Job Description

Employment Type: Full-time

Available Positions: 1

Location : On-Site

Application Deadline: Jan 5, 2026

Summary

The Director of LCMS Platforms will be responsible for providing bioanalytical support for both pre-clinical and clinical projects and partnering with our clients for project success.

Key Activities

• Lead a team of supervisors, PhD, and non-PhDs.D. scientists to ensure the development, validation, and execution of LBA-based assays (PK, ADA, PD Biomarkers) in compliance with GLP/GCLP standards.
• Directly manage supervisors and junior staff by setting clear expectations, supporting career development, and ensuring high performance.
• Train and mentor team members as needed to build scientific strength, compliance awareness, and project ownership.
• Serve as Principal Investigator (PI) on client studies, overseeing protocol development, study conduct, and reporting.
• Communicate clearly with clients and manage expectations throughout all phases of assigned projects to ensure satisfaction and alignment.
• Maintain strong relationships with global clients, supporting both ongoing and future project opportunities with responsiveness and trust.
• Provide scientific and operational leadership as Subject Matter Expert (SME) in LBA technologies, including ELISA and MSD (Meso Scale Discovery).
• Review and approve study plans, validation protocols, reports, and key regulatory documentation.
• Represent Crystal Bio Solutions at scientific conferences, industry networking events, and in client-facing presentations.
• Support business development by providing technical insights for client proposals and quote generation.
• Ensure efficient lab operations through SOP adherence, workflow improvements, and cross-functional collaboration (QA, BD, PM).

Preferred Skills

• Experience presenting at industry events or scientific meetings is preferred.
• Familiarity with LIMS (Watson preferred) and bioanalytical compliance practices.

Educations & Experience

• PhD with 10+ years, Master’s with 15+ years, or Bachelor’s with 18+ years of relevant experience in Bioanalysis within Pharma, Biotech, or CRO settings.
• At least 3–5 years of people management experience, including direct supervision of scientific staff.
• Extensive background in GLP/GCLP-regulated bioanalytical method development and validation for PK, ADA, and Biomarker assays..

Are you looking for your next opportunity? We can help.

Finding a great opportunity that fosters growth, a great culture, and leadership opportunities can be difficult. Top Quality Recruitment (TQR) connects professionals with leadership opportunities across the Packaging, Food and Beverage, Medical Devices, and Biotechnology industries. With 50+ years of experience, we believe in one-to-one communication and finding the best candidate/employer match possible.

TQR is an equal-opportunity employer that encourages diversity. We will consider all applications.

Accommodation for applicants with disabilities is available upon request.

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We thank all applicants for their interest and appreciate the time and effort involved; however, due to the large volume of resumes received only those candidates selected for an interview will be contacted. Please attached your resume to your application.

Job ID: 8084

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