Senior Chemist; Quality Control

CONTRACT PHARMACAL CORP

Town of Smithtown (NY)

On-site

USD 90,000 - 100,000

Full time

14 days+
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Job summary

CONTRACT PHARMACAL CORP is seeking a Senior Chemist to perform advanced chemical analysis for the QC laboratories, including raw materials, finished product, and environmental samples. You will document results following SOPs and contribute to method validation and investigations.

The role requires a Bachelor’s degree in a science field and at least 8 years of laboratory experience, with proficiency in HPLC/UPLC, ICP-OES/MS, UV-Vis, GC, and related techniques.

Qualifications

  • Bachelor’s degree in a science related field.
  • At least 8 years of work experience in a laboratory setting preferred.
  • Proficient in laboratory chemistry and cGMPs.
  • Able to multitask and meet tight deadlines.

Responsibilities

  • Follow all laboratory SOPs including safety, chemical handling, and data integrity.
  • Perform chemical analysis on raw materials, in-process materials, and finished product using ICP-OES/MS, UV-Vis, HPLC/UPLC, GC, titration, and other techniques.
  • Execute assay testing, content uniformity testing, impurities analyses, and validation testing with minimal errors.
  • Maintain clean and organized laboratory environment and proper waste disposal.
  • Report, review, and document results accurately and timely.
  • Mentor and train entry- and mid-level personnel and assist with instrument maintenance and calibration.

Education

Bachelor’s degree in a science related field
At least 8 years of laboratory experience

Tools

HPLC/UPLC
ICP-OES/MS
UV-Vis
GC
Dissolution
Titration
Analytical software

Job description

Description

Position Summary

The Senior Chemist is responsible for and has an advanced level of experience in performing chemical analysis for one of the assigned QC laboratories (Raw Material, Finished Product, Technical Support) which is responsible for the analysis and disposition of commercial materials (raw materials, finished product release, stability, validation, investigation), and environmental samples, as assigned, and documenting results in accordance with SOPs.

Requirements
Responsibilities

Responsibilities include, but are not limited to:

  • Follow all laboratory SOPs, including but not limited to laboratory safety, chemical handling and storage, gowning, equipment use, cGMP, GDP, data integrity, DEA requirements, etc.
  • Perform laboratory chemical analysis on raw materials, in-process materials, and/or finished product, using ICP-OES/MS, UV-Vis, Fluorescence, GC, HPLC/UPLC, titration, and other wet chemistry techniques, as assigned, in accordance with the prescribed approved analytical test method.
  • Execute assay testing, content uniformity testing, impurities analysis, validation testing (method, cleaning, process), and process/interpret data at an advanced level with minimal to no errors.
  • Maintain clean and organized laboratory working environment.
  • Disposes of used/expired/excess chemicals, solutions, solvents, etc. in dedicated waste receptacles.
  • Report well‑written, accurate and timely results.
  • Review data, calculations, notebooks, and reports.
  • Perform and assist in laboratory investigations.
  • Perform and assist in Cleaning, Method and Process validation testing and protocol/report review.
  • Maintain and troubleshoot laboratory equipment at an advanced level.
  • Suggest improvements to existing testing methods when possible.
  • Mentor and train entry‑level and mid‑level personnel on techniques performed in the lab and assist with laboratory related questions as needed.
  • Assist with routine Metrology functions, including instrument cleaning/ preventive maintenance/ calibration/ verification activities.
  • Monitor and assist with maintaining proper inventory levels of all laboratory supplies.
  • Assist with sample receiving, chemical inventory, document filing, housekeeping, etc.
  • Responsible for compliance with all rules and regulations pertaining to safety policies with the proper attitude toward safety and health, helping to ensure that all department operations are performed with the utmost regard for the safety and health for all personnel.
  • Other responsibilities as assigned by Management.
Education and Experience
  • Bachelor’s degree in a science related field.
  • At least 8 years of work experience in a laboratory setting preferred.
Skills, Knowledge, and Abilities
  • Proficient in laboratory chemistry and cGMPs.
  • Proficient in Microsoft Word, Excel, graphs/charts and databases.
  • Advanced level experience in HPLC/UPLC, ICP, Dissolution, IR, UV/VIS, and wet chemistry testing.
  • Advanced level experienced with analytical laboratory software.
  • Able to multitask and meet tight deadlines.
  • Excellent organizational skills with attention to detail.
  • Able to effectively present results.
  • Able to independently perform testing on all methods and troubleshoot most method issues with little or no help.
  • Able to independently troubleshoot complex instrument issues with little or no help.
Physical Demands
  • Required to sit and stand for long periods of time.
  • Frequently reaching with arms/hands up to 2 feet.
  • Good hand eye coordination.
  • Occasionally required to walk and kneel.
  • Must be able to lift and/or move up to 50 pounds.
  • Must be able to use close vision, distance vision, peripheral vision, color vision and the ability to adjust focus.
  • Required to reach with arms and use hands and fingers to handle or feel objects, tools and computer controls.
  • Required to stoop, kneel, crouch, stand, bend, sit, talk, hear, climb stairs.
Work Environment
  • Work environment in laboratory and production operations facilities include close proximity to heavy machinery and pharmaceutical powders.
  • Potential to move between production operations sites/areas to complete job functions; regular, ongoing travel throughout geographic areas on a continual basis as normal scope of role requiring use of personal vehicle.
  • Employee work hours/schedule and/or shift are subject to change based on business needs and Management discretion.
  • Required to be present in the laboratory to perform daily testing and collaborate with department director, manager, and peers.
Supervisory Responsibilities

None

Personal Protective Equipment or Attire Required for Position

Gowning as required by GMPs and/or SOPs.

Pay Range

$90,000 - $100,000 per year

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