BioPharma Consulting JAD Group is seeking a talented Process Development Scientist to join our dynamic team.
This role is pivotal in our mission to advance innovative solutions within the biopharmaceutical sector.
The ideal candidate will be responsible for designing and executing scientific experiments, interpreting data, and contributing to process improvements under the guidance of senior management.
Key Responsibilities: Experimental Design and Execution: Conceive, design, and conduct experimental strategies with general guidance from the supervisor.
Evaluate and interpret experimental results to ensure successful project outcomes.
Data Analysis and Interpretation: Provide thorough data analysis, interpretation, and assessment of the impact of the data on the project.
Develop and implement new protocols to address specific issues.
Compliance and Protocols: Ensure that studies are conducted in compliance with the respective protocols, guidelines, and regulations, including cGMP standards.
Scientific Development: Keep current in the field of scientific expertise, including literature and technology development.
Introduce advanced scientific methods when necessary.
Collaboration and Communication: Collaborate within and outside of the department, offering guidance and assistance in experimental design and data interpretation.
Communicate relevant observations and participate in the external scientific community.
Technical Writing: Independently author scientific reports, summary documents, complex regulatory documents, invention disclosures, and patents.
Project Management: Develop and follow timelines for project completion, contribute to department-wide efforts such as safety and recruiting, and may assume a lead role on project teams.
Supervision and Mentorship: May develop supervisory and mentoring skills to support the growth and development of junior staff.
Skills and Competencies: Advanced scientific analysis and troubleshooting skills.
Strong laboratory skills, with experience in the application of scientific theory.
Creative skills in designing and performing scientific experiments and interpreting results.
Excellent verbal and written communication skills, including technical writing.
Proven ability to motivate and supervise the activities of others.
Strong project management skills and ability to manage multiple tasks efficiently.
Computer literacy (Windows environment: Word, Excel, PowerPoint).
Advanced knowledge of cGMP regulations.
Fully bilingual (English/Spanish).
Requirements Education: Doctorate degree in Science or Engineering, or Master's degree in Science or Engineering with 5 years of scientific experience, or Bachelor's degree in Science or Engineering with 6 years of scientific experience.
Preferred Qualifications: Previous experience in process validation, formulation processes, and mixing studies.
Strong technical writing skills in English.
Demonstrated ability to work in a multidisciplinary environment and collaborate effectively across departments.
