Senior Regulatory Analyst
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Gentofte
At STG, we always encourage you to craft the career that makes you more.
Working for a company that aspires to become larger and be the undisputed and sustainable global leader in cigars, means being part of a great working environment and collaborating with people from all corners of the world in an organization you are proud of.
Summary:
Scandinavian Tobacco Group, a leading global tobacco company, is seeking a talented and experienced Senior Regulatory Affairs Specialist (Novel Categories) to join our dynamic team.
As a Senior Regulatory Affairs Specialist, you will be driving the regulatory agenda for a novel category of products primarily without the inclusion of tobacco. Additionally, you will be involved in regulatory projects including submissions to FDA on more traditional tobacco products. You will play a key global role in ensuring compliance with relevant regulations and guidelines in our industry.
You will be joining our team in Copenhagen, reporting directly to the Senior Vice President Scientific & Regulatory Affairs, but you will be working closely with our US regulatory team.
What you can expect in a Senior Regulatory Affairs Specialist at Scandinavian Tobacco Group:
Your areas of knowledge and expertise (that matter the most for this role):
What happens next?
Working for a company that aspires to become larger and be the undisputed and sustainable global leader in cigars, means being part of a great working environment and collaborating with people from all corners of the world in an organization you are proud of.
Summary:
Scandinavian Tobacco Group, a leading global tobacco company, is seeking a talented and experienced Senior Regulatory Affairs Specialist (Novel Categories) to join our dynamic team.
As a Senior Regulatory Affairs Specialist, you will be driving the regulatory agenda for a novel category of products primarily without the inclusion of tobacco. Additionally, you will be involved in regulatory projects including submissions to FDA on more traditional tobacco products. You will play a key global role in ensuring compliance with relevant regulations and guidelines in our industry.
You will be joining our team in Copenhagen, reporting directly to the Senior Vice President Scientific & Regulatory Affairs, but you will be working closely with our US regulatory team.
What you can expect in a Senior Regulatory Affairs Specialist at Scandinavian Tobacco Group:
- Monitor and interpret relevant regulatory changes, directives, and guidelines related to the food, nicotine and tobacco industry.
- Develop and implement regulatory strategies to ensure compliance with local and international regulations.
- Prepare and submit regulatory submissions, including product registrations, notifications, and dossiers.
- Collaborate with cross-functional teams to assess the impact of regulatory changes on product development and commercialization.
- Provide regulatory guidance and support to internal stakeholders, including R&D, manufacturing, marketing, and sales teams.
- Conduct regulatory assessments of new products, ingredients, and packaging materials.
- Prepare and maintain regulatory documentation, including technical files, labeling, and product specifications.
- Participate in regulatory audits and inspections, ensuring compliance with regulatory requirements.
- Stay up-to-date with industry trends, best practices, and emerging regulatory issues.
- Represent the company in interactions with regulatory authorities, industry associations, and other relevant stakeholders.
Your areas of knowledge and expertise (that matter the most for this role):
- Bachelor's degree in a scientific or regulatory-related field. A master's degree is preferred.
- Minimum of 5 years of experience in regulatory affairs within the food, FMCG or tobacco industry or a related field.
- Strong knowledge of food and/or tobacco regulations and guidelines, including EU and FDA regulations, and other regional requirements.
- Familiarity with the regulatory frameworks governing nicotine products, food or food supplements, tobacco products, including cigars, smokeless tobacco, and electronic cigarettes.
- Proven experience in preparing and submitting regulatory submissions and managing regulatory processes.
- Excellent understanding of quality management systems and regulatory compliance requirements.
- Strong analytical and problem-solving skills, with meticulous attention to detail.
- Ability to work independently and collaborate effectively with cross-functional teams.
- Excellent communication and interpersonal skills, with the ability to influence and negotiate with internal and external stakeholders.
- Proficiency in English. Additional language skills are a plus.
What happens next?
- You Apply - Join a world-leading manufacturer of cigars and pipe tobacco
- We carefully review your application. The important thing to know is that we process applications on an ongoing basis, so we encourage you to submit your application as soon as possible.
- If we are a match, you’ll receive an email or a call from our HR team
- And a final note for you to know - We'll get back to you — even if it's a no (for now)
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Gentofte.
Jobbet er oprettet på vores service den 28.7.2023, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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| Dato | Alle jobs som øvrige |
|---|---|
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