NAPS APPRENTICE

Date: Mar 26, 2026

Location: Bangalore, KA, IN

Company: bioconbiolP2

Quality Intern – Job Description

Role Title: Quality Intern

Department: Quality Assurance / Quality Control

Location: [Add Location]

Duration: 3–6 Months (customizable)


About the Role

The Quality Intern will support the Quality Assurance (QA) and/or Quality Control (QC) teams in maintaining compliance, documentation, and quality systems within a regulated environment. This role offers hands-on exposure to GMP, quality processes, audits, documentation, and laboratory/production support (based on QA/QC stream).


Key Responsibilities

1. Documentation & Compliance (QA)

  • Assist in preparing, reviewing, and updating SOPs, batch records, and quality documents.
  • Support activities related to change control, deviation management, and CAPA tracking.
  • Help maintain organized and compliant documentation systems aligned with GMP guidelines.

2. Quality Systems Support

  • Support audits (internal/external) through data gathering and document preparation.
  • Assist with training documentation and tracking quality KPIs.
  • Participate in continuous improvement projects within the Quality department.

3. Laboratory Support (QC – If applicable)

  • Assist in sample management, labeling, and basic lab activities.
  • Observe QC testing procedures (microbiology/chemistry) under supervision.
  • Help maintain laboratory records, logs, and equipment calibration files.

4. Data Analysis & Reporting

  • Compile quality metrics and prepare weekly/monthly reports.
  • Perform basic data analysis using Excel or quality tools.
  • Help identify trends in deviations, complaints, or lab results.

5. Cross-Functional Coordination

  • Coordinate with Production, Engineering, MSAT, and Supply Chain for quality data.
  • Support QA floor activities such as line clearance, in‑process checks (if applicable).
  • Participate in training sessions and team meetings.

Skills Required

  • Strong attention to detail and quality mindset.
  • Basic understanding of GMP / GLP principles (training can be provided).
  • Good communication and documentation skills.
  • Proficiency in MS Excel, Word, PowerPoint.
  • Ability to work in a structured, regulated environment.