QC Chemist
County Waterford, Munster, Ireland • Vollzeit
Bewerben Sie sich als Erste/r!
- Erfahrung
- 2+ Jahre
- Gehalt
- —
- Stellenangebote
- 1
- Veröffentlicht
- vor 8 Stunden
- Arbeitsmodus
- Im Büro
- Ausbildung
- Honours degree in Analytical Chemistry or related field
- Wieder aufnehmen
- Bewerbung erforderlich
Wo Sie arbeiten werden
Stellenbeschreibung
About Eirgen Pharma
Join Eirgen Pharma, a dynamic company established in 2005 in Waterford, Ireland, employing over 180 people. We blend the agility of a small enterprise with the ambition to manufacture and provide high-quality medicines globally within a supportive and collaborative culture focused on people.
Role Overview
As a Quality Control Chemist, you will be an integral member of the QC team responsible for analyzing all finished pharmaceutical products according to cGxP standards. This position operates in a rotating shift schedule: one week from 7am to 3pm and the next from 3pm to 11pm.
Key Duties
- Conduct timely and precise testing of raw materials, packaging, finished products, and stability samples, emphasizing finished product analysis.
- Assist with daily Quality Control laboratory operations and related activities.
- Prepare and review laboratory documentation as needed.
- Maintain strict adherence to GMP guidelines, company SOPs, regulatory, safety, and environmental protocols.
- Engage in continuous improvement efforts to optimize laboratory processes.
- Provide support during internal, customer, and regulatory inspections and audits.
- Participate in investigations concerning laboratory deviations, out-of-specification results, and incidents.
- Create, evaluate, and manage controlled documents within the document management system.
- Observe and comply with site Health & Safety regulations, including hazard identification and reporting.
Candidate Profile
- Holds an honours degree or higher in Analytical Chemistry, Pharmaceutical Science, or a related field.
- Has at least two years of experience performing HPLC testing within a Quality Control laboratory setting.
- Demonstrates experience working in a GMP-regulated pharmaceutical environment.
Why Work With Us?
- Collaborate within a dedicated analytical team focused on delivering high-quality data in a fast-paced, GMP-compliant environment.
- Gain exposure to both development-stage and commercial pharmaceutical products.
- Benefit from a quality-centered, collaborative workplace culture.
- Enjoy excellent employee benefits including pension schemes, health insurance, social club participation, and canteen amenities.
Fähigkeiten
GMP-Konformität
Einhaltung der Gesundheits- und Sicherheitsvorschriften
Document Management Systems
Regulatory Inspection Support
Deviation and OOS Investigation
Compliance-oriented
HPLC testing
Quality Control laboratory procedures
Pharmaceutical product analysis
Laboratory documentation and records management
Work styles they’re looking for
Anpassungsfähigkeit
Zeitmanagement
Teamarbeit
Liebe zum Detail
Continuous improvement in QC processes