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46 минут назад

Production Manager (Pharma Manufacturing)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
India
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR
Production Manager (Pharma Manufacturing): Planning and executing oral solid dosage manufacturing at the Goa site with an accent on production scheduling, new product introduction, cGMP compliance, HSE, and process excellence. Focus on transferring products from the mother plant, improving yields and cycle times, maintaining data integrity, and developing medium- to large-scale teams.

Location: Verna, Goa, India; onsite production role

Company

hirify.global develops medicines and healthcare solutions focused on improving patient outcomes.

What you will do

  • Plan and schedule oral solid dosage production, allocate jobs across work centers, monitor daily activities, and coordinate production requirements with cross-functional departments.
  • Manage changeovers, work-in-progress levels, documentation, and resource utilization to achieve scheduled output.
  • Lead new product transfers from the mother plant to the Goa site, including bills of materials, SAP recipes, batch schedules, reports, approvals, validation, and product registration.
  • Improve processes, cycle times, yields, capacity utilization, manufacturing costs, and product quality through process excellence initiatives and projects.
  • Maintain cGMP systems, manufacturing records, SOPs, batch documents, equipment validation, data integrity, and required training programs.
  • Ensure adherence to health, safety, and environmental policies while developing subordinate and production teams.

Requirements

  • Minimum 10 years of experience in pharmaceutical manufacturing, preferably oral solid dosage.
  • Bachelor’s or Master’s degree in Pharmacy or a Master’s degree in Science.
  • Expertise in production and operations management, performance KPIs, budget setting, monitoring, and goal achievement.
  • Knowledge of Lean and supply chain principles, EHS requirements, cGMP, and quality regulations.
  • Experience managing and developing medium- to large-scale teams, including exposure to change management and unionized workforces.
  • Understanding of new technologies, digital tools, and data analytics; cross-functional experience with Quality, Opex, Engineering, or Maintenance is advantageous.

Culture & Benefits

  • Full-time employment within a global pharmaceutical organization.
  • Equal-opportunity workplace with an emphasis on inclusion and diversity.
  • Leadership expectations include effective communication, negotiation, strategic thinking, results orientation, growth mindset, and people development.
  • Strong focus on patient commitment, product quality, GMP, HSE, and continuous improvement.

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