UCB
The Device Documentation Specialist supports drug‑device combination product development by coordinating documentation activities, tracking key deliverables, and ensuring the integrity and availability of data for design reviews and regulatory submissions. The role works cross‑functionally with technical, regulatory, and quality teams to maintain organized, traceable documentation throughout the product lifecycle.
Headquarters
Brussels, Brussels, Belgium
Company Size
5001-10000 employees
Founded
1928
UCB a global biopharmaceutical leader focuses on creating valuable solutions that improve the lives of people living with neurological and autoimmune conditions
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for UCB.
UCB didn’t post a salary, so this is our estimate from similar listings.
54% above the average for this role
Senior Regulatory CMC Drug-Device Combination Product Lead
lifelancer
Associate Director, Drug-Device Combination Development Lead (DDL)
Takeda Pharmaceutical Company Limited
Principal Scientist – Device Technical and Engineering Lead – Inhalation Programs (Director Equivalent)
MSD
Senior Director and Regulatory Platform Lead GRA CMC, Device and Drug-Device Combinations Human Factors
BioLife Plasma Services
Senior Manager, CMC Technical Writing
Avalyn Pharma
Technical Lead and Subject Matter Expert for Combination Products and Drug Delivery Devices
Scholar Rock