Sanofi

Process, Plant and C&Q Manager

Sanofi$102K — $152K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor of Engineering, Science, or comparable education
  • PMP, P.Eng, or related certifications preferred
  • 5+ years relevant experience in C&Q, construction, and large projects
  • Proven leadership in coaching technical teams and change management in C&Q
  • Strong knowledge of C&Q Lifecycle Approach, validation, and risk-based methodology
  • Familiarity with pharmaceutical industry regulations (GMP, FDA)
  • Working knowledge in biotech manufacturing processes, particularly downstream operations

Responsibilities

  • Lead investigations and develop corrective action plans for disruptions and deviations
  • Support design, construction, and startup for equipment on Tier 3 projects
  • Act as a subject matter expert during audits and ensure C&Q compliance
  • Provide technical input for cross-functional engineering projects
  • Liaise with Global Engineering on construction safety for major projects
  • Collaborate on resource planning and vendor selection for site priorities
  • Drive continuous improvement initiatives and identify operational efficiencies

Benefits

  • Comprehensive employee benefits programs
  • Opportunity for professional development
  • Collaborative and cross-functional work environment
  • Contributions to a global network impacting healthcare
  • Work on high-impact capital projects in the life sciences sector
Full Job Description

Location: Toronto, ON

About the Job

The Process, Plant and C&Q (PPC) Manager leads, provides leadership, direction and oversight to all external and internal Process and C&Q resources for Tier 3 (

Main Responsibilities:

  • Lead investigations & develop CAPAs for unplanned disruptions, breakdowns, and deviations
  • The PPC Manager supports design, construction and mechanical completion and start-up for facility and equipment on Tier 3 projects; the incumbent will ensure C&Q planning, strategy and executions are completed meeting defined budgets and timelines
  • Act as an SME for quality-related discussions during audits/inspections and provide support to Capital Projects as required; ensure C&Q standards are in compliance with regulatory requirements at all times
  • Lead technical input on projects and cross functional support for maintenance and reliability teams on engineering aspects of existing facilities.
  • This position is the primary liaison with Global Engineering for all construction safety in scope of Tier 1 and 2 projects (>5MEuro) and ensures local regulations as well as Global Minimum Requirements are followed
  • Working with ETS RMO for robust resource planning of internal and externals to ensure projects are resourced and skilled to execute on site priorities, including where applicable statements of work and vendor selections
  • Strong collaboration with Project Management, Quality, Reliability, Automation, Maintenance, HSE, Operations and support functions to achieve deliverables.
  • Collaborate with Legal and Procurement teams to ensure protections and savings for the Toronto site in contractual relationships with external suppliers
  • With consideration for efficiency, safety and quality, the PPC Manager will lead department continuous improvement initiatives and identify improvement opportunities for critical systems
  • Represent the assigned Capital Projects and business as needed in various executive/management committees as required.
  • Participate in applicable COPs and support project lessons learned to share with network
  • The PPC Manager supports front-end studies and feasibility for Tier 1 and 2 projects from a PPC perspective
  • The Document Control group resides within the organization of the PPC Manager; all site drawings, project drawings, turnover packages, both GxP and non-GxP are managed by this team
  • Supports Site Master Planning with collection of utility data, management of site plan, drawing support, site infrastructure lifecycle management, etc.
  • Team development, including maintenance of skills matrices, cross functional training initiatives and routine performance review


HSE REQUIREMENT
  • Supports all external contractor safety training
  • Ensures local regulations are understood and followed on Tier 1 and 2 projects
  • Works in collaboration with Maintenance to ensure a robust permitting program
  • Responsible for SME input to HSE Construction policies on Toronto site and contributor to Global Minimum Requirements safety standards
  • Participates in various technical HSE assessments during the project as required; every reasonable precaution is taken to ensure the health and safety of staff and contractors
  • Participates in the investigation of incidents and work-related illnesses
  • Responds promptly to all health and safety concerns or incidents and completes the appropriate documentation in a timely manner
  • Advises staff and/or contractors of any potential or actual health, safety and or environmental hazard of which they are aware
  • Ensures that protective equipment and clothing required is used by staff
  • Works within the policies, procedures and regulations as required by the Company and under the Occupational Health and Safety Act.


