- 経験
- 2年以上
- 給料
- —
- 求人情報
- 1
- 投稿済み
- 10時間前
- 作業モード
- 在任中
- 教育
- Honours degree in Analytical Chemistry or related field
- 再開する
- 応募必須
勤務地
仕事内容
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.
スキル
Work styles they’re looking for
適応力
時間管理
チームワーク
細部へのこだわり
Continuous improvement in QC processes