Life Sciences: Pharmaceuticals & Medical Technology

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a pharmacy shelf filled with lots of medicine bottles

Why should you work with us?

In a sector where precision and trust are paramount, choosing an search partner is a decision that demands absolute confidence. We provide a distinct advantage by operating on three guiding principles::

Unrivalled Industry Focus
We don't just recruit in the Life Science sector; we are embedded in it. This singular focus gives us a deep understanding of the regulatory, clinical, and quality assurance challenges you face. It provides us with an unrivalled network of accomplished leaders with experience across the pharmaceutical, medical device, and biotechnology landscape that generalist firms simply cannot access.
A True Partnership Model
When you engage Williams Manufacturing, you work directly with our senior leadership. We provide a discreet, agile, and highly confidential service, treating every search with the strategic priority it deserves. You are not one of many clients; you are our partner.
A Commitment to Excellence & Impact
Our process is measured by the long-term success of your hire. We are dedicated to securing executives who not only possess the required technical acumen to meet standards like ISO 13485 and GMP, but who will accelerate your R&D pipeline, drive innovation, and deliver the tangible growth this vital industry demands.

Chief Scientific Officer (CSO) / Head of R&D

Provides the scientific vision for the company, leading all research and development activities and managing the product or drug discovery pipeline.

Director of Quality Assurance & Regulatory Affairs (QA/RA)

Ensures all products, processes, and systems are in absolute compliance with regulatory bodies (e.g., MHRA, FDA) and quality standards like ISO 13485 and GMP.

Site Director / Head of Manufacturing

Leads a manufacturing facility, ensuring all pharmaceutical or medical device production is efficient, sterile, and compliant with all Good Manufacturing Practice (GMP) regulations.

Clinical Trials Manager

Oversees the planning, execution, and completion of clinical trials, ensuring they are conducted ethically and meet all regulatory and scientific requirements.

Commercial Director

Leads the commercial strategy, driving the successful launch and market access for new drugs or medical devices.

Head of Engineering

Manages the engineering function, responsible for the design, validation, and maintenance of specialist manufacturing equipment and cleanroom facilities.

Medical Director

Provides the primary medical expertise and leadership within the organisation, guiding clinical development and acting as a key liaison with medical professionals.

Supply Chain Director

Manages the highly regulated, often temperature-controlled, global supply chain, ensuring the integrity and traceability of all raw materials and finished products.

Product Manager (Medical Devices)

Manages the lifecycle of a specific medical device or technology, from market analysis and product development to launch and post-market surveillance.

Validation Manager

Leads the team responsible for the validation of all equipment, systems, and processes, ensuring they are fit for purpose and meet all regulatory requirements.