Senior Process Development Scientist - Pharma GMP

CIS International LLC; Juncos (PR); On-site; USD 85,000 - 115,000; Full time

Job summary

CIS International LLC in Juncos, PR seeks a Process Development Senior Scientist (Validation & Documentation) to independently conceive, design and advance experiments, interpret data and lead projects.

This on-site, 5-month contract requires strong GMP knowledge, experience with validation protocols, technical writing and collaboration across Manufacturing, Quality and Regulatory teams.

Qualifications

• Doctorate or equivalent with postdoctoral experience where applicable.
• Master's degree with 3+ years relevant scientific experience.
• Bachelor's degree with 5+ years relevant scientific experience.
• A degree in Mechanical/Chemical/Biomedical/ Biotechnology or related science preferred.
• Experience with data analysis, MS Office, JMP or Minitab, LIMS/HLEE.

Responsibilities

• Independently conducts experiments to advance projects.
• Provides advanced data analysis and interpretation.
• Leads collaborations and mentors team members.
• Plans procedures, milestones and resources for defined projects.
• Contributes to safety, quality, and documentation efforts.

Skills

Leadership

Timeline planning

Scientific analysis

Problem solving

Project management

Hypothesis development

Data interpretation

Lab skills

Bilingual English/Spanish

Education

PhD/MD/PharmD with postdoc (where applicable)

Master's degree with 3+ years relevant experience

Bachelor's degree with 5+ years relevant experience

Engineering/biomedical/science degree preferred

Proficiency with MS Office; JMP/Minitab; LIMS/HLEE

Tools

JMP

Minitab

LIMS

HLEE

Job description

CIS International LLC in Juncos, PR seeks a Process Development Senior Scientist (Validation & Documentation) to independently conceive, design and advance experiments, interpret data and lead projects.

This on-site, 5-month contract requires strong GMP knowledge, experience with validation protocols, technical writing and collaboration across Manufacturing, Quality and Regulatory teams.