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Full Time Assay Development Scientist Jobs in Iowa

Iowa City, IA Job Type: Full-Time | Exempt Position Summary Kelly Science & Clinical is seeking an ... Accurately document laboratory procedures, developmental data, and quality control metrics.

Associate Scientist On-site | Full-Time | U.S. Work Authorization Required Position Summary The ... Support the development, optimization, and validation of formulations and processes. * Prepare and ...

Participate in leadership development initiatives and continuous improvement projects * Maintain ... Must work full-time, a minimum of 80 hours each pay period. Hours are set by the manager. Rotating ...

Showing results 21-40

Full Time Assay Development Scientist information

What is a full time assay development scientist?

A Full Time Assay Development Scientist is a laboratory professional who specializes in designing, developing, and optimizing analytical assays for various scientific applications, such as drug discovery, diagnostics, or quality control. They work in research and development teams, conducting experiments, analyzing data, and troubleshooting assay protocols to ensure accuracy and reliability. Their role also involves documenting results, validating new methods, and collaborating with other scientists to support project goals. Typically, they have advanced degrees in biology, chemistry, or related fields and possess strong problem-solving and technical skills.

What are the key skills and qualifications needed to thrive as a full time assay development scientist?

To thrive as a Full Time Assay Development Scientist, you need a strong background in biochemistry, molecular biology, or a related field, typically with an advanced degree (M.S. or Ph.D.) and experience in assay design and optimization. Familiarity with laboratory techniques such as ELISA, PCR, and data analysis software, as well as experience with laboratory information management systems (LIMS), is often required. Strong problem-solving skills, attention to detail, and effective communication are essential soft skills for collaborating with cross-functional teams and troubleshooting experiments. These skills are crucial for ensuring the development of robust, reliable assays that advance research and product development objectives.

What are some common challenges faced by full time assay development scientists during the transition from research to routine clinical or commercial assays?

Full Time Assay Development Scientists often encounter challenges when translating laboratory protocols into robust assays suitable for routine clinical or commercial use. These challenges can include optimizing assay reproducibility, ensuring consistent performance across different sample types, and meeting regulatory requirements. Scientists also need to collaborate closely with quality assurance, manufacturing, and regulatory teams to validate and document procedures. Overcoming these hurdles requires strong problem-solving skills, attention to detail, and effective cross-functional communication.

What is the difference between Full Time Assay Development Scientist vs Research Associate?

AspectFull Time Assay Development ScientistResearch Associate
CredentialsBachelor's or Master's in Life Sciences, relevant experienceBachelor's or Master's in Life Sciences, entry-level experience
Work EnvironmentLaboratories focused on assay development and validationResearch labs supporting various projects, often assisting assay teams
Industry UsageCommon in biotech, pharma, and diagnostics companiesUsed across research institutions and biotech firms

The Full Time Assay Development Scientist typically has more specialized experience in designing and validating assays, working independently on development projects. In contrast, the Research Associate often supports research activities, assisting assay development under supervision. Both roles are essential in biotech and pharma industries, but the Scientist role involves greater responsibility and expertise in assay creation and optimization.

What are the most commonly searched types of Assay Development Scientist jobs in Iowa?

The most popular types of Assay Development Scientist jobs in Iowa are:

What are popular job titles related to Full Time Assay Development Scientist jobs in Iowa?

For Full Time Assay Development Scientist jobs in Iowa, the most frequently searched job titles are:

What job categories do people searching Full Time Assay Development Scientist jobs in Iowa look for?

The top searched job categories for Full Time Assay Development Scientist jobs in Iowa are:

Infographic showing various Full Time Assay Development Scientist job openings in Iowa as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Chemical Development Principal Scientist I

Cambrex

Charles City, IA

Full-time

Medical, Life, Retirement

Re-posted 6 days ago


Cambrex rating

8.1

Company rating: 8.1 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

38th of 86 rated pharmaceutical


Job description

Company Information

You Matter to Cambrex.

Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, as well as comprehensive analytical and IND enabling services. 

With over 40 years of experience and a team of 2,000 experts servicing global clients from North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances, liquid-phase peptide synthesis, solid-state science, material characterization, and highly potent APIs.

Your Work Matters.

At Cambrex, we strive to build a culture where all colleagues have the opportunity to:

  • engage in work that matters to our customers and the patients they serve
  • learn new skills and enjoy new experiences in an engaging and safe environment
  • strengthen connections with coworkers and the community

We're committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company.  We offer a competitive benefits package that includes healthcare, life insurance, planning for retirement, and more!

Your Future Matters.

Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today!

Overview:

Position is directed toward optimization of existing chemical routes and development of alternate chemistry toward key synthetic intermediates and APIs.  Carries out multistep chemical synthesis and product isolation/purification operations in the laboratory, independently or as part of an integrated team.  Chemist utilizes modern analytical tools to determine identity and purity of products made during projects.  Communication with clients in regular team meetings; prepares R&D reports at the conclusion of projects.

Responsibilities:
  • Design and carry out multistep organic syntheses, isolation, and purification of targeted products.
  • Must possess a strong understanding of modern organic synthesis methodologies.
  • Must have a thorough understanding of modern analytical and spectroscopic techniques and be able to interpret the corresponding data and spectra.
  • Ability to conduct literature searches for specific target compounds and be able to use the literature to base a design of alternate routes to these compounds. Requires ongoing professional development to keep abreast of current scientific literature and discuss these findings with colleagues.
  • Must demonstrate a proficiency to carry out laboratory syntheses and purification techniques on scales ranging from milligrams to several kilograms, and design and implement process modifications.
  • Requires excellent time management with the ability to manage projects on-time without supervision.
  • Ability to author and review comprehensive reports at the conclusion of projects for internal and customer use.
  • Work closely with other chemistry and analytical laboratory staff to coordinate project activities and resource usage.
  • Work to ensure that a spirit of teamwork and cooperation always exists within the group.
  • Conduct laboratory operations in a safe manner. Maintain familiarity with the company's chemical hygiene plan. Exhibit safety awareness and safe work practices.
  • Follow responsible actions regarding chemical disposal. Maintain compliance with all regulations at the federal, state, and local levels.
  • Must demonstrate effective communication skills (both interpersonal and presentations). Participate in project team meetings with customers.
  • Work closely with manufacturing and GMP operations to coordinate project related equipment and activities.
Qualifications / Skills:

Demonstrated ability to scale up pharmaceutical processes.

Excellent verbal and written communication/interpersonal skills, organizational skills, and the ability to work in a diverse team environment are essential.

Education, Experience, and Licensing Requirements: (Text Only)Ph.D. in Chemistry or related field with minimum 6 years of experience or M.S. in Chemistry or related field with minimum 10 years of experience or B.S. degree in Chemistry or related field with 14 years of experience in lab environment, pharmaceutical experience preferred.Employment Type: FULL_TIME

What Cambrex employees say

Pay

Benefits

Hours and flexibility

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About Cambrex

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

East Rutherford, NJ, US

Year founded

1981

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