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Development scientist skills for your resume and career
15 development scientist skills for your resume and career
1. Chemistry
Chemistry is the branch of science that tells us about the composition, properties, and structure of elements and compounds. The processes these elements undergo and how they undergo change all come under the branch of chemistry.
- Developed chemistry protocols, evaluated chemistry and instrument performance, and assessment of biochemical applications.
- Synthesized and characterized impurities, supporting medicinal chemistry research and development activities.
2. Data Analysis
- Review notebooks and data analysis for testing approval.
- Performed nucleic acid isolation, quantification, testing, data analysis, recording and reporting results under the auspices of CLIA.
3. GMP
GMP stands for Good Manufacturing Practice. It is a system that ensures that all products like food, beverages, and medicinal drugs that are produced comply with the quality standards. It helps in minimizing the risks and hazards that cannot be eliminated after the testing of final products.
- Created new protocols and laboratory procedures for design transfer into Manufacturing following GLP and GMP guidelines.
- Prepared Method Transfer documents for GMP Manufacturing.
4. HPLC
- Developed and validated custom calculations for automated HPLC reporting.
- Worked extensively on HPLC instrument maintenance & troubleshooting.
5. QC
Quality control is a set of instructions or procedures to ensure a manufactured product or a service is up to the highest quality standards. This set of quality control criteria are either defined by the clients or the company itself.
- Developed and qualified new manufacturing processes that reduced product variability and QC failure rate.
- Designed and implemented experiments to construct and characterize synthetic chromosomes for QC analyses.
6. FDA
The Food and Drug Administration (FDA) is a division of the US Department of Health and Human Services that regulates the production and sale of food, pharmaceutical products, medical equipment, and other consumer goods, as well as veterinary medicine. The FDA is now in charge of overseeing the manufacture of products like vaccines, allergy treatments, and beauty products.
- Collaborated with compliance team for FDA submission documentation.
- Contribute to audit readiness for quality audits with FDA, other Regulatory Agencies, and customers, as needed.
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Technical reports are a type of document that is used to indicate either the progress, result, or process of scientific research or the state of problems occurring within such research. A technical report may also showcase the report's overall conclusion and may also include recommendations. This kind of report does not require a peer review and isn't published officially but distributed within the organizations where it was formed.
- Authored technical reports on technology and assay development batch records and.
- Perform Verification & Validation studies per protocols and provide technical reports.
8. Clinical Trials
- Served as primary contact for ensuring quality and availability of materials for clinical trials.
- Review Clinical Trial Protocols for clinical validation and clinical utility research studies.
9. Product Development
Product development is the complete procedure of creating a product from concept until release of the final product. Product development has many stages after which a product is released into the market. Identifying the need, creating the opportunity, conceptualizing a product, and providing a solution, all are different stages of product development.
- Managed clinical IVD product development teams from conception to commercialization through Design Control process.
- Facilitated successful transfer of new reagent products from product development to manufacturing.
10. Elisa
An enzyme-linked immunosorbent assay or ELISA is an examination or test to measure and detect a person's specific antigen, antibodies, and protein. This type of test will identify if the sample component is infected with a relative disease or condition such as HIV infection, anemia, Zika Virus, and Lyme disease with just a single experiment.
- Developed and established a novel ELISA method for measuring the relative potency of an Antibody therapeutic product.
- Develop and optimize ELISA assays to determine residual Host cell protein for in-process samples.
11. PCR
PCR stands for Polymerase Chain Reaction, a tool to make millions of copies of a target part of DNA. Polymerase chain reaction involves the process of heating and cooling. The process takes place using a machine, which helps in heating and cooling off the substances. The purpose of heating exists to separate the DNA into two single strands.
- Collaborated with Product Management, Quality and other R&D groups to develop new kits and reagents for PCR product.
- Assay optimization for PCR speed and yield using Design of Experiments (DOE), and optimization for sequencing quality.
12. Cell-Based Assays
- Conducted small-scale lab automation and robotics of biochemical and cell-based assays for profiling compounds and characterizing potential drug targets.
- Purified antibodies and antigens for antibody affinity screens, biochemical and cell-based assays, immunizations, and GLP toxicology studies.
13. Assay Development
Assay development is a process in molecular biology to test or measure the activity of a drug or biochemical substance in an organic sample or organism and to screen putative compounds to determine the interaction and/or modification of the target. The aim is to standardize the assay and to be able to use it repeatedly and reproducibly.
- Authored, reviewed and approved method development reports and managed outsourced assay development activities.
- Experienced in identifying, and evaluating new technologies/ platforms for assay development.
14. GLP
GLP stands for "good laboratory practice." This refers to the integrity and quality measures that non-clinical laboratories have in place to ensure accurate research and market testing. GLP is most often used in pharmaceutical companies where new drugs must be tested before being approved for sale, but the practice can also be used in food packaging and preparation test centers.
- Conducted raw materials and excipients release testing (UPS/NF, EP, JP) under strict cGMP and GLP environments.
- Required working knowledge of cGMP and GLP practices,coordination of research with contract labs and supervisory responsibilities.
15. Test Methods
Test methods are the steps in which thorough testing is conducted in a laboratory setting.
- Developed test methods based off of NIOSH 7500.
- Developed and validated analytical test methods for small chemical entity drug substances and generation of certificate of analysis.
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What skills help Development Scientists find jobs?
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What skills stand out on development scientist resumes?
Alexandra (Sasha) Ormond Ph.D.
Associate Professor of Chemistry, Director of Dual Degree Engineering, Meredith College
What soft skills should all development scientists possess?
Alexandra (Sasha) Ormond Ph.D.
Associate Professor of Chemistry, Director of Dual Degree Engineering, Meredith College
What hard/technical skills are most important for development scientists?
Alexandra (Sasha) Ormond Ph.D.
Associate Professor of Chemistry, Director of Dual Degree Engineering, Meredith College
What development scientist skills would you recommend for someone trying to advance their career?
Scott Johnson
Professor and Director, University of Maine
What type of skills will young development scientists need?
What technical skills for a development scientist stand out to employers?
Dr. Joey Neilsen
Assistant Professor, Villanova University
List of development scientist skills to add to your resume

The most important skills for a development scientist resume and required skills for a development scientist to have include:
- Chemistry
- Data Analysis
- GMP
- HPLC
- QC
- FDA
- Technical Reports
- Clinical Trials
- Product Development
- Elisa
- PCR
- Cell-Based Assays
- Assay Development
- GLP
- Test Methods
- CMC
- Laboratory Equipment
- PowerPoint
- ICH
- IND
- Experimental Data
- Stability Studies
- Drug Substance
- Cell Lines
- GC
- Cros
- Next-Generation Sequencing
- API
- Statistical Analysis
- LC-MS
- Immunoassay
- DSC
- Technical Support
- Clinical Studies
- Method Validation
- Harvest
- Dosage Forms
- Liquid Chromatography
- Lims
- Test Results
- DOE
- Drug Products
- Biomarkers
- Analytical Method Development
- Pharmaceutical Industry
- Electrophoresis
- R
- USP
- JMP
Updated January 8, 2025