Process Development Scientist

hace 1 semana

Juncos, Puerto Rico BioPharma Consulting JAD Group A tiempo completo

Summary:

The Scientist will design, implement, and execute scientific experiments that contribute to the achievement of project and organizational goals. Under the general guidance of a supervisor, this role involves conceiving and evaluating experimental strategies, analyzing data, and ensuring compliance with applicable protocols and regulations. The Scientist will provide technical insights, contribute to innovative processes, and collaborate across departments to deliver impactful scientific outcomes.

Responsibilities:

  • Conceive, design, and execute scientific experiments to meet project objectives under general supervision.
  • Develop and implement novel protocols and advanced scientific methods to address specific challenges.
  • Conduct, monitor, and interpret experimental strategies, providing reliable data and assessments.
  • Analyze data, provide insights on its impact, and propose next steps for projects.
  • Maintain compliance with protocols, guidelines, and cGMP regulations in all scientific activities.
  • Stay updated on relevant scientific literature, technological advancements, and trends in the field.
  • Independently prepare detailed scientific reports, regulatory documents, and invention disclosures.
  • Collaborate and communicate effectively with cross-functional teams, sharing results and recommendations.
  • Represent the department on project teams and external scientific communities as needed.
  • Participate in department-wide initiatives such as safety programs, recruiting, and committees.
  • Mentor and assist team members in experimental design, data interpretation, and troubleshooting.

Skills:

  • Advanced scientific analysis, problem-solving, and troubleshooting capabilities.
  • Strong laboratory skills with creative approaches to experiment design and interpretation.
  • Proficiency in technical writing and document preparation for regulatory purposes.
  • Skilled in project management, organization, and multitasking.
  • Effective verbal and written communication skills, including negotiation and conflict resolution.
  • Proficiency in computer applications (Word, Excel, PowerPoint) in a Windows environment.
  • Demonstrated ability to lead or mentor team members and collaborate across functions.

Requirements

Education

  • Doctorate degree OR
  • Master’s degree with 5+ years of scientific experience OR
  • Bachelor’s degree with 6+ years of scientific experience

Fields of Study

  • Chemical Engineering, Biomedical Engineering, Chemistry, Biochemistry, or related life sciences.

Preferred Qualifications

  • Experience in process validation, mixing studies, and formulation processes.
  • Strong English writing and verbal communication skills; fluency in Spanish and English is required.
  • Advanced knowledge of cGMP guidelines and regulatory compliance.

Shift:

  • Full-time position requiring flexibility and adaptability to changing priorities.

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