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8 дней назад

Supervisor, CGMP Manufacturing – Downstream (Peptide Manufacturing)

100 000 - 120 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
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
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.
  • Oversee equipment readiness, qualification, preventive maintenance, vendor coordination, and real-time floor troubleshooting.
  • 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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