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analytical chemist

analytical scientist

On Site Personnel

<div>
 
 
 
 Minimum Requirements: Analytical Scientist
 
 
 
 <ul>
 <li>
 Understand urgency and initiative to drive projects/assignments to completion.
 </li>
 <li>
 Capable of developing analytical methods for chromatographic, spectroscopic, titrimetric and wet chemistry analyses.
 </li>
 <li>
 Is proficient with laboratory instrument troubleshooting.
 </li>
 <li>
 Intermediate to advanced understanding in most laboratory instrumentation such as FTIR, HPLC, ICP, GC, UV-Vis, LC-MS/MS, GC-MS, ICP-MS/OES and HPTLC.
 </li>
 <li>
 Working knowledge of:
 </li>
 <li>
 Characterization and elucidation of botanical compound structures by study of the compound structure, spectroscopic methods and mass spectrometry.
 </li>
 <li>
 Selection of analytical columns for chromatographic analyses, proper techniques or technologies and the selection for proper reagents to design effective analytical methods in timely manner.
 </li>
 <li>
 Effective sample preparation techniques to support high number of samples for testing such as liquid-liquid extraction, derivatization, chemical manipulation and mechanical manipulation.
 </li>
 <li>
 Statistical techniques, such as data trend analysis and design of experiments is highly desirable.
 </li>
 <li>
 Proficient in reviewing and interpretation of laboratory data.
 </li>
 <li>
 Principles of routine laboratory operations.
 </li>
 <li>
 Industry regulations, FDA and ICH guidelines; experience implementing and maintaining adherence to pharmaceutical and/or nutritional supplement GLP/GMP is strongly desired.
 </li>
 <li>
 Proven ability to communicate effectively and cooperatively within all levels of an organization.
 </li>
 <li>
 Excellent written and verbal communication
 </li>
 <li>
 Demonstrated aptitude to function in a dynamic fast-paced environment.
 </li>
 </ul>
 
 
 
 
 
 
 Education and Experience: Analytical Scientist
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s Degree in Chemistry or concentration in: Biochemistry, Inorganic, Physical or Polymer Chemistry preferred; or, a Master&rsquo;s/Ph.D. degree in Chemistry with a minimum of 5 years of
 </li>
 <li>
 5-7 years of experience:
 </li>
 <li>
 Method development and validation of analytical methods for nutraceuticals and/or pharmaceutical samples in a GMP environment.
 </li>
 </ul>
 
 
 
 
 
 
 
 
 
 
 Onsite Personnel is an equal opportunity employer committed to hiring a diverse workforce in an inclusive culture environment. Onsite Personnel does not discriminate based on disability, veteran status or any other basis protected under federal, state, or local laws
 
</div>

Analytical Scientist

GForce Life Sciences

<div>
 
 
 Summary
 
 
 
 Our growing, mid-sized pharmaceutical client has engaged GForce Life Sciences to provide a Scientist Consultant (QC/AS) to support the client's studies of developmental, clinical, and commercial pharmaceutical and related products
 
 
 
 
 
 
 Duties / Expectations of Role
 
 
 <ul>
 <li>
 Reviews analytical data, including raw data, of developmental, clinical, and commercial pharmaceutical and related products for accuracy and compliance with the client's GxP requirements.
 </li>
 <li>
 Initiate and monitor stability studies of developmental, clinical, and commercial pharmaceutical and related products tested by contract laboratories.
 </li>
 <li>
 Reviews, enters, and maintains stability data for developmental, clinical, and commercial pharmaceuticals and related products.
 </li>
 <li>
 Create studies in LIMS for multiple projects
 </li>
 <li>
 Enter or review sample test result data in LIMS
 </li>
 <li>
 Assists in technical investigations; enters deviations and investigations into Trackwise
 </li>
 <li>
 Maintain and manage analytical testing documentation, including protocols, reports, and data, in compliance with good documentation practices (GDP) and data integrity standards.
 </li>
 <li>
 Prepare stability reports and summaries for inclusion in INDs, NDAs, and regulatory submissions, ensuring accuracy, completeness, and adherence to regulatory requirements.
 </li>
 <li>
 Use descriptive statistical techniques to organize and summarize data
 </li>
 <li>
 Based on project needs, use statistical analysis techniques to identify patterns and trends
 </li>
 <li>
 Create graphs, profiles, and reports of testing and/or stability data and statistical analysis
 </li>
 <li>
 Assist the project team in making informed business decisions based on data insights
 </li>
 </ul>
 
 
 
 
 
