Lab Assistant

Contract Pharmaceuticals Limited; Mississauga; On-site; CAD 40,000 - 50,000; Full time

Benefits offered by this job

Benefits program

Profit-sharing plan

Paid time off

Employee assistance program

Work-life balance

On-site parking

Discounted gym membership

Job summary

CPL is seeking a QC Lab support professional to manage reference standards, reagents inventory, glassware cleaning, and GDP-compliant documentation in our non-sterile lab. You will support continuous QC testing by maintaining accurate inventory, proper waste disposal, and adherence to GDP requirements.

We offer a benefits program, deferred profit-sharing, paid time off, employee assistance, work-life balance, on-site parking, and a discounted gym membership.

Qualifications

• University degree or diploma in a science discipline (ex: Chemistry).
• GMP lab experience is preferred.
• Strong organizational and communication skills.

Responsibilities

• Organizes and maintains lab supplies and consumables for analytical testing.
• Manages inventory of reference standards and reagents, glassware cleaning and storage.
• Monitors temperature-controlled areas and ensures GDP-compliant documentation.
• Coordinates waste disposal and ensures timely replenishment of materials.
• Supports continuation of QC testing without interruption.

Skills

Organized

Communication

Team player

Adaptable

Attention to detail

Education

Science degree or diploma

Job description

Salary Range: $40,000.00 To $50,000.00 Annually

Job Type:

Current Vacancy

WHO WE ARE:

At CPL, we are passionate about pharmaceutical product development and contract manufacturing. Our aim is to be the top choice CDMO in the non-sterile liquid and semi-solid pharmaceutical products domain and ultimately bring benefits to the customers using our manufactured products.

For more than 30 years CPL has partnered with the world’s leading pharmaceutical companies to provide full-service product development and manufacturing, singularly focused on innovation and efficiency.

We recognize our employees are our number one asset and support their career growth. We also offer a benefits program, deferred profit-sharing plan, paid time off, employee’s assistance program, work/life balance, employee recognition program, on-site parking, discounted gym membership.

Job Summary:

Support QC Lab operation activities by managing reference standards and reagents inventory, cleaning and drying glassware, managing inventory of lab consumables and lab waste, monitoring temperature-controlled areas in the lab, following GDP requirements to complete the required documentation for all assigned tasks, and performing other activities to help the continuation of QC testing in the lab without interruption.

JOB RESPONSIBILITIES:

• Organizes and maintains critical laboratory supplies such as columns for HPLC and GC analysis, filters, vials, syringes, caps, and other consumables for analytical testing as per applicable methods and projects.
• Manage inventory of columns for HPLC and GC analysis ensuring that a backup column is always available for critical QC tests.
• Coordinate with buyers to ensure that critical QC reagents are replenished in a timely manner to support continuation of QC testing.
• Manage the glassware cleaning, drying and storage in designated areas. If any glassware is damaged or excessively etched, follow the appropriate procedures to discard the glassware and immediately take action to replace the glassware.
• Ensures that all reference standards and reagents are available for the analyst to execute testing. If any required material is found to be unavailable, expired or out of stock, immediately take action to replenish the material inventory.
• Manage disposal of samples, reagents, glassware, biohazard waste, and general lab waste. Sort and organize the waste as per third-party disposal service provider’s instructions. Coordinate with the warehouse team to ensure timely shipment of waste.
• Routinely check lab waste containers throughout the lab to ensure waste containers are not overflowing and that lab waste is removed in a timely manner.
• Ensure that PPE materials (disposable lab coats and safety glasses/goggles) are readily available for QC lab visitors and analysts.
• Follow assigned procedures and GDP requirements to complete all necessary documentation for assigned tasks.
• Complete other duties as assigned.

REQUIRED QUALIFICATIONS:

Education:

• A university degree or diploma in a science discipline (ex: Chemistry).

Experience:

• Prior experience in a GMP lab environment is preferred.

Knowledge, Skills, Abilities:

• Must be organized and able to handle multiple work assignments.
• Good verbal and written communication skills.
• Good understanding of GMP and GDP requirements.
• Works as an effective team member to meet departmental objectives.
• Flexible with the ability to adapt, respond quickly and manage change in a fast-paced environment.

PHYSICAL DEMANDS/WORKING CONDITIONS:

• Lab environment
• Note: lifting of some heavy items including boxes, waste containers, and glassware is expected.

CPL is an equal opportunity employer committed to diversity and inclusion. We welcome applications from all qualified individuals. CPL is committed to accommodating persons with disabilities. If you need accommodation at any stage of the application process or want more information on our accommodation policies, please contact us.

We thank all applicants for their expression of interest; however, only those selected for an interview will be contacted. No phone calls or agencies please.