Product Development Specialist

Barrington James Limited; Greater London; On-site; GBP 40,000 - 70,000; Full time

Job summary

Join a forward-thinking company as a Regulatory Product Manager, where your expertise in project management and regulatory compliance will shape innovative over-the-counter medical devices. This role combines creativity with analytical rigor, allowing you to lead impactful projects that address health concerns globally. You'll work in a collaborative environment, ensuring that products meet stringent quality and regulatory standards while contributing to meaningful healthcare solutions. If you're passionate about science and making a difference, this opportunity is for you!

Qualifications

• MSc degree in relevant field with 2+ years of project management experience.
• Strong knowledge of MDR compliance and regulatory frameworks.

Responsibilities

• Manage product development projects and ensure compliance with regulations.
• Prepare technical documentation and collaborate with business development teams.

Skills

Project Management

Regulatory Compliance

Analytical Skills

Problem-Solving

Communication Skills

Attention to Detail

Education

MSc in Pharmaceutical Science

MSc in Pharmacology

MSc in Biotechnology

Tools

MDR Compliance

ISO 14971:2019

Clinical Evaluations

Quality Management Systems

Job description

Job Title: Regulatory Product Manager

Are you ready to take on a dynamic dual role that combines creativity, analytical rigor, and global impact? This is an exciting opportunity to join an innovative team focused on developing over-the-counter (OTC) medical devices that address a variety of health concerns, including skin, throat, and nasal conditions. From inventing cutting-edge products to navigating complex regulatory landscapes, this role plays a crucial part in bringing impactful solutions to global markets.

We are seeking a talented professional with a passion for science, problem-solving skills, and a drive to make a difference. This unique role blends product development and regulatory affairs, offering the autonomy to lead projects, understand market and regulatory requirements, and transform them into high-quality self-care solutions.

Key Responsibilities:

• Manage and monitor product development projects
• Define product requirements and design controls
• Design and execute verification and validation studies, including protocols, data analysis, and test reports
• Plan and oversee PMCF studies
• Prepare and maintain technical documentation in compliance with MDR and quality management systems
• Collaborate with business development teams to align product strategies
• Provide input to senior management on project progress and regulatory considerations

Key Requirements:

• MSc degree in pharmaceutical science, pharmacology, medical biology, biotechnology, industrial design, or related field
• Minimum of 2 years of experience in project management
• At least 1 year of experience in MDR compliance
• Experience with Directive 93/42/EEC (MDD), Regulation (EU) 2017/745 (MDR), 21 CFR Part 820, and ISO 14971:2019
• Knowledge of Clinical Evaluations (MEDDEV 2.7.1 rev 4) and Clinical Investigations (ISO 14155:2011)
• Strong organizational skills with attention to detail
• Proactive and adaptable mindset
• Excellent written and verbal communication skills in both Dutch and English

This role offers the opportunity to work in a collaborative environment where innovative thinking, reliability, and dedication to excellence are valued. If you're passionate about connecting science with real-world applications and contributing to impactful healthcare solutions, we’d love to hear from you.

Interested candidates are encouraged to apply and share their vision for this role.