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Biotech Manufacturing Associate Jobs in Santa Rosa, CA

Avantor Inc.

Lab Support Specialist

Novato, CA · On-site

$28 - $30/hr

Associate's degree in Biology, Chemistry, Biotech, or a related field is preferred * Experience : 1+ year of laboratory, manufacturing, research, or laboratory support experience, or equivalent ...

AMRESCO

Lab Support Specialist

Novato, CA · On-site

$28 - $30/hr

Associate's degree in Biology, Chemistry, Biotech, or a related field is preferred * Experience : 1+ year of laboratory, manufacturing, research, or laboratory support experience, or equivalent ...

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Biotech Manufacturing Associate information

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How much do biotech manufacturing associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for biotech manufacturing associate in Santa Rosa, CA is $22.78, according to ZipRecruiter salary data. Most workers in this role earn between $17.88 and $25.48 per hour, depending on experience, location, and employer.

What is a biotech manufacturing associate?

Biotech Manufacturing Associates are professionals who work in the production of biotechnology products, such as pharmaceuticals, vaccines, and other biologically derived materials. They are responsible for operating equipment, following strict protocols, and maintaining sterile environments to ensure product quality and safety. Their duties often include preparing materials, monitoring production processes, troubleshooting equipment issues, and documenting all activities according to regulatory standards. This role is essential in ensuring that biotech products are manufactured efficiently and meet both industry and government regulations.

What are the key skills and qualifications needed to thrive as a biotech manufacturing associate?

To thrive as a Biotech Manufacturing Associate, you typically need a background in biology, chemistry, or a related field, along with experience in GMP-regulated environments. Familiarity with bioprocessing equipment, laboratory instrumentation, and documentation systems such as batch records is crucial. Attention to detail, teamwork, and strong problem-solving abilities help you excel in this collaborative and regulated field. These skills ensure the consistent production of safe, high-quality biotech products while maintaining compliance with industry standards.

What are some common challenges faced by biotech manufacturing associates, and how can they be managed effectively?

Biotech Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), troubleshooting equipment malfunctions, and working under tight production deadlines. Effective management of these challenges involves strong attention to detail, proactive communication with cross-functional teams such as quality assurance and engineering, and continuous learning to stay updated on new protocols and technologies. Developing problem-solving skills and embracing a collaborative mindset can also help associates consistently contribute to high-quality production outcomes.

What is the difference between Biotech Manufacturing Associate vs Laboratory Technician?

AspectBiotech Manufacturing AssociateLaboratory Technician
CredentialsHigh school diploma or equivalent; some roles may require associate degreeHigh school diploma or equivalent; some roles may require associate degree or certification
Work EnvironmentManufacturing floor, production lines, cleanroomsLaboratories, research facilities, testing environments
Industry UsageBiotech manufacturing, pharmaceutical productionResearch labs, quality control, testing labs

While both roles support biotech operations, a Biotech Manufacturing Associate primarily works on production and manufacturing processes in a cleanroom environment, focusing on assembling, monitoring, and maintaining manufacturing equipment. In contrast, a Laboratory Technician typically conducts experiments, tests, and quality control procedures in a laboratory setting. Both roles require attention to detail and adherence to safety protocols, but their daily tasks and work environments differ significantly.

What job categories do people searching Biotech Manufacturing Associate jobs in Santa Rosa, CA look for?

The top searched job categories for Biotech Manufacturing Associate jobs in Santa Rosa, CA are:

What cities near Santa Rosa, CA are hiring for Biotech Manufacturing Associate jobs?

Cities near Santa Rosa, CA with the most Biotech Manufacturing Associate job openings:

Biotech Manufacturing Associate jobs near you
Infographic showing various Biotech Manufacturing Associate job openings in Santa Rosa, CA as of August 2026, with employment types broken down into 1% As Needed, 66% Full Time, 29% Part Time, 2% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $47,386 per year, or $22.8 per hour.

Research Associate 1, Process Analytics and Services (Analytical Sciences)

BIOMARIN PHARMACEUTICAL

Novato, CA • On-site

Full-time

Re-posted 25 days ago

BioMarin Pharmaceutical rating

7.8

Company rating: 7.8 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

50th of 86 rated pharmaceutical

Job description

Who We Are
BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health.
Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities.
Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best - people with the right technical expertise and a relentless drive to solve real problems - and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we've produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options.
About Technical Operations
BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.

