Manufacturing Associate I

Capricor Therapeutics, Inc.; San Diego (CA); Presencial; USD 65 000 - 90 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Medical, dental, vision coverage

401(k) with company match

Paid time off and holidays

Resumo da oferta

Capricor Therapeutics is seeking a Manufacturing Associate I to join a GMP-compliant team in a cGMP cleanroom environment. You will perform routine cell culture and manufacturing tasks while ensuring precise documentation and data integrity across batch records and SOPs.

The role supports critical clinical trials and exosome development, with a rotating 12-hour schedule and potential weekend work. Capricor offers a competitive benefits package and growth opportunities.

Qualificações

• 1-3 years of experience in a cGMP/cGTP manufacturing environment.
• Experience with mammalian tissue culture and aseptic techniques.
• Working knowledge of regulatory standards in biopharmaceutical or tissue banking industries.
• Strong organizational skills and acute attention to detail in a fast-paced setting.
• Basic molecular biology and flow cytometry skills are a plus.
• Adaptability to weekend/holiday schedules as needed.

Responsabilidades

• Perform routine manufacturing tasks including media preparation, cell culture, cell counting, formulation, centrifugation, and freezing.
• Complete and ensure timely, accurate GMP documentation across batch records, forms, and protocols.
• Mentor fellow team members on cGMP documentation protocols.
• Plan, collect, analyze, and report on production data with comprehensive records.
• Author, revise, and maintain SOPs in Capricor’s document system.
• Oversee inventory, material transfers, and cleanroom procedures.
• Prepare technical summaries, protocols, and reports of production activities.
• Lead moderate-complexity CAPAs and assist with deviations and investigations.
• Take on special projects in manufacturing and development as required.

Conhecimentos

cGMP knowledge

Cell culture

Documentation

Regulatory awareness

Attention to detail

Ferramentas

Flow cytometry

Molecular biology basics

Descrição da oferta de emprego

Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.

As a Manufacturing Associate I, you’ll be a vital part of Capricor’s efforts in delivering therapies for patients in need. Supporting critical clinical trials and exosome development, you’ll perform meticulous production tasks and documentation to uphold our quality and compliance standards. This role places you in a cleanroom environment, where precision and attention to GMP standards are essential. You’ll be instrumental in ensuring that each production step is performed with accuracy, ultimately contributing to Capricor’s therapeutic success.

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

• 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.

This position follows an AWS/Panama 2-2-3 schedule, which is a rotating shift pattern designed to provide consistent coverage and extended time off.

Schedule Details

12-hour shifts

Week 1: Work Monday & Tuesday, off Wednesday & Thursday, work Friday-Sunday

Week 2: Off Monday & Tuesday, work Wednesday & Thursday, off Friday-Sunday

This creates a repeating cycle of 2 days on, 2 days off, 3 days on, then the reverse the following week.

Why Capricor?

Capricor Therapeutics is advancing cell and exosome-based therapies with a focus on serious diseases where patients and families need new treatment options. Our work is grounded in scientific rigor, collaboration, and a shared commitment to moving meaningful therapies forward. Joining Capricor means being part of a mission-driven team working at the intersection of innovation, execution, and patient impact.

Come Work With Us

At Capricor, you’ll join a collaborative environment where employees are encouraged to contribute, grow, and help build the systems, science, and operations needed to support our next stage of growth. We value people who are thoughtful, accountable, hands‑on, and motivated by work that can make a real difference.

Compensation And Benefits

The posted salary range represents Capricor’s good‑faith estimate of the salary range reasonably expected to be paid for this position at the time of hire. Final compensation will be determined based on job‑related factors, including the candidate’s relevant experience, education, skills, certifications, scope of role, location, and internal equity.

This position may also be eligible for a discretionary annual performance bonus and, depending on the level of the role, long‑term equity incentive awards in accordance with company policy.

Capricor Therapeutics offers a comprehensive benefits package that includes employer‑sponsored medical, dental, and vision coverage; company‑paid basic life and AD&D insurance; a 401(k) plan with company match; paid time off and company holidays; and paid parental leave. Additional voluntary benefits and wellness programs may also be available.