Flexible, inclusive culture - 70% remote workforce, 66% women-led teams * Learn more about our core ... MasterControl * Working experience in quality system programs * Excellent written and oral ...
Flexible, inclusive culture - 70% remote workforce, 66% women-led teams * Learn more about our core ... MasterControl * Working experience in quality system programs * Excellent written and oral ...
Remote Mastercontrol information
What is a Remote MasterControl operator?
What are the key skills and qualifications needed to thrive as a Remote MasterControl Specialist, and why are they important?
What is the difference between Remote Mastercontrol vs Remote Quality Assurance Specialist?
| Aspect | Remote Mastercontrol | Remote Quality Assurance Specialist |
|---|---|---|
| Required Credentials | GxP, FDA compliance, software validation | GxP, FDA compliance, testing methodologies |
| Work Environment | Regulatory, software validation, document management | Product testing, process audits, compliance reviews |
| Employer & Industry Usage | Life sciences, healthcare, pharmaceutical | Life sciences, manufacturing, healthcare |
Remote Mastercontrol and Remote Quality Assurance Specialist roles both require GxP and FDA compliance knowledge. While Mastercontrol focuses on document management and software validation, Quality Assurance Specialists concentrate on testing and process audits. Both roles are common in regulated industries like pharmaceuticals and healthcare, but they serve different functions within quality and compliance teams.
How does a Remote MasterControl operator typically collaborate with engineering and production teams to ensure smooth broadcast operations?
Job description
Job Description:
Document Management Specialist
The Quality Assurance & Compliance Document Management Specialist will ensure compliance with relevant guidelines and regulations in a GxP environment. The position holder, with the input from the line manager and the QA team, is responsible for Document Management in the eDMS MasterControl
Make an Impact at Veristat!
Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.
- 105+ approved therapies for marketing applications prepared by Veristat
- 480+ oncology projects in the past 5 years
- 350+ rare disease projects delivered in the past 5 years
- Flexible, inclusive culture - 70% remote workforce, 66% women-led teams
- Learn more about our core values here!
What we look for
- Bachelor's Degree in a science or related field required
- 2-3 or more years of relevant industry experience in Document Control in Quality Assurance
- 2 or more years of experience in Document Control in MasterControl
- Working experience in quality system programs
- Excellent written and oral communication skills
- Proficient in Microsoft Word, Excel and PowerPoint.
- Strong multitasking and organization skills with a high level of attention.
- Demonstrated ability to work in a cross-functional team
- Well-honed ability to work independently, think critically, take initiative and set priorities, as much as ability to work as part of a team.
- Ability to meet strict deadlines, flex with changing priorities.
- Health Authority and/or Notified Body experience a plus
Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.
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Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
About Veristat
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
501 - 1,000 Employees
Headquarters location
Southborough, MA, US
Year founded
1994