H

hims & hers

Connects patients to online medical care

Operations Engineer/ Production Scientist - Peptide Manufacturing

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeMenlo Park, CA, USAIn-person

About the Job

Requirements

  • A bachelor's degree in Chemical Engineering, Chemistry, Biochemistry, Pharmaceutical Sciences, Biotechnology, or a related field is required.
  • Three to seven years of experience in pharmaceutical, biotechnology, peptide manufacturing, API manufacturing, or related chemical processing environments is required.
  • Hands-on experience supporting GMP manufacturing operations, investigations, and process validation activities is required.
  • Direct experience with Solid-Phase Peptide Synthesis is required.
  • Experience analyzing manufacturing process data and implementing process improvements is required.
  • Technical troubleshooting skills that enable identifying root causes and implementing sustainable corrective actions are required.
  • Experience authoring or revising GMP documentation, including SOPs, batch records, technical reports, deviation investigations, CAPAs, change controls, or risk assessments is required.
  • Ability to work closely with Manufacturing, Quality, Engineering, and Supply Chain teams is required.
  • Ability to translate technical process observations into actionable recommendations is required.

Responsibilities

  • Serve as the technical process owner for peptide manufacturing operations, including Solid-Phase Peptide Synthesis, purification, and lyophilization.
  • Support manufacturing teams during batch execution and provide real-time technical troubleshooting on the manufacturing floor.
  • Monitor critical process parameters and key performance indicators across peptide manufacturing processes.
  • Collect, analyze, and trend manufacturing data to identify process variability, yield losses, bottlenecks, and improvement opportunities.
  • Develop and maintain manufacturing dashboards tracking yield, cycle time, solvent usage, throughput, batch success rate, and right-first-time metrics.
  • Evaluate coupling efficiency, resin performance, deprotection efficiency, impurity formation trends, and other process indicators related to Solid-Phase Peptide Synthesis performance.
  • Identify and implement improvements to reaction conditions, cycle parameters, manufacturing practices, and process controls.
  • Lead initiatives to improve product yield, throughput, cycle time, overall equipment effectiveness, and process robustness.
  • Apply Lean Manufacturing, Six Sigma, statistical analysis, and structured root cause analysis tools to reduce waste and process variation.
  • Lead or support investigations related to process excursions, atypical results, yield losses, manufacturing deviations, and equipment or process issues.
  • Use Fishbone Analysis, 5 Why Analysis, Failure Mode and Effects Analysis, and Statistical Process Control to identify root causes and drive corrective actions.
  • Author and revise SOPs, Master Batch Records, process descriptions, manufacturing instructions, technical reports, and process performance summaries.
  • Support deviation investigations, CAPAs, change controls, risk assessments, process validation, and continued process verification activities.
  • Ensure technical documentation is accurate, complete, and compliant with current Good Manufacturing Practice requirements.
  • Partner with Operations, Engineering, Quality, Supply Chain, and site leadership to improve manufacturing performance.
  • Support implementation of new equipment, technologies, and manufacturing systems.
  • Participate in production planning, operational excellence reviews, and process-improvement meetings.
  • Provide technical mentoring and training to manufacturing personnel on process understanding and best practices.

Desired Qualifications

  • A master's degree or Ph.D. in Chemical Engineering, Chemistry, Biochemistry, Pharmaceutical Sciences, Biotechnology, or a related field is preferred.
  • Experience in commercial-scale peptide manufacturing is preferred.
  • Experience with process monitoring, Statistical Process Control, and process capability assessments is preferred.
  • Lean Six Sigma Green Belt or Black Belt certification is preferred.
  • Experience using statistical software and data analysis tools such as Minitab, Power BI, advanced Excel analytics, or similar tools is preferred.
  • Experience in a startup or rapidly growing manufacturing organization is preferred.

About the Company

hims & hers

Connects patients to online medical care

Hims & Hers operates a consumer health platform that connects people with licensed providers for online consultations and ongoing care. Its Hims and Hers brands give customers access to services for hair loss, sexual health, mental health, skin care, and weight management, alongside prescription and nonprescription products. Providers assess patients and make treatment decisions, while the group coordinates digital records, follow-up, and fulfillment through owned and partner pharmacies. Revenue comes from product sales and subscriptions that combine recurring shipments with access to care. Hims & Hers was founded in 2017 and is headquartered in San Francisco, California.

Company size
1,001-5,000
Company stage
Post IPO Equity
Headquarters
San Francisco, California
Founded
2017

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