{"id":4258364,"url":"https://alion.io/job/agilent-technologies-manufacturing-superintendent","title":"Manufacturing Superintendent","company":{"id":6171,"name":"Agilent Technologies","domain":"agilent.com","url":"https://alion.io/company/agilent-technologies","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":84,"open_postings":52,"ghost_share":0,"stale_share":0.635,"repost_share":0.019,"time_to_fill_p50_days":34,"computed_at":"2026-11-12T10:38:37Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"senior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Charlottetown, Canada"],"countries":["CA"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":73061,"max":114158,"currency":"CAD","period":"year","gross":null,"usd_annual":80079},"salary_estimate":null,"experience_years_min":5,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GMP","optional":false}],"status":"live","first_seen_at":"2026-11-13T14:28:17Z","employer_posted_date":"2026-11-13","last_verified_at":"2026-11-13T14:28:17Z","board_verified":true,"closed_at":null,"days_open":0,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":0},"description":"Job Description\nTHIS IS A NIGHTS ONLY POSITION 7 pm-7am\nBIOVECTRA, 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.\nThe 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.\nThe responsibilities will include:\nOverseeing team leads in accomplishing overall departmental production needs and reviewing work to ensure consistency\nMentoring members of the production group and providing constructive input\nReviewing 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)\nAssisting in updates on batch production records (BPRs) to optimize process efficiencies and to assist in developing new BPR’s or work instructions\nSupporting manufacturing schedules through appropriate documentation and staging requests\nEnsuring material and/or solvent counts are completed upon request\nEnsuring the equipment and processing areas are in a ready state to meet the posted schedule\nIdentifying, troubleshooting, and resolving equipment, process and facility issues as well as contributing to process risk assessments\nParticipating in the hiring, training, and performance evaluation of employees\nParticipating in regulatory inspections and audits\nInteracting with multi-discipline units and personnel to ensure product quality and on-time delivery is adhered to\nFlexibility for after-hours consultation during manufacturing activities or during infrequent production activities will be required\nParticipating in client meetings and teleconferences\nProviding guidance and oversight to a team of employees\nWORK CONDITIONS:\n Ability to work 12-hour rotating shifts.\n Heavy lifting required (50 lbs.).\n Ability and willingness to work after hours and weekends if required.\nRequired to use a respirator.\nQualifications\nRequired:\nHigh School Diploma\nOne year demonstrated technical experience\nAbility to function and communicate in a dynamic, project driven team environment\nExperience with various software programs, spreadsheets, and word processing\nDemonstrated mature judgement and integrity of sensitive and confidential information\nHigh degree of self-motivation, independence, maturity, and decision making\nDesired:\nPost-Secondary Degree or Diploma in a scientific field\nTwo years demonstrated leadership experience\nTwo years GMP experience, protocols and FDA guidance\nFive years of related technical experience\nAdditional Details\nThis 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. 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