Benefits:

401(k)

401(k) matching

Bonus based on performance

Dental insurance

Health insurance

Vision insurance

Wellness resources

Company Overview:

Crystal Bio Solutions, a member of Crystal Pharmatech, is a leading bioanalytical and biologics CMC analytical organization with operations in the San Francisco Bay Area and New Jersey. We specialize in GLP-compliant bioanalytical and biomarker services, as well as CMC analytical support for biologics, serving biotech and pharmaceutical clients from early discovery through clinical development. We are seeking a full-time Project Manager to support our Bioanalytical and Biomarker Services at our Pleasanton, California site.

Key Responsibilities: ·

Provide oversight on the study throughout its life at CBS, including method development, method validation, sample/data analysis, and reporting.

Work closely with lab staff, data analyst, technical writing, QC, QA, Procurement and Finance to ensure studies are completed and compensated on schedule.

Maintain all communication with clients providing daily updates on all active projects while being vigilant for opportunities to earn additional business.

Work with the client to resolve sample/data discrepancies.

Monitor the progress of all assigned studies and alert management if work falls behind schedule.

Provide project trackers for client communications and lead regular teleconferences to discuss study progress.

Create project parameters and budget expectations and conduct periodic scope, schedule, and cost reviews using industry best practices, to identify needed adjustments

Coordinate client visits and where needed.

Qualifications and Educational Requirements:

Master's or bachelor's degree in biology, immunology, chemistry, pharmacology, or related scientific fields required.

Minimum of 3 years' PM-related experience. Supervisory experience in both project and people management are desirable.

Understanding of Ligand binding assays, LC-MS/MS, Cell-based assays, Immunogenicity assays, PCR and/or Flow cytometry assays is a plus.

Familiar with requirements of FDA/EMA, GLP/GCLP regulations, and ICH guidelines.

Multi-tasking capability to efficiently manage multiple projects simultaneously.

Ability to achieve objectives/timelines through collaborative efforts with coworkers, managers, and clients.

Good communication skills in both written and verbal and interpersonal skills are essential

Preferred Skills

Proficient in MS Office, PM tools (e.g., Smartsheet, MS Project, etc.)

Location: Pleasanton, California (On-site, 5 days on site)

Compensation: Compensation will be based on experience and qualifications