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Added 10 mins ago
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Senior Project Manager - Airport
AtkinsRéalis
AB · Edmonton, AB
- Full-time
…and heliport infrastructure. Based in Edmonton, Alberta, this senior role supports complex aviation projects across Canada, combining technical excellence, project leadership, and…
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PC
Project Coordinator Traveling - Ontario
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- Full-time
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- Temporary
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Added 41 mins ago
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- Full-time
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Added 41 mins ago
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Manager of Pharmacy
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Senior Chemist
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Mississauga, ON
- $40 to $45 USD / hour
- Contract
Immediately report to manager any delays in testing or if tasks cannot be completed.
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Halifax, NS · Toronto, ON · Waterloo, ON · Montreal, QC
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RQ11309 – Solutions Designer – Senior
S M Software Solutions Inc
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RQ11255 – Systems Testing/QA Specialist – Senior
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Added 2 hours ago
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Senior Manager, Quality Assurance Services
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Senior Mechanical Engineer
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Added 2 hours ago
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Apex Systems

Senior Chemist

Mississauga, ON, Canada

$40 to $45 USD / hour · Contract

Apply About employer

Applications open in a new tab.

Job details

Pay: $40 to $45 USD / hour
Job type: Contract
Apply by: Nov 26, 2026
Experience: Minimum 4 year working experience in the chemistry or chemical engineering field.
Posting language: English
Posted: Oct 27, 2026

Original job description

Job#: 3057213

Job Description:

Senior Chemist (QC)

Client: medical technology and medical device company

Contract duration: 14-month contract (potential to extend)

Location: Mississauga, Ontario

Pay Rate: $40-45/hr

Description Of Position

Responsible for performing raw materials, finished product and stability testing and ensuring records associated with Quality Control are complete. Responsible for QC method validation (in conjunction with R&D), equipment calibration/qualification and troubleshooting. Will be asked to participate in out of specification, non-conforming material and deviation investigations. Will be required to provide training and guidance to the QC team and to perform some scheduling of tasks and follow-up on completion of work.

Key Accountabilities And Responsibilities

Perform Routine, In-Process, release and stability testing, focused on simple bench tests. May be asked to perform more complex testing (e.g., using more sophisticated equipment).
May perform water bioburden testing and air sampling.
Write, update and review QC SOPs and test methods as needed.
Perform method validation/transfer sample testing when required.
Work with R&D to ensure new validated methods are converted for GMP purposes.
Develop stability schedule and monitor stability program. Review stability reports.
Schedule QC testing to ensure timelines are met.
May be asked to support equipment qualification, maintenance and the instrument calibration program.
Responsible for maintaining accurate equipment records.
Conduct out of specification investigations. Support or perform non-conformance and deviation investigations as needed.
Mentor and support junior chemists, acting as a trainer and resource as they learn.
Identify and implement improvements within the lab.
Ensure safety procedures are being followed and dispose of lab waste appropriately.
Aid in solving technical problems.
Ensure work is in compliance with GMP and established SOPs.
Store and keep track of finished product retention samples.
Monitor and order required lab solutions and equipment needed for testing.
Review test reports for QC testing.

Participate effectively as an employee of the company

Immediately report to manager any delays in testing or if tasks cannot be completed.
Work effectively in collaboration with other members of the department, or with managers and staff across the organization with whom tasks must be completed.
Work in a safe manner so as not to endanger individual health and safety, or the health and safety of others.
Work to achieve assigned tasks within the standards required (quality, quantity, time and resources).
Comply with all legal requirements, all corporate policies and procedures, and with generally accepted business and ethical practices.
Perform other duties as assigned by immediate manager.

Qualifications

Education:

Minimum a B.Sc or equivalent undergraduate degree in chemistry/chemical or related engineering area or microbiology.

Knowledge/Experience:

Understand basic QC lab practice and GMP requirements.
Minimum 4 year working experience in the chemistry or chemical engineering field.

