Process Engineering lll (Packaging)
- Mississauga, ON, Canada
$95,000 to $110,000 CAD / year · Full-time
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Job details
- Pay
- $95,000 to $110,000 CAD / year
- Job type
- Full-time
- Apply by
- Experience
- Minimum 8 years relevant pharmaceutical experience in similar roles, with focus on production floor support, technology transfer and Continuous Improvement initiatives.
- Posting language
- English
- Posted
Original job description
Current Vacancy
Who We Are
At CPL, we are passionate about pharmaceutical product development and contract manufacturing. Our aim is to be the top choice CDMO in the non-sterile liquid and semi-solid pharmaceutical products domain and ultimately bring benefits to the customers using our manufactured products.
For more than 30 years CPL has partnered with the world’s leading pharmaceutical companies to provide full-service product development and manufacturing, singularly focused on innovation and efficiency.
We recognize our employees are our number one asset and support their career growth. We also offer a benefits program, deferred profit-sharing plan, paid time off, employee’s assistance program, work/life balance, employee recognition program, on-site parking, discounted gym membership.
Job Summary
Provide technical process engineering expertise to support Manufacturing, Packaging and Maintenance departments.
Manage manufacturing and packaging Capital and Continuous Improvement (CI) projects, including the introduction of new manufacturing and packaging technology, new processes and corresponding qualification/validation activities
Job Responsibilities
- Actively supports the day-to-day operations of the Manufacturing, Packaging and Maintenance departments. Provides senior technical expertise and guidance in resolving issues and champions sustainable improvement opportunities.
- Manages assigned critical capital projects, supports new product launches and is the voice of the Engineering department in all internal and external forums.
- Prepares and executes qualification documents in accordance with GMP and CPL’s Validation Master Plan.
- Develops and actively leads strategic Engineering projects using sound project management principles, including identification, justification, risk assessment, ROI, cost management, time management, scope management and resource management.
- Prepares User Requirement Specifications (URS) for new equipment and participates in FAT (Factory Acceptance Testing) and installation processes.
- Participates in the development of capital budgets, OPEX initiatives and prioritization of Continuous Improvement projects.
- Generates manufacturing and packaging instructions for new/existing products and/or processes by adapting customer processes to CPL’s equipment and operational requirements through data obtained during line and process test runs. Uses gained knowledge to assist in the development and optimization of routings.
- Provides senior engineering support and leads troubleshooting efforts on the production floor with the help of the Maintenance department.
- Participates in customer process optimization and investigations, equipment selection and customer audits/visits.
- Supports operation of Global Track & Trace functions at CPL from customer onboarding through to management of line-level systems / equipment.
- Manages, documents and executes line trial activities.
- Stay abreast of latest process technology developments. Contribute innovation and lean thinking into manufacturing and packaging processes.
- Other duties as assigned.
- Provide technical guidance to junior engineers.
REQUIRED QUALIFICATIONS:
- Bachelor’s Degree in an Engineering discipline.
- Professional Engineer (P. Eng) designation preferred
- Minimum 8 years relevant pharmaceutical experience in similar roles, with focus on production floor support, technology transfer and Continuous Improvement initiatives.
- Good understanding of relevant unit operations in the pharmaceutical industry, their capabilities and associated processes. High preference for liquid and semi-solid dose operations.
- Working knowledge of automated / integrated production equipment and computerized systems.
- Understanding of qualification and validation of equipment, facility and processes. Capable of writing qualification documentation with minimal supervision.
- Proven ability to execute medium- to large-scale projects with minimal supervision.
- Experience managing customers, vendors and contractors with minimal supervision/guidance.
- High problem-solving capabilities, ability to address arising issues and make technical decisions within normally established guidelines with minimal supervision from management.
- Good understanding of application of codes and regulations governing the implementation of process and equipment under OBC, OHSA, Fire Code and MOE.
- Solid understanding of project management principles including project identification, justification, risk assessment, ROI, cost management, time management, scope management and resource management.
- Proficiency in Microsoft Office applications including MS Project.
- Excellent verbal and written English communication skills.
- Demonstrated leadership capabilities/competencies, ability to manage teams and reach goals without formal reporting relationships.
- Office environment (in person) and support in production area.
- Occasional off-shift hours as needed to support production schedule
We thank all applicants for their expression of interest; however, only those selected for an interview will be contacted. No phone calls or agencies please.
More about this job
Responsibilities
Provide senior engineering support to manufacturing, packaging, and maintenance operations, including production-floor troubleshooting, process optimization, and technical guidance to junior engineers. Lead capital and continuous improvement projects, technology transfers, equipment qualification and validation, line trials, and the development of manufacturing and packaging instructions.
Requirements
A bachelor’s degree in an engineering discipline is required, and a Professional Engineer designation is preferred. Candidates need at least eight years of relevant pharmaceutical experience, strong knowledge of production equipment and validation, and the ability to lead projects, solve technical problems, and communicate effectively in English.
Skills
- Pharmaceutical Process Engineering
- Packaging Engineering
- Capital Project Management
- Continuous Improvement
- Technology Transfer
- GMP Compliance
- Qualification And Validation
- Troubleshooting
- Project Management
- Risk Assessment
- Equipment Selection
- Factory Acceptance Testing
- Lean Manufacturing
- Customer And Vendor Management
- Microsoft Project
Benefits
- Deferred Profit-Sharing Plan
- Paid Time Off
- Employee Assistance Program
- Work-Life Balance
- Employee Recognition Program
- On-Site Parking
- Discounted Gym Membership
Visa sponsorship
Not detected in the job text
Categories
- Engineering
- Manufacturing
- Management & Leadership
Keywords
- Pharmaceutical Manufacturing
- Process Engineering
- Packaging
- Capital Projects
- Continuous Improvement
- Technology Transfer
- Good Manufacturing Practice
- Validation Master Plan
- Qualification
- Validation
- Factory Acceptance Testing
- Equipment Installation
- Line Trials
- Production Floor Support
- Troubleshooting
- Liquid And Semi-Solid Dosage Forms
- Automated Production Equipment
- Computerized Systems
- Risk Assessment
- Return On Investment
- Project Management
- Lean Manufacturing
- Global Track And Trace
- Microsoft Office
- Microsoft Project
- Professional Engineer
- Ontario Building Code
- Occupational Health And Safety Act
- Fire Code