Validation Engineer

Chanelle Pharma Group Limited; Ireland; On-site; EUR 40,000 - 55,000; Full time

Job summary

A pharmaceutical company in Ireland is seeking a Validation Engineer to support validation activities and ensure compliance with regulatory requirements. The position involves developing and documenting validation protocols, maintaining documentation standards, and improving validation processes. Candidates should have a degree in Engineering or Pharmaceutical Science and 2-4 years of experience in a GMP-regulated environment. An inclusive environment is fostered, welcoming diverse backgrounds.

Benefits

Inclusive workplace

Support for career breaks

Qualifications

• 2-4 years of validation experience in a GMP-regulated environment.
• Preferred experience in cleaning and equipment validation.

Responsibilities

• Develop, execute, and document validation protocols.
• Ensure compliance with GMP and regulatory guidelines.
• Support technology transfers and new product introductions.
• Maintain accurate validation documentation and support audits.
• Identify improvements in validation processes.

Skills

GMP understanding

Documentation skills

Collaborative work

Validation methodologies knowledge

Troubleshooting abilities

Education

Degree in Engineering or Pharmaceutical Science

Job description

To execute validation activities in compliance with regulatory requirements and company standards. The Validation Engineer supports the Validation Team Lead in implementing the Validation Master Plan, maintaining validation-related SOPs, and performing validation for processes, cleaning, equipment, analytical instruments, and utilities.

Location: Onsite at our facility in Loughrea.

Responsibilities

• Develop, execute, and document validation protocols and reports for process, cleaning, equipment, analytical instruments, and utilities.
• Ensure validation activities comply with GMP, regulatory guidelines, and internal procedures.
• Support technology transfers and new product introductions through validation activities.
• Maintain accurate and complete validation documentation in accordance with SOPs and regulatory requirements.
• Assist in updating and implementing validation‑related SOPs under the guidance of the Validation Team Lead.
• Ensure validation records are audit‑ready and support internal and external inspections.
• Identify opportunities to improve validation processes and enhance efficiency.
• Contribute to initiatives that align validation practices with evolving regulatory expectations.
• Work closely with manufacturing, quality, engineering, and analytical teams to coordinate validation activities.
• Provide technical support during troubleshooting and investigations related to validation.

Qualifications and Experience

• Degree in Engineering, Pharmaceutical Science, or related discipline.
• 2–4 years in validation within a GMP‑regulated environment.
• Experience in process, cleaning, and equipment validation preferred.

Skills and Competencies

• Strong understanding of GMP and validation principles.
• Excellent documentation and organizational skills.
• Ability to work collaboratively across functions.
• Solid knowledge of validation methodologies and regulatory requirements.
• Ensures accuracy and completeness in validation documentation.
• Ability to troubleshoot and resolve validation‑related issues.
• Works effectively with cross‑functional teams.
• Commitment to maintaining high standards of quality and regulatory compliance.

Applicants from diverse backgrounds, including those returning after a career break or with transferable skills from non‑traditional career paths, are encouraged to apply. We value varied experiences and are committed to fostering an inclusive environment that supports individuals with disabilities.