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Posted 23 days ago

Production Technician

@ BioVectra Inc.

Charlottetown, Prince Edward Island

$37k–$58k/yrFull-time
Apply now
SIGNALS

Overview

BioVectra Inc., now part of Agilent, is hiring a full-time Production Technician for contract manufacturing of active pharmaceutical ingredients. The role involves GMP production, filling and packaging equipment operation, and batch documentation on a 12-hour rotating day and night schedule. Pay is $37,349 to $58,358 per year CAD, plus bonus, stock and benefits eligibility.

Pay:

$37,349–$58,358 a year

Responsibilities:

  • Operate production, filling and packaging equipment
  • Weigh, measure and verify raw materials
  • Assist with validation of filtration, cleaning and sterilization
  • Maintain regulatory documentation and in-process testing records
  • Work a 12-hour rotating day and night shift

Requirements summary:

  • High school diploma or equivalent
  • Ability to lift up to 25 kg (55 lbs)
  • Strong written and verbal communication skills
  • Manufacturing experience (desired)
  • Documentation in a regulated environment (desired)
  • Experience in a cGMP-regulated environment (desired)

Tools & skills

Source and dates

Employer career site / ATS feed · workday

Employer posting date
2026-10-14
First seen by our source
2026-10-15
Source record updated
2026-11-01

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

Job details

SeniorityEntry level
DepartmentManufacturing & production
Hours per week40 (estimated)
Scheduleday, overnight
Travelair: none · ground: none
Work settingPlant or factory, Laboratory
PositionSitting and standing
Physical demandsphysical moderate · lift 55 lb · computer low
LanguagesEnglish
EducationHigh school (required)

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

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 responsibilities will include:


  • Work a 12-hour rotating shift schedule, including days and nights.
  • Comply with GMP, GDP, and Standard Operating Procedures (SOPs) while performing production and assembly processes in a manufacturing environment.
  • Operate production, filling, and packaging equipment.
  • Weigh, measure, and verify raw materials to ensure batches contain the correct ingredients and quantities.
  • Assist with the validation of processes and equipment related to filtration, cleaning, and sterilization.
  • Maintain accurate documentation to meet regulatory requirements and assist with in-process testing to ensure batches meet established specifications.

Qualifications

Required:

  • High school diploma or equivalent.
  • Ability to lift up to 25 kg (55 lbs).
  • Strong written and verbal communication skills.

Desired:

  • Manufacturing experience.
  • Experience maintaining documentation in a regulated environment.
  • Experience working in a cGMP-regulated environment.

Additional Details

This job has a full time weekly schedule.The full-time equivalent pay range for this position is $37,349.00 - $58,358.00/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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