Validation Engineer at Aphex
Waterford, County Waterford, Ireland -
Full Time


Start Date

Immediate

Expiry Date

01 Dec, 25

Salary

0.0

Posted On

02 Sep, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Iso, Regulations, Ms Project, Kpi, Pda, Completion, Gamp, Communication Skills, Compliance Regulations, Process Validation, Chemistry, Ansi

Industry

Pharmaceuticals

Description

Qualifications

  • Experience: 3-5 years’ experience working in a Healthcare manufacturing environment – ideally part of which would be in the pharmaceutical sector.
  • Natural influencer and works well as part of a multifunctional team.
  • Highly motivated and self-resilient.
  • Adaptable and flexible as well as a pragmatically minded problem solver.
  • Sees projects/tasks through to completion.
  • Capable of troubleshooting validation issues associated with projects, process development etc.
  • Competent technical knowledge of pharmaceutical plants.
  • Previous validation/product development experience would be highly advantageous for the role.
  • Knowledge of Process Validation regulations, current process validation and technical transfer industry practices, and experience of interpretation and application of guidelines and regulations.
  • Knowledge of requirements for of GAMP, ISPE Baseline guides.
  • Knowledge of steam and dry heat validation publications such as AAMI/ANSI, PDA and ISO guidelines.
  • Full understanding of relevant quality and compliance regulations
  • Able to execute projects to plan.
  • Good knowledge of quality management systems.
  • Good communication skills at organisation, team and individual levels.
  • Ability to use MS Project and SPC packages an advantage
  • Understands KPI’s for the site.
  • Previous Equipment knowledge for example pack lines, Autoclaves, Isolator Technology and fill lines would be an advantage.
  • Degree in Science (Chemistry, Micro. or Pharmacy preferred) or Engineering Chemical/Mech/Elec
Responsibilities

PURPOSE

In the Validation Engineer role, you will be required to support a new project
The Validation Engineer has a key role in ensuring the on-going validation and compliance of new equipment, systems and processes.

RESPONSIBILITIES

The following activities will be included as part of your role:

  • Executing FAT/SAT/IOQ protocols including generation of protocols and reports.
  • Designing, executing and reporting on validation studies for equipment, systems and processes.
  • Ensuring validation studies are managed in conjunction with all required * standards and legal requirements (Health & Safety, cGMP, construction, environmental etc.)
  • Providing technical interpretation and guidance of current US FDA and EU validation requirements for aseptic processing, lyophilisation, sterilisation and depyrogenation
  • Ensuring that the validation status of equipment and systems are in compliance with cGMP at all times
  • Maintaining validation documentation through the validation lifecycle
  • Participation in external regulatory inspections
  • Support Site Change Control process

Qualifications

  • Experience: 3-5 years’ experience working in a Healthcare manufacturing environment – ideally part of which would be in the pharmaceutical sector.
  • Natural influencer and works well as part of a multifunctional team.
  • Highly motivated and self-resilient.
  • Adaptable and flexible as well as a pragmatically minded problem solver.
  • Sees projects/tasks through to completion.
  • Capable of troubleshooting validation issues associated with projects, process development etc.
  • Competent technical knowledge of pharmaceutical plants.
  • Previous validation/product development experience would be highly advantageous for the role.
  • Knowledge of Process Validation regulations, current process validation and technical transfer industry practices, and experience of interpretation and application of guidelines and regulations.
  • Knowledge of requirements for of GAMP, ISPE Baseline guides.
  • Knowledge of steam and dry heat validation publications such as AAMI/ANSI, PDA and ISO guidelines.
  • Full understanding of relevant quality and compliance regulations
  • Able to execute projects to plan.
  • Good knowledge of quality management systems.
  • Good communication skills at organisation, team and individual levels.
  • Ability to use MS Project and SPC packages an advantage
  • Understands KPI’s for the site.
  • Previous Equipment knowledge for example pack lines, Autoclaves, Isolator Technology and fill lines would be an advantage.
  • Degree in Science (Chemistry, Micro. or Pharmacy preferred) or Engineering Chemical/Mech/Elec)
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