Junior Quality Control

United Consulting Hub; United States; On-site; USD 36,000 - 48,000; Full time

Job summary

United Consulting Hub is seeking a detail-oriented Junior Quality Control Analyst to support laboratory testing and quality operations in pharmaceutical and life sciences environments. This role is ideal for recent graduates seeking practical experience in analytical testing, laboratory procedures, documentation, and regulatory compliance.

You will perform routine analyses, operate lab instruments, and ensure GMP/GLP compliance, documenting results accurately and contributing to method

Qualifications

• Internship or academic laboratory experience in pharmaceutical or biotech QC.
• Basic hands-on exposure to analytical techniques (HPLC/GC/ spectroscopy).
• Understanding of data integrity principles, including ALCOA.
• Familiarity with 21 CFR Part 11 and electronic records compliance.
• Basic knowledge of LIMS or electronic laboratory management systems.

Responsibilities

• Perform routine analytical testing of raw materials, in-process samples, and finished products.
• Operate laboratory instruments including HPLC, GC, UV-Vis, and FTIR.
• Follow GMP and GLP requirements.
• Record and maintain test results accurately in notebooks and electronic systems.
• Assist with analytical method validation, equipment calibration, and qualification activities.
• Support investigations related to OOS and OOT results.
• Assist with stability testing and environmental monitoring activities.
• Collaborate with QA, Manufacturing, R&D, and cross-functional teams.

Skills

Internship/academic lab experience

Hands-on exposure to analytical tools

Data integrity: ALCOA

21 CFR Part 11 / electronic records

LIMS familiarity

Tools

HPLC

GC

UV-Vis

FTIR

Job description

We are seeking a detail-oriented and motivated Junior Quality Control (QC) Analyst to support laboratory testing and quality operations within pharmaceutical and life sciences environments. This role is well suited for recent graduates seeking practical experience in analytical testing, laboratory procedures, documentation, and regulatory compliance.

Key Responsibilities:

• Perform routine analytical testing of raw materials, in-process samples, and finished products
• Operate laboratory instruments including HPLC, GC, UV-Vis, and FTIR
• Follow GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices) requirements
• Record and maintain test results accurately in laboratory notebooks and electronic systems
• Assist with analytical method validation, equipment calibration, and qualification activities
• Support investigations related to out-of-specification (OOS) and out-of-trend (OOT) results
• Assist with stability testing and environmental monitoring activities
• Collaborate with QA, Manufacturing, R&D, and other cross-functional teams

Required Skills:

• Internship or academic laboratory experience in pharmaceutical or biotech QC
• Basic hands-on exposure to HPLC, GC, or spectroscopy techniques
• Understanding of data integrity principles, including ALCOA
• Familiarity with 21 CFR Part 11 and electronic records compliance
• Basic knowledge of LIMS or electronic laboratory management systems