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7 дней назад

Sr. Manufacturing Associate I, Label & Packaging

74 000 - 118 400$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
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
Sr. Manufacturing Associate I, Label & Packaging (GMP/Pharmaceutical Manufacturing): Executing and supporting compliant labeling and packaging operations for parenteral drug products, including vials and prefilled syringes, with an accent on line readiness, label control, documentation, and in-process verification. Focus on troubleshooting packaging equipment and systems, supporting investigations and CAPAs, coaching associates, and maintaining quality and throughput in a regulated manufacturing environment.

Location: Norwood, Massachusetts, United States; onsite manufacturing role. Only individuals who qualify as U.S. persons are eligible due to U.S. export control requirements.

Salary: $74,000–$118,400 per year, with potential discretionary bonus, incentive compensation, or equity.

Company

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

What you will do

  • Execute line setup, operation, changeovers, labeling, cartoning, kitting, aggregation, and case-packing activities according to approved SOPs and cGMP requirements.
  • Perform line clearances, room and equipment readiness checks, controlled material staging, label issuance and reconciliation, and in-process barcode, vision, print, and scan verification.
  • Complete accurate contemporaneous documentation in logbooks, batch records, MES, eBR, and labeling systems in accordance with ALCOA+ principles.
  • Identify, contain, and escalate deviations, atypical events, equipment issues, and system problems; support investigations, CAPAs, change controls, and corrective actions.
  • Train and coach associates through structured on-the-job training and peer guidance while promoting safe, compliant execution.
  • Collaborate with QA/QC, MS&T, Engineering, Supply Chain, and Digital/Systems teams on equipment readiness, engineering runs, and continuous improvement.

Requirements

  • High school diploma or GED required; an associate’s or bachelor’s degree in a scientific or technical field is preferred.
  • Typically 3–5 years of experience in GMP manufacturing or regulated operations; pharmaceutical or biotechnology labeling and packaging experience is strongly preferred.
  • Experience with packaging batch records, line clearance, in-process checks, label control and reconciliation, and equipment or system troubleshooting.
  • Ability to work independently, maintain accurate ALCOA+ documentation, support training, escalate issues, and solve shift-level problems.
  • Ability to work in controlled environments, follow gowning and PPE requirements, stand for extended periods, perform repetitive tasks, and lift up to approximately 35 pounds.
  • Must qualify as a U.S. person under U.S. export control laws; non-U.S. persons cannot be sponsored for an export control license.

Nice to have

  • Working knowledge of cGMP expectations, ALCOA+ principles, packaging batch records, logbooks, and electronic manufacturing or labeling systems.
  • Experience providing peer coaching and serving as a resource for newer associates.
  • Strong ownership, reliability, flexibility, safety focus, and commitment to continuous improvement.

Culture & Benefits

  • Healthcare and voluntary benefit programs.
  • Fitness, mindfulness, and mental health support.
  • Family planning benefits, including 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.
  • Work may include off-hours, weekends, overtime, and different shifts according to production needs.

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