1 meilleure offre (project engineer, ashburn on) (à pourvoir)

Automation Engineer
Teva —Whitchurch-Stouffville, ON
- De 98 160 $ à 122 700 $ par an
- Schémas
- CAD
- Ingénierie
- Plan d'actionnariat des employés
- Assurance Invalidité
il y a 9 jours

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Automation Engineer

Teva -
Whitchurch-Stouffville, ON

Postuler dès maintenant

Détails du poste

De 98 160 $ à 122 700 $ par an
Il y a 9 jours

Profil recherché

Étalonnage d'équipement
Veille économique
Génie chimique
Schémas
CAD
Mise en service de systèmes
Ingénierie
Conception de systèmes
Maintenance
Bonnes pratiques de fabrication (BPF)
Soutien technique
Microsoft Office
Bases de données
Esprit d'analyse
Outils d'intelligence d'affaires
Contrôleur logique programmable
Baccalauréat
Amélioration continue
Technologie d'ingénierie
Analytique des données
Contrats
Gestion de budget
Production
Implication dans la phase de mise en service
Électrotechnique
Collaboration interfonctionnelle
Procédures opératoires normalisées (PON)
Compétences en communication
Communication interfonctionnelle

Description complète du poste

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

Our Team, Your Impact

We are seeking a talented and driven Automation Engineer to join our dynamic team. In this role, you will play a critical part in designing, optimizing, commissioning, and troubleshooting automated manufacturing systems to ensure operational excellence, reliability, and efficiency. You will collaborate with cross-functional teams to support manufacturing operations, continuous improvement initiatives, and capital projects while ensuring compliance with regulatory and quality standards.

How You’ll Spend Your Day

Responsibilities include, but are not limited to:

Design, commission, optimize, and troubleshoot computer-controlled processing equipment and automated systems.
Develop, review, and approve hardware, software, and control system designs for manufacturing equipment.
Evaluate and implement process control systems, data acquisition solutions, process monitoring tools, and manufacturing support requirements, including utilities, sensors, controllers, vision systems, equipment calibration, and packaging constraints.
Implement software and hardware upgrades and assess their impact on manufacturing processes, facilities, and operations.
Execute modification and change control procedures in accordance with established protocols.
Program, configure, and troubleshoot PLC and HMI applications for automated process equipment.
Interpret and work with electrical schematics, loop diagrams, and I/O signal documentation.
Analyze operational data and present meaningful insights using Business Intelligence (BI) tools.
Develop and maintain Standard Operating Procedures (SOPs), Preventive Maintenance (PM) procedures, and calibration documentation.
Support the calibration program and collaborate with the calibration team as required.
Provide technical support to Project Engineers, particularly in the areas of process control and automation.
Manage assigned projects from initiation through completion, ensuring objectives, timelines, and budgets are achieved.
Prepare capital project requests, equipment procurement specifications, and vendor contracts in accordance with company guidelines.
Coordinate vendor inspections, Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), equipment installation, and commissioning activities.
Support qualification activities by providing required documentation and technical expertise for IQ, OQ, and PQ protocols.
Ensure systems operate according to validated requirements and remain compliant within the site's change management framework.
Meet project deadlines and complete all required reports and documentation accurately and on time.
Maintain regular communication with the Director of Engineering regarding project status, risks, and schedules.
Adhere to cGMP principles and all applicable company policies, procedures, and regulatory requirements.
Collaborate effectively within cross-functional teams to achieve departmental and organizational objectives.
Demonstrate commitment to the organization's core values and culture.
Perform all work in compliance with established safety, quality, regulatory, and compliance requirements.

Your Skills and Experience

Bachelor's degree in Electrical Engineering, Chemical Engineering, Mechatronics Engineering, Automation Engineering, or a related field. Engineering Technology diploma may also be considered.
Minimum of five (5) years of experience in the design, programming, commissioning, troubleshooting, and maintenance of industrial control systems.
Professional Engineer (P.Eng.) designation or eligibility to obtain licensure is preferred.
Strong understanding of GMP, FDA, ISO standards, validation principles, and compliance requirements within regulated environments.
Proven hands-on experience with PLC and HMI programming, troubleshooting, and support in pharmaceutical, biopharmaceutical, or highly regulated manufacturing environments.
Knowledge of advanced automation technologies, including collaborative robots (cobots), robotics, machine vision systems, Automated Guided Vehicles (AGVs), and automated warehouse systems.
Strong expertise in process control systems and manufacturing automation.
Understanding of cGMP computerized systems, software quality systems, and sanitary equipment design principles.
Proficiency with Microsoft Office applications, data analysis tools, and database management systems; CAD experience is considered an asset.
Strong analytical, problem-solving, project management, and communication skills.
Ability to work independently and collaboratively in a fast-paced manufacturing environment.

How We’ll Take Care of You

At Teva Canada we provide a rewarding and collaborative work experience, with career growth and development opportunities for employees, in a safe and caring environment! The typical hiring range for this position is $98,160-$122,700. The base pay offered may vary depending on job-related knowledge, skills, experience, education, and internal equity. In addition to base salary, this role may qualify for an annual bonus based on employment type. Certain positions may also be eligible for a sales commission structure as part of the overall compensation package. Beyond base pay, Teva also offers a comprehensive suite of wellness and benefits programs tailored to role and employment type, that continue to rank among the best in our industry! Our competitive offerings are designed to provide flexibility, security, and meaningful choices, empowering employees to thrive both personally and professionally throughout their journey with us.

As part of our commitment to well-being, employees may have access to:

Teva Canada’s choices Benefit Plan including Health, Dental, Disability, Life Insurance
Employee Assistance Program & Virtual Health Programs
Retirement Savings Programs
Employee Stock Purchase Plan (ESPP)
Time for yourself or those you care about, through paid time for Vacation, Wellness days, Care/Sick days, Teva Days and Volunteer Days
Education Assistance Program
Recognition programs such as Employee Service Awards
Employee Discounts
And much more!

More exciting details on the specific total rewards offerings to be provided at the offer stage depending on the position and employment type hiring for. This position will fill a current vacancy. Teva Canada may utilize AI- driven insights on skills and capabilities as part of our candidate recruitment process to align candidates with potentially suitable opportunities more effectively. Our recruiters and hiring managers remain the principal decision makers in the recruitment process.

Already Working @Teva?

Make sure to apply through our internal career site on Twist—your one-stop shop for career development

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

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