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Manufacturing Superintendent
Job in
Charlottetown, PEI, Canada
Listed on 2026-10-08
Listing for:
BioVectra Inc.
Full Time
position Listed on 2026-10-08
Job specializations:
-
Manufacturing / Production
Production Associate / Production Line, Pharmaceutical Manufacturing, Production Manager, Manufacturing & Industrial Operations
Job Description & How to Apply Below
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 $93,521.00 - $/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: 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:
Manufacturing
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