Manager, Diphtheria Tetanus Bulk Manufacturing


Reference No. R2729373

Place Title: Supervisor, Diphtheria Tetanus Bulk Manufacturing

Division: DTPPD Bulk

Location: Toronto, Ontario

Sanofi Vaccines

Sanofi’s world vaccines enterprise unit companions with the general public well being, medical and scientific communities to enhance entry to life-protecting vaccines and enhance vaccination protection, whereas striving to develop new and improved vaccines to reinforce well being and well-being.

At Sanofi, we chase the miracles of science to enhance folks’s lives. We consider our cutting-edge science and manufacturing, fueled by knowledge and digital applied sciences, have the potential to rework the follow of medication, turning the inconceivable into potential for tens of millions of individuals.

Place Abstract:

The Course of Upstream Supervisor, DT&PPD Manufacturing serves as the principle technical course of chief for the world associated to gear, high quality, and course of in Diphtheria and Tetanus fermentation. The position supplies management on bettering general efficiency for the upstream fermentation operations. This contains security, compliance, enterprise course of enhancements and operational actions.

Reporting to the Deputy Director, B90 Diphtheria and Tetanus Bulk Manufacturing, the Course of Upstream Supervisor supplies route to the operational group, delivers provide in response to schedule and develops and implements quick and medium time period strategic plans for the upstream manufacturing group. The Course of Upstream Supervisor works intently with B90 Managers to ship adherence to the manufacturing schedule, well timed administration of Deviations, CAPAs and CCRs to make sure steady compliance with security requirements and cGMPs.

The Course of Upstream Supervisor acts as a core member of the B90 Bulk APT, collaborating with a cross-functional group to realize the APT’s goals. 

Key Tasks:


  • Present management to a various group of workers, handle the group by organizing their every day actions, following up, speaking the plan prematurely, guarantee cohesion of the group, rejoice with the group.
  • Information of Excel, Phrase, Outlook and PowerPoint.
  • Every day presence with the group on the store ground is required.
  • Cascade data to and from workers, by verbal (+QDCI for instance) and written communication.


  • Reinforce security mindset of the store ground, determine potential near-misses and different hazards and repair earlier than occasion happens, develop checklists to standardize routine security verifications and good store ground behaviors.
  • Expertise in lean manufacturing administration programs.
  • Sturdy data and familiarity with cGMP practices, with context of pharmaceutical/biologicalmanufacturing. 

High quality:

  • Guarantee SOPs are present and adopted, guarantee BPR and logbooks are correct and reviewed with minimal delay, guarantee root reason behind course of or environmental deviations are recognized, guarantee workers coaching is full and updated.
  • Persistently implement corrective and preventive actions, in addition to course of enhancements.
  • Work with the workers to lower the human error deviations: develop possession of the deviations, enhance the group across the duties for full mistake proof options and enhance checklists.
  • Expertise in validation, aseptic processing, sterilization & disinfection. 


  • Understanding of key actions together with formulations and sterile operations.
  • Guarantee the manufacturing plan and schedule every day to 4 months for the upstream space together with oblique exercise for media washing and sterilizing, at the side of the direct actions of fermentation, taking into consideration the harvesting cleansing and purification schedule.
  • Help execution of venture actions to fulfill the enterprise wants of the location.


  • Develop workers to guarantee a excessive performing group, discovering methods to scale back additional time, present particular person suggestions on workers goals, guarantee sufficient cross coaching of workers. 
  • Personal the fermentation suites and guarantee gear/space is maintained. 
  • Present troubleshooting and problem-solving steerage for every day manufacturing and venture points, and implement preventative/corrective actions. 
  • Help growth of working funds and staffing for operations. 


  • Contain and co-operate with different departments to acquire consensus and guarantee acceptable service ranges.

Key Necessities:

  • Most well-liked post-graduate in Microbiology/Biochemistry/Engineering or Associated Science.
  • Minimal Honors BSc in Microbiology/Biochemistry/Associated Science with expertise and extra enterprise and administration coaching.
  • 36 months in Manufacturing in a pharmaceutical clear room surroundings.
  • 4 years of expertise in managing or supervising a division with greater than 5 workers.
  • Minimal 5-7 years of earlier related expertise is a minimal requirement.
  • Sturdy communication and influencing expertise, venture administration expertise, drawback fixing, robust management and administration functionality.
  • Related industries: Vaccine or Manufacturing Pharmaceutical firm.

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Sanofi is an equal alternative employer dedicated to range and inclusion. Our aim is to draw, develop and retain extremely proficient workers from various backgrounds, permitting us to profit from all kinds of experiences and views. We welcome and encourage purposes from all certified candidates. Lodging for individuals with disabilities required in the course of the recruitment course of can be found upon request.

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