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Agilent Technologies

Manufacturing Superintendent

Charlottetown, PE, Canada
Canada-Prince Edward Island-Charlottetown, Canada

Full-time

Apply on agilent.wd5.myworkdayjobs.com About employer

Applications open in a new tab.

Job details

Job type: Full-time
Posting language: English
Posted: Nov 13, 2026

Original job description

Job Description

THIS IS A NIGHTS ONLY POSITION 7 pm-7am

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.

The Manufacturing Superintendent will supervise and lead a pharmaceutical manufacturing team in the various day to day functions and activities of GMP production, purification, isolation and packaging of synthetic chemical, natural extraction, and/or fermentation related products in a dynamic multi-product-based operation following all outlined safety practices, company protocols and objectives.

The responsibilities will include:

Overseeing team leads in accomplishing overall departmental production needs and reviewing work to ensure consistency
Mentoring members of the production group and providing constructive input
Reviewing the completed BPRs (ensuring all QCs, deviations, cleaning sheets, etc. are attached to the BPR, BPR lines are signed and verified, QA review items are resolved, and label requests have been completed)
Assisting in updates on batch production records (BPRs) to optimize process efficiencies and to assist in developing new BPR’s or work instructions
Supporting manufacturing schedules through appropriate documentation and staging requests
Ensuring material and/or solvent counts are completed upon request
Ensuring the equipment and processing areas are in a ready state to meet the posted schedule
Identifying, troubleshooting, and resolving equipment, process and facility issues as well as contributing to process risk assessments
Participating in the hiring, training, and performance evaluation of employees
Participating in regulatory inspections and audits
Interacting with multi-discipline units and personnel to ensure product quality and on-time delivery is adhered to
Flexibility for after-hours consultation during manufacturing activities or during infrequent production activities will be required
Participating in client meetings and teleconferences
Providing guidance and oversight to a team of employees

WORK CONDITIONS:

Ability to work 12-hour rotating shifts.
Heavy lifting required (50 lbs.).
Ability and willingness to work after hours and weekends if required.
Required to use a respirator.

Qualifications

Required:

High School Diploma

One year demonstrated technical experience
Ability to function and communicate in a dynamic, project driven team environment
Experience with various software programs, spreadsheets, and word processing
Demonstrated mature judgement and integrity of sensitive and confidential information
High degree of self-motivation, independence, maturity, and decision making

Desired:

Post-Secondary Degree or Diploma in a scientific field
Two years demonstrated leadership experience
Two years GMP experience, protocols and FDA guidance
Five years of related technical experience

Additional Details

This job has a full time weekly schedule.The full-time equivalent pay range for this position is $73,061.00 - $114,158.00/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:

Afternoon

Duration:

No End Date

Job Function:

Manufacturing

Apply on agilent.wd5.myworkdayjobs.com About employer

More about this job

Responsibilities

The Manufacturing Superintendent will supervise and lead a pharmaceutical manufacturing team in daily GMP production activities including purification, isolation, and packaging. Responsibilities include mentoring staff, reviewing batch production records, and ensuring equipment and processing areas meet production schedules.

Requirements

Candidates must have a High School Diploma and at least one year of technical experience, with a preference for a scientific degree and two years of leadership experience. The role requires the ability to work 12-hour rotating night shifts and perform heavy lifting.

Skills

GMP production
Pharmaceutical manufacturing
Team leadership
Batch production records
Process optimization
Equipment troubleshooting
Regulatory compliance
Quality assurance
Fermentation
Synthetic chemistry
Risk assessment
Staff training
Performance evaluation
Technical documentation
Safety protocols

Benefits

Bonus
Stock
Health benefits

Visa sponsorship

Not detected in the job text

Keywords

Manufacturing
Pharmaceuticals
GMP
Fermentation
Synthetic small molecules
ADC
HPAPI
Plasmid DNA
mRNA
LNP
Sterile filling
BPR
Quality control
Process efficiency
Regulatory inspections
Audits
Respirator
Biotech
Contract development

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