GMP Specialist

Apleona GmbH; Ireland; On-site; EUR 40,000 - 60,000; Full time

Job summary

A leading facilities management company is seeking a GMP Specialist to join its team in Dublin. This role involves providing consultancy and expertise in a pharma environment, leading optimisation projects, and ensuring compliance with GMP standards. Ideal candidates should have strong GMP knowledge and experience in a lifescience setting. The company promotes a culture of continuous improvement and innovation, and the role offers the opportunity for significant professional growth.

Qualifications

• Experience working in Facilities Management/Lifescience environment.
• Strong GMP knowledge, ability to apply principles confidently.
• Membership of a relevant professional organisation is advantageous.
• Strong PC literacy with advanced proficiency in relevant software tools.

Responsibilities

• Consultancy, coaching, and expertise to site teams.
• Lead optimisation projects, innovation initiatives, and training programmes.
• Conduct inspections, audits, and sanitisation checks.
• Drive innovation across GMP services, identifying market trends.

Skills

GMP knowledge

Communication skills

Organisational skills

Time management

Reporting acumen

PC literacy

Job description

The details for the selected vacancy are shown below.

• Advert Title GMP Specialist
• Advert Text

  We are looking for a GMP Specialist to join Apleona team for pharma environment in Dublin

  Working pattern: Monday to Friday from 08:30-17:00

  Job Description

  • Provide consultancy, coaching, and expertise to internal site teams
  • Lead and support optimisation projects, innovation initiatives, internal audits, and training programmes
  • Ensuring that all documentation and logbooks entries are completed as Good Documentation Practice
  • Evaluate, harmonise, and standardise GMP compliance and cleaning practices across all Client sites.
  • Facilitate and deliver training programmes to ensure staff are fully competent in GMP standards and service requirements.
  • Conduct inspections, audits, and sanitisation checks in line with contractual requirements, KPIs, and GMP expectations.
  • Review existing GMP cleaning processes, documentation, and procedures, contributing to the implementation of standardised service models.
  • Ensure all GMP cleaning activities meet legislative requirements, industry best practices, and company standards. .
  • Keep accurate records in relation to all aspects of work and prepare reports as required.
  • Drive innovation across GMP services by identifying market trends, new technologies, and improvement opportunities.
  • Support the development and expansion of GMP service offerings, seeking opportunities for business growth
  • To undertake other duties as requested by the Line Manager

Requirements

• Experience working in Facilities Management/Lifescience environment.
• Strong GMP knowledge, with the ability to apply principles confidently across diverse operations.
• Membership of a relevant professional organisation (advantageous).
• Excellent communication, organisation, interpersonal, communication skill and time management
• A strong reporting acumen with excellent attention to detail.
• Strong PC literacy with advanced proficiency in relevant software tools
• Understanding of safe working practices and health & safety legislation.
• Flexibility with a high-level commitment to success.

We are looking forward to hearing from you!

Ref: 16021