3 Key Consulting is Hiring a Project Manager Senior, Biopharma Manufacturing (JP10103) Near Edmonton, KY

Job Title: Project Manager Senior, Biopharma Manufacturing (JP10103)Location: Edmonton, Alberta, CANADA T6X2B7Employment Type: ContractBusiness Unit: ACDM Synthetics DP/FDPDuration: 8 months with likely extensionsPosting Date: 04/21/20223 Key Consulting is hiring Senior Project Manager for a consulting engagement with our direct client, a leading global biopharmaceutical company.Job Description:Onsite at Canada location; North of Toronto (site in Whitby, ON, Canada)With minimal supervision, apply process, operational, scientific expertise, basic compliance knowledge, and analytical and troubleshooting skills to support manufacturing operations. Responsibilities include, but are not limited to the following:

Act as technical ADVISOR to manufacturing team
Support the execution of manufacturing/quality systems such as deviations, CAPAs, change controls, procedures, training, and new product introductions
Provide oversight of production runs and closely monitor high risk operations as defined by the risk assessments
Successfully detect, identify & resolve issue/defect through in-place Quality systems
Communicate newly identified risks during operation or in related Quality System documents / procedure / practices
Act as primary client contact while on site for any troubleshooting during production
Escalate as needed per escalation process
Collect information and data as provided by the local team to facilitate effective communication with the extended team
Provide periodic update on the status of the campaign
Identify optimization/improvement opportunities for the future activities

Why is the Position Open?Team need/ backfillTop Must-Have Skill Sets:

Quality records experience; deviation process. etc required
Detailed technical understanding of Oral Solid Dosage (OSD) DP/FDP unit operations
Skilled in performance of GMP production operations
Ability to communicate and collaborate with technical and management staff within manufacturing, process development, and quality
Organizational, technical writing and presentation skills\
Regulatory knowledge and interactions

Day to Day Responsibilities:Including, but not limited to providing oversight of DP and FDP productionEmployee Value Proposition:
Growth/ opportunityRed Flags:Must have GMP Knowledge.Must be able to work with 3rd party vendors/ suppliersInterview process:Pls expect 4-6 interviews:
Groups:
ACDM
QA
Packaging PD
DP-PDWe invite qualified candidates to send your resume to recruiting@3keyconsulting.com. If you decide that you’re not interested in pursuing this position, please feel free to look at the other positions on our website www.3keyconsulting.com/careers. You are welcome to also share this opportunity with anyone you think might be interested in applying for this role.