Lead and shape the future of Navamedic's new Quality and Compliance Division.

Navamedic is entering an exciting phase of growth, acquiring ownership of products with global market potential. To support this expansion, they are seeking an experienced and visionary leader to head and develop their new Quality and Compliance division.

In this role, you will take on full responsibility for all quality, environmental management systems, and QA/QC activities across the company. Your mission will be to ensure that these functions run optimally, efficiently, and in a way that adds significant value to the organization. 

The ideal candidate will bring several years of experience in compliance and quality systems within the pharmaceutical and medical device industry, having held leadership positions in this field. Success in this role requires a passion for leading teams based on trust and clear goals, while being attentive and ready to step in with support when needed.

About the company:

As a Nordic pharma company with a footprint in Northern Europe, Navamedic is a reliable supplier of medicinal products, medical devices, medical nutrition, and high-quality consumer health products to hospitals and pharmacies. Navamedic collaborates with distributors and partners to expand into new markets. All the manufacturing is outsourced. Today, the company has approximately 40 employees and has presence in 5 markets.

For more information: http://www.navamedic.com

MAIN RESPONSIBILITIES:

• Overall responsible for Quality Management Systems (QMS) at Navamedic, including quality related activities. 

• Ensure that the QMS at Navamedic are maintained and continuously improved.
• Key role in the environmental and sustainability processes meeting both legal and customer requirements.

• Identify synergies between quality systems to streamline quality work.

• Budget related to the area.

• Operative responsible for Medical Device QMS (MDR)
  • Host and follow up audits and inspections from partners and authorities
  • Qualifications/audits of service partners and manufacturer and internal audits
  • Quality agreements with service providers and manufacturers
  • Internal training 
    

KEY REQUIREMENTS:

Competence:

• Master of Science in Pharmacy or equivalent degree.

• A minimum of 10 years of experience in the pharmaceutical and medical device industry.

• At least 5 years of experience in regulatory compliance and quality systems in a leadership position.

• Extensive experience in QA systems including GMP/GDP/ ISO 13485 (MDR)/ ISO 9001 (quality) /ISO 14001 (environmental).

• Knowledge about 21CFR Part 820 (FDA) is an advantage.

• Experience from working with sustainability related topics is an advantage.
  
  

General:

• Strong commercial understanding with a strategic and business-oriented mindset, while maintaining QA integrity.

• Ensure optimal communication with external partners and ability to collaborate effectively with various functions and levels within the organization, including management.

• Proficient in project management; experience managing multiple responsibilities with minimal direction.

• Certified Quality Auditor (CQA).

• Excellent written and verbal communication skills, with strong presentation abilities.

• Fluent in English and a Nordic language, both written and spoken.

The role is reporting to CEO and is part of the extended management team.

The position can be placed either in their Stockholm or Gothenburg Office.

If you're ready to drive excellence and innovation in a fast-growing company as Navamedic, this is the opportunity for you. We look forward to your application.

Please apply through haegercarlsson.com

Questions are answered by:

Pernilla Sjöstrand +46 (0)70 – 433 84 46, pernilla@haegercarlsson.com

Julia Erginöz +46 (0)70-864 77 17, julia@haegercarlsson.com