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

QA Manufacturing Analyst

Grifols

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

Posted 10/21/2026full-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 initiatives. Proficient in supporting audits, investigations, and training while collaborating effectively with cross-functional teams.

Highest-signal resume keywords
Environmental MonitoringAseptic Regulatory RequirementsQuality Assurance SupportCleanroom Environmental MonitoringB.Sc Degree

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 SamplingSterilisation QualificationsDeviations InvestigationCAPA ManagementChange ControlValidation ActivitiesProcess ValidationMedia FillsGMP ComplianceQuality Insights
Soft Skills
Strong Communication SkillsOrganisational SkillsProactive ApproachFlexible Approach
Industry Keywords
Aseptic PharmaceuticalMedical DevicesGrade C/D EnvironmentsGrade A/B ExposureQuality MonitoringContinuous ImprovementBest PracticesTrainingAuditsInspections

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
  • Establish the Environmental Monitoring programme for aseptic manufacture and water systems for manufacturing operations

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