Chemist - Pharmaceutical
Job in
Morton Grove, Cook County, Illinois, 60053, USA
Listed on 2026-08-05
Listing for:
Actalent
Full Time
position Listed on 2026-08-05
Job specializations:
-
Quality Assurance - QA/QC
-
Science
Job Description & How to Apply Below
Job Description
This Chemist II position supports Pharmaceutical Quality Control laboratory operations. You will perform a wide range of analytical and wet chemistry testing, including HPLC and GC, to ensure products meet strict quality and regulatory standards.
This role offers structured training, hands-on analytical experience, and clear opportunities to advance into quality or analytical development paths.
Responsibilities
+ Perform routine and complex analytical testing using HPLC, GC, UV-Vis, FTIR, GC-MS, and other chromatography and mass spectrometry techniques in accordance with established procedures and Good Manufacturing Practices (GMP).
+ Conduct wet chemistry analyses, including titrations and other standard chemical tests, and interpret results in correlation with other analytical data.
+ Log in samples and specimens accurately, recording date, time, and tests to be performed, and ensure proper sample identification and traceability.
+ Prepare samples for testing by diluting, filtering, centrifuging, digesting, or otherwise processing them according to laboratory protocols.
+ Prepare and organize necessary equipment, supplies, reagents, and standards prior to testing to ensure efficient workflow.
+ Run quality control samples with known values to verify that procedures and results remain within acceptable limits and take appropriate action when deviations occur.
+ Enter test results into logs, specification sheets, and laboratory information systems with a high degree of accuracy and completeness.
+ Complete test result forms and promptly notify supervisors or appropriate stakeholders of significant or out-of-specification findings.
+ Maintain accurate, up-to-date records detailing quality control procedures, test methods, and results for all analyses performed.
+ Perform routine calibration, verification, and minor maintenance of laboratory equipment to ensure reliable and consistent performance.
+ Support preventative laboratory maintenance activities to keep instruments and equipment in optimal working condition.
+ Monitor inventory of reagents, consumables, and laboratory supplies, and inform supervisors of replenishment needs in a timely manner.
+ Stay current in the field of analytical chemistry by reading scientific literature and, as applicable, attending workshops or symposiums.
+ Maintain knowledge of and compliance with GMP operations, laboratory safety procedures, and relevant regulatory requirements.
+ Apply logical and scientific thinking to solve a wide range of intellectual and practical problems encountered in daily laboratory work.
+ Interpret and work with nonverbal scientific information such as formulas, equations, graphs, and other technical data.
+ Write clear and concise reports, business correspondence, and procedural documentation related to laboratory activities.
+ Effectively present information and respond to questions from internal stakeholders, including managers, clients, and customers, as needed.
+ Stand for extended periods, use hands to handle laboratory tools and controls, and reach with hands and arms while performing bench work.
+ Regularly lift and move up to 10 pounds and frequently lift and move up to 50 pounds of equipment, reagents, or samples as required by laboratory operations.
Essential Skills
+ Bachelor's degree (BS) or equivalent in Chemistry or a related science field from a four-year college or university, or an equivalent combination of education and experience.
+ 0-2 years of laboratory experience, with entry-level chemistry graduates strongly considered.
+ At least 1 year of HPLC experience from industry or academic settings, or equivalent analytical laboratory experience.
+
Experience with GC (gas chromatography) from school or industry is preferred.
+ Hands-on wet chemistry experience, including titration and routine bench chemistry techniques.
+ Experience working in a GMP or similarly regulated laboratory environment, or a strong understanding of GMP principles.
+ Proficiency with laboratory instrumentation such as HPLC, GC, UV-Vis, FTIR, GC-MS, and related chromatography and mass spectrometry systems.
+ Demonstrated ability to perform sample preparation techniques, including dilution, filtration, centrifugation, and digestion.
+
Experience with laboratory documentation practices, including accurate data recording and adherence to established procedures.
+ Ability to read, analyze, and interpret scientific and technical materials such as professional journals, technical procedures, and regulations.
+ Ability to write clear reports, business correspondence, and procedure manuals.
+ Ability to present information and respond to questions from internal groups, including managers, clients, and customers.
+ Strong logical and scientific reasoning skills, with the ability to solve complex analytical problems and work with abstract and concrete variables.
+ Ability to interpret and work with nonverbal scientific information, including formulas, equations, and graphs.
+…
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