Freyr Solutions Hiring Regulatory Affairs Specialist

Freyr Solutions Hiring Regulatory Affairs Specialist – Consumer Goods

Freyr Solutions seeks Regulatory Affairs Specialist (Toxicology) with 3–8 yrs experience in REACH, IUCLID, chemical & cosmetic compliance. Apply now.

Freyr Solutions is inviting applications from experienced professionals for the role of Regulatory Affairs Specialist (Toxicology) to join their Consumer Regulatory Affairs team. This position offers an exciting opportunity to contribute to global product compliance strategies, REACH registration, and IUCLID dossier development across chemicals, cosmetics, biocides, and consumer goods.

Company Overview

Freyr Solutions is a global regulatory and compliance consulting firm supporting businesses across chemicals, consumer goods, cosmetics, and biocides industries. With a strong focus on regulatory intelligence, product stewardship, and compliance management, Freyr Solutions empowers organizations to navigate complex global regulations efficiently. The company emphasizes professional growth, knowledge sharing, and fostering a culture of compliance excellence.

Job Role & Responsibilities

Regulatory Affairs Specialist (Toxicology)

• Experience Required: 3–8 years
• Location: Not specified (global compliance-focused)

Key Responsibilities:

• Manage REACH registration/support services and develop BPR-IUCLID dossiers end-to-end.
• Prepare robust summaries for human health toxicology, ecotoxicology studies, biocide efficacy, and physicochemical characterization studies.
• Ensure compliance management throughout the supply chain for raw materials.
• Assist in notification and registration processes for cosmetics and consumer products.
• Prepare and implement global strategic regulatory plans for chemicals, cosmetics, biocides, and consumer goods.
• Represent regulatory expertise in organizational processes, developing actionable compliance and registration strategies.
• Stay updated with current and emerging regulations and guidelines, recording and sharing updates.
• Conduct regulatory review, compliance gap assessments, and product stewardship activities.
• Support international business with documentation required for regulatory compliance and registration.
• Plan, review, and compile high-quality registration dossiers in line with regulatory timelines.

Eligibility / Qualifications

• Educational Background: Master’s Degree in Life Sciences, Chemistry, or Pharmaceuticals with interest in chemical, cosmetic, or biocide regulatory fields.
• Experience: 2–5 years in REACH registration and IUCLID dossier development.
• Skills Required:
  • Chemical Safety & Regulatory Affairs
  • Global REACH, IUCLID
  • MSDS authoring & review
  • Product safety and toxicology knowledge
  • Literature review and technical writing
• Preferred Attributes:
  • Research-oriented with strong analytical skills
  • Solution-oriented mindset with ability to build new capabilities
  • Effective communication, presentation, and interpersonal skills
  • Ability to manage multiple projects with attention to detail
• Relevant Courses: Regulatory Affairs, Chemical Safety, Toxicology, Product Stewardship, Cosmetic Regulations, Biocide Compliance, Global Compliance Management, Technical Writing.

Location & Salary

• Location: Flexible (global compliance-focused)
• Salary: Competitive, based on experience and expertise.

Application Process

Interested candidates can apply by sending their CV to rupali.chakraborty@freyrsolutions.com.

Steps to Apply:

1. Prepare an updated CV highlighting regulatory affairs experience.
2. Email your CV to rupali.chakraborty@freyrsolutions.com.
3. Ensure alignment with required skills, experience, and educational qualifications.

Why Join Freyr Solutions?

• Work with a global leader in regulatory compliance and consulting.
• Gain exposure to chemical, cosmetic, biocide, and consumer goods regulatory frameworks.
• Contribute to strategic compliance planning and global product registration.
• Opportunity to enhance expertise in regulatory affairs, toxicology, and dossier management.
• Engage in impactful work that ensures product safety and regulatory adherence worldwide.

FAQs

Q1: What qualifications are required for this role?
A1: Master’s Degree in Life Sciences, Chemistry, or Pharmaceuticals with regulatory interest.

Q2: How much experience is required?
A2: 3–8 years in regulatory affairs, with 2–5 years in REACH registration and IUCLID dossier development.

Q3: What are the key responsibilities of the Regulatory Affairs Specialist?
A3: REACH registration, IUCLID dossier development, regulatory compliance, product stewardship, and global regulatory strategy.

Q4: Is prior toxicology or chemical safety experience necessary?
A4: Yes, knowledge of toxicology studies, product safety, and regulatory frameworks is essential.

Q5: How can candidates apply?
A5: Send CV to rupali.chakraborty@freyrsolutions.com.

Q6: Does this role involve laboratory work?
A6: No, this is a desktop regulatory role focusing on documentation, dossier development, and compliance.

Apply Now! Advance your career in global regulatory affairs and contribute to product safety and compliance across chemicals, cosmetics, biocides, and consumer goods.

Vertical Summary Table

Category	Details
Company	Freyr Solutions
Vacancies	Regulatory Affairs Specialist (Toxicology)
Required Education	Master’s in Life Sciences, Chemistry, or Pharmaceuticals
Experience	3–8 years