At Septodont, a global leader in dental products and a key player in pharmaceutical development and contract manufacturing (CDMO), we are proud to work every day to improve patients’ health and well-being.
Present in more than 110 countries, the Group relies on the energy, expertise, and passion of 2,600 employees. With 6 international production sites, Septodont combines industrial excellence, technological expertise, and innovation to meet the needs of healthcare professionals worldwide.
In North America, our operations include facilities in Ontario, Quebec, and Pennsylvania. Our Cambridge, Ontario site is home to Novocol Pharma – a thriving center of innovation with over 40 years of expertise in sterile injectable cartridges and combination product manufacturing. Backed by a team of more than 675 dedicated professionals and modern facilities, we deliver high-quality, customer-focused solutions to partners around the world.
Beyond our expertise, our people are our greatest strength. We foster a stimulating work environment where everyone can learn, grow, and build a career that reflects their aspirations, supported by continuous training and internal mobility. As a socially responsible company, we place diversity and inclusion at the heart of our development, convinced that they enhance collective performance and foster human experience.
Joining Septodont means becoming part of a human-scale international group and contributing to a meaningful mission: improving health for as many people as possible. What if your next professional chapter started with us?
We have an opportunity Lead Hand III!
This position is starting at $34/hour.
FUNCTIONSUMMARY:
The Lead Hand III is accountable to the Production Supervisor for all compounding or filling manufacturing activities occurring on the shift. This would refer to the operation of the unit, allocation of resources, execution of development and commercial batches and effective escalation of issues relating to the equipment and work areas, quality concerns or operational deficiencies. In addition, the Lead Hand III will ensure the adequate levels of supply are stocked related to the operation including gowns, operating supplies and other PPE.
The Lead Hand III will be required to be familiar with various format parts, component size variations, compounding tank variations including all peripherals and product specific requirements associated with Pharma manufacturing. Main responsibilities are related to equipment operation, training, documentation, and continuous improvement to meet the Company’s objectives and in accordance with the requirements outlined in the Standard Operating Procedures and Good Manufacturers Practices.
Coordinates shift changeover to ensure machinery and human resources are performing/scheduled optimally. Reports any deficiencies in machinery, materials or human resources immediately to shift supervisor for timely resolution
Maintain engagement with the production schedule to help proactively organize the team for future activities
Acts as a subject matter expert for equipment, product and process related items. Understands the complexity and variation of Pharma related and product specific requirements at line and drives awareness of these items to the team
Supports the introduction of new processes and equipment by becoming an expert with the equipment/process. Participates in the generation of SOPs, guidance documents and training programs to ensure information is properly cascaded through the remainder of the team
Accountable to provide timely and pertinent updates to the Shift Supervisors and Managers
Accountable to produce a quality product, on-time and right the first time. Required to…
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