Назад
Company hidden
3 дня назад

Technical Associate, Clinical Manufacturing (Biotechnology)

24 - 40$
Формат работы
onsite
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
US
Релокация
US
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
Technical Associate, Clinical Manufacturing (Biotechnology): Operating and documenting solid dosage pharmaceutical manufacturing processes and complex production equipment with an accent on cGMP compliance, continuous manufacturing, and cross-functional coordination. Focus on executing batch records, performing operator care, applying root cause analysis, and solving routine process and equipment problems in a clinical manufacturing environment.

Location: Onsite in Andover, Massachusetts, United States. Nights and weekends may be required based on process needs. Relocation assistance may be available based on business needs and eligibility.

Salary: $24.22–$40.36 per hour, with potential overtime, weekend, holiday, and other pay premiums.

Company

hirify.global develops and manufactures medicines, with this role supporting clinical pharmaceutical manufacturing operations.

What you will do

  • Execute solid dosage manufacturing activities within continuous manufacturing and PCMM work streams.
  • Follow cGMP and safe handling procedures for pharmaceutical production.
  • Operate complex manufacturing equipment and perform associated operator care tasks.
  • Generate, assist with, and execute batch records and in-process run sheet documentation.
  • Identify and resolve moderately routine problems while ensuring accuracy, quality, and procedural compliance.
  • Coordinate with tech transfer, quality, and engineering teams and support continuous improvement using root cause analysis tools.

Requirements

  • High school diploma or GED with 2+ years of relevant experience.
  • Experience in a biotechnology manufacturing or laboratory environment.
  • Operational knowledge of computerized systems, production control systems, ERP systems, and other business systems.
  • Ability to work effectively as a member of a matrix development team.
  • Excellent oral and written communication skills and proficiency in Microsoft Office Suite.
  • Permanent authorization to work in the United States by any employer is required; U.S. work visa sponsorship is not available.

Nice to have

  • Knowledge of fermentation, downstream processing, and microbial upstream and downstream processes.
  • Experience with cGMP production of Phase I/II clinical drug substances.
  • Experience commissioning and qualifying process equipment.
  • Strong problem-solving, organizational, and attention-to-detail skills.
  • Familiarity with common AI tools and interest in applying them to improve productivity.

Culture & Benefits

  • Collaborative work across manufacturing, tech transfer, quality, and engineering functions.
  • Dynamic team environment with diverse perspectives.
  • 401(k) with hirify.global matching contributions and an additional retirement savings contribution.
  • Paid vacation, holidays, personal days, caregiver/parental leave, and medical leave.
  • Medical, prescription drug, dental, and vision coverage.
  • Physical work environment requiring extended standing, stair climbing, and lifting up to 50 pounds.

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 →