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Quality Control Analyst bei AbbVie

AbbVie · Sligo, Irland · Onsite

€36,500.00  -  €36,500.00

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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 currently recruiting a QC Analyst for our high-performing team in Manorhamilton Rd, Sligo. This is a 12 month fixed-term contract. This is also a rotating shift position.

A snapshot of your key responsibilities as a QC Analyst would be:

  • 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.
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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