Analyst, Quality Control (Contract)

Sun Pharmaceutical Industries Ltd•Brampton, ON

1d•CA$63,000 - CA$78,500•Onsite

About The Position

Driven by a bold pursuit of science and fueled by an unwavering commitment to patients, Sun Pharma is a leading global pharmaceutical company, providing high-quality medicines trusted by healthcare professionals and patients. As part of our mission to Reach People and Touch Lives, we deliver Innovative Medicines, Generics and Consumer Healthcare products that improve the lives of millions of people. With a broadly diversified portfolio of products that span multiple therapeutic areas, we improve access to effective, affordable treatments that promote better health and well-being. The main responsibility of this position is to generate accurate results while following GMP requirements. Responsible for analyzing laboratory samples using various chemical and instrumental techniques, in accordance with established compendial and in-house testing methods, while under minimum supervision.

Requirements

Ability to apply knowledge of chemistry, math, instrumentation and statistics to complete tasks.
Proficiency in various techniques and operation of instrumentation (pH meter, viscometer, Karl Fisher apparatus, UV IR spectrophotometer, Chromatography instruments).
Ability to work effectively in a team-based environment.
Proficiency with applicable software (LIMS and Empower).
Strong organizational, analytical and multi-tasking ability.
Ability to troubleshoot and resolve issues.
Excellent written and oral communication skills, particularly with analytical records, reports and investigations.
Understanding of GMP’s.

Responsibilities

Testing of raw materials by TLC, UV, IR, HPLC and GC and wet chemistry techniques as per SOP.
Document test results as per SOP and GMP.
Recognizes OOS or out of trend results and under the direction of the Supervisor assists in the completion of lab investigations.
Interpret data, communicate results and complete written reports.
Complete all GMP documentation correctly and in a timely manner.
Complete all training assignments and maintain personal training records.
Conduct (participate or lead) routine laboratory and Non-Conformance Investigations.
Initiate and follow through with actions required to close Change Controls.
Evaluate methods and procedures and suggest improvements and changes as required.
Disposes of waste solvents and orders any chemicals or laboratory supplies as required.
Flexibility to shift start time and occasional overtime.
Actively participate in laboratory housekeeping activities, ensuring a safe, clean, organized, and compliant work environment.
Other duties as assigned.
Report any adverse event received from customers for company products to the pharmacovigilance department / Drug Safety on the same day or within 1 business day.