Home › Companies › Bimeda › QC Analyst I (Afternoon Shift)
QC Analyst I (Afternoon Shift)
Bimeda · Cambridge, Ontario, N3C 2W4, Canada · On Site · Active · $48,000,000–$52,000,000 / year · BambooHR
Job facts
| Field | Value |
|---|---|
| Company | Bimeda |
| Title | QC Analyst I (Afternoon Shift) |
| Normalized title | - |
| Department / team | Quality Control |
| Location | Cambridge, Canada |
| Work model | On Site |
| Employment type | Full Time |
| Salary | $48,000,000–$52,000,000 / year |
| Status | active |
| ATS provider | BambooHR |
| Posted / first seen | 2026-05-22 / 2026-06-03 |
| Changed / last seen | 2026-06-03 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Bimeda. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through BambooHR. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Cambridge. | Open |
| Department jobs | Active postings in Quality Control. | Open |
| Work model jobs | Active On Site postings. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Bimeda |
| Source | 1e120009-f66b-4050-914e-cb1f759cda5e |
| ATS provider | BambooHR |
Description
Job Title: QC Analyst I (Afternoon Shift)
Location: Cambridge, ON (In-Office)
Position Type: Full-time regular
Shift: Afternoon Shift, Monday - Friday ( 3:00PM - 11:30PM)
Vacancy Status: This role is currently vacant
AI Disclosure in Hiring: We do not use artificial intelligence to screen, assess, or select applicants
Job Summary
Reporting to the QC Supervisor, the QC Analyst I is responsible for the analysis of raw materials, in-process, and finished product samples using various instrumental and analytical techniques while assuring compliance to cGMP, SOPs and Bimeda quality standards and requirements.
Key Role Specific Requirements
Conducts analytical (physical & chemical) testing of raw materials, in-process samples, finished products, gases and water. ie pH, Conductivity, TOC, Viscosity, Potency tests.
Samples and performs identity testing on raw materials according to the schedule or as requested, utilizing approved sampling techniques for QC and Microbiology.
Ensures that all work is carried out in compliance with company Safety Policies, Good Manufacturing Practices (GMP/GLP) and Standard Operating Procedures (SOPs).
Prepares samples for analysis according to company SOPs & GLP methods.
Performs specific analytical tests utilizing HPLC, GC, UV, IR, FTIR and other instruments.
Analyzes data, keeps the supervisor informed of discrepancies, deviations, out of specifications (OOS) and unusual trends as they occur.
Inform QC Supervisor to ensure that all reagents and supplies are replenished in a timely manner.
Ensures work areas and glassware are kept clean and tidy. Conduct basic, daily equipment calibration. Troubleshoots minor issues and maintains equipment in good working order.
Other duties as assigned.
Please note that this job description is not exhaustive, and the role holder may be required to undertake other relevant duties commensurate with the grading of the post. Activities may be subject to amendment over time as the role develops and/or priorities and requirements evolve.
What you bring to the role
1-2 years in a Pharmaceutical Analytical testing lab.
Bachelor's degree in science, chemistry, biochemistry or other related field required.
Analytical Wet Chemistry Lab experience using the following methods/equipment; titration, pH, Potency, Conductivity, Viscosity, TOC, UV, IR, GC, HPLC assays.
High integrity, excellent attention to detail, analytical thinker, ability to organize and prioritize, and work in team environment.
Excellent communication skills both verbally and written.
Competencies Required for the Role
INTEGRITY/PERSONAL CREDIBILITY – Demonstrated ability and concern that one be perceived as responsible, reliable and trustworthy.
FOSTERING COLLABORATION/TEAMWORK- is the ability to work jointly with others or together especially in an intellectual endeavor; the ability and desire to work cooperatively with others on a team; as a team leader, the ability to demonstrate interest, skill, and success in getting groups to learn to work together. Builds partnerships for global performance. Respects others.
INITIATIVE - Identifying what needs to be done and doing it before being asked or before the situation requires it.
THOROUGHNESS/DETAIL ORIENTED – Ensuring that one’s own and others’ work ad information are complete and accurate; carefully preparing for meetings and presentations following up with others to ensure that agreements and commitments have been fulfilled.
PLANNING – is the process of thinking about and organizing the activities required to achieve a desired goal.
Compensation & Benefits :
Competitive salary.
13 paid holidays.
Competitive vacation policy effective upon hire.
5 paid personal care days.
Employee Assistance Program.
Expected Salary Range: $48,000K- $52,000K /Year
About Bimeda
Bimeda is a leading global innovator, manufacturer and marketer of veterinary pharmaceuticals and animal health products and has over half a century’s experience in providing science-driven solutions to optimize the health, wellbeing and productivity of the world’s animals.
Bimeda’s global innovation program sees eight state-of-the art R&D centers across four continents collaborate on an enviable product development pipeline which anticipates the ever-evolving needs of the animal health industry.
Bimeda’s nine manufacturing facilities across seven countries allow the company to manufacture a broad range of preventative, curative and nutritional products including sterile injectables, vaccinations, nutritional boluses, feed additives, tablets, water-soluble powders, pastes and non-sterile liquids.
