Pharma Visual QA Inspector — Quality & Compliance

RXinsider LTD.; Columbia, Northern (SC, KY); Hybrid; USD 42,000 - 65,000; Full time

Job summary

RXinsider LTD. is seeking a QA Inspector to perform visual inspections of injectable products and monitor packaging areas in Columbia, SC. You will ensure batch records accuracy, promote teamwork within the QA team, and enforce adherence to cGMP, SOPs, and safety regulations.

The role requires 1–3 years of pharma QA experience and a High School Diploma. Responsibilities include line clearance, communication of quality issues to supervisors, and support for validation and manufacturing studies as

Qualifications

• Minimum 1 year of pharmaceutical QA/Production experience or 2 years related experience preferred.
• Knowledge of GMP preferred.
• Strong written and oral communication skills.
• Detail oriented with good observation skills.
• Familiarity with document control procedures and SOPs.

Responsibilities

• Monitors and performs finished product attribute inspections.
• Performs visual inspections of Outsourcing products if needed.
• Supports QA verifications of packaging and labeling.
• Maintains quality documentation and review for compliance.
• Communicates quality observations and issues to QA management.
• Adheres to cGMPs and safety regulations.
• Assist with development of solutions for quality assurance issues.
• Stay abreast of FDA requirements and SOPs.

Skills

Visual inspection

Attention to detail

Good communication

GMP knowledge

Document control

Teamwork

Adaptability

Quality auditing

Tools

MS Word

MS Excel

MS Outlook

Job description

RXinsider LTD. is seeking a QA Inspector to perform visual inspections of injectable products and monitor packaging areas in Columbia, SC. You will ensure batch records accuracy, promote teamwork within the QA team, and enforce adherence to cGMP, SOPs, and safety regulations.

The role requires 1–3 years of pharma QA experience and a High School Diploma. Responsibilities include line clearance, communication of quality issues to supervisors, and support for validation and manufacturing studies as