Quality Control Chemist

CA03 BioVectra Inc.; Windsor; On-site; CAD 50,000 - 78,000; Full time

Benefits offered by this job

Bonus eligibility

Stock options

Benefits package

Job summary

BIOVECTRA Inc. in Windsor, Nova Scotia, is seeking a Quality Control Chemist for a full-time, permanent position with 12-hour shifts rotating between days and nights. The role emphasizes analytical testing, accurate record-keeping, and instrument calibration.

Qualifications include a Chemical Technology diploma; a BS in Chemistry/Biochemistry is preferred. Proficiency with GC, HPLC, UV-VIS, PCR, and plate readers is desired, with cGMP knowledge considered an asset.

Qualifications

• Diploma from a recognized Chemical Technology program.
• Bachelor of Science degree in Chemistry, Biochemistry or related discipline preferred.
• Technical proficiency with laboratory instrumentation such as GC, HPLC, UV-VIS, PCR, Plate reader preferred.
• Knowledge of cGMP guidelines an asset.

Responsibilities

• Perform analyses using instrumental techniques such as HPLC, GC, UV-VIS, PCR, Electrophoretic assays, ELISA (Plate assays).
• Maintain accurate, real-time records of all laboratory activities.
• Perform calculations by hand or with spreadsheets or validated computer systems.
• Calibrate and maintain analytical instruments and document these activities.
• Complete paperwork/data entry for release of materials, including status labels and certificates of analysis.
• Ensure appropriate tracking and logging of samples.
• Identify test results out of specification and alert a manager or supervisor.
• Support analytical method validation/verification.
• Draft SOPs including testing procedures and sampling handling instructions.
• Additional duties assigned based on business needs.

Skills

cGMP knowledge

Education

Diploma in Chemical Technology

Bachelor of Science in Chemistry/Biochemistry

Tools

GC

HPLC

UV-VIS

PCR

Plate reader

Job description

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.

BIOVECTRA Inc. has an opening for a Quality Control Chemist. This is a full-time permanent position located in Windsor, Nova Scotia. This position works 12-hour shifts (long week/short week) rotating between days and nights.

Responsibilities

• Performing analyses using instrumental techniques such as HPLC, GC, UV-VIS, PCR, Electrophoretic assays, ELISA (Plate assays).
• Maintaining accurate, real-time records of all laboratory activities.
• Performing required calculations, by hand or with use of spreadsheets or validated computer systems.
• Performing routine maintenance and calibration of analytical instruments and documenting these activities.
• Completing paperwork/data entry for the release of materials, including status labels and certificates of analysis.
• Ensuring appropriate tracking and logging of samples.
• Identifying test results which are out of specification and alerting a manager or supervisor when this occurs.
• Supporting analytical method validation/verification.
• Technical writing of SOPs including testing procedures and sampling handling instructions.
• Additional duties assigned, based on business needs and the department supervisor's request.

Qualifications

• Diploma from a recognized Chemical Technology program.
• Bachelor of Science degree in Chemistry, Biochemistry or related discipline preferred.
• Technical proficiency with laboratory instrumentation such as GC, HPLC, UV-VIS, PCR, Plate reader preferred.
• Knowledge of cGMP guidelines an asset.

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.

• 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.

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.

Visit our career site and learn more about Agilent. Watch our video playlist to get a glimpse of life at Agilent! As a global leader in laboratory and clinical technologies, we are passionate about bringing great science to life. Our commitment to quality and innovation supports cutting-edge life science research, patient diagnostics, and ensures the safety of water, food, and pharmaceuticals. As scientists and clinicians pursue small, everyday advances and life-changing discoveries, we provide trusted answers to their most critical questions and challenges. Leveraging more than 50 years of expertise, we create advanced instruments, software, and consumables supported by teams of highly skilled and knowledgeable people. With 18,000 employees around the world, our global reach and comprehensive solutions provide the most reliable and accurate results, as well as optimal scientific, economic, and operational outcomes. We work collaboratively with our customers on their journey to make a real difference in human lives. Our culture is founded on trust, respect, and uncompromising integrity, and we pride ourselves on being a dynamic and inclusive workplace that celebrates diversity and fosters innovation. We can't wait for you to join us as we continue our mission to improve the world around us. Information about Agilent is available at Agilent.com.