Aseptic Validation Lead — Media Fill Expert (Onsite)

Akraya; Greenville (NC); On-site; USD 83,000 - 91,000; Full time

Job summary

Akraya is seeking a skilled Validation Specialist for aseptic manufacturing in Greenville, NC. This onsite role focuses on leading media fill studies and developing critical validation documentation.

You will collaborate with manufacturing, quality, and regulatory teams to ensure cGMP compliance and support process investigations, deviations, and contamination control improvements.

The contract is a 6-month W2 engagement with hourly pay range of $60–$66.

Qualifications

• Extensive experience in aseptic processing.
• Proven track record in pharmaceutical validation.
• Strong understanding of regulatory requirements.

Responsibilities

• Lead media fill study design and execution for aseptic processes.
• Author and review validation protocols, reports, and risk assessments.
• Support investigations and deviations for aseptic manufacturing.
• Collaborate with manufacturing, quality, and regulatory departments.
• Drive improvements in validation and contamination control.

Skills

Aseptic processing

Media fill studies

cGMP compliance

Validation protocols

Risk assessment

Job description

Akraya is seeking a skilled Validation Specialist for aseptic manufacturing in Greenville, NC. This onsite role focuses on leading media fill studies and developing critical validation documentation.

You will collaborate with manufacturing, quality, and regulatory teams to ensure cGMP compliance and support process investigations, deviations, and contamination control improvements.

The contract is a 6-month W2 engagement with hourly pay range of $60–$66.