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Manufacturing Superintendent

@ BioVectra Inc.

Charlottetown, Prince Edward Island

$71k–$112k/yrFull-time1+ years experience
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Overview

BioVectra Inc. is hiring a Manufacturing Superintendent to lead a GMP pharmaceutical production team on nights (7 pm to 7 am, 12-hour rotating shifts). The role supervises team leads, reviews batch production records, troubleshoots equipment and process issues, and takes part in hiring, training and regulatory audits. The posting states a full-time schedule and a pay range of $71,424 to $111,600 per year plus bonus, stock and benefits eligibility.

Pay:

$71,424–$111,600 a year

Responsibilities:

  • Superviser les chefs d'équipe et la production
  • Examiner les dossiers de production par lots (BPR)
  • Dépanner les équipements et les procédés
  • Participer à l'embauche, à la formation et à l'évaluation du personnel
  • Participer aux inspections réglementaires et aux audits

Requirements summary:

  • Diplôme d'études secondaires
  • Un an d'expérience technique démontrée
  • Capacité de travailler dans une équipe dynamique axée sur les projets
  • Expérience des logiciels, tableurs et traitement de texte
  • Deux ans d'expérience en leadership et en BPF (GMP) souhaités

Tools & skills

Source and dates

Employer career site / ATS feed · workday

Employer posting date
2026-10-07
First seen by our source
2026-10-08
Source record updated
2026-11-05

These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.

Job details

SeniorityMid level
DepartmentManufacturing & production
Experience1+ years
Manages peopleYes
Hours per week40
Scheduleevening, weekends, overnight
Travelair: none · ground: none
Work settingPlant or factory, Laboratory
PositionSitting and standing
Physical demandsphysical high · lift 50 lb · computer moderate
LanguagesEnglish
EducationHigh school (required), College diploma (preferred)
Fields of studyScientific field
Perks mentionedPerformance bonus, Stock or equity

Summary and details written by AI from the posting; the employer’s posting is the authority.

BioVectra Inc.

FieldValue
HeadquartersCharlottetown
Open jobs on Jobsy17
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 requestsEnsuring 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 $71,424.00 - $111,600.00/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:

No

Shift:

Swing

Duration:

No End Date

Job Function:

Manufacturing

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