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Eirgen Pharma

QC Chemist

Eirgen Pharma

County Waterford, Munster, Ireland · 정규직

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경험
2년 이상
샐러리
채용 공고
1
게시됨
10시간 전
작업 모드
사무실에서
교육
Honours degree in Analytical Chemistry or related field
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신청 시 필수 사항

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직무 설명

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.

Work styles they’re looking for

적응성 시간 관리 팀워크 세부 사항에 대한 주의 Continuous improvement in QC processes

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