Snr Analytical Chemist - Stability

Senior Analytical Chemist - Stability

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 lead the analytical team to deliver commercial and development analytical
testing in accordance with required timelines and perform testing in accordance with
procedure.

Responsibilities

You will:

• Supervise the analytical team and run the daily lab meetings to achieve required

• Be the technical expert on commercial and product testing where you are

• Perform technical review of documentation on behalf of the team lead as

• Attend and lead customer meetings on projects and commercial testing on

• Lead 5s/H&S/GMP inspections in the laboratory as required

• Complete laboratory investigations (Deviation/OOS/Safety) in a timely manner,

• Lead in Commercial/Validation/Transfer/Verification/Stability studies as required

• Analyse all raw materials, in process samples and finished products in a timely

• Draft/ review test methods, validation/verification/transfer protocols and

• Complete preparation for customer/ regulatory inspections and perform role of

• Prepare submission documentation in support of license applications.

• Identify and deliver improvements as part of a team within or outside the

• Report any defects/hazards as they arise
  

About you

You are qualified to a minimum of degree level (or equivalent) in chemistry, pharmaceutical
science or a related discipline and have at least five years’ experience working in a related
technical environment. You possess a broad understanding of regulatory requirements for
submission of dossiers in EU, USA, Japan and other jurisdictions, knowledge of project
management skills and are proficient in the use of HPLC/Empower & all analytical techniques.

You demonstrate key competencies including excellent communication skills - verbal &
written, attention to detail, organisational and problem solving ability, delivery of targets and
professionalism.

You will demonstrate the following behaviours – strong safety awareness, leadership,

influencing, decisiveness, teamwork & collaboration, compliance & adherence to regulations

and lean thinking.

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 further education.

Apply for the above role by sending your CV to opportunities@eirgen.com including the job title in

the subject.