team leadershipcapacgmpgmp compliancelyophilizationsppspreparative hplcpeptide manufacturing
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
Выше рынка
$100к-120к/год
$62к$82кмедиана$100к
По похожим ролям (49) ~ $82к/год
На СНГ рынке: $1.4к/мес ($1.1к - $1.6к)
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Хорошая вакансия
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Чётко описанные задачи руководителя, подробная зона ответственности в GMP-производстве и зарплата выше рыночного ориентира делают вакансию привлекательной, хотя охват и upstream, и downstream может означать высокую нагрузку.
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Широкая зона ответственностиВыше рынкаХорошие льготыПодробное описаниеБиотехнологии
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Supervisor, CGMP Manufacturing – Downstream (Peptide Manufacturing): Leading hands-on upstream and downstream peptide production at a cGMP facility, including SPPS, preparative HPLC purification, lyophilization, packaging, and production scheduling with an accent on batch compliance, equipment readiness, and on-time delivery. Focus on directing manufacturing teams, investigating deviations, supporting validation and tech transfer, and improving yield, throughput, and cost efficiency.
Location: On-site in Menlo Park, California, United States
Salary: $100,000–$120,000 per year for US-based candidates, plus equity; location-based ranges may apply outside the US.
Company
Hims & Hers is a public health and wellness platform delivering personalized healthcare access from diagnosis through treatment and delivery.
What you will do
Lead upstream cGMP peptide manufacturing, including SPPS, cleavage, filtration, precipitation, and crude peptide isolation.
Direct downstream operations including preparative HPLC purification, lyophilization, final isolation, packaging, and labeling.
Manage production schedules across multiple products, balancing equipment capacity, staffing, materials, and QC turnaround.
Lead deviation and failed-batch investigations, root-cause analysis, CAPAs, process improvements, scale-up, tech transfer, and PPQ campaigns.
Lead, coach, train, and develop chemists, operators, and technicians while maintaining GMP qualifications and shift coverage.
Requirements
Bachelor’s degree in Chemistry, Biochemistry, Chemical Engineering, or a related discipline.
At least 3 years of cGMP manufacturing experience in pharmaceutical, biopharmaceutical, or peptide manufacturing.
Hands-on experience with preparative HPLC purification and lyophilization.
At least 1 year of experience leading or supervising production teams.
Strong knowledge of cGMP batch execution, deviations, CAPAs, data integrity, and manufacturing documentation.
Strong problem-solving, communication, and organizational skills in a fast-moving manufacturing environment.
Nice to have
Commercial-scale SPPS, downstream prep HPLC, and lyophilization experience.
Experience with process validation, PPQ campaigns, and tech transfer of peptide products into GMP manufacturing.
Experience with budget oversight, capital projects, vendor management, staffing, MES, electronic batch records, and continuous improvement.
Culture & Benefits
Competitive salary and equity compensation for full-time roles.
Unlimited PTO, company holidays, and quarterly mental health days.
Medical, dental, vision, and parental leave benefits.
Employee Stock Purchase Program and 401(k) with employer matching.
Offsite team retreats and a focus on safety, ethics, wellness, accountability, and belonging.
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