About You

  • Bachelor of Engineering, Science or comparable education
  • PMP, P.Eng or other related certifications are preferred.
  • 5+ years of relevant experience in executing and managing C&Q, construction, large projects, equipment start-up and commissioning, specifically using risk-based approaches in line with current industry best practices
  • Demonstrated success leading and coaching technical teams to achieve desired technical results, particularly change management within the C&Q space
  • Strong Knowledge of C&Q Lifecycle Approach with understanding of validation using risk-based approach
  • Knowledge of the pharmaceutical industry including GMP, FDA and regional/country authorities' guidelines
  • Working knowledge of unit operations typically used in biotech and vaccine manufacturing, specifically downstream operations of bulk manufacturing including aseptic formulation, filling, inspection and packaging etc. is desirable
  • Knowledge of GxP facility finishes, process and building control systems is an asset
  • Knowledge of utility design (WFI, PW, clean steam, plant steam, clean compressed air, etc.) is an asset
  • Demonstrated success working across organizations in a highly cross-functional team environment


Competencies

  • Demonstrated leadership experience
  • Critical thinking is a must with a strong desire to challenge the status quo
  • Excellent communication skills (written and verbal) to support interactions with senior leadership, inspectors and external vendors
  • Strong interpersonal skills with demonstrated stakeholder management, conflict resolution in group dynamic
  • Strong organizational skills and ability to deal with conflicting priorities


Applications received after the official close date will be reviewed on an individual basis.

This position is for a current vacant role that is now open for applications.

AI Usage

"Artificial Intelligence" refers to any systems that use automated processes, including algorithms and machine learning, to analyze data and make predictions, inferences, decisions, or recommendations without direct human involvement. These systems may process personal information to identify patterns, improve services, or support decision-making. The Company may use Artificial Intelligence for purposes including, but not limited to, resume screening and hiring, scheduling interviews or meetings, conducting surveys, matching skills with potential job openings, interview scoring, ensuring compliance with regulations applicable to our industry, and activities related to performance evaluation. Information collected and processed by the Company's Artificial Intelligence systems may include the personal information detailed above and calendar availability. It excludes the information collected and processed for monitoring purposes. You should contact Human Resources if you have a question or concern regarding your personal information. You can also contact Canada's Privacy Officer via Sanofi's data subject request portal, Data Subject Rights Webform. The Data Subject Rights Webform can also be used to request access or correction of your personal information and file a complaint.

North America Applicants Only

The salary range for this position is:
102,600.00 - 152,600.00 (Includes target bonus)
Final compensation will be determined based on demonstrated experience, skills, location, and other relevant factors. Employees may be eligible to participate in Company employee benefits programs, and additional benefits information can be found through the (CA)LINKOR (US) LINK.

La fourchette salariale pour ce poste est la suivante:
102,600.00 - 152,600.00 (Comprend le bonus cible)
La rémunération finale sera déterminée en fonction de l'expérience démontrée, des compétences, du lieu de travail et d'autres facteurs pertinents. Les employés peuvent être admissibles à participer aux programmes d'avantages sociaux de l'entreprise, et des informations supplémentaires sur les avantages sociaux peuvent être trouvées via le lien

About Sanofi

Sanofi is a global pharmaceutical company that specializes in the research, development, and manufacturing of prescription drugs and vaccines. The company operates in over 170 countries and has a diverse portfolio of products that includes treatments for diabetes, cancer, cardiovascular disease, and rare diseases. Sanofi is committed to improving global health and has a strong focus on innovation and sustainability. The company has received numerous awards for its research and development efforts and is recognized as a leader in the pharmaceutical industry.
Learn more about Sanofi
Market Cap
$121.6 billion
Industry
Net Income
$12.3 billion
Founded
1990
5 Year Trend
+2.5%
Revenue
$37.3 billion
NASDAQ

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