Senior QC Analyst - cGMP Release Testing & Validation

Lonza; Portsmouth (NH); On-site; Confidential; Full time

Benefits offered by this job

Medical, dental and vision insurance

Paid Time Off (PTO)

Dynamic working culture

Job summary

Lonza is seeking a QC Analyst III in Portsmouth, NH, to execute critical cGMP release testing and manage investigations. This senior role requires 3-4+ years of lab experience, focusing on complex testing techniques and method validations.

The ideal candidate holds a Bachelor’s Degree in a science discipline and possesses robust communication skills. Join Lonza for a dynamic working culture and comprehensive benefits including medical insurance and PTO.

Qualifications

• 3-4+ years of direct Quality Control laboratory experience in cGMP biomanufacturing.
• Proven experience in performing various immunological assay techniques.
• Excellent written and oral communication skills.

Responsibilities

• Execute complex biological and cell-based testing.
• Lead laboratory investigations and address non-conformances.
• Train junior QC personnel and deliver hands-on training.

Skills

Quality Control laboratory experience

Cell culture maintenance

Immunophenotyping panels via flow cytometry

PCR amplification

Good Documentation Practices

Education

Bachelor’s Degree in Biochemistry, Biology, or a related field

Master’s Degree in a scientific discipline

Tools

Laboratory Information Management Systems (LIMS)

TrackWise

Job description

Lonza is seeking a QC Analyst III in Portsmouth, NH, to execute critical cGMP release testing and manage investigations. This senior role requires 3-4+ years of lab experience, focusing on complex testing techniques and method validations.

The ideal candidate holds a Bachelor’s Degree in a science discipline and possesses robust communication skills. Join Lonza for a dynamic working culture and comprehensive benefits including medical insurance and PTO.