Valtera Group Ltd
Program Lead
Skills
6 days ago
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Important information
Contract type:
Permanent
Location:
Dublin, Ireland
Work mode:
Onsite
Published on:
14 October 2026
What they need
Director, Device Program Lead
Global Device Development (GDD) | Dublin, Ireland | Hybrid, minimum 3 days a week on-site
The Valtera Group is partnering with a global pharmaceutical company on the appointment of a Director, Device Program Lead within its device development function in Dublin.
THE ROLE
GDD develops the device side of their combination products, the medicines that rely on a device to reach the patient. Much of the portfolio brings generic and complex generic injectables to market, often against tight timelines and first-to-file dynamics, alongside a growing innovation agenda.
This role leads cross-functional teams through the development and transfer of injectable drug-device products: pre-filled syringes, cartridge-based pens, autoinjectors and vial kits. It is not an administrative PMO role. The team needs a leader who can read the drug side of a programme, understanding why API viscosity, a filling challenge or an impurity profile could move a timeline, and translate that into realistic plans.
You will represent GDD in senior cross-functional forums, influencing through credibility rather than formal authority. After an initial settling-in period, you will take on line management of Program Leads.
WHAT YOU'LL DO
Lead injectable combination product programmes from feasibility through transfer to commercial manufacturing
Own the integrated view of each programme: milestones, critical path, risks, budget and resources
Work with drug product R&D to interrogate formulation, API and filling risks and reflect them in plans
Review, approve or author design review reports and design and development plans
Ensure programmes meet design control, quality and regulatory expectations for combination products
Contribute to the strategy and workplan for the Injectables Portfolio, including prioritisation across therapeutic area partners
Contribute to device CMC strategy supporting global registrations
Partner with external CMOs and teams across GDD and the wider organisation.
Report to global leadership and deliver clear executive presentations on status, risks and recommendations
Help GDD mature towards a strategic portfolio and programme management model
WHAT YOU'LL BRING
Essential
Degree in pharmaceutical science or a related discipline (pharmacy, chemistry, biochemistry). Engineering degrees considered where backed by substantial drug product experience
Extensive experience in combination product or drug delivery device development, including at least 5 years in a leadership role
Substantial drug-side experience: drug product development, formulation, technical operations, MSAT or fill-finish
A track record of leading complex cross-functional programme teams in pharma or biotech, including taking a drug delivery device programme through development, scale-up and launch
Knowledge of design controls with integrated risk management, human factors and usability engineering
Applied understanding of ISO 13485, ISO 14971, ISO 11608, ISO 11040 and 21 CFR Part 820 (QMSR)
Knowledge of pen injectors, autoinjectors, vial kits, prefilled syringes and inhalers
Experience with project planning tools (e.g. Microsoft Project, Smartsheet, Planisware) and resource, risk and budget management
Experience working with external partners, including CMOs
Strong communication skills, with experience presenting to and influencing senior leaders
Ability to work on-site in Dublin at least 3 days a week
Desirable
PFS and cartridge-based pen experience
Generics, biosimilars or other fast-moving development environments
Line management or mentoring of programme or project leads
Experience shaping portfolio governance or a PMO
Device CMC content for global regulatory submissions
Technology transfer to manufacturing sites, including global sites
Exposure to inhaled or transdermal combination products
MSc, PhD, MBA or project management qualification
WHY THIS ROLE
Genuine work at the drug-device interface on products that matter to patients
Visibility with GDD leadership and senior cross-functional forums
A clear path to line leadership and a broader portfolio remit
The chance to shape how a function manages its portfolio
Competitive salary and bonus, health insurance and pension
To discuss the role confidentially, contact Fleur Waterston, Client Partner, Valtera Group.
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