21 час назад
HPLC Analyst I (Pharmaceutical Testing)
45 000 - 55 000CAD
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
HPLC Analyst I (Pharmaceutical Testing) (HPLC/GC/LC-MS): Performing pharmaceutical analysis of APIs, raw materials, and finished products in a biopharmaceutical chemistry laboratory with an accent on chromatography, GMP compliance, and analytical instrumentation. Focus on troubleshooting instruments and methods, investigating out-of-specification results, executing USP/EP methods, and maintaining data integrity and traceability.
Location: Toronto, ON, Canada; relocation to Mississauga, ON is expected in 2026
Salary: CAD 45,000–55,000 per year
Company
is an international life sciences network providing analytical testing, laboratory, pharmaceutical, and biopharmaceutical services across multiple industries.
What you will do
- Perform analytical testing of APIs, raw materials, and finished pharmaceutical products using HPLC, GC, UPLC, LC-MS/MS, GC-MS, UV, IR, FTIR, and Karl Fischer instruments.
- Prepare samples and mobile phases, document results in laboratory records, and ensure data integrity and traceability.
- Execute USP and EP pharmacopeial methods, write protocols and SOPs, and assess compliance with compendial requirements.
- Recognize out-of-specification and out-of-trend results, support laboratory investigations, and troubleshoot analytical methods and instrumentation.
- Coordinate method transfers between R&D and QC teams and support instrument training, maintenance, and laboratory operations.
- Mentor junior staff and train new employees in instrument operation, calibration, and preventive maintenance.
Requirements
- B.Sc. degree, preferably in Chemistry, or a diploma in a related field; a strong chemistry background is mandatory.
- 5–10 years of experience working with analytical instrumentation and pharmaceutical testing.
- Proficiency with GC, HPLC, LC-MS/MS, and GC-MS, including chromatography principles and troubleshooting.
- Experience with pharmaceutical data acquisition and laboratory systems such as Empower, Chromeleon, e-LIMS, or ETQ.
- Ability to work directly from USP or EP pharmacopeia to write protocols and execute methods.
- Ability to work in a laboratory environment with standing for more than 50% of the time; shift work, overtime, evenings, and periodic weekends may be required.
Culture & Benefits
- Deadline-based, high-pressure laboratory environment supporting projects for multiple clients.
- Work performed under GMP, GLP, SOP, health, and safety requirements with appropriate PPE for hazardous materials.
- Health and dental coverage, life and disability insurance, and an RRSP with a 3% company match.
- Paid holidays and paid time off.
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