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7 дней назад

Associate Manufacturing

70 985 - 96 038$
Формат работы
onsite
Тип работы
fulltime
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Мэтч & Сопровод

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Описание вакансии

Текст:
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TL;DR
Associate Manufacturing (Biotech Manufacturing): Executing drug product packaging, device assembly, labeling, and manufacturing operations at a drug product packaging and assembly plant with an accent on GMP compliance, batch documentation, and production support. Focus on operating semi-automated equipment, performing in-process sampling and basic troubleshooting, supporting investigations and quality records, and driving continuous improvement across production lines.

Location: Thousand Oaks, California, United States; onsite production environment

Annual salary: USD 70,985.20–96,038.80

Company

hirify.global is a biotechnology company developing, manufacturing, and delivering medicines for serious illnesses across oncology, inflammation, general medicine, and rare disease.

What you will do

  • Execute drug product packaging, labeling, bottling, and assembly activities for combination products, vials, tablets, and temperature-sensitive products.
  • Operate semi-automated assembly equipment and manufacturing systems, including SAP, MES, QMTS, LIMS, EDMQ, EPIC, and LabelView.
  • Complete electronic or paper batch records, perform initial batch record reviews, conduct in-process sampling, and operate analytical equipment.
  • Support production planning, staffing, line organization, team meetings, task allocation, and production coverage across multiple shifts.
  • Serve as a subject matter expert during problem-solving sessions, process and equipment investigations, quality record triage, and support for Line Owners and NPI leads.
  • Maintain safe, clean, and compliant operations while drafting procedures, troubleshooting processes, and implementing continuous improvements.

Requirements

  • High school diploma or GED plus 2 years of manufacturing or operations experience; or an associate degree plus 6 months of experience; or a bachelor's degree.
  • Ability to interpret and apply GMP requirements, follow SOPs and manufacturing procedures, and maintain accurate documentation.
  • Ability to work various shifts, including day, swing, overnight, weekends, holidays, and 5x8-hour, 4x10-hour, or 3/4x12-hour schedules.
  • Ability to regularly lift up to 35 pounds, push or pull with up to 50 pounds of force, and stand for extended periods.
  • Ability to perform bending, reaching, climbing, kneeling, squatting, stooping, stair and ladder use, and other physical production-floor movements.
  • Ability to work in a clean room with required protective clothing and around high-pressure systems and heavy equipment.

Nice to have

  • Knowledge of CFR and regulatory requirements, mechanical systems, WIP laboratory equipment, and computers.
  • Basic statistical mathematics, chemistry, biology, physical principles, analytical methods, and purification equipment troubleshooting.
  • Strong written and verbal communication skills and the ability to prioritize work in a fast-paced environment.

Culture & Benefits

  • Collaborative, innovative, science-based environment focused on serving patients.
  • Health, dental, vision, life, disability, and flexible spending benefits for eligible employees and dependents.
  • Retirement and savings plan with company contributions, stock-based long-term incentives, and an annual bonus program.
  • Paid time-off plans and career development opportunities.
  • Sponsorship for this role is not guaranteed.

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