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Manufacturing Associate I

Capricor Therapeutics · San Diego - SD1 · On Site · Active · $25–$30 / hour · Lever

Job facts

FieldValue
CompanyCapricor Therapeutics
TitleManufacturing Associate I
Normalized title-
Department / teamCapricor Therapeutics / Manufacturing
LocationSan Diego - SD1, United States
Work modelOn Site
Employment typeFull Time (Non Exempt)
Salary$25–$30 / hour
Statusactive
ATS providerLever
Posted / first seen2026-05-13 / 2026-05-29
Changed / last seen2026-05-29 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Capricor Therapeutics.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through Lever.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in San Diego - SD1.Open
Department jobsActive postings in Capricor Therapeutics.Open
Work model jobsActive On Site postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyCapricor Therapeutics
Source2c7239d6-fc4c-4e27-958a-efe2d4c24305
ATS providerLever

Description

Responsibilities Perform routine manufacturing tasks, including media preparation, cell culture, cell counting, formulation, centrifugation, and freezing. Complete and ensure timely, accurate documentation in compliance with GMP standards across batch records, forms, and protocols. Mentor fellow team members on cGMP documentation protocols to ensure the highest standards. Plan, collect, analyze, and report on production data, maintaining comprehensive records and observations. Author, revise, and maintain SOPs through Capricor’s document change system. Oversee inventory, material transfers, and cleanroom procedures to support efficient GMP operations. Prepare technical summaries, protocols, and reports to ensure full documentation of production activities. Lead moderate-complexity CAPAs and assist with deviations and investigations to maintain quality assurance. Take on special projects in manufacturing and development as required. Requirements Bachelor’s degree in Biomedical Engineering, Biological Sciences, or a related field. 1-3 years of experience in a cGMP/cGTP manufacturing environment. Solid laboratory experience in mammalian tissue culture, along with expertise in aseptic techniques. Working knowledge of regulatory standards in biopharmaceutical or tissue banking industries. Strong organizational skills and acute attention to detail within a fast-paced, dynamic setting. Basic molecular biology and flow cytometry skills are a plus. Adaptability to work schedules that may include weekends or holidays as needed.

Full job record

Job IDe9671129e7627d4dee96f199838241f5167bdb44
Org ID06827b08-e077-436c-8800-21c4b43bf549
Source ID2c7239d6-fc4c-4e27-958a-efe2d4c24305
Board ID2c7239d6-fc4c-4e27-958a-efe2d4c24305
Providerlever
Provider Job Keyd1d33e21-fc8f-4328-9e62-31a169b5da7b
TitleManufacturing Associate I
Normalized Title
Statusactive
Activeyes
Location TextSan Diego - SD1
DepartmentCapricor Therapeutics
TeamManufacturing
Employment TypeFull-time (non-exempt)
Workplace Typeon_site
Remote Policy
CountryUnited States
Region
CitySan Diego - SD1
Salary RawUSD 25-30 per-hour-wage
Salary Min25
Salary Max30
Salary CurrencyUSD
Salary Periodhour
Source URLhttps://jobs.lever.co/capricor/d1d33e21-fc8f-4328-9e62-31a169b5da7b
Apply URLhttps://jobs.lever.co/capricor/d1d33e21-fc8f-4328-9e62-31a169b5da7b/apply
First Seen At2026-05-29 07:08:24Z
Last Seen At2026-06-06 19:46:29Z
Last Checked At2026-06-06 19:46:29Z
Last Changed At2026-05-29 07:08:24Z
Inactive At
Source Posted At2026-05-13 16:48:51Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=lever/board=capricor/date=2026-06-06/2026-06-06T19-46-28-937Z-cf3d84cc7d852ac7bf1aa24f5f70fc01441e6412f4f85430c9caa19c1ea65838.json
Event Fields
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  "last_changed_at": "2026-05-29T07:08:24.772Z",
  "active_status": "active"
}
Parsed Structured
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  "remote_policy": null,
  "salary_period": "hour",
  "workplace_type": "on_site",
  "salary_currency": "USD"
}
Extensions
{}
Native Structured
{
  "lists": [
    {
      "text": "Responsibilities",
      "content": "<div>\n\n<li>Perform routine manufacturing tasks, including media preparation, cell culture, cell counting, formulation, centrifugation, and freezing.</li>\n<li>Complete and ensure timely, accurate documentation in compliance with GMP standards across batch records, forms, and protocols.</li>\n<li>Mentor fellow team members on cGMP documentation protocols to ensure the highest standards.</li>\n<li>Plan, collect, analyze, and report on production data, maintaining comprehensive records and observations.</li>\n<li>Author, revise, and maintain SOPs through Capricor’s document change system.</li>\n<li>Oversee inventory, material transfers, and cleanroom procedures to support efficient GMP operations.</li>\n<li>Prepare technical summaries, protocols, and reports to ensure full documentation of production activities.</li>\n<li>Lead moderate-complexity CAPAs and assist with deviations and investigations to maintain quality assurance.</li>\n<li>Take on special projects in manufacturing and development as required.</li>\n\n</div>"
    },
    {
      "text": "Requirements",
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  "country": "US",
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  "updatedAt": null,
  "categories": {
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    "location": "San Diego - SD1",
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