Job Description
A QCL Shift Supervisor is required on a permanent basis to support our expanding business needs. This role will initially support Peptides manufacturing and later extend to provide supervisory support to the QCL Small Molecule shift team.
Key Responsibilities:
* Provides coaching, feedback, and administrative support for team members, including manning and work schedules.
* Plans, assigns, prioritizes, and monitors workload for shift Analysts.
* Leads daily huddles and oversees training of shift Analysts.
* Directs and coordinates day-to-day activities, schedules, and prioritizes QCL Peptides shift teams' work.
* Partners with Operations Supervisors and Analytical leadership to meet business needs.
* Serves as a QCL consult for unexpected issues and collaborates with Operations and Process Teams to resolve them.
* Creates an impact, drives results, and sets the tone for the shift team.
* Oversees performance management planning, reviews, and career planning for direct reports.
* Maintains high standards of safety and quality compliance in the area.
* Responsible for making decisions, accountable for day-to-day activities, and identifies operational problems.
* Utilizes Lean methodology to improve productivity and eliminate inefficiencies.
* Ensures analyst cover is provided to support the business.
* Coordinates PATrol troubleshooting/investigations/corrective maintenance.
* Authorizes, reviews, and approves quality documents.
* Collaborates with Lab QA to ensure Quality commitments are met.
* Influences management decisions and acts as a change agent.
* Decision-maker outside of business hours and point of escalation.
Requirements:
* Bachelor's degree in Laboratory Science or related field.
* Minimum 5 years' experience in an analytical function in a GMP setting.
* Previous experience working a shift pattern is an advantage.