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Director Bioanalytical Jobs (NOW HIRING)

MSD

Bioanalytical Associate

Gaithersburg, MD · On-site

$59K - $87K/yr

This is a laboratory-based position whose primary function is executing various types of assays with relatively high throughput in support of bioanalytical projects, under direct supervision. DUTIES ...

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$29.5K

$138.6K

$222K

How much do director bioanalytical jobs pay per year?

As of Jun 6, 2026, the average yearly pay for director bioanalytical in the United States is $138,649.00, according to ZipRecruiter salary data. Most workers in this role earn between $89,000.00 and $179,000.00 per year, depending on experience, location, and employer.

What are the typical daily responsibilities of a Director Bioanalytical?

As a Director Bioanalytical, your daily responsibilities often include overseeing the planning and execution of bioanalytical studies, ensuring compliance with regulatory standards, and managing a team of scientists and support staff. You’ll review and interpret complex data, troubleshoot analytical challenges, and coordinate closely with project managers, regulatory affairs, and external partners. Additionally, you’ll be involved in developing and validating new analytical methods and contributing to strategic decisions that support drug development pipelines. This dynamic role combines hands-on scientific oversight with high-level team leadership and cross-functional collaboration.

What are the key skills and qualifications needed to thrive in the Director Bioanalytical position, and why are they important?

To thrive as a Director Bioanalytical, you need advanced expertise in bioanalytical chemistry, method development, and regulatory compliance, typically supported by a graduate degree in a related scientific field. Familiarity with analytical platforms such as LC-MS/MS, laboratory information management systems (LIMS), and relevant regulatory guidelines (FDA, EMA) is essential. Strong leadership, project management, and effective communication skills distinguish top candidates in this role. These abilities are vital to overseeing complex studies, ensuring data integrity, and leading multidisciplinary teams in a high-stakes environment.

What is a Director Bioanalytical job?

A Director Bioanalytical oversees bioanalytical strategy, laboratory operations, and regulatory compliance for drug development and research. They manage assay development, validation, and sample analysis to support preclinical and clinical studies. This role requires expertise in bioanalytical techniques such as LC-MS/MS, ELISA, and biomarker analysis. Additionally, they ensure compliance with GLP/GCP guidelines and collaborate with cross-functional teams to drive scientific decision-making.

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What cities are hiring for Director Bioanalytical jobs? Cities with the most Director Bioanalytical job openings:
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Director Bioanalytical jobs near you
Infographic showing various Director Bioanalytical job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, and 2% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $138,649 per year, or $66.7 per hour.
Associate Director, Bioanalysis (Cell Therapy)

Associate Director, Bioanalysis (Cell Therapy)

AstraZeneca

Santa Monica, CA • Hybrid

$135K - $177K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 15 days ago

AstraZeneca rating

8.6

Company rating: 8.6 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

16th of 71 rated pharmaceutical

Job description

WHY JOIN US?

At AstraZeneca, we are dedicated to being a Great Place to Work, where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. With an ambitious goal of delivering 20 new medicines by 2030, there is no better place to make a difference in medicine, for patients, and in society.

Join us on this exciting journey to pioneer the future of healthcare. Our inclusive culture champions diversity and collaboration, and we are always committed to lifelong learning, growth, and development. As part of our team, you'll contribute to groundbreaking advancements that will shape a healthier future for people everywhere. Be a catalyst for change at AstraZeneca, where your work will have a real impact on improving people's lives.

Recognizing the importance of individualized flexibility, our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices 3 days a week. Our head office is purposely designed with collaboration in mind, providing space where teams can come together to strategize, brainstorm and connect on key projects.

Introduction to Role
Are you ready to make a significant impact in the field of cell therapy? Join our dynamic team at AstraZeneca as an Associate Director within the Cell Therapy Enterprise, where you will lead the design and implementation of robust bioanalytical strategies to support clinical assay endpoints. Your expertise will be crucial in advancing our cell therapy pipeline and transforming the lives of patients.
Accountabilities:

  • Lead design and implementation of robust bioanalytical strategies to support clinical assay endpoints, including but not limited to PK/CK/PD, immunogenicity (humoral, cellular, viral) and biomarkers related to cell and gene products to support the AstraZeneca cell therapy pipeline (CAR/TCR/in vivo).

  • Identify, evaluate scientific and operational capabilities and establish partnerships with selected specialty laboratories and CROs for generation and analysis of bioanalytical data.

  • Lead and oversee assay development, qualification/validation and tech transfer (when appropriate) of cell therapy-related bioassays at CROs or using internal capabilities.

  • Interpret and integrate complex datasets within programs and across the cell therapy portfolio. Provide written and verbal updates to key stakeholders.

  • Contribute to publication strategy, prepare data for publication or presentations in internal/external scientific conferences.


Essential Skills/Experience:

  • PhD degree in immunology, cellular and/or tumor biology or a related field with 7+ years of relevant industry experience with strong background in cell therapy

  • Demonstrated experience managing/directing analysis of clinical biospecimens to support clinical trials.

  • Proven experience in regulated bioanalysis across a range of modalities PK/CK, PD and immunogenicity assessments

  • Able to evaluate and interpret complex data sets using analysis and visualization software (i.e. Cytobank/OMIQ/FCS Express, Tableau/Spotfire/JMP), experience with AI tools is a plus.

  • Work cross-functionally and collaboratively with project stakeholders.

  • Deep understanding of cell therapy biology and up to date with latest analytical methods applicable to characterization of cell therapy products and mechanism of action.

  • Understanding of global regulatory expectations and analytical requirements to support regulatory filings.

  • Experience managing assay development teams, overseeing tech transfers, scientific quality and study conduct internally and at CROs.

  • Ability to interpret complex datasets and exceptional ability to communicate results verbally, in writing and in presentations adapting to different audiences as required.

  • Ability to prioritize multiple projects and task concurrently in a fast-paced environment.

SO, WHAT'S NEXT?

To be considered for this exciting opportunity, please complete the full application on our website at your earliest convenience - it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity. If you know someone who would be a great fit, please share this posting with them.

Where can I find out more?

  • Explore what we're building: www.evinova.com
  • Stay connected and see our impact in action: https://www.linkedin.com/company/evinova/

Apply today to bring smarter, faster clinical trials to life!

Evinova is an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination. Evinova is committed to accommodating persons with disabilities. Such accommodation is available on request in respect of all aspects of the recruitment, assessment and selection process and may be requested by emailingAZCHumanResources@astrazeneca.com.

#LI-Hybrid

The annual base pay for this position ranges from $135,058.40 - $177,264.15 USD.Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience.

In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program. Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans.

Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base pay(as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

Date Posted

21-May-2026

Closing Date

04-Jun-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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