Technical Writer

Work Schedule

Environmental Conditions

Job Description

Join Us as a Quality Assurance Specialist - Make an Impact at the Forefront of Innovation. The Clinical Quality Assurance Specialist provides broad expertise to the department in one or more specialized areas or processes in the execution of the Quality Management System (QMS). This role involves leading and attending inter-departmental meetings related to their area of expertise to develop strategies and implementation plans. The Quality Assurance Specialist II serves as a client contact for company-contracted services for large or significant programs and contributes to policy-making decisions as a resource in their area(s) of expertise.


What Youll Do:

Serve as subject matter expert for process/vendor audits or activities in several areas of expertise e.g. review computer system validation data lab investigations root cause analysis batch record review or total Quality Management.
Represent the department in client and regulatory inspections/audits and lead in development lifecycle tracking and effectiveness measurement of corrective actions.
Participate in inter-departmental meetings and contribute to policy-making decisions.
Provide training for department and/or laboratory staff.
Evaluate acceptability of data based on criteria set forth in SOPs and methods.
Review data sample result tables and analytical reports for completeness and accuracy of data.
Utilizing department checklists evaluating content of reports and compliance with reporting criteria.
Verify accuracy of analytical results and sample identification and inventories and submits data to archives.
Review complex batch records and associated documentation for completeness and accuracy of data.
May lead risk assessments.
Manage set up and filing of documents.
May mentor junior team members in area(s) of expertise.


Education & Experience Requirements:

Bachelors degree or equivalent and relevant formal academic / vocational qualification
Previous lab or QA experience that provides the knowledge skills and abilities to perform the job (comparable to 5 years).

In some cases an equivalency consisting of a combination of appropriate education training
and/or directly related experience will be considered sufficient for an individual to meet the requirements of the role.

Knowledge Skills Abilities:

* Trackwise experience preferred
Provides comprehensive expertise to the department covering one or more specialized quality management areas assuring all systems processes and their outcomes comply with applicable international and national regulations
Guidelines and fulfill client and company requirements
May lead vendor and internal audits participate in client and regulatory inspections and/or manage the administration and reporting aspects of quality management systems.
Serves as quality consultant to the organization in their area(s) of GxP expertise
Acting as a resource for training activities and policy-making decisions supporting business leaders in mitigation of risk
Being responsible for building relationships between on-site QA services and QA management of designated clients.


Working Conditions and Environment:

Work is performed in an office laboratory and/or GMP Depot environment.
For laboratory positions potential exposure to biological fluids with potential exposure to infectious organisms.
Exposure to electrical office equipment.
Personal protective equipment required such as protective eyewear garments and gloves.
Variable work hours to accommodate schedules


Why Join Us

When you join Thermo Fisher Scientific you become part of a global team that values passion innovation and a commitment to scientific excellence. Youll work in an environment where collaboration and development are part of the everyday experienceand where your contributions truly make a difference.

Apply today to help us deliver tomorrows breakthroughs.