Base: $62,500.00 - $100,625.00; bonus/equity: not ...
Fully remote
Cgmp, fda, ich, who regulations
Synthetic pharmaceutical & biopharmaceutical development
Quality and process engineering
The Specialist supports quality assurance operations by ensuring compliance with standards and regulations, contributing to testing and process improvements, supporting audits and corrective actions, and collaborating with internal teams and suppliers to resolve quality issues
Job Summary
The Specialist supports quality assurance operations by ensuring compliance with standards and regulations, contributing to testing and process improvements, supporting audits and corrective actions, and collaborating with internal teams and suppliers to resolve quality issues.
The Quality Technical Specialist provides technical and quality support to Avantor’s global customer and sales organizations.
Avantor offers a comprehensive benefits package including medical, dental, and vision coverage, wellness programs, health savings and flexible spending accounts, a 401(k) plan with company match, and an employee stock purchase program.
Matching Summary
The Specialist supports quality assurance operations by ensuring compliance with standards and regulations, contributing to testing and process improvements, supporting audits and corrective actions, and collaborating with internal teams and suppliers to resolve quality issues.
Salary
Base: $62,500.00 - $100,625.00; Bonus/Equity: Not specified; Benefits: Medical, dental, vision, 401(k) with match, ESPP, PTO, paid parental leave
Skills & Requirements
Must-have
cGMP, FDA, ICH, WHO regulations
Synthetic pharmaceutical & biopharmaceutical development
Quality and process engineering
Microsoft Office Suite proficiency
Technical and quality support
Nice-to-have
Hands-on laboratory experience
Project management skills
Customer intimacy programs
Lean principles review
Aptitude to develop technical skills
Key Requirements
BS/BA Degree in Biology, Biotechnology, Bio Engineering, Chemistry, Chemical Engineering, or related field
Minimum of three (3) years of combined experience
Experience in chemical or pharmaceutical environment
Experience in synthetic pharmaceutical & biopharmaceutical drug development and manufacturing