Analytical Sciences & Technology (AST) Analyst
Job Type: 12+ months contract
Location: Waterford
The Role
To participate in delivery of analytical projects as pertaining to business needs.
* To ensure current Good Laboratory Practices (cGLP) is adhered to in all areas of work.
* To create and maintain a safe work environment and report any unsafe conditions observed in the workplace.
Key Responsibilities
* Provide analytical chemistry expertise and support to AST-MSAT and the Site activities.
* Effective interaction with other departments on matters related to ongoing projects, particularly with Quality Assurance, Quality Control, Manufacturing, Engineering, and Program Leads.
* Participate in development, qualification, and method optimisation for the projects.
* Participate in method transfer activities as required.
* Provide updates on ongoing projects and identify improvements when needed.
* Participate in analytical and functional method improvements, manage and give updates on ongoing activities.
* Bring innovative ideas and actively research for improvements around the analytical space.
* Support other functions in investigations and troubleshooting as required.
* Assist with training of analysts in areas of expertise and knowledge, and in new methods and techniques.
* Update the AST Team Leader on potential problems and highlight improvements where possible by use of normal communication means.
* Ensure all quality documents and records are complete and current.
Compliance Related Tasks:
* Ensure laboratory areas meet current Good Laboratory Practices (cGLP) requirements.
* Ensure relevant procedures are correctly defined and followed.
* Ensure that critical chemical testing and related equipment meets current validation requirements (IQ/OQ/PQ) where required.
* Ensure safety & compliance standards are maintained to the highest standards.
* Maintain internal / external audit-ready standards.
* Maintain training compliance.
* Maintain Good Documentation Practices (GDP) at all times, including laboratory notebooks and analytical reports.
* Ensure compliance with current Good Manufacturing Practices (cGMP) at all times.
Skills and Knowledge:
* Operational experience of quality laboratories in a fast-moving manufacturing environment.
* Knowledge of quality management systems, pharmaceutical manufacturing operations, requirements for cGLP, pharmacopeial methods, and stability.
* Understand relevant quality/compliance regulations.
* Ability to manage projects to plan and budget.
* Understanding Key Performance Indicators (KPIs) for the site.
Candidates should hold appropriate RTWs for Ireland i.e., Stamp 1G, Stamp 4, Irish/British/EU passport.
For more information please apply here or contact Agnes Reena / agnes.reena@eirevo.ie Contact: 0858564199
eir evo talent is an equal opportunity employer who seeks to recruit and appoint the best available person for a job regardless of marital/civil partnership status, sex (including pregnancy), age, religion, belief, race, nationality and ethnic or national origin, colour, sexual orientation or disability. eir evo talent applies all relevant Data Protection laws when processing your Personal Data.
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Ref: EET6697
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