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17 часов назад

Project Management Associate (Oligo Production)

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

Текст:
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TL;DR
Project Management Associate (Oligo Production) (manufacturing and project management): Managing oligonucleotide manufacturing operations and customer projects with an accent on production schedules, quality, cost objectives, and GMP-compliant processes. Focus on leading validation and improvement projects, coordinating production teams, and tracking KPIs, timelines, and QC requirements.

Location: Louisville, KY, USA; full-time onsite, Monday–Friday, 8:00 a.m.–5:00 p.m.

Company

hirify.global is an international life sciences company providing analytical testing, laboratory, genomic, pharmaceutical, environmental, food, cosmetic, and clinical research services.

What you will do

  • Lead manufacturing teams and manage supervisors, team leads, production chemists, laboratory technicians, and contractors.
  • Coordinate customer and production projects, tracking timelines, costs, process implementation, deadlines, and results.
  • Develop schedules, monitor KPIs, prepare reports, and communicate progress or delays to managers and organizational stakeholders.
  • Lead validation activities for new projects and equipment, as well as Kaizen and other departmental improvement projects.
  • Maintain current bills of materials and manufacturing documentation in the electronic document management system.
  • Coordinate QC-related questions for Red Folder and VIP projects, including reviewing MS/HPLC traces before the next production step.

Requirements

  • Bachelor’s degree in engineering, chemistry, biochemistry, or a similar field.
  • At least one year of experience in manufacturing, oligonucleotide production, or a similar field.
  • Proficiency in organic synthesis and purification techniques.
  • Working knowledge of GMP, ISO, and QSR regulations, including FDA-QMS/QSR and ISO 9001 standards.
  • Experience documenting and analyzing experimental data, with strong computer, scientific, organizational, communication, and attention-to-detail skills.
  • Ability to work onsite in Louisville, Kentucky, Monday through Friday.

Culture & Benefits

  • Comprehensive medical, dental, and vision coverage.
  • Life and disability insurance.
  • 401(k) plan with company match.
  • Paid vacation and holidays.
  • Work in a life sciences organization with laboratories and operations across more than 50 countries.

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