Senior Manager – Regulatory Affairs & Scientific

J.S. Held LLC; Greater London; Hybrid; GBP 70,000 - 90,000; Full time

Job summary

A global consulting firm in the United Kingdom is seeking a Senior Manager to lead strategic operations across cosmetics and chemicals regulatory services. You will oversee cross-functional teams and manage client relationships while driving innovation in delivery. The ideal candidate has 10 years of experience in regulatory affairs, strong leadership skills, and a degree in a related field. This role offers the opportunity for remote work and a flexible time-off policy.

Benefits

Flexible work environment

Flexible Time Off Policy

Global Medical Insurance

Life Assurance

Qualifications

• 10 years in regulatory affairs or scientific operations preferably in cosmetics or consumer products.
• Proven leadership in managing multi-disciplinary remote teams.
• Strong understanding of EU / UK / US regulatory frameworks.
• Experience with IT systems supporting regulatory workflows.

Responsibilities

• Lead and mentor regulatory scientists and project managers across geographies.
• Oversee delivery of compliance services including safety assessments and Responsible Person duties.
• Manage operational budgets and resource planning for a business unit.
• Collaborate with trade associations and regulatory bodies to influence policy.
• Drive continuous improvement in remote team performance.

Skills

Proofreading

Adobe Acrobat

FDA Regulations

Manufacturing & Controls

Biotechnology

Clinical Trials

Research & Development

GLP

cGMP

Product Development

Chemistry

Writing Skills

Education

Degree in Chemistry, Biochemistry, Toxicology or related field; advanced degree preferred

Job description

The Senior Manager will lead strategic operations across cosmetics and chemicals regulatory services supporting global clients in achieving compliance across EU, UK and US markets. This role will oversee cross‑functional teams, manage client relationships and drive innovation in regulatory and IT‑enabled service delivery.

Key Responsibilities

• Lead and mentor regulatory scientists and project managers across geographies.
• Oversee delivery of compliance services including safety assessments REACH / CLP and Responsible Person duties.
• Manage operational budgets and resource planning for a business unit.
• Collaborate with trade associations and regulatory bodies to influence policy and maintain thought leadership.
• Drive continuous improvement in remote team performance and cohesion.
• Support Principal Scientist in strategic planning and business development.

Qualifications

• 10 years in regulatory affairs or scientific operations preferably in cosmetics or consumer products.
• Proven leadership in managing multi‑disciplinary remote teams.
• Strong understanding of EU / UK / US regulatory frameworks.
• Experience with IT systems supporting regulatory workflows.
• Degree in Chemistry, Biochemistry, Toxicology or related field; advanced degree preferred.

Benefits

J.S. Held understands all our employees are people and sometimes life needs flexibility. We work to always provide an environment that best supports and suits our teams needs.

• Our flexible work environment allows employees to work remotely when needed.
• Flexible Time Off Policy.
• Global Medical Insurance.
• Life Assurance.

Other Duties

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

EEO and Job Accommodations

We embrace diversity and our commitment to building a team and environment that fosters professional and personal enrichment is unwavering. We are greater when we are equal!

J.S. Held is an equal opportunity employer that is committed to hiring a diverse workforce. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age or any other characteristic protected by law.

If you are an individual with a disability and would like to request a reasonable accommodation, please email and include "Applicant Accommodation" in the subject line with your request and contact information.

Key Skills

Proofreading, Adobe Acrobat, FDA Regulations, Manufacturing & Controls, Biotechnology, Clinical Trials, Research & Development, GLP, cGMP, Product Development, Chemistry, Writing Skills

Remote Work : Yes

Employment Type : Full-time

Experience : years

Vacancy : 1