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QC Lab Analyst

AbbVie Inc.
Sligo, ie
On-site

About this role

QC Lab Analyst

Sligo, ie

Function:

Operations

Work location type:

On-Site

Job Type: Full-time

Job ID: R00151610

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

We are currently recruiting a QC Analyst for our high-performing team in Manorhamilton Rd, Sligo. This is a 12 month fixed-term contract. This role is a 12 hour rotating days and nights position.

  • Maintain and comply with Laboratory Documentation and Computerized Systems Data Integrity requirements.
  • Understand Regulations and business processes required to maintain Laboratory Data Integrity.
  • Be responsible for housekeeping duties in the lab.
  • Be responsible for the timely completion of chemical testing of raw material.
  • Ensure that all test equipment is used and maintained correctly.
  • Be responsible for raising change requests and data verification as assigned.
  • Ensure all in-process sampling and testing are completed in a timely manner.
  • Maintain up-to-date, complete, and precise records of all tests performed.
  • Adhere to cGMP and GLP requirements.
  • Assist in the resolution of quality problems as required.
  • Develop and change in-house laboratory procedures as appropriate.
  • Aid in training of new analyst.
  • Support the transfer of new products.
  • Adhere to and support all EHS & E standards, procedures and policies.

Qualifications

  • 3rd level qualification in a relevant Science discipline required.

  • A minimum of 6 months of experience in HPLC or GC.

  • Experience operating to cGMP standards utilizing laboratory equipment.

  • Previous experience in a pharmaceutical manufacturing environment is desirable but not essential

  • Equal Opportunity Employer/Veterans/Disabled.

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