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7 дней назад

Manufacturing Associate II (DP Operations)

63 200 - 100 900$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
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 Associate II (DP Operations) (cGMP/aseptic manufacturing): Performing formulation, sterile filtration, aseptic filling, visual inspection, and electronic batch record documentation in a 100% onsite pharmaceutical manufacturing environment with an accent on cleanroom operations, equipment readiness, and compliant in-process controls. Focus on executing right-first-time manufacturing, investigating deviations, maintaining ALCOA+ records, and supporting cross-functional continuous improvement on a 12-hour night shift.

Location: Norwood, Massachusetts; 100% onsite. The role requires a 12-hour night shift from 6:00 PM to 6:00 AM, with flexibility for weekends, holidays, overtime, and operational coverage. Only U.S. persons are eligible due to U.S. export control requirements, and visa sponsorship is not available.

Salary: $63,200–$100,900 per year, with potential discretionary bonus, incentive compensation, or equity subject to eligibility.

Company

hirify.global develops mRNA technology and medicines through a science-driven biotechnology platform.

What you will do

  • Perform formulation, sterile filtration, vial and syringe filling, and downstream visual inspection under cGMP and SOP requirements.
  • Prepare materials and components, check equipment, complete line clearances, and perform routine cleanroom and equipment cleaning.
  • Document manufacturing activities contemporaneously in logbooks, MES, and electronic batch records using ALCOA+ principles.
  • Execute in-process controls, record results, and maintain equipment and process parameters within established specifications.
  • Escalate deviations, atypical events, and equipment issues while supporting troubleshooting and investigations.
  • Collaborate with QA, QC, MS&T, Facilities, Supply Chain, and other functions; support SOP updates, continuous improvement, training, and peer mentoring.

Requirements

  • Associate or bachelor’s degree in a scientific field, or a high school diploma with equivalent experience.
  • Two to four years of GMP manufacturing or a similar experience is preferred; strong entry-level candidates may be trained.
  • Ability to work in cleanrooms with full gowning, stand for extended periods, and lift approximately 35 pounds.
  • Basic computer skills for batch records and training systems, with reliable and accurate documentation practices.
  • Corrected 20/20 vision and the ability to distinguish all colors across the visible spectrum; vision testing is required at hiring and annually.
  • Must be eligible to work as a U.S. person and work onsite in Norwood, Massachusetts.

Culture & Benefits

  • In-person, site-based work with direct collaboration, mentorship, and hands-on operational support.
  • Healthcare and voluntary benefit programs.
  • Fitness, mindfulness, mental health, family planning, fertility, adoption, and surrogacy support.
  • Paid vacation, volunteer days, sabbatical, global recharge days, and discretionary year-end shutdown.
  • Savings and investment programs, plus location-specific benefits.
  • Smoke-free, alcohol-free, and drug-free workplace.

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