Associate Scientist I/II/III, Analytical Services

Associate Scientist I/II/III, Analytical Services Pacific BioLabs, Hercules, California, United States Full Time, Immediate Start Overview Pacific BioLabs is an independent CRO providing cGMP/GLP testing in toxicology, biocompatibility, pharmacology, analytical chemistry, and microbiology. We are seeking energetic scientists and professionals to support our clients in the pharmaceutical, biotech, and medical device fields. The Associate Scientist I/II/III will develop and validate analytical methods and provide hands‑on technical assistance to maintain analytical equipment in good working order, while analyzing samples supporting various projects. Primary Responsibilities Develop, validate, and standardize HPLC, LC/MS, ICP-MS, GC, GC/MS, ELISA, and MSD analytical methods for isolation, detection, identification, and quantification of both drug substances and drug products of small molecules or large molecules. Review data for technical content and regulatory compliance. Analyze and evaluate material and products at all stages of the development process under stringent quality and time requirements. Prepare final reports, invention disclosures, and Standard Operating Procedures for internal and external use. Ensure analytical equipment is maintained in good working order; troubleshoot and perform minor repairs as needed. Anticipate additional resources, consumables, and equipment requirements to ensure work can be completed within the budgeted time. Maintain a safe and orderly laboratory and ensure compliance with all safety policies and practices. Stay current with the analytical chemistry literature and champion implementation of new technology. Develop and validate analytical methods for drug substances and products while ensuring laboratory equipment is maintained and compliant with cGMP/GLP standards. Review technical data, prepare final reports, and manage laboratory resources to meet project deadlines. Qualifications BSc in Chemistry or equivalent; higher degree preferred. 3–7 years of industrial experience with hands‑on GMP analytical laboratory experience. Strong understanding of analytical chemistry. Practical ability to develop methods for isolation, characterization, and quantification of drug substances and drug products using HPLC, LC/MS, ICP-MS, GC, GC/MS, ELISA, and/or MSD. Minimum 3 years working in a cGMP and/or GLP environment. Skilled in operation of data acquisition and processing software such as Agilent ChemStation, OpenLab, and other data reduction and presentation tools. Experience with the development of bioanalytical methods is a plus. Excellent written, reporting, and verbal communication skills. Proficient in Microsoft Office suite, including Word, Excel, and PowerPoint. Ability to prioritize responsibilities and multi‑task in a fast‑paced environment with changing priorities. Highly motivated and capable of working independently or under minimal supervision to deliver results under tight deadlines. Able to lift 10–25 pounds. Experience/knowledge of cGMP/GLP procedures is a plus. Hands‑on experience with Sciex LC/MS/MS is preferred. Pay & Benefits Base pay will be $63,000 to $90,000 and may vary depending on the candidate’s job‑related knowledge, skills, and experience. This position will be eligible for medical, dental, vision, life insurance, 401(k), and other benefits. Pacific BioLabs is an equal opportunity employer committed to diversity and inclusion. We are pleased to consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, or any other legally protected factor. #J-18808-Ljbffr Y-Axis