned Quality projects, CAPAs, and/or Audit Response commitments, and other initiatives to assure on time completion.
• Responsible for collaborating with appropriate departments to resolve both technical and compliance issues by providing Quality Assurance oversight.
Education/Certification/Experience:
• Bachelor's Degree, preferably in a scientific discipline (biology, chemistry or closely related field) or equivalent education/experience with a minimum of 10 years relevant progressive experience in the pharmaceutical industry.
• Requires a minimum of 3 years of experience in Quality Assurance, Quality Engineering, or Compliance role within pharmaceutical industry.
Skills/Knowledge/Abilities:
• Computer proficiency with comprehensive working knowledge of MS Office products, Learning Management Systems (LMS), EDMS and ERP systems, as well as Quality systems such as Trackwise.
• Self-directed with ability to organize and prioritize work
• Ability to communicate effectively with excellent written and oral communication skills
• Ability to interact positively and collaborate with co-workers and management
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.
#EDS014