Quality Control Analyst

  • Full-time
  • Workday Global Grade: 13

Company Description

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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on XFacebookInstagramYouTubeLinkedIn and Tik Tok.

Job Description

We are recruiting Laboratory Analyst (12 months) to join our diverse team in Cork. ( Shift Position)

Are you intrigued? Do you want to learn more?

  • Execute analysis of raw materials, in-process material, and finished product in compliance with schedule.
  • Complete analysis in accordance with SOP and standard methods.
  • Execute analysis of water, cleaning samples etc as required.
  • Execute calibrations and PM of equipment as required to ensure equipment is appropriate for use for analysis.
  • Co-ordinate maintenance schedules with external suppliers to ensure compliance with schedule and in house procedures.
  • Preparation of all solutions, reagents etc. associated with analysis.
  • Execute stock control on laboratory consumables including reagents, solvents to ensure there is adequate supply to execute tasks. Complete purchase orders as required and manage materials on receipt.
  • Participate in the preparation of QC documents including SOPs, specifications, methods.
  • Participate in training and development activities to ensure that new technologies are applied and that skill level is developed.
  • Execute validation studies and transfer studies to ensure equipment, methods and personnel are appropriately qualified.
  • Participation in QC and site projects by representing QC so as to provide an appropriate service to other departments
  • Ensure QC activities are executed in line in in-house procedures and in compliance with requirements of cGMP.
  • Ensure QC activities are executed in line with safety requirements and good laboratory practice.
  • Keep work area clean and tidy.
  • Keep up to date on regulatory development and standards by accessing in house library, accessing current Pharmacopoeias etc.
  • Participation in investigations into failures, out of trends and out of specifications as required.

Qualifications

  •  Degree in an analytical science/biochemistry/toxicology is preferred
  •  Previous experience in a laboratory environment and direct experience of bioassays and related biological analytical techniques along with HPLC analysis would be an advantage
  • Analytical approach to tasks. Good organisation skills. Technical skills in analysis are important. Microsoft office suite ( excel / word)

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

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