3 to 5 years technical experience in pharmaceutical manufacturing
Bachelor's, master's or ph.d. degree in technical field
Working knowledge of cgmp guidelines and quality by design
The role involves supporting or leading new product introductions by conducting process comparisons, development studies, and validating cleaning processes
Job Summary
The role involves supporting or leading new product introductions by conducting process comparisons, development studies, and validating cleaning processes.
Candidates are expected to demonstrate strength in technical writing for change requests, PPQ reports, and CMC sections while ensuring regulatory compliance.
The position requires providing technical expertise to resolve deviations, manage quality risk assessments, and lead process hazards analyses.
Matching Summary
The role involves supporting or leading new product introductions by conducting process comparisons, development studies, and validating cleaning processes.
Skills & Requirements
Must-have
3 to 5 years technical experience in pharmaceutical manufacturing
Bachelor's, Master's or Ph.D. degree in technical field
Working knowledge of cGMP Guidelines and Quality by Design
Experience with process optimization and sterile manufacturing
Ability to author PPQ protocols and technical reports
Nice-to-have
Strong adaptability and personal initiative
Collaboration across global company S&T network
Leadership behaviors aligned with company standards
Proactive identification of solutions for issues
Commitment to Environmental Health and Safety leadership
Key Requirements
Bachelors, Masters or Ph.D. degree in Chemical Engineering, Mechanical Engineering, Chemistry, Biological sciences or Pharmaceutical Sciences
3 to 5 years technical experience in pharmaceutical manufacturing industry
Valid work authorization not explicitly specified but VISA Sponsorship status is available