Find a jobRecruiters

Program Lead

Exclusive opportunity

Onsite

Program Lead

Valtera Group Ltd

Program Lead

Skills

RRisk Management

6 days ago

Share this opportunity

Share this opportunity to other talents of your network:
✓ Offer them a visibility boost with clients.
✓ Help your contacts find their next job.

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.

Other offers great for you!

These companies are also looking for great profiles

Data indep

Mission freelance – AI & Data Program Lead

Freelance

Paris, France

Hybrid

Skills

AI Program ManagerData & AI Program ManagementData lead

5 months ago

Quick apply

Anonyme

Technical Program Lead – Clienteling & Retail AI Platform H/F

Freelance

Paris, France

Hybrid

Skills

Architectures IA / Agentic AI et conception de plateformes IA EnterpriseLeadership techniquearchitectureinnovationdelivery

19 hours ago

Quick apply

Anonyme

Clienteling Technical Program Lead H/F

Freelance

Paris, France

Hybrid

Skills

Pilotage technique transverse entre produitarchitecture et delivery Architecture de services réutilisables / SDK / API et accompagnement de leur adoption à l’échelle

19 hours ago

Quick apply

The best place to find your next move

© 2026. All Rights Reserved.

Talents

Find a job

Create a profile

Solutions and tools