 Required experience:
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in chemistry or related science + 3-5 years work experience in a GXP environment focused on analytical laboratory testing of pharmaceuticals and related materials
 </li>
 <li>
 Familiarity in GMP environment focused on analytical laboratory testing, including HPLC, Dissolution, etc.
 </li>
 <li>
 Experience in data review
 </li>
 </ul>
 
 
 
 
 
 Nice to have
 
 
 <ul>
 <li>
 Experience with electronic document management systems &ndash; Veeva, CREDO, etc.
 </li>
 <li>
 Experience with investigation software (Trackwise preferred)
 </li>
 </ul>
 
 
 
 
 
 Term &amp; Start
 
 
 <ul>
 <li>
 12-month contract - option to extend
 </li>
 <li>
 Paid Federal Holidays for W2
 </li>
 <li>
 Health Insurance available
 </li>
 </ul>
 
 
</div>

Metric Bio

<div>
 <ol>
 <li>
 
 Experience required:
 
 </li>
 <li>
 5 &ndash; 7 years experience
 
 performing analytical method development
 
 of nutraceutical and/or pharmaceutical products in a
 
 cGMP regulated environment.
 
 </li>
 <li>
 Intermediate or mid-level experience in method development of complex nutraceutical matrices/finished products.
 </li>
 <li>
 Knowledge in the characterization and elucidation of botanical compound structures by study of the compound structure, spectroscopic methods and Mass spectrometry.
 </li>
 <li>
 Strong understanding of instrumentation such as: FTIR, HPLC, ICP, QG, UV-Vis, LC-MS, GC-MS, ICP-MS, HPTLC.
 </li>
 <li>
 Strong troubleshooting skills on HPLC and GC.
 </li>
 <li>
 
 MUST be Proficient in Empower chromatography acquisition database software.
 
 </li>
 <li>
 Strong analytical skills in laboratory techniques and fundamentals such as titration, gravimetric methods, separation techniques and others.
 </li>
 <li>
 This position will periodically support product release as part of method development responsibilities.
 </li>
 <li>
 Knowledge of industry regulations, FDA, and ICH guidelines to ensure compliance and maintain Laboratory Accreditations such as ISO 17025, NSF.
 </li>
 </ol>
 
 
 
 
 *I am working with client of mine in the Pharmaceutical sector. They are willing to help with relocation packages from anywhere in the USA.
 
</div>

<div>
 
 
 Analytical Chemist III (Nutraceuticals &amp; Pharmaceuticals)
 
 
 
 
 
 
 We are partnered with an industry leader in nutraceutical manufacturing serving both human and animal health. Headquartered in Lancaster, South Carolina&mdash;about an hour from Charlotte&mdash;the company employs 750+ staff across two production plants and five additional facilities. They are known for rigorous quality standards, rapid growth, and a strong presence at major retailers such as Costco.
 
 
 
 
 
 This role is part of a science-driven, values-oriented organization with robust cGMP-compliant operations, in-house testing, and deep investment in R&amp;D. Employees benefit from relocation support, temporary housing, career development, and long-term career stability.
 
 
 
 
 
 
 Experience Required
 
 
 
 
 Education:
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Chemistry (Biochemistry, Inorganic, Physical, or Polymer Chemistry preferred), OR
 </li>
 <li>
 Master&rsquo;s/Ph.D. in Chemistry with 3&ndash;5 years technical experience in a GMP environment.
 </li>
 <li>
 5&ndash;7 years of analytical method development in nutraceutical and/or pharmaceutical products under cGMP.
 </li>
 <li>
 Intermediate/mid-level experience in method development of complex nutraceutical matrices/finished products.
 </li>
 <li>
 Experience in characterization and elucidation of botanical compound structures using spectroscopic methods and Mass spectrometry.
 </li>
 <li>
 Proficiency with instrumentation: FTIR, HPLC, ICP, QG, UV-Vis, LC-MS, GC-MS, ICP-MS, HPTLC.
 </li>
 <li>
 Strong troubleshooting skills on HPLC and GC.
 </li>
 </ul>
 
 
 
 
 
 Required:
 
 Proficiency in Empower chromatography acquisition database software.
 
 <ul>
 <li>
 Strong foundation in laboratory techniques (titration, gravimetric methods, separation techniques, etc.).
 </li>
 <li>
 Ability to support product release as part of method development responsibilities.
 </li>
 <li>
 Knowledge of FDA and ICH guidelines to ensure compliance and maintain lab accreditations (ISO 17025, NSF).
 </li>
 </ul>
 
 
 
 
 
 Key Note:
 
 At this time, we will only consider candidates who are eligible to work in the US with no sponsorship or support needed (preferably green card holders or US Citizens).
 
 
 
</div>

Analytical Scientist III

GenScript

<div>
 
 
 About GenScript
 
 
 
 
 
 GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.
 
