Analytical Scientist Jobs in Ohio

Experience in analysis of various Biologic modalities (e.g., mAb, antibody-drug conjugate, fusion protein)

Extensive experience in separations science (e.g., SEC, RP, IEX). Experience in Molecular biology (PCR, DNA extraction) and immunoassay (ELISA) techniques.

Experience of testing strategy for late-stage program in preparation for BLA filing

Excellent written skill for drafting all the GMP related documents.

Ensure communications occur with stakeholders and partners for all the analytical topics

Author analytical method transfer/validation related protocols and reports for late stage clinical and commercial programs.

You need skills and experiences that enable you to:

Lead aspects of capability development within the Personal Health Care Analytical Chemistry organization

Lead characterization strategies for critical materials used for manufacture of our products

Or a closely related field

Your Technical Background/training Should Include

Starting Pay / Salary Range

Manage laboratories including ordering lab supplies, chemicals, and gases

Mentor, train, and guide less experienced colleagues in the instrumental analysis

VOC analysis experiences by using GC and GC-MS with optimal sample preparation techniques

Standard testing (e.g. ASTM, ISO) experience

Programming and/or software skills for data analysis (e.g. curve fitting), statistical analysis, and automation.

Experience in GC, LC or GPC

Provide technical support and assistance to product managers, R&D chemists and engineers, production and warranty group.

Communicate and provide training on analytical group capabilities and techniques.

1+ years of minimum analytical experience in a relatable industry

Responsible for developing new and improved methods and techniques in chromatography, spectroscopy, microscopy, rheology, and physical and chemical separation techniques.

Responsible for identifying, developing and implementing analytical methods and techniques to better understand and predict formulation interactions and long-term performance.

Provide and maintain a safe and clean work environment.

Associates Degree in Chemistry or related field with 0-3 years of experience in an API GMP manufacturing facility, OR

Bachelors Degree in Chemistry or related field with 0-2 years of experience in an API GMP manufacturing facility.

Learn to follow cGMP documentation and work instructions accurately and completely.

Performs basic laboratory functions including: weighing/balance use, solution preparation, pipetting, pH meter use.

Performs routine testing for the following techniques/instrumentation: appearance, FT-IR, Karl Fischer, TGA/DSC, HPLC.

Learn and perform laboratory and glassware cleaning, handling of high potent and controlled substances, and prepares samples for 3rd party testing.

Strong organizational and time management skills with emphasis on accuracy and attention to detail

2 years’ work experience in an analytical laboratory (undergraduate or graduate research experience may count toward work experience)

Excellent customer service skills and professionalism in dealing with external business partners, students, faculty and staff

Exceptional interpersonal skills with the ability to influence and build working relationships among a diverse workforce at all levels

Good knowledge in chromatography software packages is desired: Thermo Chromeleon, Thermo Xcalibur, Thermo Tracefinder, Waters Masslynx, Agilent Masshunter and Chemstation

Purdue University is an EOE/AA employer. All individuals, including minorities, women, individuals with disabilities, and veterans are encouraged to apply.

Analytical skills must include LC/MS/MS and GC/MS analysis with a familiarity of GPC and IC.

A working knowledge of at least one of the following software programs: Mass Hunter; Analyst; SCIEX OS; MassLynx; OpenLab; and/or Excalibur.

Mass spectral and chromatographic analysis of trace contaminants

Method development, Method validation and where applicable Method transfer

Sample/standard preparation, analysis and reporting data in ELN and/or LIMS

Instrument maintenance, calibration and optimization

Competitive compensation package: annual salary ranging from $45,000 to $80,000, commensurate with education, accomplishments, performance, credentials and geography

Progressive vacation policies, company holidays and paid parental leave benefits to ensure work/life balance

Performing other duties and responsibilities as prescribed by the Company

Two (2) years of relevant experience (academic or professional) preferred in cell biology, biochemistry, physiology or toxicology/pharmacology

Minimum of 1-year experience running an LC/MS/MS required

Experience using MassLynx software preferred

Six months experience in using laboratory equipment and instrumentation.

Six months experience in physical, organic, inorganic or analytical chemistry.

Six months experience in conducting clinical laboratory tests.

Six months experience in performing mathematical and statistical computations on laboratory test data.

Six months experience in generating and interpreting chemical test data by performing quantitative and/or qualitative statistical analysis.

Six months experience in selecting laboratory test methods and procedures.

AR&D Chemist or any other job title performing all listed job duties.

Catalent offers rewarding opportunities to further your career!

Conduct studies for method development, evaluation, validation, transfer and verification according to scientific justifications and current regulatory guidance;

Characterize physiochemical attributes of proteins and molecules to test for quality and stability prior to release;

Perform Quality Control testing of raw materials and in-process samples for commercial manufacturing operations;

Communicate analytical results and potential issues with supervisors and team members;

Prepare and present continuous improvement projects to management.

Apply technical knowledge and abilities to ensure all testing is performed in a compliant manner.

Communicate effectively with management regarding task completion, roadblocks, and needs.

Ability to work with management locally and globally. • Advanced ability

Review all data in accordance with applicable procedures and cGMP requirements.

Advanced ability to accurately understand, follow, interpret, and apply Global Regulatory and cGMP requirements.