Skills:

Proven good oral and written communication skills.
Advanced computer skills, e.g. proficient in the Microsoft suite (WORD [create and use templates], EXCEL, and PowerPoint), Adobe Acrobat.
Experienced in advanced analytical techniques such as HPLC, GC, ICP, etc.
Detail oriented and excellent organizational skills.
Analytical mindset and problem-solving skills.
Ability to prioritize multiple tasks.
Excellent written/oral communication and organizational skills.
Exceptional problem-solving skills and ability to “think outside the box”.

Attributes:

Ability to work autonomously.
Self-motivated and self-directed.
Adaptable and willing to take on multiple new tasks and responsibilities.
Ability to work independently as well as participating in a team of professionals.
Ability to respond to urgent situations appropriately by prioritization.
Ability to leverage relationships across other business units and with external sources.
Ability to follow-up with individuals without guidance.
Accuracy and strong attention to detail is essential.

Working Conditions

Located in Mississauga, Canada, this position requires the incumbent to spend 70-90% of the time working in the lab; the rest of the time seated at a workstation and using the keyboard and mouse of a computer to compile the data and records. On occasion, the incumbent may be required to have irregular hours.

Everforth Apex is a world-class IT services company that serves thousands of clients across the globe. When you join Everforth Apex, you become part of a team that values innovation, collaboration, and continuous learning. We offer quality career resources, training, certifications, development opportunities, and a comprehensive benefits package. Our commitment to excellence is reflected in many awards, including ClearlyRateds Best of Staffing® in Talent Satisfaction in the United States and Great Place to Work® in the United Kingdom and Mexico.

Everforth Apex Benefits Overview: In terms of professional development, Everforth Apex hosts an on-demand training program, provides access to certification prep and a library of technical and leadership courses/books/seminars once you have 6+ months of tenure, and certification discounts and other perks to associations that include CompTIA and IIBA.

© 2026 Everforth, Inc. All rights reserved.

Everforth Apex Systems is part of the Commercial Segment of Everforth, Inc.

NYSE: EFOR

4400 Cox Road

Suite 200

Glen Allen, Virginia 23060

Everforth Apex is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. Everforth Apex will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation in using our website for a search or application, please contact our Benefits Department at [email protected] or 804-523-8228. (Do not submit resumes or solicit consultants to this email address). UnitedHealthcare creates and publishes the Transparency in Coverage Machine-Readable Files on behalf of Everforth Apex.

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More about this job

Responsibilities

Perform and document quality control testing of raw materials, finished products, and stability samples, while maintaining compliance with GMP and established procedures. Support method validation, equipment calibration and qualification, investigations, stability program activities, scheduling, and training and mentoring of junior chemists.

Requirements

Requires a minimum bachelor's degree or equivalent in chemistry, chemical or related engineering, or microbiology, and at least four years of relevant work experience. Candidates should understand QC laboratory practices and GMP, have experience with advanced analytical techniques such as HPLC, GC, or ICP, and demonstrate strong communication, organization, attention to detail, and problem-solving skills.

Skills

Quality Control Testing
Good Manufacturing Practices
HPLC
Gas Chromatography
ICP
Method Validation
Equipment Calibration
Equipment Qualification
Stability Testing
Out-Of-Specification Investigations
Deviation Investigations
SOP Writing And Review
Microsoft Office
Adobe Acrobat
Problem-Solving
Laboratory Safety

Benefits

On-Demand Training
Technical And Leadership Courses
Certification Discounts

Visa sponsorship

Not detected in the job text

Keywords

Quality Control
GMP
Raw Materials Testing
Finished Product Testing
Stability Testing
HPLC
GC
ICP
Method Validation
Method Transfer
SOPs
Equipment Calibration
Equipment Qualification
Out-Of-Specification Investigations
Non-Conformance Investigations
Deviation Investigations
Water Bioburden Testing
Air Sampling
Stability Program
Retention Samples
Microsoft Word
Microsoft Excel
Microsoft PowerPoint
Adobe Acrobat
Laboratory Safety
Chemistry
Chemical Engineering
Microbiology

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