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Intern - Analytical, Microbiology & Quality Assurance

Job in Port Jervis, Orange County, New York, 12771, USA
Listing for: kdc/one
Apprenticeship/Internship position
Listed on 2026-03-04
Job specializations:
  • Quality Assurance - QA/QC
Job Description & How to Apply Below
Location: Port Jervis

Summary
This internship provides hands‑on experience in analytical chemistry, microbiology, and quality systems within a regulated manufacturing environment. Students gain exposure to raw material, bulk, and finished goods testing while developing practical skills in laboratory techniques, GMP/GDP compliance, analytical instrumentation, documentation accuracy, and problem‑solving. The role supports the Analytical Laboratory, Microbiology Laboratory, and Quality Assurance department to deliver a comprehensive understanding of product quality from start to finish.

Responsibilities
Analytical Laboratory - Raw Materials

Learn the complete raw material flow from purchasing through batching.
Understand the purpose of raw material testing and GMP/GDP compliance.
Perform hands‑on testing, including:

pH
Specific gravity
Melt point
Loss on drying (LOD)
Refractive index
Viscosity
Titrations

Interpret analytical data and properly document results.
Support laboratory investigations as needed.

Analytical Laboratory - Bulk & Finished Goods

Learn the movement and testing requirements of bulk vs. finished goods.
Understand differences between cosmetic and OTC product testing.
Operate analytical instrumentation such as:

HPLC
GC
FT‑IR
UV‑Vis

Troubleshoot analytical issues and participate in internal audits.
Assist with method validation and ensure accurate recording and interpretation of results.

Microbiology Laboratory

Conduct microbiological testing on raw materials, bulk, and finished goods.
Perform facility-wide environmental monitoring.
Analyze results for compliance with microbiological specifications and regulatory standards.

Quality Assurance Support

Provide support to the QA department under the direction of the Director of Quality.
Assist with documentation accuracy, compliance tasks, and continuous improvement activities.
Support quality systems through assigned QA projects and responsibilities.

Requirements

Currently pursuing a degree in Chemistry, Biology, Microbiology, Pharmaceutical Sciences, or a related scientific field.
Strong interest in laboratory work, quality systems, and regulated environments.
Ability to follow written procedures and Good Laboratory/Manufacturing Practices (GLP/GMP/GDP).
Strong analytical thinking, attention to detail, and problem‑solving skills.
Ability to document results clearly and accurately.
Willingness to learn and work collaboratively across multiple laboratory functions.

Benefits

Hands‑on experience with industry‑standard laboratory instruments and software.
Practical training in analytical chemistry, microbiology, and quality assurance.
Exposure to raw material, bulk, and finished goods testing workflows.
Development of professional documentation, communication, and troubleshooting skills.
Experience in a regulated manufacturing environment, preparing students for careers in quality, laboratory operations, or related scientific fields.
Mentorship from experienced laboratory and QA professionals.
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