Interim & Rekrytering
Interim & Rekrytering
Rekrytering
Rätt person på rätt plats, varje gång
Interimslösningar
För kritiska roller när ni behöver det.
Executive Management
Hitta och utveckla rätt ledare
Vår expertis
Vår expertis
Expertområden
Finance & Accounting
Marketing & Growth
Data & Tech
HR
Legal & Compliance
Sustainability & Supply Chain
Branscher
Life Science
Fastighet
Energi
Fintech
SaaS
Sustainability
Case & framgångshistorier
Så har vi hjälpt våra kunder
Vår processVi är Capa
Kontakta ossUppdrag
Vi är CapaKontaktUppdrag
Hem
Uppdrag
Combination Product Lead

Combination Product Lead

Alvotech is seeking a passionate and skilled Combination Product Lead to join our innovative Combination Products and Devices (CPD) team. The CDP team designs and develops drug delivery solutions that are reliable, accessible, and in keeping with patient needs. The Combination Product Lead works with Human Factors, Risk, Technical, and program strategy specialists to ensure the successful development, verification and validation of our products and maintenance of our combination drug product files (DHFs and DMRs).
Skicka in ansökan
Tyvärr är denna tjänst redan tillsatt för tillfället.
Vi rekommenderar dig att kika på våra andra lediga tjänster för fler möjligheter.
Lediga tjänster

Alvotech is seeking a passionate and skilled Combination Product Lead to join our innovative Combination Products and Devices (CPD) team. The CDP team designs and develops drug delivery solutions that are reliable, accessible, and in keeping with patient needs. The Combination Product Lead works with Human Factors, Risk, Technical, and program strategy specialists to ensure the successful development, verification and validation of our products and maintenance of our combination drug product files (DHFs and DMRs).

Key Responsibilities:

  • Lead the compilation of DHFs, including usability files, design verification testing, and risk assessments.
  • Draft key deliverables of the design control process.
  • Collaborate with specialists to deliver design verification, validation, and risk documentation.
  • Coordinate with regulatory bodies to compile technical files for submission, ensuring compliance with MDR 2017/745 and EU Medical Devices Directive 93/42/EC.
  • Maintain technical knowledge in the function, assembly, and testing of injection devices.
  • Stay updated on regulations related to combination drug products.
  • Author sections of global submission dossiers.
  • Contribute to process improvements and SOP drafting.
  • Maintain DHF documentation with QA.
  • Coordinate document review, updates, and approval for technical projects.
  • Perform design impact assessments for proposed design changes.
  • Schedule and manage stage reviews.

Qualifications:

  • Master’s Degree with a minimum of 7 years of relevant work experience.
  • Proven experience in life cycle management of combination products.
  • Strong knowledge of design control processes and regulatory requirements (ISO-13485, ISO-14971, MDR, 21 CFR part 4, ISO-11608, IEC-62366, ASTM 1980, ISO 23908 etc.)
  • Proficiency in risk management and design verification/validation (ISO-13485, ISO-14971)
  • Experience with technical documentation and regulatory submissions.
  • Excellent verbal and written English communication skills.
  • Ability to work independently and as part of a team.
  • Self-motivated, adaptable, and positive attitude.

What we offer:

  • An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.
  • The chance to be a part of a global and fast-growing company.
  • An international work culture that encourages diversity, collaboration and inclusion.
  • Positive, flexible, and innovative work environment.
  • Support for personal growth and internal career development.

Why Alvotech

At Alvotech, we are passionate about improving lives by increasing access to affordable biologics. We’re purpose-driven and committed to fostering an inclusive and diverse working environment that encourages curiosity, ingenuity and simplicity. We want our employees to feel inspired in their careers, challenged by interesting and meaningful work and empowered to succeed in an agile environment.

True to our Icelandic roots, we also believe that integrity, gender equality, and fairness are foundational. We strive to bring together the brightest minds regardless of backgrounds and beliefs, to deliver to our partners and patients around the world. Let’s create a healthier world together, through affordable biologic medicines.

Your Application

We look forward to your application! Please send your application as soon as possible, as the position may be filled immediately.
For any questions regarding the role, please contact Jessica Keränen, Search Partner at Capa Interim & Recruitment, at jessica.keranen@capa.se

Skicka in ansökan
Uppdrag
Aktuella tjänsterSkicka in CV
Vad vi gjort
Kundreferenser
Hur vi kan hjälpa till
Executive managementInterimRekryteringExpertområdenBranscher
Om oss
Våra experterBlogg
Kontakta ossBoka möte
Capa AgnC AB, Oxtorgsgatan 4, 111 57 Stockholm, info@capa.se
Integritetspolicy
Cookies