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Director Analytical Development Jobs in Basking Ridge, NJ

Pathos

Director, CMC - Biologics & ADC

New York, NY · On-site

$210K - $250K/yr

This individual will own upstream and downstream process development, analytical development, and ... Direct ADC-specific CMC activities including linker-payload strategy, conjugation process ...

New

Tiffany

Analyst - Development

New York, NY

$77K - $85K/yr

The Development Analyst supports the end-to-end development process by driving visibility ... Partner with PD Manager & Director / engineering leads to assess impact Product/Technical Learning:

Omnicom

Director, Analytics

New York, NY · On-site

Responsibilities Lead the development of our existing analytics products Analyze a wide range of ... days are directed by their agency or manager. Our objective is to increase this requirement ...

Neion Bio

Head of Biologics

New York, NY

$170K - $230K/yr

Lead Neion Bio's protein development function, including downstream process development, analytical development, product characterization, and regulatory strategy and interactions * Define product ...

Bridge Industrial

Development - Director

Jersey City, NJ · On-site

$150K - $180K/yr

Director, Development-East Rutherford NJ location Company Overview: Kurv Industrial ("Kurv") is a ... Zoning analysis and permitting pathways * Utility availability and infrastructure assessments

Iterative Health

Director, Analytics

New York, NY

The work spans everything from KPI definition and dashboard development to forecasting and trial ... Responsibilities Be the analytical partner operations and commercial leaders rely on Your primary ...

Iterative Health

Director, Analytics

New York, NY · On-site

The work spans everything from KPI definition and dashboard development to forecasting and trial ... Responsibilities Be the analytical partner operations and commercial leaders rely on Your primary ...

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All JobsAnalytical Development JobsDirector Analytical Development JobsDirector Analytical Development Jobs in Basking Ridge, NJ

Director Analytical Development information

See Basking Ridge, NJ salary details

$91.7K

$197.3K

$296.3K

How much do director analytical development jobs pay per year?

As of Aug 12, 2026, the average yearly pay for director analytical development in Basking Ridge, NJ is $197,260.00, according to ZipRecruiter salary data. Most workers in this role earn between $96,900.00 and $256,600.00 per year, depending on experience, location, and employer.

What are the typical daily responsibilities of a director analytical development?

A Director Analytical Development typically oversees the design, implementation, and optimization of analytical methods to support product development and quality control. This involves leading a team of scientists, ensuring projects meet regulatory requirements, troubleshooting technical challenges, and collaborating closely with cross-functional groups such as R&D, quality assurance, and manufacturing. Daily tasks often include reviewing analytical data and reports, planning project timelines, and making strategic decisions to align with organizational objectives. The role requires balancing hands-on scientific guidance with high-level management to drive innovation and efficiency within the analytical function.

What is a director analytical development?

A Director of Analytical Development oversees the strategy, development, and implementation of analytical methods to support product development and manufacturing. They lead a team of scientists, ensure regulatory compliance, and collaborate with cross-functional teams to optimize processes. Their role includes troubleshooting analytical issues, validating methods, and contributing to regulatory submissions. This position is critical in maintaining product quality and ensuring data-driven decision-making in pharmaceutical, biotechnology, or related industries.

What are the key skills and qualifications needed to thrive in the director analytical development position, and why are they important?

To thrive as a Director Analytical Development, you generally need an advanced degree in chemistry, biochemistry, or a related scientific field, along with substantial experience in analytical method development and validation, and team leadership. Familiarity with laboratory information management systems (LIMS), chromatographic and spectroscopic instrumentation, and regulatory guidelines such as ICH, FDA, and GMP is crucial. Excellent project management, strategic thinking, and interpersonal communication are standout soft skills for this position. These competencies enable effective oversight of complex analytical projects, ensure regulatory compliance, and foster team collaboration in a fast-paced R&D environment.

What job categories do people searching Director Analytical Development jobs in Basking Ridge, NJ look for? The top searched job categories for Director Analytical Development jobs in Basking Ridge, NJ are:
What cities near Basking Ridge, NJ are hiring for Director Analytical Development jobs? Cities near Basking Ridge, NJ with the most Director Analytical Development job openings:
Director Analytical Development jobs near you
Infographic showing various Director Analytical Development job openings in Basking Ridge, NJ as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, and 4% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $197,260 per year, or $94.8 per hour.

