Compliance Specialist Jobs in Orange, CT
A Compliance Specialist in the biotechnology industry is responsible for ensuring that all operations, policies, and procedures adhere to relevant legal and regulatory standards. They perform regular audits, develop and implement compliance programs, review and update internal policies, and identify any potential areas of compliance vulnerability and risk. Their role is crucial in maintaining the company's integrity and protecting it from any legal issues that could arise from non-compliance. In addition, they are responsible for training and educating staff about compliance requirements and procedures.
Key skills for a Compliance Specialist include a strong knowledge of industry regulations and guidelines, excellent attention to detail, problem-solving abilities, and strong communication and organizational skills. They should ideally have a bachelor's degree in life sciences, biotechnology or a related field. Certifications such as Certified in Healthcare Compliance (CHC) or Certified Regulatory Compliance Manager (CRCM) can be advantageous. Prior to becoming a Compliance Specialist, a professional might have roles such as Compliance Analyst, Quality Assurance Associate, or Regulatory Affairs Coordinator, which provide foundational knowledge and experience in regulatory compliance and quality assurance.
Senior Regulatory Affairs Specialist
- New Haven, CT (5 miles from Orange, CT)
- 3 days ago
- New Haven, CT (5 miles from Orange, CT)
- 3 days ago
trials, operations, and ICH Good Clinical Practices, federal regulations, and institutional processes....
RCS is the most senior, non-supervisory, position in the Research Compliance Specialist series....
Quality Assurance Associate III - Supplier Quality
- Milford, CT (4 miles from Orange, CT)
- 9 days ago
- Milford, CT (4 miles from Orange, CT)
- 9 days ago
Rentschler Biopharma is a leading global contract development and manufacturing organization (CDMO) for biopharmaceuticals. From our headquarters in Laupheim, Germany, and our site in Milford, MA,...
External Quality Assurance Associate III
- Milford, CT (4 miles from Orange, CT)
- 20 days ago
- Milford, CT (4 miles from Orange, CT)
- 20 days ago
Rentschler Biopharma is a leading global contract development and manufacturing organization (CDMO) for biopharmaceuticals. From our headquarters in Laupheim, Germany, and our site in Milford, MA,...
- Trumbull, CT (9 miles from Orange, CT)
- 30+ days ago
- Trumbull, CT (9 miles from Orange, CT)
- 30+ days ago
., Life Sciences, Biology, Chemistry, Engineering, Regulatory Science). Certificates, Licenses, Registrations. 3+ years Medical Device Regulatory experience....
- Trumbull, CT (9 miles from Orange, CT)
- 45+ days ago
- Trumbull, CT (9 miles from Orange, CT)
- 45+ days ago
Bachelors degree in chemistry, biochemistry, biology, library science, or related field preferred. Minimum of one year of regulatory experience, preferably in Consumer Packaged Goods....
YCCI Research Billing Compliance Analyst
- New Haven, CT (5 miles from Orange, CT)
- 90+ days ago
- New Haven, CT (5 miles from Orange, CT)
- 90+ days ago
Position Focus: Coordinate and conduct research billing reviews for all randomly selected clinical trials with billable services based on risk....
Demographic Data for Orange, CT
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Salary for Compliance Specialist Jobs in Orange, CT
Required or preferred licenses and certifications for Compliance Specialist positions.
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Compliance Specialists in Orange, CT offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Compliance Specialist position
- Consulting
- Decision Making
- Environmental Compliance
- Environmental Management
- Quality Systems
- ISO Certified
- Treasury
- Implementation
- Securities and Exchange Commission
- Balance Sheets
- Treasury Management
- Inspections
- ISO 13485
- Quality Management Systems
- Environmental Education
- Capital Markets
- Anti-Money Laundering
- Management Consulting
- ISO 14001
- Certified Hazardous Materials Manager
- HACCP Certified
- GxP
- Supplier Auditing
- Comprehensive Capital Analysis and Review
- 21 CFR 820
- Institutional Review Board
- ICH Guidelines
- Environmental Monitoring
- Biology
- Clinical Trials
- Biotechnology
- Environmental Science
- Genetics
- FDA Regulations
- Medical Device Sales
- Good Manufacturing Practices
- Corrective Actions & Preventive Actions
- Standard Operating Procedures
- Engineering
- Affirmative Action
- Strategy Development
- Risk Management
- Investigation
- Auditing
- Written Communication
- Documentation
- Quality Assurance
- Collaboration
- Bachelor's Degree
- Reporting
- Education Experience
- Microsoft PowerPoint
- Regulations
- Policy Development
- Project Management
- Research Skills
- Microsoft Office
- Microsoft Excel
- Problem Solving
- Time Management
- Staff Supervision
- Organization
- Scheduling
- Leadership
- Communication Skills
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