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$191.4K

$287.5K

How much do director analytical development jobs pay per year?

As of Sep 12, 2026, the average yearly pay for director analytical development in the United States is $191,412.00, according to ZipRecruiter salary data. Most workers in this role earn between $94,000.00 and $249,000.00 per year, depending on experience, location, and employer.

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 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 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.

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Director Analytical Development jobs near you
Infographic showing various Director Analytical Development job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 81% Full Time, 15% Part Time, and 2% Contract. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $191,412 per year, or $92 per hour.

Director, Analytical Development - Small Molecule

Waltham, MA • Hybrid

Ardelyx
51 - 200 employees
Learn more about Ardelyxexternal

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 22 days ago

Job description

Ardelyx is a commercial-stage biopharmaceutical company focused on redefining treatment approaches for patients with significant unmet medical needs. By combining scientific innovation with a collaborative, purpose-driven culture, we strive to create meaningful impact for patients.
 
Team Ardelyx is united by a shared mission and guided by our core values: Passionate, Fearless, Dedicated, and Inclusive.
 
We foster an inclusive environment where employees are respected, supported, and empowered to make an impact — both within our company and in the lives of patients we serve.
 
This is a hybrid role (2-3 days in office) at our Waltham, MA headquarters.
 

Position Summary: 

The Director, Analytical Development is a leader who works as a member of an integrated team at Ardelyx overseeing small molecule analytical activities involving commercial drug substance and drug product with the exception of stability program management.

This position partners cross-functionally with CMC, Quality, Manufacturing, Regulatory Affairs, Supply Chain, and external partners to ensure the successful execution of analytical strategies that support reliable product supply, regulatory compliance, and business objectives.

Responsibilities:

  • Develop and lead execution of analytical strategies; prepare RFPs, select partners, and manage the successful execution of plans consistent with objectives and compliant with cGMP requirements
  • Establish resource plans and operational budgets to meet corporate and departmental objectives
  • Effectively integrate Commercial Analytical activities with those of sister CMC functions, including Drug Substance, Pharmaceutics, Supply Chain, Quality Assurance, and Regulatory Affairs
  • Lead the preparation of analytical content for various regulatory documents (NDA, etc.) and effectively represent the function in interactions with regulatory authorities
  • Effectively and professionally represent the Commercial Analytical function on various cross-functional teams including internal project teams as well as external steering and operating teams with contract manufacturing and/or corporate partners
  • Evaluate and propose recommendations to senior leadership regarding analytical risks, opportunities, lifecycle strategies, and continuous improvement initiatives

Qualifications:

  • Bachelor’s Degree, advanced degree preferred, in chemistry or related discipline with 10+ years of industry experience or equivalent experience
  • Strong experience required in analytical chemistry and associated regulatory requirements
  • Experience working in close collaboration with technical, regulatory, quality assurance, project management, legal, finance, and supply chain functions, preferably in a cGMP operational environment
  • Experience in leading and managing outsourced analytical activities and associated operating budgets
  • Experience in preparing and defending regulatory documents
  • Excellent communication skills and the ability to present to diverse internal and external audiences are requisite
  • Periodic travel to manufacturing and other partner sites is required (approximately 10-20 % of time)
The anticipated annualized base pay range for this full-time position is $211,000 - $257,000  Ardelyx utilizes industry data to ensure that our compensation is competitive and aligned with our industry peers. Actual base pay will be determined based on a variety of factors, including years of relevant experience, training, qualifications, and internal equity. The compensation package may also include an annual bonus target and equity awards, subject to eligibility and other requirements.     
 
Ardelyx also offers a robust benefits package to employees, including a 401(k) plan with generous employer match, 12 weeks of paid parental leave, up to 12 weeks of living organ and bone marrow leave, equity incentive plans, health plans (medical, prescription drug, dental, and vision), life insurance and disability, flexible time off, annual Winter Holiday shut down, and at least 11 paid holidays.
 
Ardelyx is an equal opportunity employer.
 
We do not accept unsolicited resumes from search firms, or recruiters or similar vendors. Any such unsolicited resume submitted to any employee or through Company's career site without a valid, signed search agreement signed by Company's authorized representative will be deemed the property of the company, and no fees will be paid in the event of a hire. Company will have the right to hire any such candidate at its discretion without any financial obligation or fee owed to the vendor. Any verbal or written communication with a Company employee outside of this process will not be considered a binding agreement.