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2 дня назад

Process Engineer I (Pharmaceutical Manufacturing)

Формат работы
onsite
Тип работы
fulltime
Грейд
junior
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
Process Engineer I (Pharmaceutical Manufacturing): Facilitating technology transfer and executing engineering functions for client-specific formulation and filling operations with an accent on scale-up, GMP compliance, sterile filtration, and cleanroom processes. Focus on leading batch record activities, specifying process equipment, managing GMP investigations, and training teams on procedures and equipment operation.

Location: Albuquerque, NM, United States; onsite role

Company

hirify.global is a global contract development and manufacturing organization supporting pharmaceutical and biotech companies with the development and manufacture of life-saving treatments.

What you will do

  • Facilitate technology transfer of client processes and execute process design, scale-up, documentation, and engineering activities.
  • Lead batch record and process activities for client formulation and filling operations, including equipment preparation, bulk formulation, sterile filtration, and filling support.
  • Act as a subject-matter expert for GMP investigations, including CAPA, departures, and CCRs, from initiation through closure.
  • Specify process equipment, author equipment-operation instructions, and document process flows for cleanroom operations.
  • Develop procedures, provide training on SOPs and work instructions, and guide supporting team members.
  • Communicate engineering progress directly to clients and collaborate with internal functions while maintaining safety and compliance.

Requirements

  • Bachelor’s degree in Biology, Chemical Engineering, or a related field.
  • At least two years of experience in the pharmaceutical or biotech industry is preferred; process engineering experience is preferred.
  • Experience with aseptic fill/finish is preferred.
  • Ability to work with moderate supervision, take initiative, communicate effectively with clients and internal departments, and maintain a meticulous, organized approach.
  • Strong attention to detail and familiarity with aseptic technique and cleanroom personnel flows are desirable.
  • Working knowledge of process engineering aids such as sanitary connections, valves, and pharmaceutical process design.
  • Must pass a background check and drug screen.
  • Must be able to obtain and maintain gowning certification; media qualification may also be required.
  • May be required to wear a respirator.

Nice to have

  • Knowledge of process flows, including disposable strategies, filtration, mixing strategies, and fluid transfer between vessels.
  • Experience with aseptic fill/finish and pharmaceutical or biotech process engineering.

Culture & Benefits

  • Full-time employment with paid training, vacation, and holidays.
  • Benefits are available from the first day of employment; vacation accrual begins on the first day.
  • 401(k) program with matching contributions.
  • Education reimbursement, learning platform, and career advancement opportunities.
  • Collaborative, safety-focused environment with mentoring and guidance responsibilities.

Hiring process

  • All interested applicants must apply online.
  • hirify.global does not accept unsolicited applications from headhunters or recruitment firms without a valid, signed agreement for the specific position.

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