Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Чётко описанная стажировка в крупной mRNA-биотехнологической компании даёт практический опыт регулируемого производства и предполагает наставничество, но широкий диапазон оплаты и строгие ограничения по допуску создают неопределённость и сужают круг доступных участников.
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Разброс оплатыОграничения по допускуПонятные задачиПрактический опытПерспективная биотехнология
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Co-Op, Biopharmaceutical Manufacturing Operations (Biopharmaceutical Manufacturing): Supporting DNA manufacturing operations through documentation lifecycle management and continuous improvement in a regulated GxP environment with an accent on SOPs, batch records, process standardization, and quality practices. Focus on organizing process data, developing standard work and visual management tools, and coordinating documentation changes across Manufacturing, MSAT, QA, QC, Engineering, and Training teams.
Location: 100% onsite at the hirify.global site in Norwood, Massachusetts, United States; not eligible for remote work. Co-op term: January 18, 2027–June 25, 2027. Applicants must be available for the full duration.
Salary: $20.00–$60.00 per hour.
Company
hirify.global develops mRNA technology and infrastructure for creating and delivering medicines.
What you will do
Support documentation lifecycle management in a regulated GxP manufacturing environment, including creation, revision, review, approval, issuance, and archival.
Assist with updates to SOPs, work instructions, job aids, batch record documents, forms, templates, and training materials.
Participate in continuous improvement initiatives focused on simplification, standardization, error-proofing, and reducing rework in DNA manufacturing.
Gather and organize process maps, time studies, issue logs, deviation themes, operational feedback, and performance metrics.
Develop standard work and visual management tools such as checklists, one-point lessons, and quick reference guides.
Collaborate with Manufacturing, MSAT, QA, QC, Engineering, and Training teams and present progress updates.
Requirements
Current enrollment in a Bachelor's or Master's program in Engineering, Chemistry, Biochemistry, Biology, Biotechnology, Pharmaceutical Sciences, Data/Analytics, or a related field.
Strong analytical, problem-solving, documentation, communication, and cross-functional collaboration skills.
Comfort with common data tools such as Excel and willingness to learn quality systems and tools.
Must already hold work authorization in the United States and maintain it without future sponsorship.
Only U.S. persons eligible under applicable U.S. export control requirements.
Nice to have
GPA of 3.5 on a 4.0 scale or equivalent.
Ability to work independently and contribute effectively to high-performing teams.
Excellent written and verbal communication skills.
Culture & Benefits
In-person work environment with direct mentorship and hands-on collaboration.
Paid time off including vacation, sick time, holidays, volunteer days, and a discretionary year-end shutdown.
Subsidized commuter benefits and location-specific perks.
Free premium access to meditation and mindfulness classes.
Smoke-free, alcohol-free, and drug-free workplace.
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