Biopharma Process Development Scientist — Data-Driven & Collaborative

Inteldot; Juncos (PR); On-site; USD 90,000 - 120,000; Full time

Job summary

Inteldot is seeking a scientifically experienced professional to join our client in Puerto Rico. The role involves conceiving and executing experiments, analyzing data, and interpreting results to advance projects in a fast-paced, cGMP environment.

The candidate will monitor literature, develop new protocols, and collaborate across departments to address issues and optimize processes. Experience with regulatory documentation and cross-functional teamwork is essential.

Qualifications

• Experience with data analysis and interpretation for biopharmaceutical projects.
• Strong written and verbal communication; preparation of regulatory documents.
• Ability to design and optimize experiments in a GMP environment.
• Knowledge of validation concepts and quality systems.

Responsibilities

• Conceive, design, implement and execute scientific experiments.
• Provide data analysis and interpretation; track trends and impacts on projects.
• Monitor literature and technology developments relevant to the function.
• Develop and implement new protocols to address issues.
• Collaborate with department or project teams under supervision.
• Support deviations, investigations and root cause analysis as needed.
• Assist with experimental design and data interpretation across teams.

Skills

Data analysis

Cross-functional collaboration

Biopharmaceutical knowledge

Regulatory writing

Education

Doctorate

Master’s + 2 years of experience

Bachelor + 4 years experience

Tools

JMP

Job description

Inteldot is seeking a scientifically experienced professional to join our client in Puerto Rico. The role involves conceiving and executing experiments, analyzing data, and interpreting results to advance projects in a fast-paced, cGMP environment.

The candidate will monitor literature, develop new protocols, and collaborate across departments to address issues and optimize processes. Experience with regulatory documentation and cross-functional teamwork is essential.