M-F, 8am - 5pm
100% onsite at Oneonta
Top/Required Skills:
- Associates or Bachelors and minimum of 2 years relevant work experience, preferably in a manufacturing environment
- Previous experience using ETQ or other Document Management software preferred
- Proficiency in Microsoft office
- Experience in ISO 9001 or other Quality System standards
- ISO 13485 and 21 CFR 820 Quality Management Systems knowledge highly preferred
- Extremely organized with ability to use multiple resources in comparing documentation
This position is to assist with a major project in Oneonta with changes to the documentation system and preparing for an audit.
Summary:
Responsible for administration of quality management system documents and records required for Life Sciences processes. Responsible for initiation of document changes, distributions, notifications and fulfilling internal and external document distribution.
Description of Work:
- Generates, reviews, and maintains quality system documents including procedures, work instructions, job aids, certificate of conformances, etc. in compliance with ISO 13485, ISO 9001, and 21 CFR 820 standards.
- Initiates Change Controls and Document Change Requests to update procedures and processes.
- Works within departments and with various departments to update processes and procedures.
- Assists in managing the document review and retention processes.
- Supports or leads continuous improvement initiatives for document control related processes.
- Supports other Quality Assurance functions as needed (internal audit, CAPAs, etc.)
- Other duties as required
Minimum Qualifications:
- Associate or bachelor's Degree, 2 years of work equivalent experience (work in a manufacturing environment is preferred).
Skills/Experience:
- Previous experience using ETQ or other Document Management software preferred
- Proficiency in Microsoft office
- Experience in ISO 9001 or other Quality System standards
- ISO 13485 and 21 CFR 820 Quality Management Systems knowledge highly preferred
- Must be detail oriented and accurate in execution of work
- Able to work well both independently and in a group setting
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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100% onsite at Oneonta
Top/Required Skills:
- Associates or Bachelors and minimum of 2 years relevant work experience, preferably in a manufacturing environment
- Previous experience using ETQ or other Document Management software preferred
- Proficiency in Microsoft office
- Experience in ISO 9001 or other Quality System standards
- ISO 13485 and 21 CFR 820 Quality Management Systems knowledge highly preferred
- Extremely organized with ability to use multiple resources in comparing documentation
This position is to assist with a major project in Oneonta with changes to the documentation system and preparing for an audit.
Summary:
Responsible for administration of quality management system documents and records required for Life Sciences processes. Responsible for initiation of document changes, distributions, notifications and fulfilling internal and external document distribution.
Description of Work:
- Generates, reviews, and maintains quality system documents including procedures, work instructions, job aids, certificate of conformances, etc. in compliance with ISO 13485, ISO 9001, and 21 CFR 820 standards.
- Initiates Change Controls and Document Change Requests to update procedures and processes.
- Works within departments and with various departments to update processes and procedures.
- Assists in managing the document review and retention processes.
- Supports or leads continuous improvement initiatives for document control related processes.
- Supports other Quality Assurance functions as needed (internal audit, CAPAs, etc.)
- Other duties as required
Minimum Qualifications:
- Associate or bachelor's Degree, 2 years of work equivalent experience (work in a manufacturing environment is preferred).
Skills/Experience:
- Previous experience using ETQ or other Document Management software preferred
- Proficiency in Microsoft office
- Experience in ISO 9001 or other Quality System standards
- ISO 13485 and 21 CFR 820 Quality Management Systems knowledge highly preferred
- Must be detail oriented and accurate in execution of work
- Able to work well both independently and in a group setting
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.