Técnico PPLM; Product & Process Lifecycle

Puesto: Técnico PPLM (Product & Process Lifecycle)
Location: Alcalá de Henares

Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter – one filled with bold ambitions and enormous opportunity.

Our trusted portfolio of brands – including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum – lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science.

Now it’s time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose – to deliver better everyday health with humanity – at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture.

About the role

As a PPLM Technician you will lead the Product & Process Lifecycle Management of products manufactured on site.

Key Responsibilities Acts as site Product & Process Lifecycle SME, maintaining the site product/process & cleaning state by assessing impact of new products, processes, or changes against the existing site cleaning matrix and existing process. Coaches and develops the Technical team to ensure that cleaning and manufacturing validation execution demonstrates that the process produces the expected results in a reproducible manner, and that proper monitoring is in place to ensure the processes remain in a validated state of control.

Prepares and maintains site validation master plan (SVMP), with other relevant site areas, such as Engineering, Quality and Technical departments.

Ensure validation activities are completed on time and compliant to Haleon and Health Authority standards (e.g., MHRA)
Understands and ensures compliance to evolving expectations of:
Equipment and Facility C&Q, Process/Packaging validation, Cleaning validation, Continued Process validation (CPV) and Computer System validation

Prepares and reviews Technical documentation as required: trials, TRA, PCS, Validation documentation, investigations.

Supports I&T area according to site priorities.

Actively collaborate with other site relevant areas such as Manufacturing, Quality and Engineering for projects: material simplification, productivity, CAPEX integration with processes and materials.

Lead and support the improvement projects related to the manufacturing process of products.

Participate in the PCT (Performance Centric Teams) and supports HAPS deployment mindset as required.
· Evaluates Validation impact on change controls for manufacturing and validation activities.

Own and manage compliance records, including deviations, CAPAs, change controls, and events.

Support person responsible for complaints during investigations/Investigation of complaints.

Risk identification related to Technical, Safety, Quality, Supply, etc.

Proactively solving problems to eliminate recurring issues.

Project management for projects assigned.

Minimum Requirements :

Basic Qualifications:

Bachelor’s degree in engineering, industrial pharmacy, chemistry, or other appropriate scientific or pharmaceutical discipline

Minimum of 2 years of demonstrated experience GMP regulated Technical role, with strong experience in process and cleaning validation

Use of problem solving and continuous improvement tools

Project management.

Data analytics and Statistics Fluent in English and Spanish are required

Preferred Qualifications:

Experience in field or plant operations

Experience implementing FDA and/or GMP regulations

Ability to articulate business vision to staff, peers, and senior executives

Understanding of production forecasts and SAP systemsSAP, e , Serialization, Workday, Veeva,…