Reach your career goals with Eirgen Pharma, your future could be here
Would you like to be part of a company that has the courage, innovation, and capability to improve and enhance patient lives across the globe?
A growing and innovative company based in Waterford, Eirgen Pharma develops and supplies specialty care medicines to patients in more than 50 countries worldwide. Our guiding principle is to improve and enhance the lives of patients, whether they be reached directly or through our contract manufacturing and development customers across the pharmaceutical industry.
Eirgen’s Waterford campus consists of a state-of-the-art and globally-accredited manufacturing environment which provides tableting, capsule, soft gel manufacturing and packaging capabilities. Our R&D function accommodates our development and analytical scientists working on the next generation of treatments for the company and its clients.
About the Job
In this role you will support QC and Stability by ensuring all raw materials, packaging, finished products and Stability samples are analysed in accordance with cGxP.
You will:
- Test and complete write up of QC raw material, packaging, finished product and stability samples in a timely & efficient manner.
- Support all other on-going laboratory functions & requirements.
- Prepare and review stability summary sheets where required.
- Ensure that all work carried out is in compliance with the required standards conforming to company, cGxP, SOPs, regulatory regulations and guidelines, safety and environmental guidelines.
- Identify and make recommendations for improvements as part of a team within or outside the department in order to ensure continuous improvement.
- Check own work and that of others for accuracy.
- Assist in the preparation for internal / customer/ regulatory inspections.
- Be involved in internal investigations e.g. Out of Specifications, Incidents & Deviation investigations, etc.
- Draft, review or revise documentation within EirGen documentation management system
- Report any Deviations/Out of Specifications to Senior Chemist and complete in a timely manner
- Implement safety requirements as per site documentation including SOPs, Safety Statement and COPs
- Report any defects.
About you
You are qualified to a minimum of honours degree level in Analytical Chemistry, Pharmaceutical science or related discipline while two years’ experience working in a related technical environment is preferable but not essential. You possess strong analytical ability and are proficient in the use of HPLC, Dissolution testing & associated problem solving.
You have a broad understanding of regulatory requirements for submission of dossiers in EU, USA, Japan and other jurisdictions. You also have knowledge of Microsoft products including, Excel, Word & Power Point. You possess excellent written & verbal communication skills, have strong attention to detail and work effectively on your own as well as with others.
You will draw from many skills including adaptability, planning, multi-tasking and time management. You have the ability to form positive relationships and enjoy collaborating, gaining knowledge, continuous improvement and solving problems.
Working at Eirgen – What to expect
At Eirgen, we have developed a diverse, people-centric, high performance culture where people are enabled to achieve their potential.
If you are working at Eirgen, then we think you’ve got something special. Our employees are high-performing and work as part of a cohesive team, they are dedicated people who are driven to succeed and are rewarded with competitive salaries and an attractive range of benefits including opportunities for career progression and continuing education.
Apply for the above role by sending your CV to opportunities@eirgen.com including the job title in the subject.