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Filling Supervisor - Afternoon Shift (Pharmaceutical Manufacturing)

72Β 080 - 108Β 120CAD
Π€ΠΎΡ€ΠΌΠ°Ρ‚ Ρ€Π°Π±ΠΎΡ‚Ρ‹
onsite
Π’ΠΈΠΏ Ρ€Π°Π±ΠΎΡ‚Ρ‹
fulltime
Π“Ρ€Π΅ΠΉΠ΄
lead
Английский
b2
Π‘Ρ‚Ρ€Π°Π½Π°
Canada
Вакансия ΠΈΠ· списка Hirify.GlobalВакансия ΠΈΠ· Hirify Global, списка ΠΌΠ΅ΠΆΠ΄ΡƒΠ½Π°Ρ€ΠΎΠ΄Π½Ρ‹Ρ… tech-ΠΊΠΎΠΌΠΏΠ°Π½ΠΈΠΉ
Для мэтча ΠΈ ΠΎΡ‚ΠΊΠ»ΠΈΠΊΠ° Π½ΡƒΠΆΠ΅Π½ Plus

ΠœΡΡ‚Ρ‡ & Π‘ΠΎΠΏΡ€ΠΎΠ²ΠΎΠ΄

Для мэтча с этой вакансиСй Π½ΡƒΠΆΠ΅Π½ Plus

ОписаниС вакансии

ВСкст:
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TL;DR
Filling Supervisor - Afternoon Shift (Pharmaceutical Manufacturing): Supervising pharmaceutical filling operations in an Alliston manufacturing facility, coordinating production deadlines while maintaining product quality and GMP compliance with an accent on team development, automated equipment, and regulatory requirements. Focus on training and mentoring employees, troubleshooting production equipment, completing NCRs and CAPAs, and implementing improvements to reduce costs or improve quality.

Location: Alliston, Ontario, Canada; onsite manufacturing facility

Salary: $72,080–$108,120 annually, including base salary and estimated target incentive payout.

Company

hirify.global is a multinational healthcare and medical products company focused on developing and manufacturing products that save and sustain lives.

What you will do

  • Supervise filling operations and coordinate production activities to meet deadlines while maintaining product quality.
  • Train, mentor, and develop team members through daily coaching and feedback.
  • Set up, adjust, troubleshoot, and repair automated production equipment.
  • Provide technical support for quality and equipment issues and complete NCR and CAPA activities.
  • Identify and implement value improvement projects to reduce product costs or improve quality.
  • Ensure production activities comply with GMPs, SOPs, specifications, regulatory requirements, and budgeted labor standards.

Requirements

  • High school diploma or GED.
  • 3–5 years of manufacturing and supervisory experience in a GMP-regulated facility.
  • Previous supervisory experience in pharmaceutical manufacturing.
  • Knowledge of GMP, ISO standards, and regulatory and corporate requirements.
  • People management, coaching, team development, communication, analytical, and problem-solving skills.
  • Intermediate proficiency with Word, Excel, and PowerPoint; working knowledge of SOPs, specifications, blueprints, PCS documents, and BOMs.

Culture & Benefits

  • Collaborative, multidisciplinary manufacturing environment focused on safety, cleanliness, quality, and accountability.
  • Training, conferences, certifications, and support for advanced degrees.
  • Opportunities for progression from role to role or level to level.
  • Work takes place in a high-energy facility with robust processes supporting employee health and safety.

Hiring process

  • Selected candidates participate in an interview process.
  • Interview results are provided within 45 days of the interview.

Π‘ΡƒΠ΄ΡŒΡ‚Π΅ остороТны: Ссли Ρ€Π°Π±ΠΎΡ‚ΠΎΠ΄Π°Ρ‚Π΅Π»ΡŒ просит Π²ΠΎΠΉΡ‚ΠΈ Π² ΠΈΡ… систСму, ΠΈΡΠΏΠΎΠ»ΡŒΠ·ΡƒΡ iCloud/Google, ΠΏΡ€ΠΈΡΠ»Π°Ρ‚ΡŒ ΠΊΠΎΠ΄/ΠΏΠ°Ρ€ΠΎΠ»ΡŒ, Π·Π°ΠΏΡƒΡΡ‚ΠΈΡ‚ΡŒ ΠΊΠΎΠ΄/ПО, Π½Π΅ Π΄Π΅Π»Π°ΠΉΡ‚Π΅ этого - это мошСнники. ΠžΠ±ΡΠ·Π°Ρ‚Π΅Π»ΡŒΠ½ΠΎ ΠΆΠΌΠΈΡ‚Π΅ "ΠŸΠΎΠΆΠ°Π»ΠΎΠ²Π°Ρ‚ΡŒΡΡ" ΠΈΠ»ΠΈ ΠΏΠΈΡˆΠΈΡ‚Π΅ Π² ΠΏΠΎΠ΄Π΄Π΅Ρ€ΠΆΠΊΡƒ. ΠŸΠΎΠ΄Ρ€ΠΎΠ±Π½Π΅Π΅ Π² Π³Π°ΠΉΠ΄Π΅ β†’