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QA SOP Analyst (Documentation Specialist) - Remote at Remote, Remote, USA
Email: [email protected]
Role:                     QA SOP Analyst (Documentation Specialist)

Rate:                   $60hr c2c Okay with H1s

Duration:             12 Months

Location:             Remote

Candidate should be from California to Mid-West Not accepting far East candidates

 MOSTLY REMOTE BUT NEED TO ATTEND SOME ONSITE MEETINGS. (Foster City, CA)

 Pharma, Medical, Life science or Biotech industry background is required

 Primary responsibilities for role:

Develop SOP's for over 20 different laboratory systems/equipment and a new digital platform. Client is going from a Paper-Based system to a digital platform system.

Interface with SME's that are implementing the new digital platform and the Laboratory Technicians.

Attend required onsite/remote meetings.

Update client and PTS Advance management on progress and any areas that have become a bottleneck which is causing delays.

Requirements:

Education and Experience by level:

Minimum Education: Bachelor's Degree

At least 4+ years of technical documentation experience within the Life Science industry including gathering required information and developing documentation to include SOPs, implementation plans, admin guides

3+ years of experience managing technical documentation including version control and developing processes to make document creation and maintenance more efficient

2+ years of experience reviewing technical documentation to identify areas of improvement and quality

Demonstrates strong technical documentation skills and ability to adapt to changing circumstances.

Displays flexibility with assignment.

Completes SOP's in a timely manner and can identify and present to management areas that are causing project delays.

Communicates effectively and promptly at all levels of the organization, supporting department objectives and management decisions.

Able to promote team approach.

Application Question(s):

What level of experience do you have with developing SOP's within a Laboratory Environment

Have you developed SOP's for a Pharmaceutical, Biotech and/or Medical Device company

Have you ever developed SOPs for any lab equipment

Any experience with QMS, Trackwise or similar system

Have you ever worked in a supervisory role

Thanks,

Ashley

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Siliconstar Tech, 320 Decker Drive, Suite 100, Irving, Texas 75062 Phone: 972 256 8154

Keywords: quality analyst California
[email protected]
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Mon Jan 29 23:53:00 UTC 2024

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