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

Batch Record Reviewer


Reference:AMC21394 Location: Cork
Qualification:DegreeExperience:See description
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Documentation Specialist


Electronica Batch Record Reviewer
11 month Contract
Hybrid role - Cork
AMC21394

We are currently on the lookout for a Operations Technical Specialist to support a Vaccine IPT team in a biotechnology manufacturer based in Cork. In this role you will be responsible for completing electronic batch record reviews.

You will have:

  • 1-3 years experience in a n operational role in a pharmaceutical or highly regulated environment
  • BSc in Biochemistry, Microbiology, Chemistry, Engineering or related field
  • Experience in Batch Record reviews
  • Working knowledge of GxP systems eg. GLIMS, eVAL and DeltaV

In this role you will:
  • Manage Batch Record reviews
  • Provide support for troubleshooting and leading SPS for shop floor issues
  • Manage EHS and Quality investigations and oversee batch record reviews
  • Offer technical support for Operations and changes
  • Lead cross-functional teams for troubleshooting and investigations within Vaccines IPT
  • Write technical reports and conduct investigations
  • Complete continuous improvement projects for manufacturing operations
  • Utilize Lean Six Sigma and Lean methodologies
  • Represent the department on project teams
  • Ensure compliance with EHS policy, cGMP, and other regulations
  • Maintain highest standards for Compliance (Quality and Safety)
  • Participate in risk assessments, audits, regulatory inspections, and incident investigations
  • Uphold Quality, Compliance, and Safety standards through compliance with Manufacturing Division QMS requirements, including ownership where applicable.

If interested in this posting please feel free to contact Angela McCauley on +353 (0)87 693 0951 or angela.mccauley@lifescience.ie for further information or apply directly by uploading your CV.