Globally, the company focuses on the development, manufacture and commercialization of quality Bimeda-branded products while also being the partner of choice for contract manufacturing and R&D services for prominent companies within the animal health industry.
More info at www.bimedacareers.com
Equal Opportunity & Accessibility
At Bimeda we are committed to fostering an inclusive, barrier-free and accessible environment. Part of this commitment includes arranging accommodations to ensure an equitable opportunity to participate in the recruitment and selection process. If you require an accommodation, we will work with you to meet your needs. We are committed to an inclusive and accessible recruitment process. We are an equal-opportunity employer and assess candidates based on skills and experience. Recruitment records are retained in accordance with Ontario law.
Full job record
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| Org ID | 969abde4-a059-4a43-bf9d-a9b455a2c5ed |
| Source ID | 1e120009-f66b-4050-914e-cb1f759cda5e |
| Board ID | 1e120009-f66b-4050-914e-cb1f759cda5e |
| Provider | bamboohr |
| Provider Job Key | 562 |
| Title | QC Analyst I (Afternoon Shift) |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Cambridge, Ontario, N3C 2W4, Canada |
| Department | Quality Control |
| Team | — |
| Employment Type | full_time |
| Workplace Type | on_site |
| Remote Policy | — |
| Country | Canada |
| Region | — |
| City | Cambridge |
| Salary Raw | Salary Range: $48,000K- $52,000K /Year About Bimeda Bimeda is a leading global innovator, manufacturer and marke |
| Salary Min | 48,000,000 |
| Salary Max | 52,000,000 |
| Salary Currency | USD |
| Salary Period | year |
| Source URL | https://bimeda.bamboohr.com/careers/562 |
| Apply URL | https://bimeda.bamboohr.com/careers/562 |
| First Seen At | 2026-06-03 10:26:05Z |
| Last Seen At | 2026-06-06 10:28:33Z |
| Last Checked At | 2026-06-06 10:28:33Z |
| Last Changed At | 2026-06-03 10:26:05Z |
| Inactive At | — |
| Source Posted At | 2026-05-22 00:00:00Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=bamboohr/board=bimeda/date=2026-06-06/2026-06-06T10-28-31-235Z-d256df6cd6115c62248069825580dc13de218638385be94f31a9f940b50fdda2.json |
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"description": "<p><span style=\"font-family: Inter, sans-serif\"><span style=\"font-weight: bold\">Job Title:</span> QC Analyst I (Afternoon Shift)</span><br><span style=\"font-family: Inter, sans-serif\"><span style=\"font-weight: bold\">Location:</span> Cambridge, ON (In-Office)</span><br><span style=\"font-family: Inter, sans-serif\"><span style=\"font-weight: bold\">Position Type: </span>Full-time regular</span></p>\n<p><span style=\"font-weight: bold\">Shift:</span> Afternoon Shift, Monday - Friday (<span style=\"font-family: Inter, sans-serif\">3:00PM - 11:30PM)</span><br><span style=\"font-family: Inter, sans-serif\"><span style=\"font-weight: bold\">Vacancy Status:</span> This role is currently vacant</span><br><span style=\"font-family: Inter, sans-serif\"><span style=\"font-weight: bold\">AI Disclosure in Hiring: </span>We do not use artificial intelligence to screen, assess, or select applicants</span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 15px\"><br></span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 15px\"><span style=\"font-weight: bold\">Job Summary </span></span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 15px\">Reporting to the QC Supervisor, the QC Analyst I is responsible for the analysis of raw materials, in-process, and finished product samples using various instrumental and analytical techniques while assuring compliance to cGMP, SOPs and Bimeda quality standards and requirements.</span></p>\n<p><br></p>\n<p><span style=\"font-size: 12pt; font-weight: bold\">Key Role Specific Requirements</span></p>\n<ul>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 15px\">Conducts analytical (physical & chemical) testing of raw materials, in-process samples, finished products, gases and water. ie pH, Conductivity, TOC, Viscosity, Potency tests.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 15px\">Samples and performs identity testing on raw materials according to the schedule or as requested, utilizing approved sampling techniques for QC and Microbiology.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 15px\">Ensures that all work is carried out in compliance with company Safety Policies, Good Manufacturing Practices (GMP/GLP) and Standard Operating Procedures (SOPs).</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 15px\">Prepares samples for analysis according to company SOPs & GLP methods.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 15px\">Performs specific analytical tests utilizing HPLC, GC, UV, IR, FTIR and other instruments.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 15px\">Analyzes data, keeps the supervisor informed of discrepancies, deviations, out of specifications (OOS) and unusual trends as they occur.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 15px\">Inform QC Supervisor to ensure that all reagents and supplies are replenished in a timely manner.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 15px\">Ensures work areas and glassware are kept clean and tidy. Conduct basic, daily equipment calibration. Troubleshoots minor issues and maintains equipment in good working order.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 15px\">Other duties as assigned.</span></li>\n</ul>\n<p><br></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 15px\"><span style=\"font-size: 15px\"><em><span style=\"font-size: 13px\">Please note that this job description is not exhaustive, and the role holder may be required to undertake other relevant duties commensurate with the grading of the post. Activities may be subject to amendment over time as the role develops and/or priorities and requirements evolve. <br><br></span></em></span></span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 15px\"><span style=\"text-decoration: underline\"><span style=\"font-weight: bold\">What you bring to the role</span></span></span></p>\n<ul>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 15px\">1-2 years in a Pharmaceutical Analytical testing lab.