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Rising Pharma Holdings Inc.
Decatur, IL | Full Time
$56k-74k (estimate)
2 Months Ago
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Quality Control Chemist
$56k-74k (estimate)
Full Time 2 Months Ago
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Rising Pharma Holdings Inc. is Hiring a Quality Control Chemist Near Decatur, IL

Job Summary:
Perform the sampling of raw materials, chemical and physical analysis of raw material, bulk formulations, finished products, stability samples, and any non-routine samples.

Duties:

  • Sampling and testing of raw materials per approved procedure.
  • Physical and chemical testing of bulk and (pre-fill, finished product, and stability) product.
  • Upkeep of laboratory notebook.
  • Maintaining the work area in an orderly manner.
  • Maintaining Lab inventory like list of standards, chemical, reagent etc.
  • Recording daily activity like PH verification, balance verification, temperature and humidity monitoring of lab stability chambers, freezer, refrigerator etc.
  • Experience in the operation of handling QC major instruments like HPLC, GC, UV, IR, Auto titrator, etc.
  • Perform Finished product/in-process/cleaning validation and raw material analysis independently. Complete testing within specified timeframes and document results accurately
  • Coordinate with vendor for instrument PM, calibration and qualification activity. Provide necessary support.
  • Maintain and monitor lab GLP activity like instrument calibration/qualification schedule, Preparation of instrument operating procedure, coordinate with metrology team and vendor for scheduling period calibration/qualification activity etc.
  • Performs calibration of lab instruments whenever possible.
  • Cleaning of laboratory glassware.
  • Responsible for writing SOP for instrument operation/ calibration etc.
  • Provide necessary support for OOS/OOT investigation.
  • Preparation of stability schedule, Protocol, and report per ICH requirements.
  • Adhere to regulatory guidelines (e.g., FDA, ICH, GMP) and company quality standards during testing and documentation.
  • Ensure adherence to Good Laboratory Practices (GLP), Good Documentation Practices (GDP), and Good Manufacturing Practices (GMP) during testing procedure.

Skills:

  • Ability to meet attendance standards.
  • At times it may be necessary to work additional hours to get the required tasks accomplished to meet deadlines.
  • Working knowledge of MS Word, Excel, Outlook, and Power Point.
  • Working knowledge of Adobe Acrobat.
  • Excellent conceptualizing, analytical, and problem-solving skills.
  • While performing the duties of this job, the employee is regularly required to sit, stand, walk, talk, and hear. The employee is required to use hands to finger, handle, or feel. Specific vision abilities required by this job include close vision for written work and PC use.
  • Requires eye-hand coordination and manual dexterity. Requires normal range of hearing and vision to record, prepare and communicate appropriate reports.
  • Will come in contact with hazardous materials. Employee is expected to work with hazardous materials in a safe manner and use all safety precautions.
  • Effective written and oral communication skills.
  • Ability to receive instructions and follow work rules and company policies.
  • Strong organizational, planning, and communication skills.
  • Using logic and reasoning to identify solutions to problems.
  • Ability to multi-task, set priorities, and meet strict deadlines.
  • Ability to lead, motivate, coach, and teach others.
  • Ability to accurately communicate ideas, facts, and technical information.
  • Ability to meet deadlines and effectively deal with office stress.
  • Ability to follow safety and security practices.

Education and Experience:

  • Bachelor's Degree from a four-year accredited college or university with a Major in Chemistry or equivalent.
  • Prefer, two years of industry experience involving analytical or wet chemistry test procedures in a quality control environment.
  • Experience with, Infra-Red (IR), Ultraviolet/Visible Spectroscopy, Particle Size Analysis, KF Titration, and wet chemistry skills are required.
  • Familiarity with High Pressure Liquid Chromatography, Gas Chromatography (GC), and HPLC/GC analytical software is preferred, but not required.
  • Familiarity with GLP/GMP guidelines.
  • Good Communication and writing skills.
  • Familiarity with out-of-specification (OOS) investigation.
  • Computer literate.
  • Experience with USP/EP monographs.

Job Type: Full-time

Benefits:

  • 401(k)
  • 401(k) matching
  • Dental insurance
  • Disability insurance
  • Flexible spending account
  • Health insurance
  • Health savings account
  • Life insurance
  • Paid time off
  • Vision insurance

Schedule:

  • Day shift
  • Monday to Friday

Education:

  • Bachelor's (Required)

Ability to Relocate:

  • Decatur, IL 62522: Relocate before starting work (Required)

Work Location: In person

Job Summary

JOB TYPE

Full Time

SALARY

$56k-74k (estimate)

POST DATE

03/29/2024

EXPIRATION DATE

05/01/2024

Show more

Rising Pharma Holdings Inc.
Full Time
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2 Months Ago

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The following is the career advancement route for Quality Control Chemist positions, which can be used as a reference in future career path planning. As a Quality Control Chemist, it can be promoted into senior positions as a Biologist II that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Quality Control Chemist. You can explore the career advancement for a Quality Control Chemist below and select your interested title to get hiring information.