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Manager Analytical Development Jobs (NOW HIRING)

Legend Biotech is seeking a Scientist I, Analytical Development as part of the Research and ... Collaboration, consensus and alignment with management are required for decisions related to ...

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NJ · On-site

$220 - $293/hr

Position Summary Rocket Pharma is seeking an experienced Senior Director, Analytical Development to ... Strong time management skills with the ability to prioritize tasks across multiple projects to meet ...

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Manager Analytical Development information

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$33K

$77.4K

$133K

How much do manager analytical development jobs pay per year?

As of Aug 13, 2026, the average yearly pay for manager analytical development in the United States is $77,438.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,500.00 and $90,500.00 per year, depending on experience, location, and employer.

What are the typical day-to-day responsibilities for a manager analytical development?

As a Manager Analytical Development, your typical day involves overseeing laboratory teams, managing analytical method development and validation projects, and ensuring compliance with relevant quality standards. You’ll often collaborate with R&D, quality assurance, and production departments to support product development timelines and troubleshoot analytical challenges. Additionally, you may conduct data reviews, prepare regulatory documentation, and participate in meetings to drive project progress. Your role also includes mentoring team members and optimizing lab workflows for productivity and accuracy.

What is a manager analytical development?

A Manager Analytical Development oversees the development, validation, and implementation of analytical methods to support product development and manufacturing. They ensure compliance with regulatory standards, manage a team of scientists, and collaborate with cross-functional departments to drive innovation and efficiency. Their role is critical in ensuring product quality, consistency, and regulatory approval.

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

To excel as a Manager Analytical Development, you typically need an advanced degree in chemistry, biochemistry, or a related field, along with experience in analytical method development and leadership. Familiarity with laboratory information management systems (LIMS), chromatographic software (HPLC/UPLC), and regulatory standards such as ICH and FDA guidelines is common. Outstanding project management, team leadership, and communication skills help you effectively coordinate cross-functional projects and mentor staff. These competencies enable delivery of high-quality analytical solutions, ensure regulatory compliance, and drive successful product development.

What does a Manager Analytical Development do?

A Manager of Analytical Development oversees the design, validation, and implementation of analytical methods used to test and ensure the quality of pharmaceutical or biotech products. They lead teams of scientists, coordinate method development projects, and ensure compliance with regulatory standards such as GMP and FDA guidelines. The role often requires expertise in analytical techniques, laboratory management, and relevant certifications.
More about Manager Analytical Development jobs
What cities are hiring for Manager Analytical Development jobs? Cities with the most Manager Analytical Development job openings:
What are the most commonly searched types of Analytical Development jobs? The most popular types of Analytical Development jobs are:
What states have the most Manager Analytical Development jobs? States with the most job openings for Manager Analytical Development jobs include:
Infographic showing various Manager Analytical Development job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $77,438 per year, or $37.2 per hour.

Manager/Sr. Manager, Analytical

Soleil Labs, LLC

South San Francisco, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 21 days ago


Job description

Department / Function: CMC/Analytical

Work Location: This is an on-site position based at our corporate Headquarters (South San Francisco)


Position Summary:
TCG Labs-Soleil is looking for an experience analytical lead to join our CMC team. We are seeking a highly skilled and self-motivated professional to lead analytical development and quality control activities for our expanding portfolio of development programs. In this exciting role, you'll be working closely with internal teams and CDMOs to develop fast and efficient plans for analytical development and method qualification for biologics programs. As the primary point of contact, you will be responsible for providing general analytical oversight at CDMOs to support the on-time delivery of clinical materials.

