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6 дней назад

Manufacturing Representative - Day Shift

32 - 50$
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
Manufacturing Representative - Day Shift (Oligonucleotide Manufacturing): Commissioning, qualifying, and validating equipment and systems while manufacturing oligonucleotide APIs in a GMP-regulated facility with an accent on tech transfer, scale-up, and process equipment operation. Focus on troubleshooting complex manufacturing systems, maintaining regulatory documentation, and establishing procedures and training materials for a new operation.

Location: US-CO-Frederick. Candidates must work Monday–Friday, 8 am–5 pm during startup and training, then transition to a custom 3x12 or 4x10 shift based on business needs.

Pay: $31.92–$49.88 per hour, plus eligibility for bonus, stock, and benefits.

Company

hirify.global is expanding oligonucleotide manufacturing capabilities through a new facility supporting therapeutic development.

What you will do

  • Support commissioning, qualification, and validation of new manufacturing equipment and systems.
  • Manufacture oligonucleotide APIs in a GMP-regulated environment.
  • Assist with technology transfer and process scale-up from Technical Services to Manufacturing.
  • Operate, maintain, calibrate, and troubleshoot critical process equipment and laboratory instruments.
  • Write and revise SOPs and other regulatory documentation.
  • Collaborate with Engineering, Validation, and Quality on CAPAs, deviations, change controls, and technical issues.

Requirements

  • Associate’s or Bachelor’s degree in a scientific or technical field, or equivalent experience.
  • At least 1 year of pharmaceutical or GMP manufacturing experience.
  • Strong attention to detail, documentation, math, and troubleshooting skills.
  • Ability to follow SOPs and safety protocols and work with complex equipment.
  • Experience in chemical processing, PSM-regulated, cleanroom, or FDA-regulated manufacturing environments is highly desired.
  • Availability for the stated startup and subsequent custom shift schedules.

Nice to have

  • Familiarity with oligonucleotide synthesis, HPLC, UFDF, or lyophilization.
  • Mechanical aptitude and experience maintaining manufacturing equipment.

Culture & Benefits

  • Hands-on role supporting the startup of a new manufacturing operation.
  • Opportunity to help establish best practices and training materials for future team members.
  • Bonus, stock, and benefits eligibility.
  • Work focused on integrity, trust, respect, teamwork, accountability, and quality.

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