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Analytical Development Biotech Jobs in Frederick, MD

... analytical solutions -we are modernizing clinical trials and accelerating the development of life ... in biotech and pharma. Responsibilities * Drive net-new business development by securing new ...

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Analytical Development Biotech information

See Frederick, MD salary details

$28.8K

$53.1K

$80.5K

How much do analytical development biotech jobs pay per year?

As of Aug 24, 2026, the average yearly pay for analytical development biotech in Frederick, MD is $53,112.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,300.00 and $59,700.00 per year, depending on experience, location, and employer.

What is analytical development in biotech?

Analytical Development in biotech refers to the process of designing, developing, and validating methods to analyze biological products, such as proteins, antibodies, or cell therapies, during various stages of drug development and manufacturing. These methods are essential for ensuring the safety, quality, potency, and purity of biotechnological products. Professionals in this field work closely with research, production, and regulatory teams to ensure that analytical methods meet industry standards and comply with regulatory requirements. Analytical Development is a critical part of bringing new biopharmaceutical products from the lab to the market.

What are the key skills and qualifications needed to thrive as an analytical development biotech professional?

To thrive as an Analytical Development Biotech professional, you need a strong background in analytical chemistry, biochemistry, or a related field, typically supported by at least a bachelor's or master's degree. Familiarity with analytical instrumentation such as HPLC, GC, mass spectrometry, and relevant quality systems like GMP or ICH guidelines is crucial. Strong problem-solving, attention to detail, and effective communication are important soft skills for collaborating across multidisciplinary teams. These competencies ensure accurate data generation, regulatory compliance, and successful development of biotechnological products.

What are some typical challenges faced by analytical development professionals in the biotech industry?

Analytical Development professionals in biotech often encounter challenges such as developing robust methods for novel biologics, ensuring regulatory compliance, and adapting to rapid technological changes. They frequently work within cross-functional teams, collaborating closely with research, manufacturing, and quality assurance groups to optimize assay performance and troubleshoot issues. Staying current with evolving regulatory standards and balancing project timelines with method validation requirements are also common aspects of the role.

What is the difference between Analytical Development Biotech vs Quality Control Analyst?

AspectAnalytical Development BiotechQuality Control Analyst
CredentialsBachelor's/Master's in Life Sciences, Chemistry, or related fieldsBachelor's in Chemistry, Biology, or related fields; often requires GMP training
Work EnvironmentResearch labs, development departments, collaborative teamsQuality labs, manufacturing facilities, compliance-focused settings
Industry UsageDeveloping and optimizing analytical methods for biotech productsTesting and ensuring product quality and compliance with standards

Analytical Development Biotech focuses on creating and refining analytical methods during product development, while Quality Control Analysts primarily test products to ensure they meet quality standards. Both roles require similar educational backgrounds and work in laboratory settings, but their core responsibilities differ in the product lifecycle.

What are popular job titles related to Analytical Development Biotech jobs in Frederick, MD?

For Analytical Development Biotech jobs in Frederick, MD, the most frequently searched job titles are:

What job categories do people searching Analytical Development Biotech jobs in Frederick, MD look for?

The top searched job categories for Analytical Development Biotech jobs in Frederick, MD are:

What cities near Frederick, MD are hiring for Analytical Development Biotech jobs?

Cities near Frederick, MD with the most Analytical Development Biotech job openings:

Infographic showing various Analytical Development Biotech job openings in Frederick, MD as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 20% Part Time, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $53,112 per year, or $25.5 per hour.

