Perform Chemistry analysis of In process / Final product as per schedule and in accordance with regulatory requirements. Also perform analysis on Stability samples from a wide range of products
Documenting all testing activities, results and raw data on time, accurately and legibly
Use of laboratory IT systems including LIMS and Empower
Reviews and interprets test results
Adhering to all company standards in the areas of safety, housekeeping and quality, notifying management of any discrepancies
Ensure good housekeeping and good laboratory practices
Rotating shifts monthly
Work with team, Supervisors, Quality Manager and Laboratory Manager to ensure compliance to Quality Management System

3rd Level Qualification in a Science Discipline, preferably Chemistry related.
1-2 Years’ experience working as an Analyst in a GMP/GLP environment.
1-2 Years’ experience of working with a range of Analytical Equipment specifically HPLC and GC and well as other laboratory techniques is preferred.
Good knowledge and understanding of Data Integrity from Laboratory perspective.
Excellent communication, organization, time-management and teamwork skills
Demonstrate ability to work on one’s own initiative.

Behaviours/Value:

Relationship Building: establishing excellent working relationships with all functions within the business
Communication: excellent communication and presentations skills, both written and oral. Articulate the quality requirements in a clear, concise and persuasive manner.
Planning & Organizing: excellent analytical skills. Ability to plan and schedule.
Decision Making: identify and understand issues, problems and opportunities whilst providing a viable solution.
Adaptability; Able to work in a fast, dynamic, environment whilst being able to adjust readily to meet unexpected constraints.

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.

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