PPLM Technician: Lifecycle Master for GMP Ops

Haleon; Alcalá de Henares; Presencial; EUR 45.000 - 61.000; Jornada completa

Descripción de la vacante

Haleon is seeking a PPLM Technician to lead the Product & Process Lifecycle Management of products manufactured on site. You will supervise validation programs, maintain the validation master plan, and ensure compliance with MHRA and Haleon standards while coordinating with Engineering, Quality and Technical teams.

The role requires a scientific background (engineering/pharma), GMP experience, data analytics, and strong communication skills in English and Spanish to drive continuous improvement

Formación

• 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

Responsabilidades

• 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&C, 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.
• 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.

Conocimientos

Data analytics

Statistics

Problem solving

Continuous improvement

Project management

Teamwork

Communication

Bilingual English/Spanish

GMP

Educación

Bachelor's degree in engineering/industrial pharmacy/chemistry

Herramientas

SAP

eBR

Serialization

Workday

Veeva

MyLearning

Office

Descripción del empleo

Haleon is seeking a PPLM Technician to lead the Product & Process Lifecycle Management of products manufactured on site. You will supervise validation programs, maintain the validation master plan, and ensure compliance with MHRA and Haleon standards while coordinating with Engineering, Quality and Technical teams.

The role requires a scientific background (engineering/pharma), GMP experience, data analytics, and strong communication skills in English and Spanish to drive continuous improvement