Quality Control Analyst

Agilent Technologies; Charlottetown; On-site; CAD 50,000 - 78,000; Full time

Benefits offered by this job

Bonus eligibility

Stock options

Benefits

Job summary

BIOVECTRA, part of Agilent, is seeking a skilled analytical laboratory professional to support development and manufacturing of pharmaceutical therapies. You will perform analytical testing (HPLC, GC, UV-Vis, NMR), maintain records, and contribute to data reporting in a fast-paced CGMP environment.

Ideal candidates have post-secondary science education, prefer a Bachelor’s in chemistry/biology, and can handle routine maintenance, documentation, and safe handling of hazardous materials.

Qualifications

• Post-secondary education in a scientific field.

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.

Skills

HPLC

GC

NMR

Titrimetry

Gravimetry

KF analysis

cGMP

Lab documentation

Data reporting

Safety handling chemicals

Education

Post-secondary education in a scientific field

Bachelor’s degree in Chemistry, Biology, Biochemistry, or related science

Tools

HPLC

GC

KF analysis

Job description

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/locations

Agilent 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:

No

Shift:

Swing

Duration:

No End Date

Job Function:

Quality/Regulatory