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Sr. Counsel - Regulatory (m/f/x)

Avantor

Schwabmünchen

Vor Ort

EUR 80.000 - 120.000

Vollzeit

Vor 5 Tagen
Sei unter den ersten Bewerbenden

Zusammenfassung

A leading global science company is seeking a Senior Counsel to join its European legal team in Germany or the UK. The ideal candidate will provide strategic legal counsel on EU regulations, ensuring product compliance and mitigating risks. With a strong background in pharmaceutical or highly regulated industries, candidates should have a law degree and extensive legal experience. This role offers the opportunity to make a significant impact on innovative products that improve lives.

Leistungen

Opportunities for career growth
Commitment to diversity and inclusion

Qualifikationen

  • 10+ years of legal experience, preferably from a leading law firm or multinational corporation.
  • 5–7 years specializing in European regulatory law within highly regulated industries.
  • Proficiency in English and at least one other European language.

Aufgaben

  • Provide expert legal advice on EU regulations and compliance.
  • Engage with regulatory authorities and draft regulatory responses.
  • Develop and implement compliance strategies for regulations.

Kenntnisse

Strong analytical and problem-solving abilities
Excellent communication and negotiation skills
Ability to work effectively in cross-functional teams

Ausbildung

Law degree (LLM or equivalent)
Jobbeschreibung
The Opportunity

Senior Counsel (m/w/d) – Europe (Germany or UK). This is a brand-new position to shape legal processes and be a member of Avantor's European legal team. You will report to the VP & Deputy General Counsel, Regulatory, and help navigate complex regulatory frameworks across Europe, with a strong emphasis on product regulatory compliance and trade regulations. You will provide strategic legal counsel to Regulatory Affairs, Quality Assurance, and Commercial leadership, and support other Avantor lawyers to mitigate legal risks. Ideal candidates have experience in pharmaceutical, medical device, chemical, or other highly regulated industries and possess strong business acumen to influence policy development and mitigate legal risk in a dynamic global environment.

Location: Germany or UK preferred.

Join Avantor and make a significant impact as we innovate together.

What we’re looking for
  • Education: Law degree (LLM or equivalent) and registered as an attorney in at least one European jurisdiction.
  • Experience: 10+ years of legal experience, preferably from a leading law firm and/or multinational corporation, with 5–7 years specializing in European regulatory law within the pharmaceutical, chemical, medical device, or other highly regulated industries. Experience collaborating across a matrixed business and legal environment.
  • Expertise: In-depth knowledge of EU regulatory frameworks, including CLP, REACH, and GMP guidelines.
  • Skills: Strong analytical and problem-solving abilities, excellent communication and negotiation skills, and the ability to work effectively in cross-functional teams.
  • Languages: Proficiency in English is required; at least one other European language is preferred.
How you will thrive and create an impact
  • Legal Advisory: Provide expert legal advice to senior management and legal colleagues on European regulations, including REACH, CLP, MDR/IVDR, GMP, pharmaceutical and/or medical device law, import/export, and environmental regulations.
  • Regulatory Liaison: Engage with regulatory authorities (e.g., EMA, ECHA, NCAs), draft regulatory responses, facilitate audits, and advocate for the company in policy discussions.
  • Compliance Oversight: Develop and implement strategies to ensure adherence to European regulatory requirements, including EU and international trade regulations, customs classifications, Incoterms, duty drawback processes, and trade sanctions. Conduct investigations as directed.
  • Quality Assurance: Direct support for compliance audits, corrective actions, and continuous improvement initiatives.
  • Regulatory Submissions: Assist in preparing and reviewing submissions to regulatory authorities such as the EMA, ECHA, or national agencies.
  • Stakeholder Communication: Collaborate with internal and external stakeholders, including government bodies, industry associations, and cross-functional teams, to address regulatory issues.
  • Policy Monitoring: Develop and implement internal policies to ensure ongoing regulatory compliance; stay updated on legislative changes and industry trends, assessing impact and recommending proactive measures.
  • Risk Management: Identify and mitigate legal risks related to regulatory compliance, including field actions.
  • Training and Education: Conduct training sessions to increase awareness of regulatory requirements within the organization.
Why Avantor?

Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges advances life-changing science.

The work we do changes people’s lives for the better, bringing new patient treatments and therapies to market and enabling medical devices that help people hear, see, and live better. This is an opportunity to contribute your talents and grow your career at Avantor.

We are committed to a diverse, equitable and inclusive culture with learning experiences to support your career growth and success. Apply today!

EEO Statement

We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by law.

If you need a reasonable accommodation for any part of the employment process, please contact us by email at recruiting@avantorsciences.com and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis.

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