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Added 14 mins ago
Principal Geotechnical Engineer
WSP in Canada
Saskatoon, SK
Full-time
…engineering presence across Saskatchewan. As a Principal Geotechnical Engineer , you'll leverage your established industry relationships, reputation, and expertise to develop new client…
Added 14 mins ago
Senior Engineer Digital Power Systems Vancouver
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Full-time
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Added 44 mins ago
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Senior Water Resources Engineer
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Senior Water Resources Engineer
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Added 44 mins ago
Digital Architect – Data - GOAPRDJP00000987
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Added 44 mins ago
Principal Geotechnical Engineer
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Full-time
…engineering presence across Saskatchewan. As a Principal Geotechnical Engineer , you'll leverage your established industry relationships, reputation, and expertise to develop new client…
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Senior Water Resources Engineer
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Digital Architect – Data - GOAPRDJP00000987
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AB · Edmonton, AB
Full-time
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Added 44 mins ago
Digital Architect – Data - GOAPRDJP00000987
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Senior Product Designer - Okta Privileged Access
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Added 1 hour ago
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Added 1 hour ago
GTM Engineer Intern (Remote)
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Amaris Consulting | Part of Mantu

Process Engineer

Whitby, ON, Canada

Job type: Full-time
Apply by: Oct 28, 2026
Posting language: English
Posted: Sep 28, 2026

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Original job description

We are seeking a Process Engineer to support a portfolio of 6–7 commercial-stage pharmaceutical client accounts within an Oral Solid Dose (OSD) manufacturing environment. This role combines process engineering expertise, GMP documentation, and technical subject matter expertise, with direct collaboration with clients and regulatory stakeholders. The position is primarily desk-based, with most of the time focused on technical analysis, GMP documentation, and client and regulatory correspondence. Floor presence is limited and primarily required for escalated troubleshooting.

Location: Whitby, ON

Work Mode: Onsite, 5 days/week

Duration: 6 months, with possible extension

Key Responsibilities

Act as the on-site technical SME for an assigned client portfolio, troubleshooting manufacturing issues escalated from the floor that operations cannot resolve independently (occasional floor presence, approximately 30 minutes per day)
Generate and maintain GMP technical documentation, including batch records, technical and investigation reports, feasibility protocols, and scale-up reports
Serve as the direct technical point of contact for clients and regulatory/quality auditors, answering process- and equipment-related questions on behalf of operations
Maintain continuity on active client initiatives handed off from the outgoing process engineer
Coordinate as needed with technical writers (documentation support) and technical project leads (scale-up and tech transfer projects)

Qualifications

1–2 years of hands-on OSD process engineering or manufacturing experience, OR approximately 5 years of general pharmaceutical GMP experience (e.g., liquid dose, sterile) for candidates without direct OSD background
Technical knowledge of core OSD unit operations and equipment, including: Granulation: fluid bed, high shear, roller compaction; Compression: tablet presses (e.g., Elizabeth Hata, Korsch) and capsule filling; Coating: film/cosmetic coating, O'Hara pans.
SAP experience required
Comfort ramping up on proprietary systems and the QMS platform (TrackWise); training provided at start
Strong client-facing communication skills
Ability to represent operations confidently to external clients and auditors
Strong technical analysis and documentation abilities

Expected Compensation Range:

100K. The final compensation offered will be determined based on the candidate’s level of experience, skills, and qualifications, in compliance with applicable pay transparency requirements.

Canadian Experience Requirement:

No Canadian work experience is required for this position. Candidates are encouraged to apply regardless of previous Canadian experience.

Artificial Intelligence (AI) Disclosure:

No Artificial Intelligence (AI) tools are used in the screening, assessment, or selection of candidates for this position. All stages of the recruitment process are conducted by human recruiters and hiring managers.

Statement Regarding Job Vacancy:

This position is a Job creation, created to support ongoing project needs.

Recruitment Process & Feedback Timeline:

Candidates will receive feedback on their application within a maximum of 45 days from the date of application or from their most recent interview stage.

Why choose us

An international community bringing together more than 110 different nationalities
An environment where trust is central: 70% of our leaders started their careers at the entry level
A strong training system with our internal Academy and more than 250 modules available
A dynamic work environment that frequently comes together for internal events (afterworks, team buildings, etc.)
Amaris Consulting promotes equal opportunities. We are committed to bringing together people from diverse backgrounds and creating an inclusive work environment. In this regard, we welcome applications from all qualified individuals, regardless of sex, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

Apply About employer

More about this job

Responsibilities

Serve as the technical subject matter expert for assigned pharmaceutical client accounts, troubleshooting escalated manufacturing issues and responding to client and auditor questions. Prepare and maintain GMP documentation, support ongoing client initiatives, and coordinate documentation, scale-up, and technology transfer activities.

Requirements

Candidates need either 1–2 years of hands-on OSD process engineering or manufacturing experience, or approximately five years of general pharmaceutical GMP experience. Required qualifications include SAP experience, knowledge of OSD equipment and unit operations, strong technical documentation and analysis skills, and confidence communicating with clients and auditors.

Skills

OSD Process Engineering
Pharmaceutical Manufacturing
GMP Documentation
Process Troubleshooting
Granulation
Tablet Compression
Capsule Filling
Coating
SAP
TrackWise
Technical Analysis
Client Communication
Regulatory Audits
Batch Records
Scale-Up
Technology Transfer

Visa sponsorship

Not detected in the job text

Keywords

Oral Solid Dose
Pharmaceutical Manufacturing
Good Manufacturing Practice
Process Engineering
Batch Records
Technical Reports
Investigation Reports
Feasibility Protocols
Scale-Up Reports
Fluid Bed Granulation
High-Shear Granulation
Roller Compaction
Tablet Presses
Capsule Filling
Film Coating
Cosmetic Coating
O'Hara Coating Pans
SAP
TrackWise
Quality Management System
Troubleshooting
Regulatory Audits
Client Communication
Scale-Up
Technology Transfer

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