Markham, On Qc analyst level Jobs – 15 Openings This Week

Laboratory QC Analyst Level 2
Shields Pharma Inc. —Markham, ON
- $53,000–$65,000 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Dental care
- Vision care
Quick apply
3d
KYC Analyst - Corporate Banking
MUFG —Toronto, ON
- Full-time
- Microsoft Word
- Microsoft Excel
- Analysis skills
Quality Control Analyst
Kingfisher International Inc —Stouffville, ON
- $55,000–$65,000 a year
- Overtime
- Microsoft Office
- Analysis skills
- Bachelor's
- Disability insurance
- Dental care
Quick apply
Quality Control Analyst, Mortgages
Neo Financial —Toronto, ON
- $65,000–$75,000 a year
- Full-time
- Quality Control
- Organizational skills
- Communication skills
- Paid time off
- Life insurance
Quick apply
Statistical Programmer Analyst
SCiAN Services —Toronto, ON
- Full-time
- Master's degree
- Bachelor's
- Communication skills
Senior Compensation Advisor
TELUS —Toronto, ON
- $86,000–$160,000 a year
- Full-time
- Bilingual
- Google Suite
- English
GCMSMS ANALYST II - Eurofins BioPharma Product Testing Toronto, Inc.
Eurofins Canada BioPharma —Toronto, ON
- $55,000–$70,000 a year
- Overtime
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Designated paid holidays
- Disability insurance
Quick apply
HPLC Analyst - Eurofins BioPharma Product Testing Toronto, Inc.
Eurofins Canada BioPharma —Toronto, ON
- $50,000 a year
- Overtime
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Designated paid holidays
- Disability insurance
Quick apply
Senior Actuarial Analyst - Research & Development
Wawanesa —North York, ON
- $90,000–$110,000 a year
- Part-time
- Hybrid work
- English
- Databases
- Bachelor's
9d
Analytical Chemist II – HPLC/GC (Temporary Contract) - Eurofins Cosmetics & Personal Care, Inc.
Eurofins Canada Cosmetic Testing —Toronto, ON
- $24.04–$26.44 an hour
- Overtime
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Quick apply
9d
Bilingual Lease Analyst (FR/ENG)
BGIS —Markham, ON
- $63,397–$79,246 a year
- Full-time
- Hybrid work
- Bilingual
- Microsoft Word
- Microsoft Excel
Actuarial Consultant - Research & Development
Wawanesa —North York, ON
- $120,000–$145,000 a year
- Part-time
- Hybrid work
- English
- Databases
- Bachelor's
9d
Senior Specialist - Quality Engineering
LTM —Toronto, ON
- $130,000–$150,000 a year
- Databases
- SQL
- Presentation skills
- Disability insurance
- Dental care
Quick apply
OOS Investigator - Eurofins BioPharma Product Testing, Inc.
Eurofins Canada BioPharma —Toronto, ON
- $55,000 a year
- Immediate opening
- Laboratory experience
- Microsoft Office
- Bachelor's
- Designated paid holidays
- Disability insurance
Quick apply
Principal Engineer- EMT and Special Studies
DNV —Toronto, ON
- $180,000–$235,000 a year
- Full-time
- Hybrid work
- AutoCAD
- Engineering
- English
- Designated paid holidays
- Disability insurance

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Laboratory QC Analyst Level 2
Shields Pharma Inc. —Markham, ON
Minimum M.Sc. or B.Sc. degree in Chemistry, Pharmaceutical, Analytical Chemistry or similar applied scientific disciplines with at least of 4 years direct hands…
$53,000–$65,000 a year
Quick apply
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qc analyst level jobs near markham, on

Laboratory QC Analyst Level 2

Shields Pharma Inc. -
Markham, ON

Quick apply

Job details

Permanent | Full-time
$53,000–$65,000 a year
3 days ago

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Laboratory experience
Microsoft Office
Master's degree
Analysis skills
Bachelor's
Chemistry
Computer skills
Communication skills

Full job description

About Shields Pharma Inc.

Shields Pharma Inc. is a Health Canada approved GMP organization located in Markham, Ontario.

We offer Laboratory R&D and QC testing services as well as production and formulation of certain psychedelic therapeutics for treatment of certain mental health disorders such as anxiety, depression, obsessive-compulsive disorder, PTSD, and problematic substance.

Shields Pharma Inc. is an equal opportunity employer committed to diversity and inclusion for everyone. We are continuously looking for smart-minded, skilled, qualified, experienced, independent, reliable, and detail-oriented candidates to join our successful team.

Our people are at the heart of everything we do.

You can count on;

Safety as our first core value,
Integrity,
Accountability, and
Continuous Training and skill development.

Position Title: Laboratory QC Analyst Level 2

Reports to: Director of Laboratory Operation and Laboratory Manager

Job Summary

The main responsibility of this position is to generate accurate results while following GMP requirements. Responsible for analyzing laboratory raw material, in-process, and finished products samples using various chemical and instrumental techniques, in accordance with compendial; USP, BP, EP, and JP methods and specifications and established in-house testing methods, while under minimum supervision.

The Quality Control Analyst is responsible to operating, maintaining, performing and basic troubleshooting of analytical instruments, including; Dissolution, HPLC, UPLC, LC/MS, GC, GC/MS, ICP-MS, etc.

