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Analytical Development Biotech Jobs (NOW HIRING)

Ph.D. with 0-3 years of relevant experience in pharmaceutical or biotech settings * M.S. with 4+ ... Proven ability to lead analytical activities for drug development programs. * Strong knowledge of ...

D. with 0-3 years of relevantexperiencein pharmaceuticalor biotech settings * M.S. with 4+ years of ... Proven ability to lead analytical activities for drug development programs. * Strong knowledge of ...

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Analytical Development Biotech information

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$29K

$53.4K

$81K

How much do analytical development biotech jobs pay per year?

As of Jun 27, 2026, the average yearly pay for analytical development biotech in the United States is $53,418.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,500.00 and $60,000.00 per year, depending on experience, location, and employer.

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 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, and why are they important?

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.
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What cities are hiring for Analytical Development Biotech jobs? Cities with the most Analytical Development Biotech job openings:
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What job categories do people searching Analytical Development Biotech jobs look for? The top searched job categories for Analytical Development Biotech jobs are:
Infographic showing various Analytical Development Biotech job openings in the United States as of June 2026, with employment types broken down into 83% Full Time, 4% Part Time, 2% Temporary, 10% Contract, and 1% Nights. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $53,418 per year, or $25.7 per hour.
Senior Scientist, Analytical Development

Senior Scientist, Analytical Development

Aurion Biotech Inc.

Cambridge, MA

$155K - $170K/yr

Other

Medical, Retirement, PTO

Posted 16 days ago


Job description

Description

JOB TITLE: Senior Scientist, Analytical Development

LOCATION: Cambridge, MA

SALARY RANGE: $155,000 to $170,000


ABOUT THE POSITION

Aurion Biotech is seeking a highly motivated Senior Scientist, Analytical Development in Cambridge, MA. This position will serve as an integral part of a multidisciplinary team to develop, qualify, and transfer in-process control, characterization, and release assays to support early and late-stage clinical manufacturing and testing of cell therapy products. The individual in this role will work collaboratively with the Research, Process Development, Quality and other groups to make sure assays meet the timeline of characterization and release of cell therapy products.


KEY RESPONSIBILITIES

  • Conduct various independent laboratory experiments including but not limited to Flow Cytometry, cell counting, dPCR, qPCR, ELISA, cell-based potency assays etc. to satisfy the overall AD objectives.
  • Collaborate cross-functionally with other functions including Cell Production, Process Development, Manufacturing, and Quality. 
  • Author method qualification SOP, method qualification report and test method SOP and other technical documents to support regulatory submissions and other groups.
  • Track progress toward project milestones and ensure that deliverables are met.
  • Responsible for the development, optimization, qualification, and transfer of GMP-compliant analytical methods and materials that meet US FDA and/or EU regulatory requirements for clinical stage, cell therapy products.
  • Train other groups to execute various in-house assays. 
  • Experience with Quality Control and regulatory requirements for late-stage method development and documentation are highly preferred.
  • Other duties as assigned.


ABOUT AURION BIOTECH 

With offices in Seattle, Boston, and Tokyo, Aurion Biotech is a clinical-stage biotech company, whose mission is to restore vision to millions of patients with life-changing regenerative therapies. The Company's first candidate is for the treatment of corneal edema secondary to endothelial dysfunction, and one of the first clinically validated cell therapies for corneal care; it was recently granted regulatory approval from Japan's PMDA. Aurion Biotech is the recipient of the prestigious Prix Galien award for best start-up in biotech. The Company is preparing for clinical trials in the U.S. We are growing rapidly and seek to hire highly motivated candidates from diverse backgrounds, cultures, and experiences, who share our values:

  • Stewardship: We make the world a better place for our patients, our communities, our clinicians, and our colleagues. We act responsibly as individuals, as employees, and as a company. 
  • Transformation: We embrace our challenges, our successes, and our failures. We are curious, we take risks, and we collaborate. 
  • Grit: We break down walls and strive to achieve the impossible. We are persistent and resilient, and we deliver on our commitments.

Aurion Biotech has a lot to accomplish in the next few years, and this role is key to our success. Privately held, Aurion Biotech is backed by Alcon, the global leader in eye care. To learn more about Aurion Biotech, visit www.aurionbiotech.com


LIFE AT AURION BIOTECH

We want our people to wake up every morning excited and energized for work. We value employees, which is why we invest in making life at Aurion Biotech healthy, fun, and rewarding:

  • Robust Benefits: We offer full health insurance to employees and their families, and all the acronyms: 401(k) matching, EAP, FSA, and generous PTO.
  • Total Rewards: We offer competitive compensation packages to ensure all Aurion employees are rewarded for their hard work.
  • Perks and Fun: Paid parking, subsidized commuter passes, in-office catered lunches, team events, and community projects are just a few ways that we bond, celebrate each other, have fun, and live our values.

Requirements

QUALIFICATIONS AND EDUCATION

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the education, experience, knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • A PhD and 3-5 years' experience or an MS degree and 6-8 years of experience in a relevant discipline (immunology, biochemistry, cell biology, biotechnology, or related field) in the pharmaceutical industry and academia, and specifically in gene and cell therapy.
  • Experience with biological therapeutic products is critical, experience specifically with cell therapy technologies is preferred.
  • Demonstrated track record with analytical development supporting early and late-stage development of cell therapies.
  • Deep technical understanding of analytical method development for key assays (Flow Cytometry, automated cell counting, dPCR, qPCR, ELISA, cell-based potency) and associated requirements (validation, stability programs, comparability assessments, etc.) across development is required.

REQUIRED SKILLS, KNOWLEDGE, AND ABILITIES

  • The ability to work in a dynamic, fast-paced, matrix environment, manage priorities and maintain timelines for multiple projects.
  • Demonstrated ability to technically trouble shoot and resolve assay challenges to successfully produce cell therapy products at a high-performance rate.
  • Demonstrated ability to develop, qualify/validate and transfer biologics analytics into manufacturing processes and product testing that meet customer needs is required.
  • The ability to work both independently and in a matrix team environment is essential.
  • Must have strong interpersonal and communication skills, be a team player and be willing to work in an environment where individual initiative, accountability to the team, and professional maturity are required.
  • Knowledge of Manufacturing to develop and innovate next-generation analytical tools for characterization.
  • Familiar with data analytics software such as FlowJo, JMP, and GraphPad Prism.