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Analytical Technology Specialist II

AbbVie Inc

Missouri

On-site

USD 60,000 - 90,000

Full time

8 days ago

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Job summary

AbbVie Inc is seeking an Analytical Technology Specialist for a 12-month fixed-term contract at their Westport site. This role involves conducting Cell-Based Potency Assay testing and overseeing various laboratory duties. Ideal candidates will have a Bachelor's or higher in a Biological Science, along with strong analytical skills and experience in laboratory practices within a regulated environment.

Qualifications

  • Practical experience in mammalian cell culture and techniques
  • GMP experience is advantageous but not essential
  • Sound understanding of ELISA based methods

Responsibilities

  • QC Testing of commercial product via Cell Based Potency Assay
  • Routine lab duties including equipment maintenance and inventory management
  • Support regulatory inspections as required

Skills

Communication
Analytical Skills

Education

Bachelors of Science
Master’s Degree
Ph.D in a Biological Science

Tools

ELISA methods

Job description

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 atwww.abbvie.com. Follow @abbvie onX,Facebook,Instagram,YouTube,LinkedInandTik Tok.

Job Description

At our Westport site in Co. Mayo, we are now hiring an Analytical Technology Specialist to join our talented and ambitious team, on a12months fixed term contract.

The role centers on conducting Cell-Based Potency Assay (CBPA) testing, ad-hoc investigational & development testing.

With an exciting pipeline of products and a great salary and benefits package, this may be the ideal opportunity to develop your career with an industry leader.

So if you are interested in joining this team, read below to find out more…

In your new role, you will:

  • QC Testing of commercial product via Cell Based Potency Assay and related ELISA methods
  • Routine lab duties including critical reagent qualifications, inventory management and equipment maintenance
  • Interdepartmental co-ordination - support product release, drive completion of defined projects etc.
  • Support and execute Method Transfer and Validation activities associated with key biological drug product projects.
  • Assay performance monitoring and trending
  • Compiling and review of Laboratory documentation (e.g. SOPs, methods, validation documentation etc.).
  • Perform lab duty tasks to maintain a high standard of housekeeping within the laboratory.
  • Support regulatory inspections as required.
  • Supporting Root Cause Analysis Investigations
  • Adhere to and support all EHS procedures and policies.
  • Support and lead Laboratory projects to ensure timelines are met successfully.
Qualifications

To succeed in this role, you will have the following Education and Experience:

  • Bachelors of Science, Master’s Degree or Ph.D in a Biological Science
  • Practical experience of mammalian cell culture and basic techniques (Passaging, freeze-down, drug treatments) is an advantage
  • Previous GMP experience is advantageous but not essential
  • Sound scientific/practical understanding of ELISA based methods
  • A clear understanding of working within a regulated environment.
  • Excellent communication and presentations skills, both written and oral.
  • Strong analytical skills with the ability to plan and schedule workloads.
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, visithttps://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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