QC Chemist, Stability

Job Description

BIOVECTRA, now a part of Agilent, is recognized as a leader in the contract development and manufacturing space of active pharmaceutical ingredients specializing in clinical-to-commercial scale production for microbial fermentation, synthetic small molecules including ADC, HPAPI, plasmid DNA, mRNA, LNP and sterile filling capabilities. With over 650 employees at both the Windsor, NS and Charlottetown, PEI sites, BIOVECTRA supports over 100 clients, including over 20 top pharma and biotech companies.

BIOVECTRA joined Agilent in 2024 and is part of Agilent’s Advanced Manufacturing Partnerships Division (AMPD), which also contains Agilent’s Nucleic Acid Solutions Division. With BIOVECTRA, Agilent aims to align advanced manufacturing capabilities, expertise, and resources to foster greater innovation and operational excellence. Within AMPD, you will have the opportunity to work with cutting-edge technologies and collaborate with a team of dedicated professionals committed to revolutionizing advanced manufacturing, making a significant impact in the industry and, most importantly, improving patient care through the manufacture of better therapeutics. 

The candidate will be responsible for:   

• Performing analyses using instrumental techniques such as HPLC, GC, UV-VIS and other instrumental techniques. 
• Performing analyses using bench chemical techniques such as TLC, titrimetry and gravimetry. 
• Maintaining accurate, real-time records of all laboratory activities. 
• Performing required calculations, by hand or with use of spreadsheets or validated computer systems. 
• Completing paperwork and updating computerized systems to report the analytical results from the analysis of stability stations. 
• Ensuring appropriate tracking and logging of stability samples. 
• Identifying test results which are out of specification and alerting a manager or supervisor when this occurs. 
• Adhering to BIOVECTRA's Health and Safety Policy. 
• Performing additional duties assigned, based on business needs and the department supervisor’s request. 

Qualifications

The successful candidate for this position should have:  

Required:

• Post secondary education in a scientific discipline
• One year of relevant laboratory experience

Desired:

• Bachelor of Science (Chemistry)
• Technical proficiency with laboratory instrumentation such as GC, HPLC, UV-VIS
• Good oral and written communication skills
• Knowledge of cGMP guidelines

Additional Details

This job has a full time weekly schedule.The full-time equivalent pay range for this position is $26.91 - $47.10/hr 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:

No

Shift:

Day

Duration:

No End Date

Job Function:

Quality/Regulatory