Supervisor Analytical Operations (Afternoon Shift)

Work Schedule Second Shift (Afternoons) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials Job Description Title: Supervisor Analytical Operations (Afternoon Shift) As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Division/Site Specific Information Position is onsite and will sit/work at the Whitby, Canada site and will support the Drug Product Division at Thermo Fisher Scientific. Discover Impactful Work: Supervise the activities of an Analytical Operations (AO) Group, within Laboratory Operations, ensuring that all Standard Operating Procedures (SOP), current Good Manufacturing Practices (c GMP), current Good Laboratory Practices ( c GLP ) , C orporate   Q uality   S tandards   and client objectives/timelines are achieved.   Supervise a Team of   10-14   Scientists who   are responsible for   the execution of product evaluation/ CofA   release and   commercial S tability testing in support of client projects   and timelines .   A Day in The Life:     Ensure cGMP and Environmental Health & Safety compliance, as well as good laboratory housekeeping   and documentation   practices   of   direct reports.   Provide technical leadership for analytical challenges.   Conduct   weekly   direct report   team huddles   in order to   facilitate   problem solving and communication.  Maintain accountability of the team   for   standard work, compliance, scientific integrity ,   documentation   and project execution.   Convey results of analytical studies to colleagues and clients and provide scientific input with regards to unexpected results, overall product   stability   and formulation development efforts.    Ensure that all AO laboratory documentation within the group   is   completed to the highest quality standards, in compliance with Attributable Legible Contemporaneous Original and Accurate (ALCOA) and documented Right- First - Time   (RFT).   Ensure all testing ( i.e.   raw material, finished product, in-process, intermediate, micro, purified water)   is completed   in accordance   with   approved test methods and   SOP’s .     Ensure   all LIMS Certificate of Analysis ( CofA ); Analytical Release   Form   (ARF) and Control Procedure (CP) are current and   accurate .    Ensure Follow-Up Stability Testing (FUST) and any other commercial Stability stud y testing   are completed on time   to avoid deviations .   Ensure customer complaints are supported as needed.   Ensure   commercial product Out-Of-Specification (OOS) or Unexpected/Out-Of-Trend (OOT) investigations are supported for phase 1 lab testing   and approval of the Lab Incident Records .   Ensure External Lab test results are received   in a timely manner   including any results received from Patheon-Toronto Regional Operations (TRO)   Design and   monitor   progress against the schedules for each Scientist in the   g roup . E nsure that studies are completed   in accordance with   project timelines, On Time Delivery (OTD)   dates   and client expectations.   Supervise the training of all   Scientists   within   the group   to ensure   their   proficiency   and competency i n conducting   studies assigned to them . Each Scientist should be provided with   a