hims & hers

2 weeks ago

Quality Specialist, Peptide API & Development

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 22 hours agoStatus: Live

Job Summary

Support Quality operations at a peptide-focused API manufacturing and development site by executing and maintaining core GMP quality systems. Own day-to-day document control, training administration, and the lifecycle of deviations, investigations, CAPAs, and change control. Review GMP records for accuracy and compliance, assist batch record reviews, and help ensure inspection readiness across manufacturing, lab, warehouse, and support areas.

Location: Menlo Park

Workplace: Onsite

Employment Type: Full time

Job Function: Quality & Regulatory (Non-Software)

Key Responsibilities

•Support day-to-day execution of site Quality Systems, including document control, training, deviations, CAPA, change control, and record management.
•Review GMP records for completeness, accuracy, and compliance with approved procedures and Good Documentation Practices.
•Assist with issuing, tracking, reconciliation, and archival of controlled documents (SOPs, forms, logbooks, protocols, reports).
•Support batch record review activities for peptide API manufacturing and escalate issues to Quality leadership.
•Assist in tracking and coordinating deviations, investigations, CAPAs, change controls, and action items to closure.

Pay and Benefits

Salary: USD 95,000 - 115,000 annually

Equity and Bonus:Equity

Perks:Health InsuranceDentalVisionPaid LeaveParental Leave401k

Key Requirements

•Bachelor’s degree in Chemistry, Biology, Biochemistry, Pharmaceutical Sciences, or related field (preferred).
•2–5+ years of experience in Quality, manufacturing, laboratory, or document control roles in pharmaceutical/biotech/GMP-regulated environments.
•Working knowledge of cGMP principles, Good Documentation Practices, and basic quality systems concepts.
•Strong organizational skills to manage multiple priorities and follow through on details.
•Preferred experience using electronic quality systems, document management systems, or training systems.

Experience:2+ yearsPharmaceuticalBiotechGMP-regulatedDocument controlPeptide APISterile operationsStartup environment

Education:Bachelor's in Chemistry, Biology, Biochemistry, Pharmaceutical Sciences, or related field

Skills:Detail-orientedExecution-focusedQuality mindsetCollaborationAdaptable

Company Brief

hims & hers

A telehealth and consumer wellness platform offering personalized care and products across sexual health, hair, mental health, dermatology, weight loss and primary care via digital consultations, prescriptions, and fulfillment.

Industry: HealthTech

Company Size: Enterprise (1,001+ employees)

Revenue: USD 1B+

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: San Francisco, United States

Founded: 2017

Glassdoor: 2.9

Website LinkedIn Glassdoor

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hims & hers

2 weeks ago

Quality Specialist, Peptide API & Development

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 22 hours agoStatus: Live

Job Summary

Location: Menlo Park

Workplace: Onsite

Employment Type: Full time

Job Function: Quality & Regulatory (Non-Software)

Key Responsibilities

•Support day-to-day execution of site Quality Systems, including document control, training, deviations, CAPA, change control, and record management.
•Review GMP records for completeness, accuracy, and compliance with approved procedures and Good Documentation Practices.
•Assist with issuing, tracking, reconciliation, and archival of controlled documents (SOPs, forms, logbooks, protocols, reports).
•Support batch record review activities for peptide API manufacturing and escalate issues to Quality leadership.
•Assist in tracking and coordinating deviations, investigations, CAPAs, change controls, and action items to closure.

Pay and Benefits

Salary: USD 95,000 - 115,000 annually

Equity and Bonus:Equity

Perks:Health InsuranceDentalVisionPaid LeaveParental Leave401k

Key Requirements

•Bachelor’s degree in Chemistry, Biology, Biochemistry, Pharmaceutical Sciences, or related field (preferred).
•2–5+ years of experience in Quality, manufacturing, laboratory, or document control roles in pharmaceutical/biotech/GMP-regulated environments.
•Working knowledge of cGMP principles, Good Documentation Practices, and basic quality systems concepts.
•Strong organizational skills to manage multiple priorities and follow through on details.
•Preferred experience using electronic quality systems, document management systems, or training systems.

Experience:2+ yearsPharmaceuticalBiotechGMP-regulatedDocument controlPeptide APISterile operationsStartup environment

Education:Bachelor's in Chemistry, Biology, Biochemistry, Pharmaceutical Sciences, or related field

Skills:Detail-orientedExecution-focusedQuality mindsetCollaborationAdaptable

Company Brief

hims & hers

Industry: HealthTech

Company Size: Enterprise (1,001+ employees)

Revenue: USD 1B+

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: San Francisco, United States

Founded: 2017

Glassdoor: 2.9

Website LinkedIn Glassdoor