Quality Control Laboratory Analyst

2 months ago

Strathroy, Canada Catalent Full time

Quality Control Laboratory Analyst

Position Summary

Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee.

This position is located in Strathroy, Ontario, one of two sites located in Canada offering softgel development and manufacturing capabilities for the Pharmaceutical and Consumer Health industries. We have a broad range of integrated formulation, manufacturing, analytical and packaging services to offer full-service turnkey solutions.

Reporting to the Quality Control Laboratory Supervisor, the Quality Control Laboratory Analyst is responsible for coordinating and performing laboratory activities/projects including performing analysis of raw materials, finished products and stability samples. The Quality Control Laboratory Analyst is part of a scientific team that assists in the advancement of pharmaceutical products produced by the organization.

Regular working hours: 8:00 AM-4:30 PM or 8:30 AM-5:00 PM with a 30-minute unpaid lunch

The Role:

 Responsible for the testing of raw materials, finished products and stability samples by instrumental and wet chemistry methods and described in compendia references or in-house methods .

Train, advise and assist laboratory personnel as required. (e.g. methods, procedures, tests, etc.)

Maintain adequate levels of laboratory supplies.

Calibrate and maintains instruments according to relevant SOPs.

Comply with SOPs and GMPs at all times.

Maintain the laboratory environment in a safe and clean manner such as laboratory cleaning, glassware washing, storing of supplies, disposal of waste, etc.

 May be asked to work extended hours (overtime), especially when problems occur or when deadlines must be met.

Other duties as assigned.

The Candidate:

College diploma in Chemistry required. Bachelor’s degree in chemistry or related field preferred.

2+ years of experience as a lab analyst is preferred.

Experience working in a pharmaceutical and/or GMP facility is an asset.

Strong technical/scientific background.

Knowledge of laboratory techniques, terminology, equipment and materials.

Effective attention to detail and a high degree of accuracy.

Demonstrate applicable ethics and due diligence.

Good communication (written and verbal), and interpersonal skills.

While performing the responsibilities of the job, the employee is required to talk and hear.

The employee is often required to sit and use their hands and fingers, to handle or feel and to manipulate keys on a keyboard.

Use of manual dexterity is required. The employee is often required to stand, walk, reach with arms and hands, bend or twist, and to stoop, kneel, crouch or crawl.

Vision abilities required by this job include close vision.

The employee is required to stand for long periods of time and occasionally bend and lift

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