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 international 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 boost well being and well-being.

At Sanofi, we chase the miracles of science to enhance individuals’s lives. We imagine our cutting-edge science and manufacturing, fueled by information and digital applied sciences, have the potential to rework the apply of medication, turning the inconceivable into doable for hundreds of thousands of individuals.

Place Abstract:

The Course of Upstream Supervisor, DT&PPD Manufacturing serves as the primary technical course of chief for the realm associated to tools, high quality, and course of in Diphtheria and Tetanus fermentation. The function gives management on enhancing total efficiency for the upstream fermentation operations. This consists of 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 gives route to the operational crew, delivers provide based on schedule and develops and implements quick and medium time period strategic plans for the upstream manufacturing crew. 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 crew to realize the APT’s targets. 

Key Tasks:


  • Present management to a various group of staff, handle the crew by organizing their day by day actions, following up, speaking the plan upfront, guarantee cohesion of the crew, rejoice with the crew.
  • Information of Excel, Phrase, Outlook and PowerPoint.
  • Each day presence with the crew on the store ground is required.
  • Cascade data to and from employees, via 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.
  • Robust information 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 employees coaching is full and updated.
  • Persistently implement corrective and preventive actions, in addition to course of enhancements.
  • Work with the employees 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 day by day to 4 months for the upstream space together with oblique exercise for media washing and sterilizing, together with the direct actions of fermentation, taking into consideration the harvesting detoxing and purification schedule.
  • Help execution of venture actions to satisfy the enterprise wants of the location.


  • Develop employees to guarantee a excessive performing crew, discovering methods to cut back extra time, present particular person suggestions on employees targets, guarantee enough cross coaching of employees. 
  • Personal the fermentation suites and guarantee tools/space is maintained. 
  • Present troubleshooting and problem-solving steering for day by day manufacturing and venture points, and implement preventative/corrective actions. 
  • Help improvement of working price range and staffing for operations. 


  • Contain and co-operate with different departments to acquire consensus and guarantee applicable 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 staff.
  • Minimal 5-7 years of earlier related expertise is a minimal requirement.
  • Robust communication and influencing expertise, venture administration expertise, drawback fixing, sturdy management and administration functionality.
  • Related industries: Vaccine or Manufacturing Pharmaceutical firm.

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Sanofi is an equal alternative employer dedicated to variety and inclusion. Our objective is to draw, develop and retain extremely gifted staff from various backgrounds, permitting us to learn from all kinds of experiences and views. We welcome and encourage purposes from all certified candidates. Lodging for individuals with disabilities required throughout the recruitment course of can be found upon request.

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