Job Description

QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

Log on now to our website http://www. qrcgroup.com to learn more about our services and solutions!

We are seeking a Process Development Scientist to provide technical support for commercial bio pharmaceutical manufacturing operations, with a primary focus on formulation and aseptic filling processes. This role is responsible for process monitoring, troubleshooting manufacturing issues, supporting investigations, and driving continuous process improvements while ensuring compliance with quality and regulatory requirements. The scientist will collaborate with cross-functional teams to support safe, efficient, and compliant manufacturing operations.

Qualifications

Requirements

• Must meet one of the following education and experience requirements: Doctorate (Ph.D.) in a scientific discipline; or Master's degree in a scientific discipline with 2+ years of relevant scientific experience; or Bachelor's degree in a scientific discipline with 4+ years of relevant scientific experience.
• Experience in a commercial bio pharmaceutical manufacturing environment, preferably supporting formulation and aseptic filling operations.
• Understanding of protein science, formulation processes, and aseptic filling operations
• Experience with process monitoring, data analysis, trending, and statistical software (e.g., JMP)
• Experience supporting deviations, investigations, root cause analysis, and product impact assessments.
• Experience providing direct manufacturing floor support in a fast-paced, GMP-regulated production environment.
• Strong technical writing skills with experience preparing documentation for regulatory inspections and audits.
• Excellent communication, presentation, problem-solving, and project management skills.
• Demonstrated ability to collaborate effectively with cross-functional teams.
• Bilingual proficiency in English and Spanish (written and verbal).
• Work schedule: 8:00 am to 5:00 pm (admin shift). However, staff will support a 24/7 formulation and filling operations, and irregular shifts, including extended hours (12 hrs), nights, weekends, or holidays may be required based on business needs.

Additional Information

All your information will be kept confidential according to EEO guidelines.