 
 
 
 GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.
 
 
 
 
 
 About ProBio
 
 
 
 
 
 ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio&rsquo;s total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing.&nbsp;
 
 
 
 
 Job Summary:
 
 
 
 
 We are seeking a detail-oriented and proactive
 
 Analytical Associate Scientist or Scientist
 
 to join our US Protein Department. This role involves performing analytical testing and characterization of protein products to support research, development, and production activities. The ideal candidate will have a strong background in analytical chemistry, biochemistry, or biotechnology, with practical laboratory experience and familiarity with regulatory standards.
 
 
 
 
 Key Responsibilities:
 
 
 
 <ol>
 
 <li>
 Perform routine and non-routine analytical testing on protein samples using techniques such as HPLC, SDS-PAGE, ELISA, UV-Vis spectroscopy, and others as required.
 </li>
 
 <li>
 Prepare reagents, standards, and samples according to established protocols.
 </li>
 
 <li>
 Record, analyze, and interpret data with accuracy and integrity; prepare detailed reports and documentation.
 </li>
 
 <li>
 Maintain and calibrate laboratory instruments and ensure compliance with quality standards and safety regulations.
 </li>
 
 <li>
 Assist in method development, validation, and troubleshooting of analytical procedures.
 </li>
 
 <li>
 Collaborate with cross-functional teams to support project timelines and deliverables.
 </li>
 
 <li>
 Participate in the review and update of SOPs, batch records, and other quality documentation.
 </li>
 
 <li>
 Support continuous improvement initiatives and additional tasks as assigned by the supervisor.
 </li>
 
 </ol>
 
 
 
 Qualifications:
 
 
 
 <ol>
 
 <li>
 BS/MS in analytical chemistry, biochemistry, biotechnology, or related with 2+ years of relevant experience in protein purification/characterization.
 </li>
 
 <li>
 Hands-on experience with analytical instruments such as HPLC, SDS-PAGE, ELISA, UV-Vis, or similar is preferred.
 </li>
 
 <li>
 Strong attention to detail, organizational skills, and commitment to data integrity.
 </li>
 
 <li>
 Ability to work independently and collaboratively in a fast-paced team environment.
 </li>
 
 <li>
 Good communication skills and the ability to clearly document and present data.
 </li>
 
 <li>
 Experience working in a CRO or CDMO setting is an advantage.
 </li>
 
 </ol>
 
 
 &nbsp;
 
 
 
 
 #GS
 
 
 
 
 &nbsp;
 
 
 
 GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
 
 
 
 
 
 GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
 
 
 
 
 &nbsp;
 
 
 
 
 
 Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.&nbsp;
 
 
 
</div>

Analytical Associate Scientist/Scientist

ALKU

<div>
 
 
 Analytical Method Establishment Scientist
 
 
 
 
 Overview:
 
 
 
 A mid-sized pharmaceutical company is seeking a skilled
 
 Method Establishment Scientist
 
 to support the implementation and training of
 
 High Voltage Leak Detection (HVLD) instrumentation
 
 . This individual will be responsible for establishing methodologies, drafting technical documentation, and training laboratory personnel to ensure successful adoption of HVLD technology within the organization.
 
 
 
 Key Responsibilities:
 
 
 <ul>
 <li>
 Lead method establishment and execution of testing using HVLD instrumentation for container closure integrity testing (CCIT).
 </li>
 <li>
 Train and mentor laboratory staff and quality team members on the proper use, maintenance, and troubleshooting of HVLD equipment.
 </li>
 <li>
 Draft and revise SOPs, protocols, and reports related to HVLD operations and CCIT methodologies.
 </li>
 <li>
 Collaborate with Quality and Laboratory teams to ensure compliance with regulatory expectations and internal standards.
 </li>
 <li>
 Provide technical expertise in CCIT methods and support validation activities as required.
 </li>
 <li>
 Ensure documentation is complete, accurate, and audit-ready.
 </li>
 </ul>
 
 
 Qualifications:
 
 
 
 
 <ul>
 <li>
 Strong background in
 
 Quality and Laboratory operations
 
 within the pharmaceutical or biotech industry.
 </li>
 <li>
 Hands-on experience with
 
 HVLD instrumentation
 
 and CCIT methods is required.
 </li>
 <li>
 Proven ability to draft SOPs, protocols, and technical reports.
 </li>
 <li>
 Experience training and mentoring technical staff.
 </li>
 <li>
 Strong understanding of cGMP and regulatory compliance requirements.
 </li>
 <li>
 Excellent communication and documentation skills.
 </li>
 </ul>
 
 
</div>

Analytical Method Establishment Scientist

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