Chemist, Quality Control

Sun Pharmaceutical Industries Ltd•Brampton, ON

8d•CA$56,500 - CA$71,000•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. Reaching People. Touching Lives.

Requirements

Bachelor of Science
Minimum 1 year experience in Pharmaceutical Laboratory environment preferred
Ability to apply knowledge of chemistry, math, instrumentation and statistics to complete tasks
Knowledge of 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
Knowledge of applicable software (LIMs, Empower and Excel)
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

Assist the QC Analyst in performing laboratory testing by preparing reagents, solutions, HPLC systems for analysis and issuing required documentation for testing.
Perform Wet chemistry, KF, UV/VIS, HPLC and GC testing of Raw materials.
Prepare testing documentation package, including project checklist, sample list, certificate of analysis, testing method templates, testing methods (SOP), labels, samples, HPLC column, and standards.
Manage inventory of reagents and solutions (VS, TS solutions: including preparation and standardization).
Manage inventory of laboratory supplies (vials, glassware, syringes, paper, etc).
Assist with standards maintenance: drying, issuing, sign-out.
Maintain inventory usage of HPLC / GC columns.
Prepare HPLC testing solutions (Mobile Phase, Internal Standard solution, Sample Solvent, buffers, etc).
Control resolution solutions.
Complete all GMP Documentation correctly and in a timely manner.
Complete all training assignments and maintain personal training records.
Assist with Non Conformance Investigations.
Assist with completion of Corrective and Preventive Actions (CAPA’s).
Participate in Internal, Customer, Regulatory and Safety Audits.
Perform 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 (Only applicable to customer facing roles).