Process Development Scientist, Analytical Services

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 Process Development Scientist, Analytical responsibilities will include:

• Providing timely analytical support for process development projects.
• Developing appropriate in-process QC procedures in conjunction with Process Development Scientists.
• Developing modern analytical methodologies using quality by design (QbD) and design of experiments (DoE) methodologies to identify and understand design space and critical instrument parameters.
• Training and supervising fellow scientists, technicians and students in analytical methodology.
• Transferring technology to technical staff, as a member of the project team working effectively with both the Process Development and Quality groups.
• Maintaining accurate, real-time records of all laboratory activities.
• Executing assigned housekeeping responsibilities.
• Additional duties assigned, based on business needs and the department supervisor’s request.

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Qualifications

Required:

• Bachelor of Science in Chemistry.
• One year of HPLC Experience.

Desired:

• Master or Ph.D. in Chemistry.
• Method development, validation or qualification.

• Cgmp Experience.

• Strong Technical Writing.

Additional Details

This job has a full time weekly schedule.The full-time equivalent pay range for this position is $63,345.00 - $98,976.00/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:

Occasional

Shift:

Day

Duration:

No End Date

Job Function:

R&D