toronto on quality control laboratory chemist Jobs – 4 Openings This Week

Quality Control Laboratory Chemist
Apollo Health And Beauty Care —Toronto, ON
- $52,000–$55,000 a year
- Full-time
- Laboratory experience
- Bachelor's
- Computer skills
- Dental care
Quick apply
3d
Production Analytical Chemist (ICP-MS and ICP-OES)
Entegris —Scarborough, ON
- $95,000–$110,000 a year
- 8 hour shift
- Laboratory experience
- Master's degree
- Bachelor's
- Dental care
- Vision care
Quality Control Chemist (FTC)
Bora Pharmaceutical Services —Mississauga, ON
- $46,430–$58,040 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Laboratory experience
- Dental care
- Paid time off
R&D Lab Technician (Afternoon Shift)
Apollo Health And Beauty Care —Toronto, ON
- $45,000–$48,000 a year
- Full-time
- Laboratory experience
- Dental care
Quick apply

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Production Analytical Chemist (ICP-MS and ICP-OES)
Entegris —Scarborough, ON
This knowledge is required to troubleshoot, develop, and optimize analytical methods for routine and non-routine QC analysis to support the Manufacturing and…
$95,000–$110,000 a year

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Quality Control Laboratory Chemist

Apollo Health And Beauty Care -
Toronto, ON

Quick apply

Job details

Full-time
$52,000–$55,000 a year
3 days ago

Qualifications

Statistics
Laboratory experience
Bachelor's
Chemistry
Computer skills
Business
Communication skills

Full job description

Benefits:

Gym Access
Dental insurance
Health insurance

We're Hiring!

The Quality Control Laboratory Chemist provides technical support in documenting and reviewing of raw materials, in-process products, finished goods and water samples as well as supporting method development needs. Sample testing may be required.

JOB RESPONSIBILITIES

Perform physical and chemical analyses on raw materials, in-process samples, finished products and Stability samples.

Operate complex laboratory equipment such as HPLC, GC, ICP-OES, FTIR, Auto titrator ,TOC etc.

Participates in analytical methods development and validation.

Reviews notebooks and raw data for GMP/GLP/GDP compliance.

Review data, analyzes results, and maintains accurate and up-to-date records.

Writes and executes laboratory equipment qualification protocols and set up Qualification program for new instruments with some guidance.

Assists in reviewing technical documents for content and conformance to USP such as Technical Documents and Vendor Qualification Documents.

Writes technical documents including but not limited to laboratory equipment operation and calibration, test methods, validation protocols, transfer protocols and reports.

Performs calibration and maintenance on existing equipment.

Investigates and troubleshoots analytical issues.

Creates and updates raw material and finished product specifications.

Assists in maintaining the laboratory in compliance with SOP, GMP, GLP and GDP.

Participates in project related meetings.

Coordinates analytical methods transfer from contract laboratories as appropriate.

Interacts with other departments and outside testing laboratories to ensure proper analytical testing.

Periodically reviews SOP for compliance with GMP/GLP and revises if necessary.

Performs physical and analytical testing of raw material, in-process & finished products, stability and water samples.

Performs other assignments as directed by Quality Control Laboratory Team Lead/Supervisor.

Flexible Shift working as business needs

JOB REQUIREMENTS

Bachelor’s degree in chemistry, Pharmaceutical Sciences, or a related field

Minimum of 3+ years of experience in a pharmaceutical laboratory environment

Solid understanding and hands-on experience with GMP and GLP standards

Knowledge of US FDA, Health Canada regulations, and ICH Guidelines

Demonstrated proficiency in general chemistry principles and laboratory practices

Experience with analytical instrumentation, including HPLC, GC, ICP, UV-VIS, FTIR, titrations, and related techniques

Strong computer skills with the ability to document, analyze, and report data accurately

Excellent written and verbal communication skills

High attention to detail with strong quality-focused documentation practices

Ability to multitask, prioritize workload, and manage shifting priorities effectively

Capable of performing routine and new procedures with minimal supervision

Strong interpersonal skills with the ability to interact effectively across all levels of the organization and influence decisions when needed

Good understanding of statistics with the ability to analyze and present data clearly and effectively

Apollo Health & Beauty Care Ltd. will ensure accommodations are available in consultation with candidates during all stages of the recruitment process. The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job. Duties outlined in this job description may not be all-inclusive, and can be modified at any time if requested by management. Apollo is committed to providing accommodations for people with disabilities in all parts of the hiring process. Apollo will work with applicants to meet accommodation needs that are made known in advance.

We thank all applicants for their interest however only those meeting the minimum qualifications will be interviewed.

Vacancy Status: This posting represents an existing vacancy, and we are actively recruiting to fill this position.

Quick apply

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quality control laboratory chemist jobs in toronto on

Quality Control Laboratory Chemist

Production Analytical Chemist (ICP-MS and ICP-OES)

Quality Control Chemist (FTC)

R&D Lab Technician (Afternoon Shift)

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