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Quality control analyst

Cork
AbbVie
Quality control analyst
€60,000 - €80,000 a year
Posted: 28 October
Offer description

Join to apply for the Quality Control Analyst role at AbbVie


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 X, Facebook, Instagram, YouTube, LinkedIn 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 preventive maintenance of equipment to ensure it 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. Complete purchase orders as required and manage materials on receipt.
* Participate in the preparation of QC documents including SOPs, specifications, and 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.
* Participate 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 with 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 the in‑house library and current pharmacopoeias.
* Participate in investigations into failures, out‑of‑trends and out‑of‑specifications as required.


Qualifications

* Degree in analytical science, biochemistry, toxicology or related field 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 and technical skills in analysis.
* Proficiency with 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


Seniority level

* Entry level


Employment type

* Full‑time


Job function

* Quality Assurance


Industries

* Pharmaceutical Manufacturing and Biotechnology Research
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