Onsite Process Engineer in Whitby
Job in
Whitby, Oshawa, Ontario, Canada
Listed on 2026-10-03
Listing for:
AMARIS GROUP SA
Full Time
position Listed on 2026-10-03
Job specializations:
-
Pharmaceutical
Validation Engineer, Pharmaceutical Manufacturing, Pharma Engineer
Job Description & How to Apply Below
Contribute your process engineering expertise with Amaris Consulting as a key onsite Process Engineer in Whitby, Ontario. Engage in GMP documentation, technical analysis, and direct client support daily.
This role targets candidates with 1-2 years in OSD manufacturing or 5 years in general pharmaceuticals. You will manage GMP documentation and work closely with clients and regulatory stakeholders. Your troubleshooting skills will be crucial as you navigate technical inquiries and support operational excellence.
Key Responsibilities:
• Serve as the on-site technical SME for assigned clients
• Generate and maintain GMP technical documents and reports
• Act as the direct contact for clients and auditors
• Support active initiatives and manage documentation handovers
• Collaborate with technical writers on project needs
Requirements:
• 1-2 years of OSD experience or 5 years in GMP roles
• Strong knowledge of OSD unit operations
• SAP proficiency is required
• Excellent client-facing communication skills
• Ability to confidently support external stakeholders
Utilize your engineering skills to ensure operational efficiency and compliance for Amaris’s clients in the pharmaceutical space.
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