Hims & Hers

Operations Engineer - Peptide API

Hims & Hers$90K — $120K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Chemical Engineering, Chemistry, Biochemistry, or related field.
  • 2+ years of experience in pharmaceutical, biotechnology, or chemical manufacturing.
  • Experience in peptide synthesis or complex chemical manufacturing is strongly preferred.
  • Hands-on experience troubleshooting manufacturing processes and equipment.
  • Working knowledge of cGMP principles and quality systems.

Responsibilities

  • Support daily peptide API manufacturing operations, focusing on solid-phase peptide synthesis (SPPS) and HPLC purification.
  • Troubleshoot manufacturing and process issues in real-time to minimize downtime.
  • Assist in executing production batches with equipment setup and process monitoring.
  • Analyze manufacturing performance metrics to implement process improvements.
  • Support scale-up activities and technology transfers from R&D to manufacturing.
  • Identify opportunities to optimize processes and reduce waste.
  • Maintain accurate GMP documentation, including SOPs and batch records.

Benefits

  • Unlimited PTO, company holidays, and quarterly mental health days.
  • Comprehensive health benefits including medical, dental & vision, and parental leave.
  • Employee Stock Purchase Program (ESPP).
  • 401k benefits with employer matching.
  • Offsite team retreats.
Full Job Description
About the Role:

We are looking for a hands-on Operations Engineer to support and scale manufacturing operations in a peptide API facility. This role will work closely with the Operations Manager to execute daily production, troubleshoot processes, and help build robust, GMP-compliant systems. The ideal candidate is technically strong, highly adaptable, and eager to take ownership in a fast-paced, developing environment operating within applicable regulatory frameworks.

You Will:
  • Support daily peptide API manufacturing operations, including solid-phase peptide synthesis (SPPS), purification (HPLC), and lyophilization.
  • Troubleshoot manufacturing and process issues in real time to minimize downtime and maximize batch success.
  • Assist in the execution of production batches, including equipment setup, process monitoring, and batch documentation.
  • Analyze manufacturing performance, including yield, cycle time, and deviations, and implement process improvements to enhance efficiency and robustness.
  • Support process scale-up activities and technology transfers from R&D into commercial manufacturing.
  • Identify opportunities to optimize manufacturing processes, reduce waste, and improve operational performance.
  • Author and maintain SOPs, batch records, technical reports, and other GMP documentation.
  • Support deviation investigations, CAPAs, change controls, and continuous improvement initiatives.
  • Ensure accurate, timely, and compliant documentation in accordance with cGMP requirements.
  • Assist with equipment commissioning, qualification (IQ/OQ/PQ), calibration, preventive maintenance, and maintenance coordination.
  • Partner with Engineering to troubleshoot equipment issues and support equipment upgrades and reliability initiatives.
  • Collaborate closely with QA/QC to ensure product quality, regulatory compliance, and inspection readiness.
  • Operate within applicable, evolving regulatory frameworks
  • Support internal and external audits while adhering to all safety, environmental, and quality standards.
  • Partner cross-functionally with R&D, Engineering, Quality, and Supply Chain to ensure seamless manufacturing operations and successful introduction of new materials and processes.


You Have:
  • Bachelor's degree in Chemical Engineering, Chemistry, Biochemistry, or a related scientific discipline.
  • 2+ years of experience in pharmaceutical, biotechnology, or chemical manufacturing.
  • Experience supporting peptide synthesis, API manufacturing, or similarly complex chemical manufacturing processes strongly preferred.
  • Prior experience working in a startup or other fast-paced, high-growth manufacturing environment is a plus.
  • Hands-on experience troubleshooting manufacturing processes and equipment in a production environment.
  • Strong understanding of chemical manufacturing principles with the ability and desire to learn peptide manufacturing processes.
  • Experience executing process improvements and translating technical plans into operational results.
  • Working knowledge of cGMP principles, including documentation, compliance, and quality systems.
  • Strong attention to detail with a commitment to maintaining accurate GMP documentation and high-quality standards.
  • Ability to adapt quickly to changing priorities and thrive in a dynamic, evolving environment.
  • Excellent collaboration and communication skills, with the ability to work effectively across Engineering, Manufacturing, Quality, R&D, and Supply Chain teams.
  • Willingness to work flexible hours as needed to support manufacturing operations and production schedules.


Our Benefits (there are more but here are some highlights):
  • Competitive salary & equity compensation for full-time roles
  • Unlimited PTO, company holidays, and quarterly mental health days
  • Comprehensive health benefits including medical, dental & vision, and parental leave
  • Employee Stock Purchase Program (ESPP)
  • 401k benefits with employer matching contribution
  • Offsite team retreats

About Hims & Hers

Hims & Hers is a telehealth company that provides personalized healthcare services to consumers. The company offers a range of products and services, including prescription medications, over-the-counter treatments, and medical consultations. Hims & Hers was founded in 2017 and is headquartered in Los Angeles, California.
Learn more about Hims & Hers
Size
500 employees
Industry
Net Income
-$39 million
Founded
2017
5 Year Trend
+100%
Revenue
$69 million
NASDAQ

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