# Associate Site Investigation Specialist

**Company**: GSK
**Location**: Upper Merion Biopharm
**Work arrangement**: onsite
**Job type**: full-time
**Category**: Operations
**Industry**: Healthcare

**Apply**: https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/Upper-Merion-Biopharm/Associate-Site-Investigation-Specialist_450879?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/associate-site-investigation-specialist-a8e2f6ff-017/

## Description

The Associate Site Investigation Specialist is responsible for identifying and analysing non-conformances to determine their root causes and develop corrective and preventive actions (CAPA) in alignment with GSK Global Standards.

**Key Responsibilities:**

- Serve as the Lead Investigator for deviations using standardised processes and GSK Orange Belt Training and Certification program

- Utilise DMAIC problem-solving and GSK Production System (GPS) tools to improve efficiency and prevent non-compliance events

- Conduct thorough investigations of deviations and quality events

- Identify root causes and implement effective CAPAs

- Collaborate with cross-functional teams to gather information and support CAPAs

- Prepare comprehensive investigation reports documenting findings and CAPAs

- Provide training and support for effective system utilisation

- Adhere to ALCOA principles for documentation tasks

- Own deviation and environmental monitoring investigations and CAPA management

**Basic Qualifications:**

- Bachelor of Arts or Bachelor of Science

- 1+ years of experience in a GMP-regulated manufacturing environment or related industry

**Preferred Qualifications:**

- Bachelors of Science, Engineering or Biotechnology

- Orange Belt Certification

**Work Arrangements:** This role is 5 days on-site at a GSK manufacturing or laboratory site in the United States.

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## Skills

### Required
- Bioprocessing
- Cell Line Development
- Experimental Methods
- Technical Writing
- Technology Transfer

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