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Associate Scientist Analytical Development Jobs in Raleigh, NC

PSG Global Solutions

Associate Scientist II

Durham, NC · On-site

Proven experience dealing with large data sets and designing/analyzing metabolic process development studies is a plus. * The candidate must be able to work independently as well as closely with ...

Actalent

Scientist

Durham, NC

Analytical Development Scientist This role focuses on supporting process development teams through advanced analytical testing and assay development in a fast-paced laboratory environment. The ...

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Associate Scientist Analytical Development information

See Raleigh, NC salary details

$18

$34

$55

How much do associate scientist analytical development jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for associate scientist analytical development in Raleigh, NC is $34.92, according to ZipRecruiter salary data. Most workers in this role earn between $27.12 and $39.71 per hour, depending on experience, location, and employer.

What does an associate scientist analytical development do?

An Associate Scientist in Analytical Development is responsible for designing, conducting, and analyzing experiments to develop and validate analytical methods used in the testing of pharmaceutical products. They work closely with cross-functional teams to ensure the quality and consistency of drug formulations by using various laboratory techniques such as chromatography, spectroscopy, and wet chemistry. Their role is critical in supporting drug development, regulatory submissions, and ensuring products meet industry standards.

What are some common challenges an associate scientist analytical development might face when working on new drug formulations?

Associate Scientists in Analytical Development frequently encounter challenges such as developing robust analytical methods for complex or novel drug formulations and ensuring these methods meet regulatory standards. Balancing tight project timelines with the need to thoroughly validate methods can also be demanding. Additionally, they often need to troubleshoot unexpected results and collaborate closely with cross-functional teams—including formulation scientists and quality assurance—to resolve technical issues and deliver reliable data. These challenges require strong problem-solving skills and adaptability.

What are the key skills and qualifications needed to thrive as an associate scientist analytical development, and why are they important?

To thrive as an Associate Scientist Analytical Development, you need a solid background in chemistry, biochemistry, or a related field, often supported by a bachelor’s or master’s degree. Familiarity with analytical techniques like HPLC, GC, mass spectrometry, and relevant laboratory information management systems (LIMS) is typically required. Strong problem-solving skills, attention to detail, and effective teamwork are important soft skills for this role. These competencies ensure accurate data generation, regulatory compliance, and successful collaboration in the development of pharmaceutical products.

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

AspectAssociate Scientist Analytical DevelopmentAssociate Scientist Quality Control
Required CredentialsBachelor's or Master's in Chemistry, Biology, or related field; relevant laboratory experienceBachelor's or Master's in Chemistry, Biology, or related field; laboratory experience often focused on testing
Work EnvironmentResearch and development labs, method development, process optimizationQuality control labs, testing, sample analysis, compliance with regulations
Employer & Industry UsagePharmaceutical, biotech companies, focus on method developmentPharmaceutical, biotech companies, focus on product testing and quality assurance

Associate Scientist Analytical Development primarily focuses on developing and optimizing analytical methods for new or existing products, while Associate Scientist Quality Control concentrates on testing and ensuring the quality of products before release. Both roles require similar educational backgrounds but differ in daily tasks and focus areas within the industry.

What are popular job titles related to Associate Scientist Analytical Development jobs in Raleigh, NC?

For Associate Scientist Analytical Development jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Associate Scientist Analytical Development jobs in Raleigh, NC look for?

The top searched job categories for Associate Scientist Analytical Development jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Associate Scientist Analytical Development jobs?

Cities near Raleigh, NC with the most Associate Scientist Analytical Development job openings:

Associate Scientist Analytical Development jobs near you
Infographic showing various Associate Scientist Analytical Development job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $72,637 per year, or $34.9 per hour.

Associate Scientist, AS&T

Asklepios BioPharmaceutical, Inc.

Durham, NC • On-site

Full-time

Re-posted 9 days ago

Job description

AskBio Inc., a wholly owned and independently operated subsidiary of Bayer AG, is a fully integrated gene therapy company dedicated to developing life-saving medicines and changing lives. The company maintains a portfolio of clinical programs across a range of neuromuscular, central nervous system, cardiovascular, and metabolic disease indications with a clinical-stage pipeline that includes investigational therapeutics for congestive heart failure, limb-girdle muscular dystrophy, multiple system atrophy, Parkinson's disease, and Pompe disease. AskBio's gene therapy platform includes Pro10™, an industry-leading proprietary cell line manufacturing process, and an extensive array of capsids and promoters. With global headquarters in Research Triangle Park, North Carolina, and European headquarters in Edinburgh, Scotland, the company has generated hundreds of proprietary capsids and promoters, several of which have entered pre-clinical and clinical testing.
Our vision: Pioneering science to create transformative molecular medicines.
Our mission: Lead innovative science and drive clinical outcomes to transform people's lives.
Our principles:
  • Advance innovative science by pushing boundaries.
  • Bring transformative therapeutics to patients in need.
  • Provide an environment for employees to reach their fullest potential.

Our values:
  • Be a Pioneer. We are not afraid of the impossible and to innovate to make gene therapies accessible to those in need.
  • Cultivate Collaboration. Strive to be the best teammate, actively listen, openly communicate, and embrace diverse points of view.
  • Embrace Responsibility. We are humbled by the enormity of our mission. We hold a relentless commitment to advance science and clinical outcomes for our patients, families, and caregivers.
  • Raise the Bar. Continuously drive improvements and efficiencies. Seek and provide constructive feedback. Have a bias for learning and action.
  • Act with Uncompromising Integrity. Be honest, transparent, and committed to doing what's right in every situation. Make clear commitments and follow through.

