Job description

Yoh is hiring a Scientist II, Analytics – Product Development for our pharmaceutical client in Corona, CA. In this role, you will provide analytical support for pharmaceutical product development programs, helping advance the development and approval of generic drug products for U.S. and international markets. The Scientist II will perform analytical testing, method development, validation and verification, laboratory equipment maintenance, technical documentation, and data review while collaborating with internal product development teams, CROs, and CMOs. The ideal candidate will have a strong foundation in analytical chemistry and hands-on experience with HPLC, GC, UV-Vis, FTIR, Karl Fischer, and other pharmaceutical laboratory techniques. Industry: Pharmaceutical / Product Development Location: Corona, CA Compensation: $65,000 - $75,000 per year; based upon experience Type: Direct Hire Job Functions Perform analytical testing of raw materials, in-process samples, finished products, and stability samples using compendial and non-compendial methods. Perform method development, evaluation, validation, and verification using HPLC, GC, and other analytical laboratory techniques. Utilize analytical techniques including wet chemistry, spectrometry, chromatography, and physical testing. Perform testing using instrumentation including HPLC, GC, UV-Vis, FTIR, Karl Fischer, balances, and other laboratory equipment. Accurately document laboratory testing according to Good Documentation Practices (GDP), company procedures, and applicable regulatory requirements. Analyze testing results and communicate findings to management in a timely manner. Write, review, and execute study plans, analytical protocols, validation protocols, technical transfer protocols, and associated reports. Author technical documents including Standard Operating Procedures (SOPs), method validation protocols/reports, and method transfer protocols/reports. Review laboratory documentation, including notebooks and instrument logbooks, for calculations, data entry accuracy, and regulatory compliance. Perform preventive maintenance, calibration, qualification, and routine monitoring of laboratory equipment and analytical instruments. Maintain laboratory Quality Systems related to samples, standards, reagents, equipment qualification, preventive maintenance, periodic calibration, stability chambers, and controlled-environment storage cabinets. Prepare sample and standard reconciliation reports and other laboratory reports as required. Assist with analytical data management, including data review and control charting. Collaborate with internal product development teams, CROs, and CMOs to establish timelines, understand analytical work requests, resolve technical issues, and communicate results. Support the creation of study designs, method development protocols and reports, and technology transfer protocols and reports. Provide timely analytical support for R&D activities associated with the development and approval of generic pharmaceutical products for U.S. and international markets. Utilize Microsoft Word, Excel, Outlook, and related software for data analysis, technical documentation, and communication. Maintain strict compliance with laboratory procedures and applicable compliance programs. Maintain a clean and safe laboratory work environment, including proper cleaning and storage of laboratory equipment and glassware. Perform additional responsibilities as assigned by management. Education, Licensure and/or Experience Bachelor's degree in a science-related field required; advanced degree preferred. Minimum of three (3) to six (6) years of relevant professional experience. Minimum of one (1) year of experience in a relevant area of Pharmaceutical R&D. Strong knowledge of basic analytical chemistry principles and techniques. Hands-on experience with analytical instrumentation and techniques, including HPLC, GC, UV-Vis, FTIR, Karl Fischer, wet chemistry, chromatography, and spectrometry. Experience with analytical method development, validation, verification, and/or method transfer. Familiarity with pharmaceutical R&D environments, terminology, procedures, and regulatory expectations. Knowledge of Good Documentation Practices and laboratory compliance requirements. Experience preparing and reviewing analytical protocols, reports, SOPs, and other technical documentation. Proficiency with Microsoft Word, Excel, Outlook, and similar programs. Strong written and verbal English communication skills. Strong interpersonal skills with the ability to collaborate effectively with internal teams and external partners, including CROs and CMOs. Ability to organize and manage analytical activities while meeting established project timelines. Strong attention to detail and commitment to accurate laboratory documentation and data integrity. #IND-SPG Estimated Min Rate : $65000.00 Estimated Max Rate : $75000.00 What’s In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include: Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week) Health Savings Account (HSA) (for employees working 20+ hours per week) Life & Disability Insurance (for employees working 20+ hours per week) MetLife Voluntary Benefits Employee Assistance Program (EAP) 401K Retirement Savings Plan Direct Deposit & weekly epayroll Referral Bonus Programs Certification and training opportunities Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply. Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Visit yoh.com to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice: yoh.com Stay Safe During Your Job Search Fraudulent recruiting communications have become increasingly common. Emails from Yoh recruiters will only come from an @yoh.com email address. Yoh will never ask candidates to pay fees, purchase equipment, send gift cards, or transfer funds as part of the recruiting or hiring process. If you receive a communication that appears suspicious or requests payment, contact Yoh directly before responding or sharing personal information.

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401k