Careers

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Innovotech aims to empower health product companies to turn innovation into impact through rigorous, science-based data. We’re a team of passionate thinkers and creative problem solvers who thrive on collaboration and curiosity.

Our Team:

Works at the forefront of practical research and technology, solving real-world problems for our clients
Brings ideas and expertise to help shape solutions that impact health technology products
Relies on diverse perspectives, quality and rigorous work, with freedoms to explore new possibilities
Is a talented and unified group of professionals who support, inspire, and celebrate our successes

Current Job Opportunities

Junior Laboratory Analyst

The Opportunity

We are seeking a motivated and detail-oriented Junior Laboratory Analyst to join our analytical laboratory team. This entry-level opportunity is ideal for a recent graduate or early-career professional with a strong interest in analytical chemistry and laboratory sciences.

Working under the guidance of experienced analysts, the successful candidate will perform routine chemical testing, support laboratory operations, maintain analytical instrumentation, and contribute to the quality systems that ensure compliance with applicable regulatory requirements. This role offers excellent hands-on experience with analytical techniques, laboratory instrumentation, and quality systems within a regulated environment.

Key Responsibilities

Conduct routine analytical testing of samples in accordance with approved Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMP), and established test methods.
Prepare samples, reagents, standards, and solutions required for analytical testing.
Accurately record, review, and report laboratory data and test results.
Support microbiological testing activities as required under supervision.
Participate in laboratory investigations and troubleshooting activities related to analytical results and laboratory processes.
Perform routine maintenance, calibration, verification, and validation activities on laboratory instrumentation and equipment.
Assist with troubleshooting analytical instruments and coordinating service requirements.
Ensure analytical equipment is maintained in a qualified and operational state.
Maintain accurate laboratory records, logbooks, and controlled documentation.
Work in accordance with GMP requirements and laboratory quality standards.
Develop and maintain familiarity with applicable regulatory guidance and compendial requirements, including ICH, USP, FDA, EMA, and Health Canada regulations.

Qualifications

Diploma or Bachelor’s degree in Chemistry, Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline.
Strong attention to detail and commitment to data accuracy and integrity.
Excellent problem-solving and organizational skills.
Effective written and verbal communication skills.
Ability to work independently while contributing positively to a team environment.
Willingness to learn new laboratory techniques, instrumentation, and quality processes.

Quality Assurance Assistant

The Opportunity

We are seeking a detail-oriented and motivated Quality Assurance Assistant to join our growing team. This role provides essential support to the quality system by managing documentation, tracking samples and materials, maintaining quality records, and assisting with investigations and audits. The successful candidate will play a key role in ensuring compliance with internal procedures and applicable regulatory requirements.

This position is ideal for someone who enjoys working in a structured environment, has strong administrative and organizational skills, and is interested in quality systems within a regulated industry.

Key Responsibilities

Receive, log, track, and organize incoming samples.
Prepare and distribute testing reports and quality documentation.
Receive materials and assist with equipment commissioning activities.
Issue, process, and maintain controlled documentation, including:
- Standard Operating Procedures (SOPs)
- Controlled Forms
- Equipment Logs
Maintain and update Quality Assurance databases and records.
File, archive, and organize quality documentation in both electronic and paper formats.
Assist with internal and external audits by gathering and organizing required documentation.
Collect documentation and trend data for investigations and quality system reports.
Support the completion of quality system records, including:
- Deviations
- Out-of-Specification (OOS) investigations
- Corrective actions and investigations
Monitor and remain current with applicable regulatory requirements and guidance documents, including Health Canada, FDA, ICH, USP, and EP standards.
Coordinate shipping, scanning, copying, shredding, and other administrative activities.
Order and maintain inventory of office and department supplies.
Provide general administrative support to the Quality Assurance team as required.

Qualifications

Diploma or certificate in a science, quality, business administration, or related field, or an equivalent combination of education and experience.
Strong attention to detail and commitment to accuracy.
Excellent organizational and document management skills.
Proficiency with Microsoft Office applications, particularly Word, Excel, and Outlook.
Strong written and verbal communication skills.
Ability to manage multiple priorities and meet deadlines.
Ability to work independently as well as collaboratively within a team.

We’re always interested in meeting people who are curious about the work we do.
If you don’t see a role that fits today, introduce yourself below.

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