Supervisor, Laboratory Quality Control

AbbVie; Westport (CT); On-site; USD 65,000 - 95,000; Full time

Job summary

An innovative company is seeking a QC Lab Supervisor to lead a dynamic team in Westport. This role involves overseeing laboratory operations, ensuring compliance with regulatory standards, and driving continuous improvement in testing practices. The ideal candidate will have a solid background in analytical chemistry, with experience in HPLC and Empower systems. Join a forward-thinking organization that values integrity and innovation, where your contributions can make a significant impact on healthcare solutions. If you are passionate about science and leadership, this opportunity is perfect for you.

Qualifications

• 4+ years of analytical experience in the pharmaceutical industry.
• Experience with HPLC, GC, and LCMS preferred.
• Strong communication and time-management skills.

Responsibilities

• Supervise laboratory operations and ensure compliance with regulations.
• Document testing activities and results accurately.
• Identify performance improvement opportunities in the lab.

Skills

Analytical Skills

HPLC

GC

LCMS

GCMS

Data Integrity

Communication Skills

Time Management

Teamwork

Education

3rd Level Qualification in a Science Discipline

Tools

LIMS

Empower

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 at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

We are now hiring a QC Lab Supervisor to join our team in Westport for a 12 month Fixed-Term-Contract. You will lead the QC Chemistry Analysis and Release testing team and ensure the continued success of the team. Ensure that technical and systems excellence is maintained in the laboratory by ensuring own skills are maintained, by coaching and training analysts to ensure right first time behavior and by implementing improved working practices in terms of efficiency, compliance and Right First Time.

• Supervise Daily Laboratory operations, ensuring personnel execute their responsibilities in strict accordance with relevant regulatory guidelines. Support the weekly and daily production schedules and participate in the daily Tier 1 meeting to review shift production.
• Documenting all testing activities, results and raw data on time, accurately and legibly
• Use of laboratory IT systems including LIMS and Empower
• Adhering to all company standards in the areas of safety, housekeeping and quality, notifying management of any discrepancies
• Work with team, Supervisors, Quality Manager and Laboratory Manager to ensure compliance to Quality Management System
• Identify and understand issues, problems and opportunities whilst providing a viable solution.
• Have a people centred approach to their management style whilst upholding the values and ethos of Abbvie
• Executing and / or supporting projects as assigned by the laboratory manager.
• Developing and changing of in-house laboratory procedures as appropriate.
• Adheres to and supports all EHS & E standards, procedures, and policies.
• Ensuring that the agreed compliance timelines, such as CAPA due dates are adhered to and identify recovery paths when required to bring test schedules back into alignment with plant requirements.
• Identifying opportunities in laboratory performance improvements and working with the laboratory manager to rectify.
  
  

Qualifications

• 3rd Level Qualification in a Science Discipline, preferably Chemistry related.
• Minimum 4 years analytical experience in the pharmaceutical industry.
• Experience in an analytical role with experience in HPLC, GC, LCMS, GCMS, Automatic titration, Identification techniques preferred.
• Experience and good knowledge of Empower.
• 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
  
  

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