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

Purpose:

The primary function is to support the Quality Control Laboratories with independent, effective and timely testing services and able to ensure that tasks are performed according to requirements with review/verification of results and problem solving for issues identified.

Major Responsibilities:

Responsible for the timely completion and data verification of all testing of raw material, intermediates, in-process control samples and final productMaintain up-to-date, complete and precise records of all tests performedEnsure that all test equipment is used and maintained properly in GMP environmentActs as an SME for simple to complex instruments and techniques where neededLead and perform any method transfer or method validation protocols or equipment qualifications and support the transfer of new productsUnderstands, implements and maintains cGMP and 6S conceptAble to present clearly and lead confidently during audits and site leadership inquiriesWrite/revises procedures as necessary and make recommendations for process improvementEffectively perform a multitude of laboratory techniques for which they are trained on with minimal errorTrains new analysts and technicians on all instruments/techniques, as well as routinely reviewing that all API lab personnel are adhering to proper GMP standardsResponsible for assisting the lab supervisor in following up with corrective actionsResponsible for ownership of laboratory investigation - Able to lead the whole laboratory investigation and work alongside with QA for success closure of investigationParticipate in tier meeting for manufacturing updates on incoming raw materials/in-process samples and final APIUnderstands and maintains a safe work environment for themselves and others in accordance with procedural requirements by driving all EHS standards, procedures and policies
Qualifications
Bachelor of Science majoring in Biology, Chemistry, Biochemistry or related scientific degreeAt least 5 years of experience in a QC LabAt least 1-3 years of experience in a pharmaceutical manufacturing environmentStrong GMP background and proficient with using laboratory equipmentHighly motivated, independent and able to work under pressurePossess good interpersonal and communication skillsStrong analytical, problem solving and writing skillsTeam motivator – able to motivate and be role model for less experienced peersTotal commitment to quality and maintaining a high standard of work at all times
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