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?
This position is starting at $30/hour PLUS shift premium.
Work Authorization: Applicants must be legally authorized to work in Canada for the duration of employment. This position is not eligible for employer-sponsored immigration support.
FUNCTION SUMMARY:
The Lead Hand 1 is accountable to the Production Supervisor for all activities relating to the operation, repair and maintenance of equipment and work area. In addition the Lead Hand 1 will ensure the adequate levels of supply are stocked related to the operation. Main responsibilities are related to equipment operation, training, documentation, and in-process IPQC testing to meet the Company’s objectives and in accordance with the requirements outlined in the Standard Operating Procedures and Good Manufacturers Practices.
PRIMARY DUTIES AND RESPONSIBILITIES:
Coordinates shift changeover to ensure machinery and human resources are optimal. Reports any deficiencies in machinery, materials or human resources immediately to shift supervisor for timely resolution
Actively participates in and supports the continuous improvement initiatives projects
Performs the operator’s duties if necessary
Ensures the availability of component and supply
Takes corrective action to fix documentation errors and to coach the related operators on documentation practices
Ensures that the area is clean and organized
Assists the other departments if required
Issues, investigates and rectifies Quality Assurance deviations and other procedures
Responds to and troubleshoots equipment alarms and take corrective action and/or involving maintenance
Participates in revision of departmental SOP’s and other GMP documents
Conducts on-the-job training including review of related SOP’s for new employees. Works with Production Supervisors and Production Manager to identify/solve any production problems and training needs in the area
Enters accurate AX transactions as it relates to the job duties
Assists in coordinating, planning and scheduling of employee work rotations
Completes and/or reviews documentation entries in batch record and logbooks
Coordinates and communicates priorities with other shifts
Follows GMP and regulatory requirements and ensures quality standards are met
Observes and supports all safety guidelines and regulations
Demonstrates the Company Mission, Vision and Values Statements, policies, and current standard business practices
Performs other related duties as required
BASIC REQUIREMENTS
Education
Experience
1 year experience in pharmaceutical manufacturing or a related environment. Previous leadership experience is an asset
Demonstrated leadership and interpersonal skills with the ability to positively interact with interdepartmental teams
Ability to work independently in a fast paced environment
Strong communication skills, both written and verbal
Analytical and problem solving skills
Ability to work on all shifts
Work Authorization: Applicants must be legally authorized to work in the country where the position is based for the duration of employment. This position is not eligible for employer-sponsored immigration support.
We are committed to diversity and inclusion, and thank all applicants in advance; however, we will be corresponding only with those selected for an interview.
In accordance with the Ontario Human Rights Code and the Accessibility for Ontarians with Disabilities Act, we are committed to providing an inclusive and barrier free recruitment and selection process.
Recruitment Fraud – please be aware of recruitment fraud. Novocol Pharmaceutical of Canada Inc. will never ask for banking information, money or any personal information up front. We will only respond to official applications submitted through our careers site. In addition, we will only use official corporate e-mail addresses (septodont.com or novocolpharma.com) to communicate with applicants. Should you be contacted without submitting an application, please delete the message and advise your e-mail provider.
