Manager/Sr. Manager, Analytical

Soleil Labs, LLC; South San Francisco (CA); On-site; USD 145,000 - 190,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

Life Insurance

Disability Insurance

HSA

FSA

401k

PTO

Job summary

TCG Labs-Soleil in South San Francisco, CA on-site, is seeking an experienced analytical lead to join our CMC team. You will lead analytical development and quality control activities for our expanding portfolio, working with internal teams and CDMOs to plan analytical development and method qualification for biologics programs.

As the primary contact, you will provide analytical oversight at CDMOs to support on-time delivery of clinical materials, manage stability and investigations, and guide

Qualifications

• Bachelor’s, Master’s, or Ph.D. in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, Chemical Engineering, or a related scientific discipline.
• Minimum years of experience: 8 (BS), 6 (MS), 4 (PhD) in analytical development, quality control, or pharmaceutical/biotech labs.
• 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, OOT, 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.

Responsibilities

• Lead the development, qualification, and transfer of analytical methods 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 guidelines.
• Manage stability trending activities using statistical and scientific evaluation.
• Manage troubleshooting and root cause investigations related to analytical methods and laboratory results.
• Manage method qualification activities at CDMOs.
• Review and approve analytical data, investigations, deviations, OOS/OOT, CAPAs, protocols, and reports.
• Contribute to regulatory submissions including INDs, IMPDs, and related documentation as 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.

Skills

Analytical method development

HPLC/UPLC/LC-MS

Quality control

Data integrity

Regulatory compliance

Cross-functional collaboration

Project management

Education

Bachelor’s/Master’s/PhD in a related science

Experience 8/6/4 years in analytical development/QC/pharma labs

Biologics/biotech lab experience

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 [e-mail].

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 [e-mail] with the Subject Heading: Staffing Agency Request.