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3 дня назад

Senior Process Development Associate (Enzyme Manufacturing)

75 000 - 85 000$
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
Senior Process Development Associate (Enzyme Manufacturing): Building and optimizing recombinant protein expression and purification processes for routine enzyme manufacturing with an accent on scalable process design, experimental development, and quality requirements. Focus on identifying critical process parameters, managing process risks, validating equipment and systems, and supporting manufacturing through technical documentation and training.

Location: Boulder, Colorado, onsite. Local candidates preferred. Applicants must be eligible to work in the United States; visa sponsorship requirements will be assessed during the application process.

Salary: $75,000–$85,000 base compensation annually, plus bonus and equity.

Company

hirify.global develops and manufactures genomic and enzyme-related products.

What you will do

  • Build, optimize, and transfer recombinant protein expression and purification processes into routine manufacturing.
  • Design and execute experiments, document results, and develop scalable processes based on product requirements.
  • Identify process risks, critical process parameters, and critical-to-quality attributes, then develop appropriate controls and mitigations.
  • Support process, equipment, and computer-system validation, material qualification, and process updates for on-market products.
  • Author work instructions, batch record templates, and production documentation; prepare and deliver operator training.
  • Collaborate with R&D, Production, IT, Quality Assurance, and other cross-functional teams.

Requirements

  • Bachelor’s degree, ideally in Biochemistry or Biochemical Engineering, with at least 5 years of relevant process development or bioprocess manufacturing experience; or a master’s degree with 3 years of experience.
  • Experience with recombinant protein expression, protein purification, chromatography, and basic protein biochemistry.
  • Technical understanding of PCR, next-generation sequencing, risk management, FMEA, measurement systems analysis, Gauge R&R, DOE, SPC, regression analysis, ANOVA, and t-tests.
  • Experience with ISO 9001 and/or ISO 13485 standards or a structured quality management system.
  • Strong scientific communication, problem-solving, organization, task management, and cross-functional collaboration skills.
  • Ability to work onsite in Boulder, Colorado, and eligibility to work in the United States are required.

Culture & Benefits

  • Collaborative work across R&D, Production, IT, and Quality Assurance.
  • Flexible Time Off and paid holidays.
  • Medical coverage with the employer covering 75% of the base plan, plus dental, vision, and employee assistance benefits.
  • Paid parental leave and employer-paid life and AD&D insurance.
  • 401(k) retirement plan with a 4% employer match.

Hiring process

  • Submit a PDF letter of motivation and resume or curriculum vitae.
  • Applications are reviewed on a rolling basis until the position is filled.
  • Selected candidates must provide three professional references; pre-employment checks may apply.

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