BioMarin Pharmaceutical

(CW) Research Associate (Contract/Temporary)

BioMarin Pharmaceutical$75K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's or Master's degree in relevant scientific discipline (Biochemistry, Biology, Chemical Engineering) with 2-6 years of industry experience.
  • Proven experience in purifying recombinant enzymes, proteins, antibodies, or peptide therapeutics.
  • Hands-on operation of ÄKTA Pure, ÄKTA Avant, or similar chromatography systems.
  • Familiarity with protein analytical techniques including SEC-HPLC, RP-HPLC, CE-SDS, SDS-PAGE, and UV/Vis spectroscopy.
  • Experience with tangential-flow filtration (TFF) and ultrafiltration/diafiltration (UF/DF) is preferred.

Responsibilities

  • Independently execute purification experiments for recombinant enzymes and therapeutic biologics.
  • Optimize purification workflows using various chromatography methods including affinity and ion exchange.
  • Perform concentration and buffer exchange using advanced filtration techniques.
  • Evaluate purification performance and recommend process improvements.
  • Analyze and interpret analytical data to support decision-making and process optimization.

Benefits

  • Join a leading organization in biopharmaceutical research and development.
  • Gain hands-on experience in advanced biologics purification.
  • Support early-stage exploratory research programs.
  • Work collaboratively within multidisciplinary teams in a dynamic environment.
Full Job Description
Description

Senior Research Associate I (Temporary) - Biologics Purification & Characterization

BioMarin Pharmaceutical Inc. - Worldwide Research & Development
Position Type: Temporary, Full-Time ONSITE

Position Summary
The Therapeutics Process Development & Characterization (TPDC) group is seeking a highly motivated Temporary Senior Research Associate I to support biologics purification and analytical characterization, with a primary focus on recombinant enzymes and additional exposure to therapeutic proteins, antibodies, and peptide-based modalities.
This is a primarily laboratory-based role involving hands-on purification and characterization of biologics using established chromatography and filtration workflows. The successful candidate will independently execute purification experiments, troubleshoot technical challenges, analyze experimental data, and contribute to activities supporting multiple early-stage and exploratory research programs across BioMarin. The position also supports laboratory operations through routine instrument maintenance.
The ideal candidate is detail-oriented, scientifically curious, highly organized, and capable of working independently while collaborating effectively within multidisciplinary project teams.

Duties & Responsibilities
Protein & Biologic Purification
Independently perform purification of recombinant enzymes and other therapeutic biologics, including proteins, antibodies, and peptides, using ÄKTA Pure and ÄKTA Avant chromatography systems.
Execute and optimize purification workflows including:
Affinity chromatography
Ion exchange chromatography (AEX/CEX)
Size-exclusion chromatography (SEC)
Hydrophobic interaction chromatography (HIC)
Desalting and buffer exchange
Perform concentration and buffer exchange using tangential-flow filtration (TFF), ultrafiltration/diafiltration (UF/DF), or centrifugal filtration.
Evaluate purification performance and recommend process improvements to enhance yield, purity, and recovery.
Troubleshoot chromatography, filtration, and purification processes with minimal supervision.
Prepare buffers, reagents, and chromatography columns according to established procedures.
Perform routine instrument checks, preventative maintenance, and basic troubleshooting of purification equipment.

Analytical Characterization
Perform analytical assays to assess purity, identity, concentration, and quality of biologics, including:
SDS-PAGE
CE-SDS
SEC-HPLC
RP-HPLC
UV/Vis spectrophotometry
Additional protein and peptide analytical methods as required
Interpret analytical data to support purification process optimization and project decision-making.
Analyze experimental results using GraphPad Prism, JMP, Microsoft Excel, or similar software.
Communicate experimental findings through technical summaries, presentations, and discussions with cross-functional project teams.
Support analytical method development, qualification, or technology transfer activities as needed.

General Laboratory Responsibilities
Maintain accurate and complete electronic and/or paper laboratory notebooks.
Follow established SOPs and document deviations with guidance.
Communicate results, observations, and progress updates clearly within the team.
Contribute to a safe, clean, and well-organized laboratory environment in compliance with BioMarin safety standards.

Education & Experience
Senior Research Associate I
Bachelor's degree in Biochemistry, Biology, Chemical Engineering, or a related scientific discipline with 4-6 years of relevant industry experience, or
Master's degree in a related scientific discipline with 2-4 years of relevant industry experience.
Demonstrated experience purifying recombinant enzymes, proteins, antibodies, or peptide therapeutics.
Hands-on experience operating ÄKTA Pure, ÄKTA Avant, or equivalent FPLC chromatography systems.
Experience with protein analytical techniques including SEC-HPLC, RP-HPLC, CE-SDS, SDS-PAGE, and UV/Vis spectroscopy.
Experience with tangential-flow filtration (TFF) and ultrafiltration/diafiltration (UF/DF) is preferred.

Desired Skills
Experience in protein purification and biologics characterization.
Demonstrated ability to independently plan, execute, troubleshoot, and optimize purification experiments.
Strong analytical and problem-solving skills with excellent attention to detail.
Experience with electronic laboratory notebooks (Benchling or similar) and data analysis software such as GraphPad Prism or JMP.
Excellent written and verbal communication skills with the ability to present technical data effectively.
Ability to manage multiple priorities while maintaining high-quality scientific documentation.
Strong collaboration skills and the ability to work effectively within multidisciplinary research teams.

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.

Ireland Safety Responsibility
Support the organisation's commitment to environmental protection, injury prevention, and continual improvement of EHS management systems. Actively contribute to a safe and environmentally responsible workplace by identifying hazards, reporting incidents and participating in EHS initiatives and training.

About BioMarin Pharmaceutical

BioMarin Pharmaceutical Inc. is a biotechnology company that develops and commercializes innovative therapies for patients with serious and life-threatening rare and ultra-rare genetic diseases. The company's portfolio consists of seven commercialized products and multiple clinical and pre-clinical product candidates. BioMarin's products are used to treat patients suffering from rare genetic diseases such as phenylketonuria, achondroplasia, and Batten disease. The company was founded in 1997 and is headquartered in San Rafael, California.
Learn more about BioMarin Pharmaceutical
Size
3,045 employees
Market Cap
$19.2 billion
Industry
Net Income
$859.1 million
Founded
2003
5 Year Trend
+10.6%
Revenue
$1.8 billion
NASDAQ

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