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Product Development Specialist

Pharmiweb

London

On-site

GBP 100,000 - 125,000

30+ days ago

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Job summary

An innovative team is seeking a Regulatory Product Manager to lead the development of OTC medical devices. This dynamic role combines creativity and analytical skills to navigate complex regulatory landscapes and bring impactful solutions to global markets. You will manage product development projects, define requirements, and ensure compliance with MDR and quality management systems. If you are passionate about science and eager to make a difference in healthcare, this is a unique opportunity to contribute to meaningful self-care solutions in a collaborative environment.

Qualifications

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

Responsibilities

  • Manage product development projects and define product requirements.
  • Prepare technical documentation in compliance with MDR.

Skills

Project Management

Problem-Solving

Regulatory Compliance

Communication Skills

Attention to Detail

Education

MSc in Pharmaceutical Science

MSc in Pharmacology

MSc in Medical Biology

MSc in Biotechnology

MSc in Industrial Design

Tools

MDR Compliance

ISO 14971:2019

Directive 93/42/EEC

Regulation (EU) 2017/745

Clinical Evaluations

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

Key Requirements:
  1. MSc degree in pharmaceutical science, pharmacology, medical biology, biotechnology, industrial design, or related field
  2. Minimum of 2 years of experience in project management
  3. At least 1 year of experience in MDR compliance
  4. Experience with Directive 93/42/EEC (MDD), Regulation (EU) 2017/745 (MDR), 21 CFR Part 820, and ISO 14971:2019
  5. Knowledge of Clinical Evaluations (MEDDEV 2.7.1 rev 4) and Clinical Investigations (ISO 14155:2011)
  6. Strong organizational skills with attention to detail
  7. Proactive and adaptable mindset
  8. 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.

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