QA Control Documents Senior Coordinator

Summary of Responsibilities :

Follow applicable departmental Standard Operating Procedures and Work Instructions.

Complete required trainings according to required timelines.

Administer controlled documents ensuring availability to the end user.

Track and report metrics as determined by management according to required timelines.

Assist with implementation of new / revised processes and procedures.

Demonstrated ability to communicate effectively.

Perform checks to ensure quality of work completed.

Ensure timely escalation and resolution management of issues impacting controlled document release.

Ensure Regulatory Compliance and Quality Assurance (RC and QA) responsibilities as indicated in applicable controlled documents are followed.

All other duties as needed or assigned.

Qualifications (Minimum Required) :

3 years in regulatory environment (experience in GXP roles).

Demonstrated ability to plan prioritize organize and communicate effectively.

Demonstrated ability to pay attention to detail.

Strong analytical skills.

Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Experience (Minimum Required) :

3 years in regulatory environment (experience in GXP roles).

Strong interpersonal skills with ability to work well with others.

Ability to deliver consistent high quality of work.

Ability to use computer and departmental tools.

Physical Demands / Work Environment :

Tasks involve sitting in front of a terminal for many hours during the working day.

Learn more about our EEO & Accommodations request here .

Required Experience :

Senior IC

Key Skills

Continuous Integration,Quality Assurance,FDA Regulations,Root cause Analysis,TFS,Food Processing,ICH Q10,Jira,Software Testing,Quality Management,Selenium,Github

Employment Type : Full-Time

Experience : years

Vacancy : 1