Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Grifols

Environmental Monitoring Analyst

Grifols

. Support the Quality Monitoring Supervisor and act as delegate when required .

Posted 11/9/2026full-timeDublin • IrelandJuniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in quality assurance within the aseptic pharmaceutical and medical device industries, focusing on environmental monitoring, regulatory compliance, and continuous improvement practices. Strong collaboration and communication skills are essential for supporting cross-functional teams and training initiatives.

Highest-signal resume keywords
Quality Assurance SupportEnvironmental MonitoringGMP ComplianceAseptic Regulatory RequirementsTraining and Continuous Improvement

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Environmental SamplingCleanroom QualificationDeviation InvestigationCAPA ManagementProcess ValidationMedia FillsQuality AuditsSterilisation QualificationChange ControlQuality Insights
Soft Skills
Strong Communication SkillsOrganisational SkillsProactive ApproachFlexible Approach
Certifications & Qualifications
B.Sc Degree
Industry Keywords
Aseptic PharmaceuticalMedical DevicesGrade C/D EnvironmentsGrade A/B ExposureGMP Compliance

About the role

Key responsibilities & impact
  • Support the Quality Monitoring Supervisor and act as delegate when required
  • Collaborate with cross-functional teams to deliver monitoring activities and share quality insights
  • Perform environmental and water sampling, supporting cleanroom and sterilisation qualifications
  • Contribute to investigations (deviations, CAPA, change controls) and provide QA support to manufacturing
  • Support audits, inspections, product quality reviews, and GMP compliance across the site
  • Assist with training, continuous improvement, and implementation of best practices
  • Participate in validation activities, including media fills and process validation
  • Support additional quality activities as needed

Requirements

What you’ll need
  • Minimum of B.Sc Degree or equivalent third level education.
  • 1-2 years’ experience working in an aseptic pharmaceutical/medical devices industry.
  • Solid understanding of aseptic regulatory requirements.
  • Experience in Grade C/D environments, with exposure to Grade A/B an advantage.
  • Experience in cleanroom environmental monitoring within aseptic pharma or medical device setting.
  • Strong communication and organisational skills, with a proactive and flexible approach.

Benefits

Comp & perks
  • Highly competitive salary
  • Annual performance based bonus %
  • Shares options scheme
  • Group pension scheme - Contribution rates are (3%/ 5%/ 7%) and company will match
  • Private Medical Insurance for the employee
  • Ongoing opportunities for career development in a rapidly expanding work environment
  • Succession planning and internal promotions
  • Education allowance
  • Wellness activities - Social activities eg. Padel, Summer Events