Lead Hand II

Septodont; Cambridge; On-site; CAD 36,000 - 52,000; Full time

Benefits offered by this job

Shift premium

Job summary

Septodont's Cambridge, Ontario site is seeking a Lead Hand II responsible for equipment repair, maintenance, and ensuring ready supplies for the filling operation. The role emphasizes training, IPQC, and strict adherence to GMP and SOPs.

You will supervise shifts, troubleshoot alarms, review batch records, and support continuous improvement initiatives while maintaining aseptic practices and gowning certification.

Qualifications

• Minimum one year in pharmaceutical manufacturing or related environment.
• Experience in leadership is an asset.
• Strong communication skills, both written and verbal.

Responsibilities

• Coordinate shift changeovers to optimize machinery and staffing.
• Perform operator duties when needed and train new employees.
• Maintain GMP compliance and accurate documentation in batch records.

Skills

Leadership

Communication

Documentation

Troubleshooting

Training

Education

High school diploma

College certification

Tools

AX ERP

Job description

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 for you!Shift Available: Night Shift - Sunday to Thursday - 10pm to 6am - Shift Premium $3/hourThis position is starting at $32/hour, PLUS shift premium.FUNCTION SUMMARY:The Lead Hand II is accountable to the Production Supervisor for all activities relating to the repair and maintenance of equipment and work area. In addition the Lead Hand II will ensure the adequate levels of supply are stocked related to the filling operation including gowns and other PPE. 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 resolutionActively participates in and supports the continuous improvement initiatives projectsPerforms the operator’s duties if necessaryEnsures the availability of component and supplyTakes corrective action to fix documentation errors and to coach the related operators on documentation practicesEnsures that working areas are clean and organizedAssists the other departments if requiredIssues, investigates and rectifies Quality Assurance deviations and other proceduresTroubleshoots equipment alarms and take corrective action and/or involving maintenanceParticipates in revision of departmental SOP’s and other GMP documentsConducts 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 areaEnters accurate AX transactionsAssists in coordinating, planning and scheduling employee work rotationsCompletes and/or reviews documentation entries in batch record and logbooksCoordinates and communicates priorities with other shiftsFollows all Aseptic practices and behavior while involved in Aseptic processesUnderstands the first air principal to avoid cross contamination of products and their componentsUnderstands basic MicrobiologyFollows proper cleaning and sanitization techniquesMaintains annual Gowning CertificationFollows GMP and regulatory requirements, and ensures quality standards are metObserves and supports all safety guidelines and regulationsDemonstrates the Company Mission, Vision and Values Statements, policies, and current standard business practicesPerforms other related duties as requiredBASIC QUALIFICATIONS:EducationHigh school completion, college certification/diploma or working towards completion.Experience1 year experience in pharmaceutical manufacturing or a related environment. Previous leadership experience is an assetDemonstrated leadership and interpersonal skills with the ability to positively interact with interdepartmental teamsAbility to work independently in a fast paced environmentStrong communication skills, both written and verbalWork 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.