Key Responsibilities:
- Supervise all validation programs ensuring adherence to timelines and quality benchmarks.
- Manage the development and timely completion of validation protocols and reports.
- Ensure activities align with site plans and comply with regulatory standards.
- Respond to regulatory inquiries and manage associated documentation.
- Lead team meetings and resource planning to enhance efficiency and achieve performance goals.
- Oversee training and skill development within the team.
- Represent the department during audits and ensure continuous audit readiness.
- Work closely with other departments to support operational planning and execution.
- Serve as the subject matter expert for all validation activities.
- Coordinate and process regulatory requests related to validation.
Qualifications :
- Candidates must hold a relevant degree in Chemistry or a comparable scientific field.
- A minimum of five years professional experience within the pharmaceutical industry.
- Self-motivated and highly organized with a disciplined work ethic.
- Excellent communication and interpersonal skills.
- Forward thinking and detail orientated.
- Proficiency in Empower (or equivalent systems) and LIMS.
Additional Information :
Expected Behaviors:
- Integrity flexibility working under own initiative
- Strong analytical ability and associated problem solving
- Results and performance driven
- Good time management & attention to detail
- Professionalism; with the client contractors and colleagues at all times
- Compliance with SGS and client policies and procedures
To apply please submit your CV.
Candidates must be immediately eligible to work in Ireland this is a site based role.
We are an equal opportunity employer and value diversity at our company.
Remote Work :
No
Employment Type :
Contract