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Associate Scientist Product Development Jobs in Washington

ATCC

Senior Scientist

Manassas, VA

$120K - $140K/yr

This onsite role in Manassas, VA leads research initiatives, supports product development and ... Scientific Technical Expertise in Bacteriology and Infectious Disease: Lead bacteriology and ...

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Associate Scientist Product Development information

What are some common challenges faced by an associate scientist in product development, and how can they be addressed?

Associate Scientists in Product Development often encounter challenges such as balancing tight project timelines with the need for thorough experimental design and data analysis. They may also need to quickly adapt to changing project priorities or troubleshoot unexpected results in the lab. Collaborating effectively with cross-functional teams, such as quality assurance, manufacturing, and regulatory affairs, is essential to overcome these hurdles. Proactively communicating progress, seeking feedback, and staying organized can help Associate Scientists navigate these challenges and contribute successfully to product advancement.

What does an associate scientist in product development do?

An Associate Scientist in Product Development plays a crucial role in researching, designing, and testing new products or formulations in industries like pharmaceuticals, biotechnology, or consumer goods. They conduct laboratory experiments, analyze data, and collaborate with cross-functional teams to improve product performance and ensure regulatory compliance. Their work helps bring innovative and safe products to market efficiently.

What is the difference between Associate Scientist Product Development vs Associate Scientist Quality Control?

AspectAssociate Scientist Product DevelopmentAssociate Scientist Quality Control
CredentialsBachelor's or Master's in Life Sciences, Chemistry, or related fieldBachelor's or Master's in Life Sciences, Chemistry, or related field
Work EnvironmentResearch labs focused on product formulation and innovationLaboratories conducting testing and quality assurance of products
Industry UsageUsed in pharmaceutical, biotech, and consumer goods companiesCommon in manufacturing and quality assurance departments
Search IntentComparing roles in product development and formulationLooking into quality testing and compliance roles

Associate Scientist Product Development and Associate Scientist Quality Control are both entry-level roles in the life sciences industry. While they share similar educational backgrounds, the former focuses on creating and improving products, whereas the latter emphasizes testing and ensuring product quality. Both roles are essential in bringing safe, effective products to market, but they differ in daily tasks and objectives.

What are the key skills and qualifications needed to thrive as an associate scientist in product development?

To thrive as an Associate Scientist in Product Development, you typically need a degree in chemistry, biology, or a related field along with strong laboratory and analytical skills. Familiarity with laboratory information management systems (LIMS), analytical instrumentation (such as HPLC or GC), and relevant regulatory guidelines is often required. Attention to detail, teamwork, and effective problem-solving are vital soft skills for success in collaborative and fast-paced environments. These abilities ensure the accurate development, testing, and optimization of products while maintaining compliance and fostering innovation.
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Associate Scientist Product Development jobs near you

Health Care Life Sciences Regulatory Associate (Mid-Level) - DC

Greenberg Traurig

Washington, DC • On-site

$260K - $390K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 4 days ago

Greenberg Traurig rating

9.4

Company rating: 9.4 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

3rd of 34 rated law firms

Job description

Greenberg Traurig (GT), a global law firm, has an exciting full-time employment opportunity for a 3rd-6th year associate to join a life sciences/product regulatory group within the Health Care Practice of our DC office. We offer competitive compensation and an excellent benefits package. GT is consistently among the top firms on the Am Law Global 100; the associate will have the opportunity to work with clients, large and small, from a variety of industries across the world.
Responsibilities

  • Advise life sciences, biotechnology, and technology clients on U.S. FDA or other regulatory matters, including product development, approval pathways, commercialization strategies, and life-cycle management
  • Support complex cross-border regulatory strategy or corporate transactions, including mergers and acquisitions, strategic alliances, and licensing
  • Conduct regulatory due diligence in connection with transactional matters involving advanced technology and life sciences companies
  • Assist clients in developing and implementing compliance strategies across multiple jurisdictions, including the United States, Europe, and Asia
  • Monitor and analyze legislative and regulatory developments affecting clients' businesses and prepare client alerts, memoranda, and strategic guidance
Required Qualifications
  • Three to six years of experience at a law firm, government agency, or comparable in-house legal department
  • Substantive experience in life sciences product regulatory law, including familiarity with FDA regulatory pathways and compliance requirements
  • Demonstrated ability to manage complex matters and work effectively in a fast-paced, client-driven environment
  • Strong research, writing, and analytical skills with the ability to distill complex regulatory issues into clear, actionable advice
  • Admission to one or more state bars is required
Preferred Qualifications
  • Experience with cell and gene therapy, immuno-oncology, or advanced biotechnology regulation
  • Familiarity with CMS reimbursement and pricing frameworks, including coverage determinations, coding, and payment policy as they relate to innovative life sciences products
  • Experience advising on cross-border regulatory matters in one or more international markets
  • Familiarity with national security and trade policies impacting the life sciences and semiconductor sectors
  • Professional fluency in Japanese or Mandarin is a strong plus

Submissions from search firms will only be accepted through our web portal for third-party submissions; for access, contact Mike Balzotti.
The expected pay range for this position is:
$260,000 - 390,000 per year
Actual pay will be adjusted based on experience, location, and other job-related factors permitted by law. Full time employees may be eligible for a discretionary bonus, health insurance with an optional HSA, short term disability, long term disability, dental insurance, vision care, life insurance, Healthcare and Dependent Care Flexible Spending Accounts, 401K, vacation, sick time, and an employee assistance program. Additional voluntary programs include: voluntary accident insurance, voluntary life, voluntary disability, voluntary critical illness and cancer insurance and pet insurance. Commuter and Transit programs may also be available in certain markets.
GT is an EEO employer with an inclusive workplace committed to merit-based consideration and review without regard to an individual's race, sex, or other protected characteristics and to the principles of non-discrimination on any protected basis.

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