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Pharmaceutical Development Scientist Jobs in Iowa

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Pharmaceutical Development Scientist information

What does a pharmaceutical development scientist do?

A Pharmaceutical Development Scientist is responsible for researching, designing, and developing new drugs and medications. They work on formulating drug compounds, ensuring their safety and efficacy through laboratory testing, and optimizing production processes. These scientists collaborate with regulatory agencies to ensure compliance and play a key role in advancing medicines from concept to market. Their work is critical in improving healthcare outcomes and meeting regulatory standards.

What are the key skills and qualifications needed to thrive as a pharmaceutical development scientist?

To thrive as a Pharmaceutical Development Scientist, you need a solid background in chemistry, biology, or pharmaceutical sciences, often supported by an advanced degree such as a Master's or Ph.D. and relevant laboratory experience. Familiarity with analytical instrumentation (like HPLC and mass spectrometry), regulatory compliance systems (such as GMP), and data analysis software is crucial. Strong problem-solving, attention to detail, and effective teamwork and communication skills set top professionals apart. These abilities are vital for developing safe, effective medications and ensuring regulatory compliance in a highly collaborative and precise environment.

What are some common challenges pharmaceutical development scientists face when transitioning a drug from the lab to large-scale manufacturing?

Pharmaceutical Development Scientists often encounter challenges related to scaling up a drug formulation from laboratory experiments to full-scale production. This process requires careful optimization to ensure that the product maintains its efficacy, safety, and quality while being manufacturable at a commercial scale. Issues such as ingredient compatibility, process reproducibility, and regulatory compliance frequently arise, demanding collaboration with cross-functional teams in manufacturing, quality assurance, and regulatory affairs. Adaptability and problem-solving skills are essential for overcoming these hurdles and ensuring successful product development.

What is the difference between Pharmaceutical Development Scientist vs Formulation Scientist?

AspectPharmaceutical Development ScientistFormulation Scientist
CredentialsBachelor's or Master's in Pharmacy, Chemistry, or related fields; often requires experience in drug developmentBachelor's or Master's in Pharmacy, Chemistry, or related fields; focus on formulation techniques
Work EnvironmentResearch labs, development departments, pharmaceutical companiesResearch labs, manufacturing, pharmaceutical companies
Industry UsageInvolved in early-stage drug development, formulation, and process optimizationSpecializes in creating and testing drug formulations for stability and delivery

The main difference is that Pharmaceutical Development Scientists focus on the overall development and process optimization of new drugs, while Formulation Scientists concentrate specifically on designing and testing drug formulations. Both roles require similar educational backgrounds and work environments, but their core responsibilities differ within the drug development process.

What are popular job titles related to Pharmaceutical Development Scientist jobs in Iowa?

For Pharmaceutical Development Scientist jobs in Iowa, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Development Scientist jobs in Iowa look for?

The top searched job categories for Pharmaceutical Development Scientist jobs in Iowa are:

What cities in Iowa are hiring for Pharmaceutical Development Scientist jobs?

Cities in Iowa with the most Pharmaceutical Development Scientist job openings:

Analytical Development Scientist II

Cambrex

Charles City, IA • On-site

Full-time

Medical, Life, Retirement

Re-posted 23 days ago


Cambrex rating

8.1

Company rating: 8.1 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

39th 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:

The Scientist II will provide analytical support for multiple project teams. This individual will collect and analyze data to support the development, validation and transfer of analytical methods for APIs, API intermediates and raw materials. Strict compliance with cGMP guidelines is required to perform most job tasks.

Responsibilities:
  • Safely and effectively collect analytical data to help develop, establish, and validate analytical
  • testing methodologies used to control raw materials, production intermediates, and final products
  • Perform analytical chemistry assays based on new and existing methodologies
  • Operate analytical instrumentation such as HPLC, GC, GC/MS, LC/MS, FTIR, Titrator, Particle
  • Size Analyzer
  • Maintain laboratory notebooks documenting work
  • Maintain compliance with GMP SOPs and DEA regulations
  • Transfer documented analytical methods to the QC and Process Support Group departments
  • Set up new or existing analytical methods for compound identification, purity and potency testing.
  • Coordinate off-site testing as necessary
  • Conduct testing of analytical samples for the Chemical Development Department as needed.
  • Collect analytical data to help qualify reference materials.
  • May also perform other duties as required
Qualifications / Skills:
  • Analytical Chemistry Knowledge: Basic understanding of the principles of Analytical Chemistry, some practical laboratory experience
  • Cross Discipline Knowledge: Basic understanding of the principles of cross-functional departments, including organic chemistry.
  • GMP/Regulatory Knowledge: Basic understanding of GMP; with manager assistance can help to answer client inquiries related to SOP or regulatory guidance.
  • Instrumentation: Good fundamental understanding and ability to use/investigate issues with HPLC,GC.
  • Communication: Good written and oral communication skills, demonstration of successful interdepartmental communication.
  • Problem Solving: Ability to support laboratory investigations with manager support.
  • Time Management: Reasonable ability to handle one or more tasks or projects, often with supervision.
  • Leadership: Shares ideas with peers.
  • Technical Documentation and Review: Ability to write technical documents with assistance.
  • External Influence: Occasionally participates in internal project team meetings, as needed; demonstrated ability to work within a team matrix.
  • Industry Credibility and Rapport: Known as a solid scientific contributor within the department/group.
  • Operational Excellence: Demonstrated interest in improvements of operational aspects of the group/team.
  • Change Orientation: Provides constructive feedback for Cambrex initiatives
Education, Experience, and Licensing Requirements: (Text Only)- M.S. in Chemistry or related field with minimum 2 years of experience or B.S. degree in Chemistry or related field with 6 years of experience in lab environment, pharmaceutical experience preferred. - Excellent verbal and written communication/interpersonal skills, organizational skills, and the ability to work in a diverse team environment are essential.  Employment Type: FULL_TIME

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Benefits

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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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