The Manufacturing Engineer will be responsible for assigned duties related to the design, procurement, installation, commissioning and qualification of new pharmaceutical processes and equipment. The Manufacturing Engineer is responsible for commissioning manufacturing systems and inspecting the construction and operation of the equipment. Working closely with maintenance, the engineer will provide sound advice as a subject matter expert. This position will ensure all projects are delivered to meet the project timelines, budgets and applicable quality standards (GXP, ISO, ICH) as well as the applicable regulatory legislation (OHS, CSA, NFPA, CEPA, etc).
- Prioritizing and executing assigned project deliverables, including adherence to budgets and schedules, coordinating project startup, commissioning and qualification activities with internal and external groups.
- Startup of new process equipment and instrumentation, troubleshooting equipment and instrumentation during commissioning activities.
- Assembling and reviewing Turn Over Packages (TOP) for systems and equipment. Developing Equipment Qualification protocols and execution of these protocols. Data collection and statistical analysis.
- Developing and updating ACAD drawings. Reviewing and updating "As Built" drawings in coordination with outside contractors.
- Coordinating project startup, commissioning and validation activities with internal and external groups.
- Supporting trades people (electrical, mechanical, and structural) by providing advice or guidance.
- Conferring with vendors to determine product specifications, purchase equipment, materials or parts, materials of construction (“MOC”) and evaluate products according to quality standards.
- ·Processing, equipment and engineering improvements/modifications to existing manufacturing equipment. This includes mechanical, electrical and instrumentation installation and improvements.
- ·Researching technical information for the installation, installation, maintenance, and operation of instruments and equipment. Determining the critical testing requirements for instrumentation and equipment prior to qualification.
- ·Assisting maintenance department with repair, calibration, and sourcing replacement parts, as required.
- ·Participating in project meetings between engineering, manufacturing and client.
- Participate in P&D, HAZOP, PHA and other design reviews
- Organizing project paperwork, drawings and files
- ·Additional duties assigned, based on business needs and the department supervisor’s request
Education:
- Bachelor of Science in Engineering (Mechanical/Chemical preferred)
- Six Sigma or Lean Certification would be an asset
- PMP is considered an asset
- Red Seal trade or CET designation considered an asset
Experience:
- 5+ experience in a pharmaceutical manufacturing or similar regulated environment.
- Hands on experience with the starting up and commissioning instruments and process equipment.
- Possesses financial acumen, understands business metrics, and how to impact results. Ability to communicate effectively, both written and orally.
- Basic understanding of fire and building codes and applicable quality and regulatory standards.
Preferred Skills/Qualifications:
- Ability to communicate effectively with departments and personnel.
- Excellent computer skills; including Excel, Word, MS Project and AutoCAD.
- Ability to anticipate issues and trends which could impact clients and projects.
- Energetic team player but able to work effectively independently.
- Ability to function effectively under ongoing pressure and flexibility to change.
- Enthusiastic and willing to expand on responsibilities and professional abilities.
- Project management experience would be an asset.
Additional Details
This job has a full time weekly schedule.The full-time equivalent pay range for this position is $82,882.00 - $129,503.00/yr CAD plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locationsAgilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.Travel Required: OccasionalShift: DayDuration: No End DateJob Function: ManufacturingSkills Required
- Bachelor of Science in Engineering (Mechanical or Chemical preferred)
- 5+ years' experience in pharmaceutical manufacturing or similar regulated environment
- Hands-on experience with startup and commissioning of instruments and process equipment
- Ability to communicate effectively, both written and orally
- Possesses financial acumen and understands business metrics
- Basic understanding of fire and building codes and applicable quality and regulatory standards (GxP, ISO, ICH)
- Excellent computer skills, including Excel, Word, MS Project and AutoCAD
- Six Sigma or Lean Certification
- PMP certification
- Red Seal trade or CET designation
- Project management experience
Agilent Technologies Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Agilent Technologies and has not been reviewed or approved by Agilent Technologies.
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Retirement Support — The core U.S. package highlights a generous 401(k) match as a strength. Retirement programs are positioned as competitive within the company’s total rewards.
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Equity Value & Accessibility — An Employee Stock Purchase Plan at a discount provides accessible equity and augments total compensation. Ownership opportunities are presented as a notable advantage alongside retirement benefits.
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Leave & Time Off Breadth — Flexible Time Off, company holidays, a personal holiday, and paid volunteer time create a broad leave offering. Time off can accrue into multiple weeks in the first year, supporting flexibility.
Agilent Technologies Insights
What We Do
Analytical scientists and clinical researchers worldwide rely on Agilent to help fulfill their most complex laboratory demands. Our instruments, software, services and consumables address the full range of scientific and laboratory management needs—so our customers can do what they do best: improve the world around us. Whether a laboratory is engaged in environmental testing, academic research, medical diagnostics, pharmaceuticals, petrochemicals or food testing, Agilent provides laboratory solutions to meet their full spectrum of needs. We work closely with customers to help address global trends that impact human health and the environment, and to anticipate future scientific needs. Our solutions improve the efficiency of the entire laboratory, from sample prep to data interpretation and management. Customers trust Agilent for solutions that enable insights...for a better world.
