Thermo Fisher Scientific
Principal Operational Process and Compliance Specialist
Thermo Fisher Scientific, North, South Carolina, United States, 29112
Employer Industry: Life Sciences and Clinical Research
Why consider this job opportunity:
Salary eligible for a variable annual bonus based on performance results
Comprehensive Total Rewards package including medical, dental, and vision plans
At least 120 hours of paid time off (PTO) annually, plus paid holidays and parental leave
Opportunities for career growth and professional development
Supportive work environment that values employee wellness and work-life balance
What to Expect (Job Responsibilities):
Lead mid-to-large scale process improvement projects across various departments Conduct in-depth risk assessments and develop strategies for quality concerns Establish and maintain governance frameworks for quality and compliance practices Analyze trends to provide insights for process optimization and compliance improvement Collaborate with senior leadership to align process improvements with business priorities What is Required (Qualifications):
Bachelor's degree or equivalent relevant qualification Minimum of 8+ years of experience in clinical research or related fields Strong understanding of process improvement practices and regulatory guidelines Excellent investigative, analytical, and negotiation skills Effective oral and written communication skills in English How to Stand Out (Preferred Qualifications):
Significant clinical research experience in all phases of the clinical study lifecycle Familiarity with clinical management technologies and systems Proven ability to direct and promote teamwork in a multi-disciplinary setting Strong creative and critical thinking skills We prioritize candidate privacy and champion equal-opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. If you encounter any employer not adhering to these principles, please bring it to our attention immediately.
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Lead mid-to-large scale process improvement projects across various departments Conduct in-depth risk assessments and develop strategies for quality concerns Establish and maintain governance frameworks for quality and compliance practices Analyze trends to provide insights for process optimization and compliance improvement Collaborate with senior leadership to align process improvements with business priorities What is Required (Qualifications):
Bachelor's degree or equivalent relevant qualification Minimum of 8+ years of experience in clinical research or related fields Strong understanding of process improvement practices and regulatory guidelines Excellent investigative, analytical, and negotiation skills Effective oral and written communication skills in English How to Stand Out (Preferred Qualifications):
Significant clinical research experience in all phases of the clinical study lifecycle Familiarity with clinical management technologies and systems Proven ability to direct and promote teamwork in a multi-disciplinary setting Strong creative and critical thinking skills We prioritize candidate privacy and champion equal-opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. If you encounter any employer not adhering to these principles, please bring it to our attention immediately.
#J-18808-Ljbffr