Analyst III, QC Analytical

Emergent BioSolutions•Canton, MI

21h

About The Position

This is a laboratory testing position with the major responsibilities include daily testing per SOP, protocol-driven non-routine testing, peer data review, writing/revising standard operating procedures, scheduling lab activities, investigating aberrances and providing/implementing compliant solutions, technical writing, and general laboratory maintenance and upkeep. Emergent is a leading public health company that delivers protective and life-saving solutions to communities around the world. Here, you will join passionate professionals where our culture is informed by our values and commitment to protecting and saving lives.

Requirements

Has core understanding of applicable compliance/guidance/regulations (ISO, USP, FDA, EU).
Demonstrates proficiency in moderately complex methods such as ELISA, Cell Culture, Plaque assays, CCIT, KF, pH, etc.
Bachelors or Master’s degree in a scientific discipline
Minimum of 5 years of related experience
Hands-on experience with one or more assays and instruments: cell-based toxin neutralization assays, animal handling and dosing, and cell culture
Strong technical and communication skills: oral/written and listening
Personal Competencies: Self-awareness, Integrity, Team Player, Creative, and Flexible.
Computer skills (MS Office, JMP statistical software, Visio, MS Project)

Responsibilities

Executes laboratory tests and other lab activities to ensure timely delivery of results to internal and external customers.
Work with Management to coordinate scheduling of laboratory activities
Ability to Investigate and determine Root Cause associated with laboratory deviations.
Executes Change Controls, CAPAs, and Effectiveness Checks
Executes validation studies; obtain and interpret validation data.
Maintains laboratory equipment as per established procedure
Initiates change and continuous improvement using LEAN practices such as 5S and Kaizen.
Works with facilities/metrology to conduct and document execution of work orders to ensure GMP compliant state of labs and equipment.
Uses GMP and scientific expertise to lead internal (department and site) audit activities.
Performs as supporting personnel and/or acts as lead under guidance of management or higher level scientific personnel.
May provide guidance to lower level personnel.
Performs laboratory instrument calibration in accordance with established procedures.
Represents QC in vendor relations, including contract support and working with vendors during validation (IOPQ) and calibration.
May perform scheduling to ensure critical QC metrics are consistently met for product turnaround times.
Reviews and Verifies QC data.
Author/revise and contributes test methods; SOPs; specifications; protocols, technical studies or reports.
Author laboratory investigations and non-conformance.
Supports CAPA and change control through participation in project planning and collaboration.
Works on problems of diverse scope requiring evaluation of identifiable factors.
Exercises judgment within defined procedures and practices to determine appropriate action.
Receives no instruction on routine work, general instructions on new assignments.
Actively participate in self-development
Follow through on commitments, Situational Leadership or additional accountability tools
Able to complete required tasks and associated documentation with minimal error
Maintain positive attitude in a changing work environment
Effectively communicate with all levels of manufacturing and support staff
Actively participate in department / level meetings
Escalate issues through the proper channels
Live the Core Values