Compliance Manager
at Thermo Fisher Scientific
Wilmington, North Carolina, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 28 Jul, 2024 | Not Specified | 01 May, 2024 | 5 year(s) or above | Critical Thinking,Training,Management Skills,Risk Assessment,Communication Skills,Travel,Root | No | No |
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Description:
JOB DESCRIPTION
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
EDUCATION
- Bachelor’s degree or equivalent and relevant formal academic / vocational qualification
EXPERIENCE
- 5+ years of quality assurance experience that provides the knowledge, skills, and abilities to perform the job or equivalent combination of education, training, & experience.
‘In some cases an equivalency, consisting 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
- Detailed knowledge of GCP and appropriate regional research regulations and guidelines
- Proficiency in a conducting GxP audits
- Excellent oral and written communication skills
- Strong problem solving, critical thinking, risk assessment and impact analysis abilities
- Confirmed experience in root cause analysis
- Demonstrated organizational and time management skills
- Flexible and able to multi-task and prioritize complex demands/workload
- individuals with prior experience in Clinical Quality Assurance/Compliance – GCP audit, inspection, consultancy experience is necessary.
- Travel under 25%
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:5.0Max:10.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Wilmington, NC, USA