close

Did you know that your Internet Explorer is out of date?

To get the best possible experience using our website we recommend that you upgrade to a newer version or download another web browser.
A list of the most popular web browsers can be found below. Just click on the icons to get to the download page.

crome
Google Chrome
IE
Internet Explorer
firefox
Mozilla Firefox
opera
Opera

Your browser will need to close to complete the installation and you will need to manually reload the site when finished
Apply for this job

Name:

Surname:

Email:

Phone:

Cv:

Salary Expectations:

Education:

Experience:

Current Location:

Notice Period:

Write here your cover note:


If you would like us to create a jobseeker account for you, giving you access to
account management, job alerts and one-click applications, then please tick this box

If you are having difficulty you can always email your cv to applications@lifescience.ie
Details

Manufacturing Biotech Associate 24/7 Shift


Reference:AS20487 Location: Meath
Qualification:DegreeExperience:See description
Job Type:Fixed Term ContractSalary: Not Disclosed

Manufacturing Biotech Associate 24/7 Shift
AS20487
11 Months
Meath

We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Meath. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.

Duties:

  • Support operations team to consistently deliver on specific Key Performance Indicators (KPIs), e.g. Environmental Health and Safety (EHS) metrics, Production Plan, Overall Equipment Effectiveness (OEE), compliance and team training.
  • Execute commercial manufacturing processes according to established work instructions and
  • Standard Operating Procedures (SOPs).
  • Ensures that all assigned task related to manufacturing documentation support is in accordance with good manufacturing practices.
  • Routinely talk about any safety issues you are concerned about.
  • Work as part of a dedicated process team where flexibility and teamwork are a key requirement.
  • Generate SOPs/ Work Instructions (WIs) to ensure compliance with regulatory standards.
  • Maintain/ support a high standard of safety/ Good Manufacturing Practice (GMP) compliance at all times.
  • Determine solutions by referencing relevant past experiences as part of problem solving activities.
  • Get actively involved by participating in inspections, GEMBA’s and Go-See’s.
  • Act as a team member on process deviation reviews and Gemba walkdowns.
  • Mentor new members of staff in specific plant activities.
  • Be prepared to answer auditor questions during site walkdowns.
  • Engage in implementing innovative solutions that drive a high performance organisational culture that accommodates rapid growth and highly dynamic expectations ensuring attainment of site operational and development goals.
Education and Experience :
  • Level 7 qualification in a science or engineering discipline, or level 6 with a minimum of 4+ years’ experience in a GMP Manufacturing environment.
  • Experience of Upstream/ Downstream Processing.
  • Start-up experience in a large-scale commercial drug substance facility, or similar.
  • A proven ability to work with automated systems such as Manufacturing Execution System (MES), Systems Applications and Products (SAP), Delta V etc.
If interested in this posting please feel free to contactAvishek Singhon +353 (0)87 282 7991 or Avishek.singh@lifescience.ie for further information.