Director, Process & Analytical Development

Jobtailor

Walkersville, MD โ€ข On-site

$180 - $270/hr

Other

Posted 2 days ago

New


Job description

  • Provide overall leadership for analytical development, process development, and project-specific manufacturing activities within the ADS US organization
  • Ensure the ADPD organization delivers services and products safely, compliantly, on time, in full, and within budget
  • Lead, coach, and develop a high-performing ADPD organization
  • Define and execute strategic direction through long-term planning, portfolio management, resource allocation, organizational design, and performance management
  • Establish capabilities, infrastructure, and talent for future manufacturing operations and business growth
  • Contribute to the Sales & Operations Planning (S&OP) process
  • Oversee development and project-specific manufacturing activities against Safety, Quality, Compliance, Delivery, and Cost expectations
  • Own organizational budgets, resource planning, and operational performance
  • Drive Lean maturity, Operational Excellence, and continuous improvement
  • Lead strategic initiatives and transformation programs
  • Partner with R&D, Manufacturing, MSAT, Engineering, Quality, Automation, Supply Chain, and Commercial teams
  • Evaluate, acquire, and implement new technologies
  • Establish governance processes, performance metrics, and decision-making frameworks
  • Support site startup, facility expansion, validation, and capital investment initiatives
Requirements
  • Masterโ€™s degree in engineering, Life Sciences, Chemistry, Pharmaceutical Sciences, or a related field required
  • 15+ years of progressive leadership experience within pharmaceutical, biotechnology, CDMO, or related life sciences environments
  • Deep understanding of small molecule and bioconjugate technologies
  • Extensive leadership experience in Process Development, Analytical Development, Technical Operations, Manufacturing, or related GMP-regulated organizations
  • Strong understanding of pharmaceutical manufacturing operations, cGMP requirements, technology transfer, validation, operational readiness, and commercialization activities
  • Experience supporting facility startup, expansion projects, greenfield or brownfield investments, and large-scale capital programs
  • Proven success leading organizations through growth, transformation, and operational scale-up initiatives
  • Strong technical knowledge and experience in small molecule drug substance manufacturing
  • Ability to collaborate across Engineering, Quality, MSAT, Automation, Manufacturing, EHS, HR, Finance, and Commercial functions
  • Ability to translate business requirements into practical, scalable operational solutions
  • Strong executive presence and ability to communicate readiness, risks, performance, and recommendations to senior leadership
  • Experience building organizations, developing talent, and preparing teams for future needs
  • Understanding of Lean Manufacturing, Six Sigma, Operational Excellence, automation, digital systems, and data integrity principles
  • Capability in portfolio management, strategic planning, budget ownership, and resource allocation
  • Ability to navigate ambiguity, manage competing priorities, and lead in a fast-paced environment
  • Strong leadership, communication, problem-solving, and decision-making skills
  • Ability and willingness to transition to an East Coast or Midwest U.S. site location as project needs evolve
  • Willingness and ability to travel to EMEA and NA approximately 25โ€“30% of the time
Core Competencies

Demonstrates extensive leadership in Process Development, Analytical Development, and Technical Operations within GMP-regulated environments, with a strong focus on operational excellence, strategic planning, and budget management. Capable of driving transformation initiatives and collaborating across multiple functions to achieve business growth and compliance.

Highest-signal resume keywords
  • Leadership Experience in Pharmaceutical Manufacturing
  • Process Development and Analytical Development
  • Understanding of cGMP Requirements
  • Lean Manufacturing and Six Sigma Expertise
  • Strategic Planning and Budget Management
ATS Optimization Keywords Hard Skills
  • Process Development
  • Analytical Development
  • Technical Operations
  • Small Molecule Drug Substance Manufacturing
  • Technology Transfer
  • Validation
  • Operational Readiness
  • Commercialization Activities
  • Portfolio Management
  • Resource Allocation
Soft Skills
  • Leadership
  • Communication
  • Problem-Solving
  • Decision-Making
  • Collaboration
Industry Keywords
  • Pharmaceutical
  • Biotechnology
  • CDMO
  • GMP-Regulated Organizations
  • Facility Startup
  • Capital Investment
  • Sales & Operations Planning
  • Operational Excellence
  • Transformation Programs
  • Compliance
Tools & Technologies
  • Lean Manufacturing
  • Six Sigma
  • Digital Systems
  • Data Integrity Principles
  • Automation
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