gmpprocess engineeringpharmaceutical manufacturingtechnology transferbiotechcleanroomsterile filtrationaseptic fill finish
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Обязанности понятны и дают практический опыт в стерильном фармпроизводстве, переносе процессов и GMP. При этом в CDMO-проектах задачи могут меняться в зависимости от клиента.
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Работа на производствеПонятные обязанностиПоддержка развитияПроекты для клиентов
Оценка от Hirify AI
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Описание вакансии
Текст:
Hirify AI/Оригинал
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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