Job Description We are now looking for a QC Supervisor to join our team on our Westport site for a 12 month Fixed Term Contract.
The Microbiology Supervisor is responsible for the planning, supervision and control of a Microbiology testing team involved in the routine microbiology laboratory activities including environmental monitoring of cleanrooms; microbial analysis site utilities and testing of raw material, commercial, clinical and development batches..
The position holder will ensure a continued "on the floor" presence within the laboratory area and business unit cleanrooms actively engaging with, challenging and motivating team members and business unit personnel.
As the Supervisor you will use your This position supervises a team of QC technicians and reports to the QC Manager.
Responsibilities: Provide guidance to direct reports to ensure activities are completed as per schedule and in a GMP compliant manner and in line with regulatory (QA and EHS) and corporate requirements.
Maintain strong relationships with management and colleagues both within the site business units and the quality function, direct reports and customers.
Articulate the necessary aseptic and micro requirements in a clear, concise and persuasive manner.
Provide motivation to the team and take appropriate corrective action on individual/team performance where required.
Hold performance meetings according to company policy.
Update TMS and take appropriate action where an individual's attendance / timekeeping is below the expected standard.
Actively participate in the training and certification of new employees.
Ensure that all aspects of the area of responsibility are fully staffed and that any constraints are managed appropriately.
Coach and develop team members to support the Company's succession planning Represent the company in Ministries of Health inspections as deemed necessary as a subject matter expert in the field of Microbiology Foster an environment of continuous improvements for the QC area by identifying and implementing efficiencies and quality improvements.
Lead all new product introductions from a microbiology perspective, including but now limited to method validation, validation of cleanrooms, laboratory equipment validations, maintenance and calibration of business unit cleanroom monitoring system.
Qualifications 3 Years of experience in a QC environment within the pharmaceutical industry.
Proven track record in direct people management Scientific qualification in relevant discipline Knowledge of laboratory GMP standards.
Extensive knowledge of microbiology tasks and associated regulatory standards and guidance.
Ability to anticipate, understand and address the changing regulatory environment of the Pharma/Medical Device industry.
Assess implications of new regulatory guidance and implement necessary changes as they relate to Micro and aseptics.
Ability to articulate clearly when dealing with external bodies Excellent conflict handling skills Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie's policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.
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
