| Company: | GenQuest BioScience, Inc. |
|---|---|
| Type: | Full Time |
| City: | Mountain View |
The selected candidate will have responsibility for the maintenance and continuous improvement for the Corporate Training Program. The Coordinator is responsible for development and delivery of the cGMP Training Program, including Initial and annual cGMP Training. The coordinator will evaluate, identify and recommend training gaps and opportunities. Develop, support and promotes informal cGMP learning and related educational opportunities. Additional core responsibilities include development of site training plan, monitoring and archiving of personnel training files. The Coordinator will track personnel training activity completion including SOPs/courses and report training metrics on a timely basis to management. The Coordinator will partner with technical subject-matter experts (SME) to conduct SOP training needs assessments and maintain company training profiles that define target audience, learning objectives and effectiveness measures to effectively meet these needs. This person will have a strong working knowledge of regulatory, corporate and industry cGMP training requirements and trends. Ensures internal programs and requirements meet and/or exceed regulatory requirements. This person will keep abreast of new regulatory/technical developments and training methodologies to support continuous improvement.
Skills Required: Must be flexible, adaptable to change, tight deadlines, time constraints, and rapid shifts of direction and/or priority with a customer-oriented approach to problem-solving. Strong ability to maintain detailed and accurate records. Highly proficient in the use of a wide variety of computer applications including MS Word, Excel, PowerPoint, Visio, database management systems, and project management software. Proficient with electronic documentation systems. Ability to work as a team or independently with little or no instruction. Receive general instructions on new assignments
Qualifications include a Bachelors degree or equivalent experience, with a minimum of 5 to 8 years related experience in quality assurance. Familiarity with pharmaceutical and medical device standards, both GMP and ICH guidelines. Experience with Agile preferred.
How to Apply:
Resumes must be sent via e-mail only and as a file attachment in either MS Word or Rich Text format to: jobs@genquestbio.com
To learn more about this position, follow us on Twitter or to preview other opportunities, please visit our website at: www.genquestbio.com/careers.htm
Skills Required: Must be flexible, adaptable to change, tight deadlines, time constraints, and rapid shifts of direction and/or priority with a customer-oriented approach to problem-solving. Strong ability to maintain detailed and accurate records. Highly proficient in the use of a wide variety of computer applications including MS Word, Excel, PowerPoint, Visio, database management systems, and project management software. Proficient with electronic documentation systems. Ability to work as a team or independently with little or no instruction. Receive general instructions on new assignments
Qualifications include a Bachelors degree or equivalent experience, with a minimum of 5 to 8 years related experience in quality assurance. Familiarity with pharmaceutical and medical device standards, both GMP and ICH guidelines. Experience with Agile preferred.
How to Apply:
Resumes must be sent via e-mail only and as a file attachment in either MS Word or Rich Text format to: jobs@genquestbio.com
To learn more about this position, follow us on Twitter or to preview other opportunities, please visit our website at: www.genquestbio.com/careers.htm
