Compliance Specialist Jobs in New Jersey
Qualifications: B.S. degree in a scientific, health sciences or technical discipline required (e.g., engineering, bioengineering, biology, chemistry)....
International Regulatory Compliance Specialist
- Mount Laurel, NJ
- 1 day ago
- Mount Laurel, NJ
- 1 day ago
One of our food & beverage manufacturing clients is seeking an International Regulatory Compliance Specialist to join their team on site in Mount Laurel, NJ....
Senior Business Management Specialist - Compliance Operations
- Mount Laurel, NJ
- 1 day ago
- Mount Laurel, NJ
- 1 day ago
Work Location: New York, New York, United States of America Hours: 40 Pay Details: $110,760 - $178,880 USD TD is committed to providing fair and equitable compensation opportunities to all...
Immediate need for a talented AVP-Compliance Officer. This is a 08+months contract opportunity with long-term potential and is located in Jersey City, NJ (Onsite). Please review the job...
Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and...
Regulatory Affairs Specialist Advertising/Promo
- Bridgewater, NJ
- 6 days ago
- Bridgewater, NJ
- 6 days ago
Regulatory Affairs Specialist Advertising & Promotion Location: Bridgewater, NJ / Hybrid Industry: Pharmaceuticals / Life Sciences Track: Technical (No Direct Reports) Pay Rate: $61-$91/hour...
Alternate Locations:** Radnor, PA (Pennsylvania); Boston, MA (Massachusetts); Dover, NH (New Hampshire); Fort Wayne, IN (Indiana); Work from Home **Work Arrangement:** Hybrid Preferred : Preferred...
Remote WorkRegulatory Affairs Specialist - Advertising/Promo
- Bridgewater, NJ
- 6 days ago
- Bridgewater, NJ
- 6 days ago
Regulatory Affairs Specialist Advertising & Promotion Location: Bridgewater, NJ / Hybrid Industry: Pharmaceuticals / Life Sciences Track: Technical (No Direct Reports) Pay Rate: $61-$91/hour...
Sr. Regulatory Affairs Specialist - Franklin Lakes, NJ
- Franklin Lakes, NJ
- 8 days ago
- Franklin Lakes, NJ
- 8 days ago
Summary Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and its no small...
Job Title: Technical Writer Compliance Job Description We are seeking a skilled Technical Writer Compliance professional who will be responsible for writing and completing investigations and...
This is an opportunity to join Ascot Group - one of the world's preeminent specialty risk underwriting organizations. Designed as a modern-era company operating through an ecosystem of...
Company :** Highmark Health **Job Description :** **JOB SUMMARY** This job works collaboratively riskacross Highmark Health clinical areas to support clinical quality auditing, The Senior Risk...
Regulatory Affairs Specialist** Kelly Science and Clinical is seeking a **Regulatory Affairs Specialist** **for** our client a leading medical device company in Bridgewater, NJ. If youre...
Regulatory Affairs Specialist Kelly Science and Clinical is seeking a Regulatory Affairs Specialist for our client a leading medical device company in Bridgewater, NJ. If youre passionate about...
Quality Assurance and Regulatory Affairs Specialist Description The Quality Assurance and Regulatory Affairs Specialist will be responsible for supporting local Quality and Regulatory strategies,...
Demographic Data for New Jersey
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Compliance Specialist Online Courses and Training Opportunities
Title Synonyms
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Salary for Compliance Specialist Jobs in New Jersey
Required or preferred licenses and certifications for Compliance Specialist positions.
Highest Education Level
Compliance Specialists in New Jersey offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Compliance Specialist position
- ICH GCP
- Medical Affairs
- 21 CFR 820
- Internal Audits
- Institutional Review Board
- Scientific Research
- TrackWise
- ICH Guidelines
- Environmental Monitoring
- Stem Cells
- Biomedical Engineering
- Drug Development
- Change Control
- GxP
- Quality Systems
- Good Clinical Practice
- ISO 13485
- Quality Management Systems
- Good Laboratory Practice
- Biochemistry
- Cell Culture
- Biotechnology
- Animal Care
- Microbiology
- Medical Device Sales
- Biology
- Corrective Actions & Preventive Actions
- Clinical Trials
- Good Manufacturing Practices
- Clinical Research
- FDA Regulations
- Standard Operating Procedures
- Product Development
- Engineering
- Strategy Development
- Risk Management
- Implementation
- Written Communication
- Driving
- Auditing
- Collaboration
- Investigation
- Interpersonal Skills
- Documentation
- Education Experience
- Reporting
- Quality Assurance
- Policy Development
- Filing
- English
- Problem Solving
- Bachelor's Degree
- Microsoft Office
- Regulations
- Microsoft Excel
- Research Skills
- Organization
- Scheduling
- Leadership
- Communication Skills
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