SUMMARY
The Analytical Sciences department is seeking a Research Associate 1 to join the Process Analytics & Services (PAS) function. This is a hands-on laboratory role supporting analytical testing and characterization of therapeutic candidates across process development, early clinical, late-stage, and commercial programs.

The selected candidate will execute a variety of GxP and non-GxP analytical methods to support drug substance and drug product process development, method lifecycle activities, and cross-functional technical investigations. This role requires strong laboratory execution, data analysis, and collaboration skills in a fast-paced, multi-disciplinary environment.

KEY RESPONSIBILITIES

Analytical Testing & Data Execution

  • Perform routine and non-routine analytical testing to support process development (Drug Substance and Drug Product) and lifecycle programs
  • Execute assays including:
    • Chromatographic methods (e.g., HPLC/UPLC)
    • Capillary electrophoresis (CE) and gel-based electrophoresis (e.g., SDS-PAGE)
    • Spectrophotometric methods (e.g., UV/Vis, FTIR)
    • Plate-based assays (e.g., ELISA) and cell-based bioassays
    • Basic nucleic acid and compendial physicochemical testing
  • Accurately document test results in accordance with GMP/GLP and internal procedures
  • Analyze and interpret analytical data and communicate results clearly

Method Lifecycle & Laboratory Support

  • Support method qualification, optimization, validation, and transfer activities under supervision
  • Assist with drafting and updating technical documents (e.g., analytical procedures, protocols, reports)
  • Support troubleshooting of analytical methods and laboratory workflows
  • Maintain laboratory equipment and ensure readiness of reagents, standards, and materials

Process Development & Cross-Functional Support

  • Provide analytical testing support for process development, manufacturing, and investigation activities
  • Collaborate with cross-functional teams including:
    • Drug Substance Technologies (DST)
    • Formulation and Drug Product Technologies (FPT)
    • Manufacturing Sciences & Technology (MSAT)
    • Manufacturing, Quality Control, and Quality teams
  • Support in-process, release, and stability-related analytical testing

Compliance & Inspection Readiness

  • Ensure all work is performed in accordance with GxP requirements and BioMarin procedures
  • Maintain laboratory documentation and data in an inspection-ready state
  • Support regulatory inspections, audits, and site readiness activities

Data Management & Communication

  • Document experimental plans, results, and conclusions clearly and accurately
  • Maintain organized electronic records to ensure traceability and data integrity
  • Present data and progress updates in team meetings

Continuous Improvement & Team Support

  • Contribute to improvement of laboratory processes, workflows, and documentation practices
  • Support training and knowledge sharing within the team as appropriate

REQUIRED SKILLS

  • Hands-on experience with one or more analytical techniques (e.g., HPLC/UPLC, CE, ELISA, spectrophotometry)
  • Basic understanding of GMP/GLP principles and data integrity expectations
  • Ability to analyze and interpret data
  • Strong written and oral communication skills
  • Strong organizational skills with the ability to manage multiple tasks
  • Ability to work independently and collaboratively in a team environment

PREFERRED SKILLS

  • Hands-on experience with chromatographic (LC/HPLC/UPLC) and capillary electrophoresis (CE) methods
  • Exposure to biopharmaceutical development or protein characterization
  • Experience with bioassays or cell-based assays
  • Familiarity with analytical method lifecycle activities (e.g., qualification, troubleshooting, validation, or transfer)
  • Experience working in a cross-functional or fast-paced environment

EDUCATION & EXPERIENCE

  • Bachelor's degree in Biochemistry, Chemistry, Biology, Analytical Chemistry, or related field
  • 1-2 years of relevant experience in a pharmaceutical or biotechnology environment
  • Master's degree is a plus but not required

ADDITIONAL INFORMATION

  • This is a fully onsite laboratory role
  • Routine work includes handling chemicals and biological materials with appropriate safety practices
  • May require occasional flexibility to support operational needs
EQUIPMENT
Operation of standard laboratory equipment for biochemistry and for cellular assays

REPORTING STRUCTURE

  • Reports to: Sr. Manager, Process Analytics & Services
  • No supervisory responsibilities

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.

Employment Type: Fulltime-Regular

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