Analytical support
  • Lead the development and implementation of phase-appropriate analytical control strategies for gene therapy products, integrating scientific expertise, regulatory expectations, and product knowledge to ensure robust product characterization and lifecycle support.
  • Apply advanced scientific knowledge and broad analytical expertise to direct lifecycle management of complex bioanalytical methods, including but not limited to PCR/ddPCR, ELISA, cell-based potency assays, NGS, HPLC, and AUC, driving method evolution, troubleshooting complex technical challenges, and enabling program objectives.
  • Guide the design and execution of scientifically sound method qualification, validation, transfer, and comparability strategies for rAAV programs, leveraging comprehensive understanding of regulatory requirements, assay performance, and product development considerations.
  • Integrate and interpret analytical data across multiple programs and functional disciplines to identify trends, assess method variability and provide strategic recommendations that support product quality, process understanding, and decision-making.
  • Apply statistical methodologies and scientific judgment to evaluate assay performance, capability, robustness, and lifecycle suitability, developing innovative approaches to address complex analytical challenges and improve data-driven decision-making.
  • Drive continuous improvement and innovation in analytical sciences through the advancement of emerging technologies, digitalization, automation, and novel scientific approaches, guiding the development of new procedures, enhancing operational efficiency, and strengthening analytical capabilities across the organization

Tech transfer and external partner management
  • Lead analytical method transfers across CDMOs, CROs, and internal QC laboratories, applying broad scientific expertise and strategic oversight to ensure successful implementation, knowledge transfer, and sustained method performance throughout the product lifecycle
  • Author, review, and approve transfer protocols, validation strategies, technical reports, and scientific justifications, ensuring alignment with regulatory expectations, quality standards, and program objectives while advancing best practices in analytical sciences
  • Serve as the Analytical Sciences & Technology (AS&T) subject matter expert for external partners, leveraging technical knowledge and cross-functional understanding to establish scientific alignment, resolve complex analytical issues, and drive effective outcomes across organizational boundaries.
  • Lead troubleshooting and resolution of cross-site analytical challenges by integrating scientific principles, data-driven approaches, and multidisciplinary expertise to ensure method consistency, robustness, comparability, and compliance across global laboratory networks.

Quality support
  • Provide scientific oversight for complex analytical investigations, including OOS, OOT, and deviation events, applying technical expertise, data-driven methodologies, and multidisciplinary knowledge to aid in the identification of root causes, assess impact, and develop effective resolution strategies.
  • Partner with Quality, Manufacturing, Regulatory, and other functional areas to develop, and implement, scientifically sound CAPAs, ensuring sustainable improvements, operational excellence, compliance, and alignment with company objectives.
  • Drive inspection readiness by providing scientific leadership in the evaluation, documentation, and resolution of analytical quality events, ensuring robust investigation practices, regulatory compliance, and continuous improvement across the analytical lifecycle.

Regulatory
  • Author and review analytical sections of global regulatory submissions (IND, BLA, MAA), leveraging expertise in analytical control strategies and regulatory requirements to support successful product development and registration
  • Participate in the development and continuous evolution of analytical control strategies, integrating multidisciplinary scientific insights, product knowledge, and emerging regulatory guidance to ensure robust product quality, control, and lifecycle management.
  • Support regulatory interactions, inspections, and responses as an analytical SM

Minimum Requirements
  • Bachelor's degree in biology, microbiology, molecular biology, biotechnology or related field with 8+ years of relevant work experience, or a Master's degree with 4+ years of relevant work experience
  • Demonstrated experience working in matrix organizations and independent management of cross-functional initiatives
  • Ability to influence without direct authority across teams and functions
  • Hands-on experience supporting GMP environments
  • Experience with method validation, transfer, and lifecycle management
  • Knowledge of analytical methods supporting biologics manufacturing
  • Understanding ICH, FDA, and EMA requirements for gene therapy products.
  • Excellent written and verbal communication skills
  • High attention to detail and data integrity mindset
  • Strong problem-solving and investigative skills

Preferred Education, Experience and Skills
  • Industry experience with strong focus on gene therapies analytical methodologies
  • Experience with stability studies and impurity profiling
  • Project management and prioritization skills
  • Experience supporting regulatory filings and agency interactions
  • Knowledge of Quality by Design (QbD) and risk-based approaches

AskBio Inc. (AskBio) is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status or any other protected status prohibited under Federal, State or local laws. All employment decisions are based on valid job-related requirements. If you are a qualified individual with a disability or a disabled veteran and are unable or limited in your ability to use or access our website, you may request a reasonable accommodation to express interest in a specific opening by calling us at (919) 561-6210 or sending us an email at careers@askbio.com.
Agencies: Please do not contact any employee at AskBio about this requisition. Any resume submitted by a recruitment agency to any employee at AskBio, through any medium, will be deemed the sole property of AskBio unless the agency was engaged by AskBio Talent Acquisition team to recruit for that position. All agencies must have a prior executed service agreement with AskBio prior to any search engagement. If a candidate who was submitted outside of the AskBio agency process is hired by AskBio, no fee or payment of any kind will be paid to the agency.

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