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 15px\">Bachelor's degree in science, chemistry, biochemistry or other related field required.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 15px\">Analytical Wet Chemistry Lab experience using the following methods/equipment; titration, pH, Potency, Conductivity, Viscosity, TOC, UV, IR, GC, HPLC assays.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 15px\">High integrity, excellent attention to detail, analytical thinker, ability to organize and prioritize, and work in team environment.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 15px\">Excellent communication skills both verbally and written.</span></li>\n</ul>\n<p><br></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 15px\"><span style=\"text-decoration: underline\"><span style=\"font-weight: bold\">Competencies Required for the Role </span></span></span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 15px\"><span style=\"font-weight: bold\"><span style=\"color: #c00000\">INTEGRITY/PERSONAL CREDIBILITY</span> </span>– Demonstrated ability and concern that one be perceived as responsible, reliable and trustworthy.</span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 15px\"><span style=\"font-weight: bold\"><span style=\"color: #c00000\">FOSTERING COLLABORATION/TEAMWORK- </span></span>is the ability to work jointly with others or together especially in an intellectual endeavor; the ability and desire to work cooperatively with others on a team; as a team leader, the ability to demonstrate interest, skill, and success in getting groups to learn to work together. Builds partnerships for global performance. Respects others.</span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 15px\"><span style=\"font-weight: bold\"><span style=\"color: #c00000\">INITIATIVE</span> - </span>Identifying what needs to be done and doing it before being asked or before the situation requires it.</span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 15px\"><span style=\"font-weight: bold\"><span style=\"color: #c00000\">THOROUGHNESS/DETAIL</span> </span><span style=\"font-weight: bold\"><span style=\"color: #c00000\">ORIENTED </span></span>– Ensuring that one’s own and others’ work ad information are complete and accurate; carefully preparing for meetings and presentations following up with others to ensure that agreements and commitments have been fulfilled.</span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 15px\"><span style=\"font-weight: bold\"><span style=\"color: #c00000\">PLANNING</span> </span>– is the process of thinking about and organizing the activities required to achieve a desired goal.<br></span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt; font-weight: bold\"><span style=\"color: rgb(51, 51, 51)\"><br></span></span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt; font-weight: bold\"><span style=\"color: rgb(51, 51, 51)\"><span style=\"font-weight: bold\">Compensation & Benefits</span>:</span></span></p>\n<ul>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Competitive salary.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">13 paid holidays.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Competitive vacation policy effective upon hire.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">5 paid personal care days.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Employee Assistance Program.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Expected Salary Range: $48,000K- $52,000K /Year</span></li>\n</ul>\n<p><br></p>\n<p><span style=\"font-family: Inter, sans-serif; font-weight: bold\">About Bimeda</span></p>\n<p><span style=\"font-family: Inter, sans-serif\">Bimeda is a leading global innovator, manufacturer and marketer of veterinary pharmaceuticals and animal health products and has over half a century’s experience in providing science-driven solutions to optimize the health, wellbeing and productivity of the world’s animals.</span></p>\n<p><br></p>\n<p><span style=\"font-family: Inter, sans-serif\">Bimeda’s global innovation program sees eight state-of-the art R&D centers across four continents collaborate on an enviable product development pipeline which anticipates the ever-evolving needs of the animal health industry.</span></p>\n<p><br></p>\n<p><span style=\"font-family: Inter, sans-serif\">Bimeda’s nine manufacturing facilities across seven countries allow the company to manufacture a broad range of preventative, curative and nutritional products including sterile injectables, vaccinations, nutritional boluses, feed additives, tablets, water-soluble powders, pastes and non-sterile liquids.</span></p>\n<p><br></p>\n<p><span style=\"font-family: Inter, sans-serif\">Globally, the company focuses on the development, manufacture and commercialization of quality Bimeda-branded products while also being the partner of choice for contract manufacturing and R&D services for prominent companies within the animal health industry.</span></p>\n<p><br></p>\n<p><span style=\"font-family: Inter, sans-serif\">More info at <a href=\"https://www.bimedacareers.com/\" target=\"_blank\" rel=\"noopener noreferrer\">www.bimedacareers.com</a></span><br><br><span style=\"font-family: Inter, sans-serif; font-weight: bold\">Equal Opportunity & Accessibility</span><br><span style=\"font-family: Inter, sans-serif\">At Bimeda we are committed to fostering an inclusive, barrier-free and accessible environment. Part of this commitment includes arranging accommodations to ensure an equitable opportunity to participate in the recruitment and selection process. If you require an accommodation, we will work with you to meet your needs. <span style=\"font-size: 12pt\">We are committed to an inclusive and accessible recruitment process. We are an equal-opportunity employer and assess candidates based on skills and experience. Recruitment records are retained in accordance with Ontario law.</span></span></p>",
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