Responsibilities:
Analytical Development
Lead the development, optimization, qualification, and transfer of analytical methods for drug substances and drug products at CDMOs and external partners.
Design and oversee analytical strategies to support process development, comparability studies, and stability programs.
Ensure analytical methods are scientifically sound, phase-appropriate, and compliant with ICH, FDA, EMA, and other applicable regulatory guidelines.
Manage stability trending activities using statistical and scientific evaluation.
Manage troubleshooting and root cause investigations related to analytical methods and laboratory results.
Quality Control
Manage method qualification activities at CDMOs.
Review and approve analytical data, laboratory investigations, deviations, OOS/OOT results, CAPAs, protocols, and reports.
Contribute to regulatory submissions including INDs, IMPDs, and related documentation by serving as a QC reviewer.
Coordinate analytical activities with external laboratories, CDMOs, and testing partners.
Provide technical expertise and risk assessments to support change controls and manufacturing investigations.

Qualifications:
Bachelor's, Master's, or Ph.D. in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, Chemical Engineering, or a related scientific discipline.
A minimum of 8(with BS) / 6(with MS) / 4(with PhD) years of experience in analytical development, quality control, or pharmaceutical/biotech laboratory operations.
Strong expertise in analytical techniques such as HPLC, UPLC, CE, UV/Vis, bioassays, and mass spectrometry.
Extensive experience with analytical method development, qualification, validation, and transfer following ICH guidelines.
Experience managing laboratory investigations including deviations, OOS (Out-of-Specification), OOT (Out-of-Trend), CAPA, and root cause analysis.
Experience with stability studies, specification setting, and product lifecycle management.
Strong understanding of data integrity principles and laboratory documentation practices.
Demonstrated ability to manage multiple projects, timelines, and cross-functional collaborations.
Ability to travel to domestic and international sites as required.
Experience overseeing external CROs, CMOs, or contract testing laboratories preferred.
Experience in biologics and sterile products preferred.
Experience in developing project and CMC timelines preferred.
Ability to work independently and effectively in a dynamic, fast-paced, collaborative environment as a member of a cross-functional team.


Company Overview

TCG Labs-Soleil, established in partnership with The Column Group, a science-focused venture capital firm, is pioneering a novel 'venture capital-biotech' model. Our core mission is to efficiently translate scientific insights into therapeutic solutions for patients facing serious diseases. This model supports scientific entrepreneurs from the initial idea to clinical proof of concept (PoC) by combining a dedicated fund (TCG Labs) with our independent, evergreen R&D center led by a top-tier scientific team (Soleil). Together, we create an integrated ecosystem that fosters the development of single-asset portfolio companies, strategically poised for transacting after clinical PoC.

For more details, visit TCGLSoleil.com and follow us on LinkedIn

EEO Statement

TCG Labs-Soleil is an Equal Opportunity Employer. We do not discriminate against qualified applicants based upon any protected group status, including but not limited to race, religion, color, creed, sex (including breastfeeding and related conditions), gender identity/gender expression, pregnancy (including childbirth and related conditions), national origin, ancestry, age, marital status, military or veteran status, sexual orientation, genetic information, physical or mental disability or medical condition as defined by applicable equal opportunity laws. Any request for accommodation can be directed to contact@tcglsoleil.com.

Benefits and Compensation

TCG Labs-Soleil provides a competitive benefits package that includes access to Medical, Dental, and Vision Insurance, Life Insurance, Short and Long Term Disability, Health Savings Account (HSA), Flexible Spending Accounts (FSA), 401k plan and PTO.

The anticipated salary range for fully qualified candidates applying for this role will be $145,000-$190,000 annually (not including discretionary bonus, equity, and benefits). The final salary offered will be dependent on several factors that include but are not limited to relevant previous experience including duration and type of experience within the industry, education, and internal equity.

Staffing Agencies

TCG Labs-Soleil does not accept unsolicited agency resumes and will not pay fees to any third-party agency or firm that doesn't have a signed agreement with TCG Labs-Soleil. Please do not send agency CVs/resumes through TCG Labs-Soleil website or TCG Labs-Soleil Employees. Inquiries must be sent to contact@tcglsoleil.com with the Subject Heading: Staffing Agency Request.