Associate Scientist - Analytical Development

Yoh Services LLC; Corona (CA); On-site; USD 42,000 - 60,000; Full time

Benefits offered by this job

Medical Benefits

401K Retirement Savings

EAP Program

Direct Deposit & weekly payroll

Annual bonus opportunities

Job summary

Yoh Services LLC is seeking an Associate Scientist, Analytics – Product Development for our pharmaceutical client in Corona, CA. You will support Product Development and R&D programs focused on generic drug development for U.S. and international markets.

You will perform routine analytical testing, assist with method development and validation, maintain records, operate HPLC, GC, UV-Vis, FTIR, and Karl Fischer.

Qualifications

• Bachelor's degree in Chemistry or related field.
• Entry level to two years of laboratory experience; pharmaceutical, academic, internship, or related analytical lab experience preferred.
• Familiarity with analytical instrumentation such as HPLC, GC, UV-Vis, FTIR, Karl Fischer or similar.
• Exposure to analytical method development, validation, verification, or transfer is preferred but not required.
• GDP familiarity and good documentation practices are preferred.

Responsibilities

• Perform routine analytical testing under supervision of senior personnel.
• Test raw materials, in-process samples, finished products, and stability samples.
• Assist with analytical method development, validation, verification, and transfer activities.
• Operate laboratory instrumentation including HPLC, GC, UV-Vis, FTIR, Karl Fischer and other equipment.
• Document testing accurately per GDP and SOPs, and communicate results to team.

Skills

HPLC

GC

UV-Vis

FTIR

Karl Fischer

GDP

Data entry

Excel

Communication

Education

Bachelor's degree in Chemistry or related field

Job description

Yoh is hiring an Associate Scientist, Analytics – Product Development for our pharmaceutical client in Corona, CA. In this role, you will support Product Development and R&D programs focused on the development and approval of generic drug products for U.S. and international markets. The Associate Scientist will perform routine analytical testing, assist with method development and validation activities, maintain laboratory documentation, and support laboratory equipment and Quality Systems under the guidance of senior scientists. This is an excellent opportunity for an early-career scientist to develop hands-on pharmaceutical R&D experience with analytical techniques and instrumentation including HPLC, GC, UV-Vis, FTIR, and Karl Fischer.

Industry: Pharmaceutical / Product Development

Location: Corona, CA

Compensation: $50k - $60K

Type: Direct Hire

Job Functions

• Perform routine analytical testing under the direction and supervision of senior scientific personnel.
• Test raw materials, in-process samples, finished products, and stability samples using established compendial and non-compendial methods.
• Assist with analytical method development, evaluation, validation, verification, and method transfer activities.
• Perform analytical techniques including wet chemistry, spectrometry, chromatography, and physical testing.
• Operate laboratory instrumentation including HPLC, GC, UV-Vis, FTIR, Karl Fischer, balances, and other analytical equipment following established procedures.
• Prepare samples, standards, reagents, and solutions required for analytical testing.
• Accurately document laboratory testing in accordance with Good Documentation Practices (GDP), company procedures, and applicable regulatory requirements.
• Record, analyze, and communicate analytical results to senior scientists and management.
• Assist with the preparation and execution of study plans, protocols, and reports.
• Support preparation of technical documentation, including SOPs, analytical methods, validation documentation, and method transfer documentation.
• Maintain laboratory notebooks, instrument logbooks, and other required records to ensure accuracy, completeness, and data integrity.
• Assist with preventive maintenance, calibration, qualification, and routine monitoring of laboratory equipment and analytical instruments.
• Support laboratory Quality Systems, including sample, standard, and reagent management.
• Assist with monitoring stability chambers and controlled-environment storage equipment.
• Prepare sample and standard reconciliation documentation and other laboratory reports as required.
• Support QC data management activities, including data entry, data review, and control charting.
• Collaborate with Product Development and other cross-functional team members to support project timelines and analytical testing requirements.
• Provide timely analytical support for R&D activities associated with the development of generic pharmaceutical products for U.S. and international markets.
• Follow established laboratory procedures, safety requirements, Quality Systems, and compliance programs.
• Maintain a clean, organized, and safe laboratory environment, including proper cleaning and storage of laboratory equipment and glassware.
• Perform additional laboratory responsibilities as assigned by management.

Education, Licensure and/or Experience

• Bachelor's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, Biology, or another related scientific discipline required.
• Entry level to two (2) years of laboratory experience; pharmaceutical, academic, internship, or related analytical laboratory experience preferred.
• Basic understanding of analytical chemistry principles and laboratory techniques.
• Academic or professional hands-on experience with analytical instrumentation such as HPLC, GC, UV-Vis, FTIR, Karl Fischer, or similar laboratory equipment preferred.
• Familiarity with wet chemistry, chromatography, spectrometry, and physical testing techniques.
• Exposure to analytical method development, validation, verification, or method transfer is preferred but not required.
• Basic understanding of Good Documentation Practices (GDP) and laboratory documentation requirements preferred.
• Pharmaceutical R&D, GMP, GLP, or other regulated laboratory experience is a plus.
• Ability to accurately follow written analytical methods, SOPs, protocols, and laboratory procedures.
• Strong attention to detail and commitment to accurate data collection and documentation.
• Strong organizational and time-management skills with the ability to manage multiple laboratory assignments.
• Effective written and verbal communication skills.
• Ability to work effectively under the guidance of senior scientific personnel and collaborate within a cross-functional team.
• Proficiency with Microsoft Word, Excel, Outlook, and similar software applications.
• Motivated to learn new analytical techniques, instrumentation, and pharmaceutical development processes.

Physical Job Requirements

• Pharmaceutical R&D laboratory and office environment.
• Regularly required to perform hands-on laboratory testing and operate analytical instrumentation and equipment.
• Regular handling of laboratory glassware, chemicals, samples, standards, and reagents in accordance with established safety procedures.
• Regular use of computers and related systems for data entry, analysis, documentation, and communication.
• Ability to stand or sit for extended periods while performing laboratory activities.
• Must be able to maintain a clean, organized, and safe laboratory workspace.

Estimated Min Rate: $42000.00

Estimated Max Rate: $60000.00

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 https://www.yoh.com/applicants-with-disabilities 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.

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