Назад
Company hidden
9 часов назад

Sr Manager Contract Manufacturing Specialists Team Lead (Manufacturing)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior/lead
Английский
b2
Страна
Singapore
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Sr Manager Contract Manufacturing Specialists Team Lead (Manufacturing): Overseeing contract manufacturing specialists and managing manufacturing operations, site performance, technology transfers, and business process improvements with an accent on cGMP compliance, regulatory requirements, and cross-functional leadership. Focus on coordinating complex transfers, managing deviations and CAPA records, monitoring contract-site performance, and implementing practical AI-enabled workflow solutions.

Location: Singapore, Singapore

Company

hirify.global is a biotechnology company focused on using biology and technology to improve outcomes for patients with serious illnesses.

What you will do

  • Lead and coach a team of contract manufacturing specialists.
  • Oversee manufacturing operations, including budgets, contracts, scopes of work, supply agreements, deviations, CAPA records, and change controls.
  • Monitor contract-site performance metrics, identify improvement opportunities, and oversee procurement and invoice payments.
  • Manage department-wide projects and technology transfers from conception through implementation and close-out.
  • Coordinate transfer risk management, timelines, escalations, and cross-functional activities.
  • Lead business process improvements and implement practical AI-enabled solutions to standardize workflows and reduce manual effort.

Requirements

  • Doctorate degree with 2 years of directly related experience, Master's degree with 6 years, or Bachelor's degree with 8 years.
  • At least 8 years of experience in protein, active pharmaceutical ingredient, drug substance, drug product, or packaging manufacturing.
  • At least 8 years of working knowledge of cGMP principles, FDA and other regulatory guidelines, and validation principles.
  • At least 5 years of experience in people leadership and team management.
  • Experience leading cross-functional and matrixed teams, with strong writing, presentation, and interpersonal skills.
  • Availability to travel as required by business needs and ability to fulfill the medical requirements of the role.

Culture & Benefits

  • Work in an environment that values innovation, collaboration, inclusion, and professional growth.
  • Medical check expenses required for the role are covered by the company.
  • Reasonable accommodations are available during the application and interview process and for essential job functions.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →