Regulatory Specialist
Apply NowCompany: Ascent Industries Co
Location: Danville, VA 24540
Description:
POSITION DESCRIPTION
Job Title: Regulatory Affairs and Quality Systems Specialist
Reporting: Continuous Improvement Leader
Date: July 2024
Duties and Responsibilities:
Skills, Qualifications, Experience, Special Physical Requirements:
Job Title: Regulatory Affairs and Quality Systems Specialist
Reporting: Continuous Improvement Leader
Date: July 2024
Duties and Responsibilities:
- Ensure regulatory compliance and maintain high-quality standards across multiple sites.
- Stay abreast of relevant regulations, guidelines, and standards applicable to specialty chemicals.
- Monitor and review new and existing laws, regulations, and guidelines relevant to our products.
- Analyze the impact of regulatory changes on our operations and products.
- Interpret and communicate regulatory requirements to internal stakeholders.
- Conduct regulatory assessments for new products and changes to existing products.
- Provide regulatory guidance and support to resolve compliance issues and inquiries.
- Work closely with R&D, Production, Supply Chain, and Sales teams to ensure regulatory compliance and quality standards are met throughout the product lifecycle.
- Prepare regulatory requirements and updates for entry into the site ERP system.
- Develop training materials on regulatory and quality topics for employees.
- Prepare and/or update regulatory affair supplier questionnaires for produced materials as requested for new and existing customers.
- Develop, maintain, and update accurate SDS for our product portfolio.
- Distribute new and updated SDS's to internal and external customers as required
- Ensure SDS compliance with global regulatory requirements (e.g., OSHA, REACH, GHS).
- Assist in the implementation, maintenance, and improvement of the Quality Management System.
- Conduct internal audits and support external audits related to regulatory compliance, quality assurance, and ISO9001 compliance.
- Be the process expert and owner of the company's QMS software and associated processes.
- Maintain accurate documentation related to regulatory compliance and quality assurance activities.
- Other duties as directed by the management.
Skills, Qualifications, Experience, Special Physical Requirements:
- Bachelor's degree in chemistry, Chemical Engineering, Regulatory Affairs, or a related field (advanced degree preferred).
- Proven experience (3+ years) in regulatory affairs and quality assurance within the specialty chemicals industry.
- Strong knowledge of global regulations and standards (e.g., REACH, OSHA, GHS).
- Experience creating SDS and familiarity with SDS authoring software.
- In depth knowledge of ISO9001 compliance related to specialty chemicals
- Strong computer skills and experience with a QMS software system
- Excellent analytical skills and attention to detail.
- Effective communication and interpersonal skills to collaborate across departments and with regulatory agencies.
- Ability to prioritize tasks, manage multiple projects simultaneously, and meet deadlines.