Senior Regulatory Affairs Specialist

Sinclair Pharma plc; California (MO); Remote; USD 90,000 - 120,000; Full time

Job summary

A leading global medical aesthetics organization is seeking a Senior Regulatory Affairs Specialist to manage regulatory activities and support product lifecycle management. This remote position is ideal for candidates based in California, with a focus on achieving regulatory compliance and collaboration with stakeholders.

Qualifications

• 3-5 years’ experience in Regulatory Affairs.
• Experience working with internal and external stakeholders.

Responsibilities

• Support regulatory activities for product lifecycle management.
• Maintain or obtain product authorizations and registrations.

Skills

Proficiency in English

Knowledge of regulatory legislation

Excellent computer skills

Strong communication skills

Education

University Degree in a scientific or engineering field

Job description

Job Details: Senior Regulatory Affairs Specialist

Full details of the job.

Vacancy Name: Senior Regulatory Affairs Specialist

Vacancy No: VN462

Employment Type: Full-Time

Location: Remote - California

Sinclair is currently recruiting for a Senior Regulatory Specialist for the USA. The Senior Regulatory Specialist is responsible for regulatory activities supporting product lifecycle management at Sinclair. They will support various responsibilities within the organization to achieve targets and maintain or obtain product authorizations and registrations, including supporting global markets as part of the Regulatory team.

Location: Remote with a preference for California-based candidates

About Sinclair

Founded in 1971, Sinclair is a global medical aesthetics organization offering an extensive product range. With in-house manufacturing and a network of distributors, our products are sold in 55 countries worldwide. This is a great time to join Sinclair as we expand our product range and enter new markets.

Our Vision: Providing aesthetic excellence globally.

Our Mission: Driving product quality, customer satisfaction, innovation, and investing in people.

Our Values:

• Act with Integrity
• Results-driven
• Innovation-centered
• One company, one goal
• Own it!

Skills & Experience – Do You Have What it Takes?

Essential:

• University Degree in a scientific or engineering field (desirable but not essential)
• 3-5 years’ experience in Regulatory Affairs
• Proficiency in English and regional languages
• Knowledge of regulatory legislation for medical devices
• Excellent computer and administrative skills
• Experience working in an office environment with internal and external stakeholders

Desirable:

• Knowledge in dermatology/aesthetics
• Understanding of pharmaceutical and biologic regulations
• Critical thinking and business acumen
• Ability to manage multiple tasks in a fast-paced environment
• Effective team collaboration skills

Personal Attributes:

• Well-organized, target-oriented, flexible
• Ability to work under pressure with minimal supervision
• Strong communication skills
• Confidentiality management
• Attention to detail in documentation
• Supportive of project teams and management
• Ability to establish relationships with local affiliates and partners

Core Competencies:

• Achievement-oriented
• Adaptability
• Mentorship and learning ability
• Integrity and ethics
• Cross-disciplinary cooperation

Application Details

If you meet these requirements and are interested, please apply. Note that high application volume may close the role early.

By applying, you consent to personal data processing for job-related decisions. For questions, email [e-mail].

Additional Information

Sinclair does not accept unsolicited CVs from recruitment agencies; such CVs will be considered property of Sinclair.