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Bioduro Jobs (NOW HIRING)

Quality Engineer Manager

Irvine, CA · On-site

$110K - $160K/yr

The company was recently formed through the acquisition of Irvine operations from BioDuro and is operating as a newly established, independent entity. As a result, Forma's standalone online presence ...

Quality Engineer Manager

Irvine, CA · On-site

$110K - $160K/yr

The company was recently formed through the acquisition of Irvine operations from BioDuro and is operating as a newly established, independent entity. As a result, Forma's standalone online presence ...

Bioduro information

See salary details

$15K

$241.3K

$387K

How much do bioduro jobs pay per year?

As of Jul 31, 2026, the average yearly pay for bioduro in the United States is $241,295.00, according to ZipRecruiter salary data. Most workers in this role earn between $200,000.00 and $300,000.00 per year, depending on experience, location, and employer.

What are some typical projects that a scientist at BioDuro might work on, and how does cross-functional collaboration play a role?

At BioDuro, scientists often work on contract research projects involving drug discovery, preclinical development, or pharmaceutical manufacturing. These projects typically require close collaboration with colleagues in chemistry, biology, and analytical teams, as well as regular communication with clients to ensure project goals are met. Cross-functional teamwork is essential, as scientists coordinate with project managers, quality assurance, and regulatory specialists to deliver high-quality results under tight timelines. This collaborative environment not only enhances problem-solving but also provides opportunities to learn from experts in various fields.

What are the key skills and qualifications needed to thrive at BioDuro, and why are they important?

To thrive at BioDuro, professionals typically need a background in life sciences such as biology, chemistry, or pharmaceutical sciences, often with a relevant degree. Familiarity with laboratory instrumentation, Good Laboratory Practices (GLP), and data analysis software like LIMS or ELN is highly valuable. Strong teamwork, attention to detail, and effective communication are crucial soft skills in this collaborative and regulated environment. These abilities ensure accurate scientific results, regulatory compliance, and efficient project delivery in a fast-paced contract research setting.

What jobs can I do with biology and chemistry?

With a background in biology and chemistry, you can pursue roles such as research scientist, laboratory technician, quality control analyst, or pharmaceutical sales representative. These jobs often require laboratory skills, knowledge of scientific methods, and sometimes certifications or advanced degrees depending on the position.

How many employees does BioDuro have?

BioDuro is a contract research organization that employs several hundred staff members, including scientists, researchers, and support personnel. The company focuses on drug discovery and development services, often requiring specialized skills and certifications. Exact employee numbers can vary over time due to business growth and restructuring.

What does BioDuro do?

BioDuro is a contract research organization that provides drug discovery and development services, including chemistry, biology, and formulation. Employees in this field often work with laboratory tools, follow strict safety protocols, and may require scientific or technical certifications. The company supports pharmaceutical and biotech clients in advancing their research projects.

What is a Bioduro and what do they do?

Bioduro is not a job title, but rather the name of a company specializing in pharmaceutical research, drug development, and manufacturing services. BioDuro (now part of BioDuro-Sundia) provides contract research and development services to pharmaceutical and biotechnology companies, helping them bring new drugs to market faster and more efficiently. Employees at BioDuro may have various roles such as scientists, researchers, project managers, or quality assurance specialists, all contributing to the advancement of drug discovery and development.

Is BioDuro a Chinese company?

BioDuro is a contract research organization that was founded in China and has operations there. It provides drug discovery and development services to pharmaceutical companies worldwide. As a company, it has a significant presence in China, but it also operates internationally.

What is the difference between Bioduro vs Biotech Research Associate?

AspectBioduroBiotech Research Associate
Required CredentialsBachelor's degree in biology, chemistry, or related field; laboratory experienceBachelor's or master's degree in life sciences; laboratory skills
Work EnvironmentLaboratories, research facilities, pharmaceutical companiesResearch labs, biotech firms, academic institutions
Industry UsagePrimarily in biotech and pharmaceutical sectors for drug developmentIn biotech, pharma, and research institutions for experimental work

Both Bioduro and Biotech Research Associates work in laboratory settings within the biotech and pharmaceutical industries. Bioduro often focuses on contract manufacturing and drug development support, while Biotech Research Associates typically conduct experimental research and data analysis. Understanding these differences helps job seekers identify roles aligned with their skills and career goals.

