Quality Assurance Specialist - GMP & Continuous Improvement

en-careers-hovione; East Windsor Township (NJ); On-site; USD 92,000 - 147,000; Full time

Benefits offered by this job

Health coverage (medical, dental, etc)

401(k)

Job summary

Hovione in New Jersey seeks a Quality Assurance Specialist to ensure cGMP compliance across projects and products. You will support supplier qualification, audits, deviations, and change controls, while maintaining the Quality Management System to keep the site audit-ready.

Candidates should have a university degree in chemistry or related field, 3–5 years of QA GMP experience, fluent English, and strong documentation skills.

Qualifications

• Bachelor's degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences or similar
• 3–5 years of QA GMP experience in the pharmaceutical industry
• Experience with Regulatory Affairs and GMP standards
• Fluency in English
• Strong documentation skills and attention to detail

Responsibilities

• Ensure cGMP compliance across projects and products
• Support supplier qualification, audits, deviations, and change control
• Maintain Quality Management System and keep site audit-ready
• Prepare for internal and external site audits and inspections
• Collaborate with stakeholders to ensure regulatory requirements are met
• Generate QA reports and KPIs for the team

Skills

GMP knowledge

English fluency

Documentation skills

Attention to detail

Education

University degree in Chemistry or related field

Tools

MS Office

Job description

Hovione in New Jersey seeks a Quality Assurance Specialist to ensure cGMP compliance across projects and products. You will support supplier qualification, audits, deviations, and change controls, while maintaining the Quality Management System to keep the site audit-ready.

Candidates should have a university degree in chemistry or related field, 3–5 years of QA GMP experience, fluent English, and strong documentation skills.