Process Engineer

Amaris Consulting

• $100K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 1-2 years in OSD process engineering or 5 years in general pharmaceutical GMP experience
  • Technical knowledge of granulation, compression, and coating equipment
  • Proficiency with SAP required
  • Capacity to learn proprietary systems and TrackWise QMS
  • Excellent client-facing communication skills
  • Confident representation of operations to clients and auditors
  • Robust technical analysis and documentation capabilities

Responsibilities

  • Act as on-site technical SME for troubleshooting manufacturing issues
  • Generate and maintain GMP technical documentation
  • Serve as direct contact for clients and regulatory auditors
  • Ensure continuity on client initiatives from outgoing engineers
  • Coordinate with technical writers and project leads as needed

Benefits

  • Onsite work environment fostering team collaboration
  • Potential for contract extension beyond initial 6 months
  • No Canadian work experience required to apply
  • No use of AI in recruitment process ensuring human oversight
  • Timely feedback on applications within 45 days
Full Job Description
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, ONWork Mode: Onsite, 5 days/weekDuration: 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.

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