Biotechnology, Life Sciences, Medical Devices, Scientific Instruments, Software

Quality Control Analyst

Canada-prince Edward Island-charlottetown, PEOnsiteFull TimeCA$49,848–CA$77,888 /yrPosted 15 days ago

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Required skills

HPLC
GC
UV-Vis
NMR
TLC
titrimetry
gravimetry
laboratory records
calculations
data reporting

Nice to have

Chemistry
Biology
Biochemistry
related science
cGMP-regulated environment
analytical skills

Role summary

BIOVECTRA, part of Agilent, is seeking a Quality Control Analyst to join their collaborative team in a fast-paced laboratory environment. This role involves performing various analytical and bench chemistry tests using techniques such as HPLC, GC, UV-Vis, NMR, TLC, titrimetry, and gravimetry. Responsibilities include maintaining accurate records, preparing documentation, managing samples, identifying OOS results, and ensuring safe handling of materials. The position requires a post-secondary education in a scientific field and offers a full-time schedule with a competitive salary range.

Job Description

About BIOVECTRA

BIOVECTRA, part of Agilent, is a leading contract development and manufacturing organization supporting the production of life-changing pharmaceutical therapies. Join a collaborative team working with innovative technologies in a fast-paced laboratory environment.

Key Responsibilities

Perform analytical testing using HPLC, GC, UV-Vis, and NMR.
Conduct bench chemistry testing, including TLC, titrimetry, and gravimetry.
Maintain accurate laboratory records and documentation.
Perform calculations and support data reporting.
Conduct routine instrument maintenance and calibration.
Prepare material release documentation and Certificates of Analysis.
Track and manage laboratory samples.
Identify and report out-of-specification (OOS) results.
Safely handle chemicals, solvents, APIs, and other hazardous materials.

Qualifications

Minimum Qualifications

Post-secondary education in a scientific field.

Preferred Qualifications

Bachelor's degree in Chemistry, Biology, Biochemistry, or a related science.
Experience with HPLC, GC, and Karl Fischer (KF) analysis.
Experience working in a cGMP-regulated environment.
Ability to work effectively in a fast-paced laboratory setting.

Ideal for candidates with strong analytical skills, attention to detail, and a passion for supporting the development and manufacture of life-changing therapeutics.

Additional Details

This job has a full time weekly schedule.The full-time equivalent pay range for this position is $49,848.00 - $77,888.00/yr CAD plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locationsAgilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.

Travel Required:

Shift:

Swing

Duration:

No End Date

Job Function:

Quality/Regulatory

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