More about Bioduro jobs
What cities are hiring for Bioduro jobs? Cities with the most Bioduro job openings:
What states have the most Bioduro jobs? States with the most job openings for Bioduro jobs include:
Infographic showing various Bioduro job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% Physical job distribution, with an average salary of $241,295 per year, or $116 per hour.

Quality Assurance Specialist

Forma Life Sciences

Irvine, CA • On-site

$71K - $85K/yr

Full-time

Medical, PTO

Posted 6 days ago


Job description

What We Do

Forma is a next-generation Contract Development and Manufacturing Organization (CDMO) based in Irvine, California. The company was recently formed through the acquisition of the Irvine operations from BioDuro and is operating as a newly established, independent entity. As a result, Forma’s standalone online presence is still being built.

We are a lean, entrepreneurial organization of approximately 60 employees focused on drug product development and manufacturing for pharmaceutical and biotechnology clients.

Why Forma?

Unlike large, highly layered organizations, Forma operates with a hands-on, execution-driven model. Our teams work closely across functions to solve complex technical and operational challenges, move quickly, and deliver consistently high-quality results.

Employees at Forma are expected to take on meaningful responsibility, collaborate directly with colleagues and clients, and contribute to building scalable systems and processes as the company grows. This is an environment well suited to individuals who value autonomy, technical excellence, and the opportunity to help shape a growing organization.

Requirements

Job Overview/Summary

The Specialist supports Quality Assurance activities regarding materials management, manufacturing, testing, packaging, labeling, facilities, and equipment ensures compliance to GMP regulatory requirements.

Essential Functions and Responsibilities

  • Primary person responsible for review and approval of all batch records.
  • Work directly with clients to obtain approvals on batch records and client notifications.
  • Work with cross functional stake holders to ensure timely closure of batch associated deviations.
  • Supply Chain/Materials Management Support – Support Materials Management in assignment of material codes, review/approval of raw material and packaging component specifications, and materials disposition. Ensure suppliers of raw materials and services are approved according to the vendor management program.
  • Audits and Regulatory Inspections – Participate and assist with internal and external audits and regulatory inspections. Work with the QA group to ensure inspection-readiness for all GMP operations, including compliance with CFRs, GMPs, company policies and procedures.
  • Analytical Support – Provide hands-on support for data review/approval of analytical testing data summaries (such as in-process, release, stability, method validation, and cleaning validation/verification testing, environmental monitoring data) and ensure tasks are tracked and timelines are met. Participate in laboratory investigations and ensure corrective and preventive actions are implemented.
  • Support quality exceptions including review/approval of deviations, CAPA, non-conformances, risk/impact assessment, and change management.
  • Safety – Comply with all safety regulations and Mechanical/Electrical/Fire Hazards encountered in Manufacturing/Laboratory Areas
  • Other duties as deemed appropriate by the Supervisor or Head of Quality.
  • This job description is subject to change at any time.

Required Qualifications

  • Bachelor’s degree in science-related field is preferred.
  • Minimum 5 years of experience in Quality Assurance
  • Hands-on experience performing production line clearance, review/approval master and executed production batch records, review/approval of deviations and implementation of corrective and preventive actions.
  • Working knowledge of applicable CFR, ICH, and GMP regulations.
  • Ability to apply and enforce GMP compliance to all aspects of the position.
  • Detailed attention in job performance.
  • Excellent written and verbal communication.

Preferred Qualifications

  • Detailed attention in job performance
  • Good attitude, work ethic and natural leadership
  • Achievement of an advanced degree or certification
  • Excellent written and verbal communication

Benefits

Position Benefits

We offer full health benefits, paid vacation and sick leave, an aggressive bonus structure, and market-competitive salaries to all our employees. In addition, Forma provides employees with a variety of engaging employee events.

The salary range for this position is $71,000-$85,000 annually. Actual compensation will be determined based on the selected candidate’s experience, qualifications, skills, and overall fit for the role.