Supervisor, Manufacturing
Sanofi is hiring a Supervisor, Manufacturing. Level rates it ; you can apply on Sanofi.
Level's read on this job
- Little AI ●○○○ is how Level rates this role: aI is not part of the work.
- The posting mentions manufacturing, gmp and leadership among its tools and skills.
- Level classes it as a mid-level role.
- Sanofi has 1,100+ other open roles on Level.
AI in this role
Lead the startup and operation of manufacturing areas to produce engineering and commercial batches while ensuring compliance.
Job Title: Supervisor, Manufacturing
Hiring Manager: Manager, Manufacturing
Location: Tuas, Singapore
About the Job
Sanofi Manufacturing and Supply organization is preparing its future through an ambitious program named Modulus. The Modulus Project is at the cornerstone of Sanofi strategy as it aims at creating a new manufacturing concept consisting of a new generation of evolutive multi-product facilities, modular, adaptable and agile, leveraging new disruptive technologies, to better address vaccine business challenges as well as Specialty Care Biologics products. One of these two Modulus is implemented in Singapore in a new Greenfield site, with a design identical to the one in Neuville (France). The facilities will also have highly digitalized and automated capabilities which is a key enabler for operations using technologies such as autonomous guided vehicles (AGVs), cobots and cloud systems.
The manufacturing team in Sanofi Modulus, Singapore is seeking to expand the team and has an open position as Supervisor, Manufacturing, responsible for the operations in either Central Manufacturing Services (CMS) or Process Manufacturing (PM) team.
The role will report to the Manager, Manufacturing. In this role, you will be responsible to lead the startup and operation of the manufacturing areas to produce engineering and PPQ batches with the aim of commercial production. In line with this, you will be responsible to provide field leadership to the team of biotechnologist who will be your direct reports. The working hour of this role is 12-hour rotating shifts (day and night) and also include weekends and public holidays.
The Supervisor, Manufacturing will (not limited to the following):
Ensure compliance with GMP, safety regulations, and company procedures.
Train, develop, and evaluate team members' performance.
Troubleshoot equipment and process issues.
Maintain accurate production records and documentation.
Initiate and implement continuous improvement initiatives.
Manage inventory and resource allocation in the manufacturing operations.
Collaborate closely with cross functional teams to operate the manufacturing process manufacturing process lifecycle and supporting deviation investigations line including management of changes and CAPA implementation, management
As a fronter or Subject Matter Expert (SME) to support the team for regulator inspection audits.
Performance Standards: Duties & Responsibilities
Key Areas
Action Areas, Deliverables and Outcomes
Weightage (Total 100%)
Team Management and Leadership 50%
Hire, train and manage direct team reports.
Manufacturing Operations 50%
Lead and perform operations on the production floor.
Ensure compliance to applicable HSE and quality guidelines.
About You
Pre-requisites
Knowledge, Skills & Competencies / Language
Team management
Self-starter and independent worker who can operate and perform in cross functional setting.
Possess analytical and critical thinking skills with the ability to problem solve and navigate through complexity and ambiguity.
Able to work in fast paced and dynamic conditions with tight timelines.
Excellent analytical, consultative, and diagnostic skills with ability to make sound, data-based business decisions.
Effective communication skills necessary to interact with internal stakeholders (includes strong presentation skills).
Good technical writing skills.
Qualifications / Requirement
Bachelor's Degree or equivalent with at least 8 years of relevant experience.
Biotechnology/Pharmaceutical with At least 2 years of people leadership experience in Manufacturing area.
Experience with cGMP documentation and record maintenance.
Strong troubleshooting, problem solving and prioritization skills are required.
Familiarity and prior working experience with Single Use Systems would be preferred.
Previous work experience in a digitalized and automated facility operated by DeltaV and MES would be preferred.
Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
How we rate this
Supervisor, Manufacturing at Sanofi rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.
Little AI. AI is not part of the work.
- ●●●● Builds AI80 to 100
- ●●●○ Works on AI60 to 79
- ●●○○ Uses AI40 to 59
- ●○○○ Little AI0 to 39
Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.
Prepare for this job
Built from this posting and from similar jobs on Level.
Skills and AI tools this role asks for
Questions you could be asked
- Tell me about a project where manufacturing was part of your work. What did you do?
- Tell me about a project where gmp was part of your work. What did you do?
- Tell me about a project where leadership was part of your work. What did you do?
- Tell me about a project where troubleshooting was part of your work. What did you do?
Adapt your resume
- List these exact terms on your resume: Manufacturing, Gmp, Leadership, and Troubleshooting. An applicant tracking system matches the wording, not the idea.
- Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.
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