Compliance Specialist Jobs in Wisconsin
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.
., biology, chemistry, physics) or engineering and minimum four (4) years of progressive regulatory and quality experience in the pharmaceutical industry); or equivalent combination of education and...
Job Description In Strategy & Consulting we work with C-suite executives, leaders and boards of the world's leading organizations, helping them reinvent every part of their enterprise to drive...
We're here to better our world with biology. Join us as our new Senior QA IT Compliance Specialist Our Global Quality Systems team is a part of our Global Quality Management & Systems area....
Compliance Specialist III Location: Madison, Wisconsin Department: WISCONSIN STATE LABORATORY OF HYGIENE/EHD*EHD RESEARCH PROGRAM Category: Compliance, Legal, and Protection Employment Type: Onsite...
Specialiste en conformite QC / QC Compliance Specialist
- Montreal, WI
- 16 days ago
- Montreal, WI
- 16 days ago
QC Compliance Specialist Jubilant HollisterStier, a subsidiary of Jubilant Pharma Holdings Inc., is currently recruiting a QC Compliance Specialist to join our team! What do we offer?...
We are seeking two Senior IT Compliance Specialists to take a leading role in driving compliance maturity, process optimization, and business impact across our IT landscape....
Principal Scientist - Sterility Assurance Lead
- Pleasant Prairie, WI
- 29 days ago
- Pleasant Prairie, WI
- 29 days ago
, Biochemistry, Biochemical Engineering, Chemical Engineering, or other related scientific discipline Additional Skills/Preferences: 5+ years supporting cGMP manufacturing preferred (specifically within...
Auditeur de conformite I/II/III / Compliance Auditor I/II/III
- Montreal, WI
- 45+ days ago
- Montreal, WI
- 45+ days ago
Auditeur de conformite I/II/III Jubilant HollisterSiter, une filiale de Jubilant Pharma Holdings Inc., recrute actuellement pour un poste du Auditeur de confirmite I/II/III pour joindre notre...
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Required or preferred licenses and certifications for Compliance Specialist positions.
Highest Education Level
Compliance Specialists in Wisconsin 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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