Chemist I

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 18-month contract opportunity for a Chemist I.

Location: 25 Wolseley Court, Cambridge

Employment Type: Contract (18 months)

Schedule: Monday – Friday, 2:00 pm - 10:00 pm

Hours: 40 per week

Pay: $30.45/hour

FUNCTION SUMMARY:

The Chemist I position is an entry-level position and is accountable to the Department Supervisor. The Chemist I is responsible for performing various analytical activities associated with incoming materials, bulk, finished products, stability and complaints testing.

PRIMARY DUTIES AND RESPONSIBILITIES:

• Perform routine and non-routine analytical testing of incoming materials, in-process samples, bulk product, finished product, stability samples, complaints and other assigned samples in accordance with approved methods, specifications and internal procedures.
• Conduct chemical, functional and compendial testing using appropriate laboratory techniques, instrumentation and approved references, including internal methods and applicable pharmacopeial standards.
• Complete testing for special studies, investigations, validation activities, bulk hold studies, cleaning validation and process validation samples as assigned.
• Review analytical data and testing performed by other analysts, ensuring results are accurate, complete and compliant with GMP, data integrity and quality requirements.
• Maintain, calibrate and use laboratory equipment and instrumentation in accordance with approved procedures and safety requirements.
• Notify management of deviations, out-of-trend, suspect or out-of-specification results in a timely manner and support related investigations, documentation and follow-up actions.
• Support internal and external audits by providing records, technical information and laboratory support as required.
• Perform analytical method transfer activities from CDMO and R&D laboratories to the Stability and Analytical Services department, as assigned.
• Follow all GMP, regulatory, quality, safety and company requirements, including current policies, procedures, mission, vision and values.
• Perform other related duties as assigned.

BASIC REQUIREMENTS:

Education

• Degree or diploma in Chemistry or related discipline.

Experience

• One to two years of experience in pharmaceutical or related industry is an asset.
• Strong attention to detail.
• Proven analytical skills with the ability to solve problems.
• Proficient time management skills with the ability to manage multiple priorities.
• Ability to work in a self-directed team environment.
• Proficiency with Microsoft Office application especially Excel.
• Experience with Empower and LIMS is an asset.

What we Offer:

• Excellent compensation/benefits package
• Discounted gym memberships

• Programs supporting work life balance (EAP)
• Corporate Discounts and PERKS

• Employee recognition program

• Social events and spirit days
• Paid time off
  

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.