Snr Analytical Chemist - Stability at EirGen
Waterford, County Waterford, Ireland -
Full Time


Start Date

Immediate

Expiry Date

26 May, 25

Salary

0.0

Posted On

26 Feb, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

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.

Responsibilities

You will:

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

targets

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

assigned

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

required

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

behalf of your team

  • Lead 5s/H&S/GMP inspections in the laboratory as required
  • Complete laboratory investigations (Deviation/OOS/Safety) in a timely manner,

identifying root cause in line with expected timelines

  • Lead in Commercial/Validation/Transfer/Verification/Stability studies as required
  • Analyse all raw materials, in process samples and finished products in a timely

and efficient manner to ensure quality and efficacy of the product.

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

reports as applicable

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

SME during inspections.

  • Prepare submission documentation in support of license applications.
  • Identify and deliver improvements as part of a team within or outside the

department in order to ensure continuous improvement.

  • Report any defects/hazards as they arise
Loading...