Essential Functions

Perform raw material, in-process, finished product, and stability sample testing using instrumental analytical, wet chemicals, and physical analytical methods and techniques following the written procedure or compendial methods.
Prepare analytical equipment for experiments; Including reagents, standards, test solutions, and mobile phase as required by the test procedure.
Perform analytical method Transfer, Verification, Validation and Stability testing.
Maintain accurate documentation including lab reports, records of procedures, results, and data analysis in accordance with Good Documentation Practices (GDP) guidelines
Ordering general lab supplies (chemicals/non-chemicals) when required.
Document analytical test results in lab notebooks; Ensure the data generated is accurate and meets the specifications, report results on the testing worksheets (finished products and raw materials) according to standard operating procedures in a timely manner, meeting specified deadlines.
Maintain laboratory lab-books, equipment logbooks, and trackers on daily basis in accordance with department policies and procedures.
Demonstrate sound knowledge of Pharmaceutical Compendial (i.e., USP, BP, EP, JP, etc.) General Chapters’ methods
Effectively manage the prioritization to meet multiple goals and timelines.
Demonstrate a strong understanding of cGMP, cGLP, Health Canada, FDA, ICH, and other regulatory guidelines
Be able train new or existing personnel as identified by QC management.
Notify any aberrant/OOS/OOT results to QC management and participate to investigate results following the SOP.
Conduct laboratory instruments qualification, calibration, and preventive maintenance when requested
Be able to work in a collaborative, fast-paced environment.

Position Requirements: (Work Status, Qualification, Knowledge, and Experience)

Must possess Permanent Canadian residency with work permit and/or Canadian citizenship.
Must be living in Canada, preferably in Toronto area
Minimum M.Sc. or B.Sc. degree in Chemistry, Pharmaceutical, Analytical Chemistry or similar applied scientific disciplines with at least of 4 years direct hands-on experience working in pharmaceutical disciplines.
Solid knowledge and expertise (including operation, Qualification, trouble-shooting, and maintenance) working with laboratory instrumentation such as Dissolution, HPLC, GC, ICP-MS, UV-VIS, FT-IR, TOC, TLC, KF, etc.
Familiarity to LC/MS/MS instrumentation and Nitrosamine impurity analysis would be an advantage
Possess extensive experience and in-depth technical knowledge in the method validation, and application of analytical methods used to support pharmaceutical product development and quality control. This includes a strong focus on assay determination, related substances (impurities) analysis, and residual solvents (organic volatile impurities) testing, aligned with ICH, USP, EP, and regulatory expectations.
Well versed in understanding USP, BP, EP, and JP, methods and specifications.
In-depth knowledge and competency in cGMP/GMP (Good Manufacturing Practices), GDP (Good Documentation Practices), GXP, FDA CFR 211, ICH, and ALCOLA+ regulation and quality system guidelines.
Strong attention to detail
Strong problem solving and analytical skills including decision analysis and implementation
Computer Proficiency with MS office (Excel, Word, PowerPoint), Spreadsheets, etc.
Strong ability to function as a team member; ability to communicate effectively with team members and other plant personnel, both verbally and in writing
Track record of multi-tasking, being detail-oriented, trouble-shooting/problem solving abilities, working in a fast-paced environment with minimal instruction on routine work and moderate instruction on new assignments.
Be punctual, team player, fast learner, and have strong Interpersonal and communication skills.

How To Apply

Please reference “Laboratory QC Analyst Level 2” in subject line and submit resume with cover letter to [email protected]

We welcome and encourage applications from all qualified applicants. We are committed to adhering to our company objectives and requirements outlined above. Kindly refrain from applying if you are not qualified.

We thank all applicants for their interest, however, only those qualified and selected shall be contacted for an interview.

No phone calls please.

Pay: $53,000.00-$65,000.00 per year

Benefits:

Dental care
Extended health care
On-site parking
Vision care

Application question(s):

Minimum M.Sc. or B.Sc. degree in Chemistry, Pharmaceutical, Analytical Chemistry or similar applied scientific disciplines with at least of 4 years direct hands-on experience working in pharmaceutical disciplines
Solid knowledge and expertise (including operation, Qualification, trouble-shooting, and maintenance) working with laboratory instrumentation such as Dissolution, HPLC, GC, ICP-MS, UV-VIS, FT-IR, TOC, TLC, KF, etc.
Extensive experience and in-depth technical knowledge in the method validation, and application of analytical methods used to support pharmaceutical product development and quality control. This includes a strong focus on assay determination, related substances (impurities) analysis, and residual solvents (organic volatile impurities) testing, aligned with ICH, USP, EP, and regulatory expectations
Well versed in understanding USP, BP, EP, and JP, methods and specifications
In-depth knowledge and competency in cGMP/GMP (Good Manufacturing Practices), GDP (Good Documentation Practices), GXP, FDA CFR 211, ICH, and ALCOLA+ regulation and quality system guidelines.

Work Location: In person

Quick apply

Refine Your Search

qc analyst level jobs in markham, on

Laboratory QC Analyst Level 2

KYC Analyst - Corporate Banking

Quality Control Analyst

Quality Control Analyst, Mortgages

Statistical Programmer Analyst

Senior Compensation Advisor

GCMSMS ANALYST II - Eurofins BioPharma Product Testing Toronto, Inc.

HPLC Analyst - Eurofins BioPharma Product Testing Toronto, Inc.

Senior Actuarial Analyst - Research & Development

Analytical Chemist II – HPLC/GC (Temporary Contract) - Eurofins Cosmetics & Personal Care, Inc.

Bilingual Lease Analyst (FR/ENG)

Actuarial Consultant - Research & Development

Senior Specialist - Quality Engineering

OOS Investigator - Eurofins BioPharma Product Testing, Inc.

Principal Engineer- EMT and Special Studies

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