Director, CMC - Biologics & ADC

Pathos

New York, NY • On-site

$210K - $250K/yr

Full-time

Posted 2 days ago

New

Job description

Drug development shouldn't be guesswork, not when patients are waiting.
Pathos is building a next-generation biotech with AI at the core. Not as a feature, but as the operating system for how medicines get developed. We believe most drugs don't fail because the science was wrong. They fail because they were tested in the wrong patients, with the wrong assumptions, in trials that couldn't answer the real question: who benefits, and why?
Pathos exists to change that. We're building the largest foundation model in oncology and pairing it with proprietary AI systems, deep oncology expertise, and 200+ petabytes of multimodal data linked to patient outcomes, so we can make development decisions with more precision, much earlier.
This is not theoretical. We're well-capitalized and have the leadership to build a generational company. We invest in and advance our own clinical-stage programs, using our AI platform to sharpen trial design, patient selection and biomarker strategy. So therapies reach the patients most likely to benefit, sooner.
How We Build
Pathos does not operate like a traditional biotech. There is no middle management. There are no layers of approval. The company is designed, from the ground up, around small teams of 2-4 subject matter experts who each command hundreds of AI agents to do the work that used to require dozens of people.
Everyone builds. Everyone ships. Every function at Pathos - from clinical execution to asset selection to the foundation model itself - runs on this model. Our product velocity delivers meaningful outcomes in hours instead of weeks. This is not a future aspiration. It is how we operate today.
The people who thrive here are operators: deep experts who can specify what needs to happen, orchestrate AI agents to execute at scale, and make high-judgment calls that compound over time. If you have spent your career building and shipping AI systems at scale, this is the environment where that experience becomes a superpower.
About the Role
We are seeking a Director, CMC - Biologics & ADC to lead the chemistry, manufacturing, and controls strategy for our antibody and antibody-drug conjugate (ADC) oncology programs. This individual will own upstream and downstream process development, analytical development, and ADC conjugation/manufacturing - from early clinical supply through late-stage development - ensuring phase-appropriate quality, robust and scalable processes, and regulatory-ready documentation. This is a foundational hire on the Pathos CMC/Technical Operations team. You will help build and scale the chemistry, manufacturing, and controls function from an early stage, working shoulder-to-shoulder along with the Head of CMC with Research, Clinical, Regulatory, and Quality colleagues in a fast-moving, resource-conscious environment. You are equally comfortable rolling up your sleeves on technical detail and operating strategically across a portfolio.
What You Will Do
CMC Strategy & Program Leadership
  • Define and execute the end-to-end biologics/ADC CMC strategy for one or more oncology programs, spanning antibody drug substance, conjugation, and drug product.
  • Serve as the CMC program lead and single point of accountability, representing CMC on cross-functional program teams alongside Research, Clinical, Regulatory, and Quality.
  • Translate program goals and timelines into phase-appropriate development plans, budgets, and risk-mitigation strategies.

Upstream & Downstream Process Development
  • Expert in biologics cell line and drug substance development.
  • Lead upstream process development for antibodies - cell line development oversight, media/feed optimization, and fed-batch/perfusion bioreactor processes from bench through scale-up.
  • Lead downstream process development - harvest/clarification, Protein A and polishing chromatography, viral clearance, ultrafiltration/diafiltration, and formulation.
  • Apply QbD and risk-based approaches to establish robust, scalable, and controllable processes and control strategies.

ADC Conjugation & Manufacturing
  • Direct ADC-specific CMC activities including linker-payload strategy, conjugation process development, and drug-to-antibody ratio (DAR) control.
  • Oversee ADC drug substance and drug product manufacturing, including handling of high-potency payloads and appropriate containment (OEB) controls.
  • Coordinate the multi-component supply chain (antibody intermediate, linker-payload, conjugated drug substance, and drug product) across specialized CDMOs.
  • Experience with high-concentration development is a plus
  • Lyophilization experience is a plus

Analytical Development & Characterization
  • Own the analytical strategy for antibodies and ADCs - method development, qualification/validation, specifications, and stability.
  • Direct product characterization and comparability, including purity/impurities, aggregation, charge variants, glycosylation, potency/bioassays, DAR, free-drug, and other ADC-critical quality attributes.
  • Design and execute studies to assess protein stability, aggregation, degradation pathways, viscosity, and developability under relevant formulation conditions.

External Manufacturing, Regulatory & Quality
  • Select, manage, and technically oversee CDMOs for antibody and ADC manufacture, leading tech transfer, scale-up, engineering, and GMP campaigns.
  • Ensure timely, phase-appropriate clinical supply (Phase 1-3) and lead process performance/validation to support late-stage development and commercialization.
  • Author and review CMC sections of regulatory filings (IND, IMPD, briefing documents, and later BLA/MAA modules) and support health-authority interactions.
  • Partner with Quality to ensure GMP compliance, manage deviations and change control, and support audits.

Who You Are
Required Qualifications
  • Ph.D. in Biochemistry, Chemical/Biochemical Engineering, Biotechnology, or a related field (or an M.S./B.S. with commensurate additional experience).
  • 8-10+ years of biopharmaceutical CMC experience with demonstrated depth in antibody upstream AND downstream process development and analytics.
  • Hands-on experience with ADC manufacturing - conjugation chemistry, linker-payload handling, DAR control, and high-potency containment.
  • Direct experience in oncology drug development.
  • Proven track record across the full development lifecycle: phase-appropriate development for Phase 1-3 as well as hands-on experience with late-stage development.
  • Experience in BOTH a small/emerging biotech and a large pharma environment, with the versatility to operate effectively in each.
  • Demonstrated success managing CDMOs and leading technical transfer, scale-up, and GMP manufacturing for biologics and/or ADCs.
  • Strong command of ICH, FDA, and EMA guidance for biologics/ADCs and phase-appropriate GMP expectations, with experience authoring CMC regulatory submissions.

Preferred Qualifications
  • Experience taking a biologic or ADC oncology asset through pivotal/late-stage development and toward registration (BLA/MAA).
  • Familiarity with site-specific/next-generation conjugation, novel payload classes, or bispecific antibody formats.
  • Experience with comparability strategies and control of ADC-specific critical quality attributes across process changes.
  • Comfort operating in a data- and technology-forward organization; interest in leveraging AI/ML to accelerate CMC decision-making.

What Success Looks Like
  • Reliable, phase-appropriate clinical supply of antibody and ADC material that never gates the clinical program.
  • Robust, scalable processes and well-controlled critical quality attributes that de-risk late-stage development.
  • Clean, defensible CMC regulatory submissions and successful health-authority interactions.

Location
This is a hybrid role, requiring 3 days per week onsite, in our NYC Headquarters.
The pay range for this role is:
210,000 - 250,000 USD per year (New York Office - ACLS East Tower)

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