Manufacturing Associate I

Capricor Therapeutics, Inc.; San Diego (CA); On-site; USD 34,440 - 41,328; Full time

Job summary

Capricor Therapeutics, Inc. is looking for a Manufacturing Associate I in San Diego, CA, to support critical clinical trials and exosome development. This role requires precision in a cleanroom environment, performing tasks like media preparation and documentation to maintain compliance standards. Candidates should have a Bachelor’s degree in Biomedical Engineering or a related field, along with 1-3 years of experience in a cGMP setting. The position offers hourly pay ranging from $25 to $30, with a rotating AWS/Panama schedule of 12-hour shifts.

Qualifications

• 1-3 years of experience in a cGMP/cGTP manufacturing environment.
• Solid laboratory experience in mammalian tissue culture.
• Strong attention to detail in a fast-paced setting.

Responsibilities

• Perform routine manufacturing tasks like media preparation.
• Complete timely and accurate documentation in compliance with GMP.
• Mentor team members on cGMP documentation protocols.

Skills

Aseptic techniques

Organizational skills

Mammalian tissue culture

Basic molecular biology

Flow cytometry skills

Education

Bachelor’s degree in Biomedical Engineering or related field

Job description

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

• 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.

$25 - $30 an hour

Schedule Details

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.

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.