Process Development Scientist ID 35470

Inteldot; Juncos (PR); On-site; USD 65,000 - 85,000; Full time

Job summary

Inteldot in Puerto Rico is seeking candidates for an Administrative Shift role. This position focuses on designing and executing scientific experiments to meet project goals under general supervision.

The ideal candidate will have relevant biopharmaceutical manufacturing experience, strong bilingual communication skills, and proficiency in data analysis. Educational requirements include a Doctorate or Masters plus scientific experience.

Qualifications

• Relevant experience in biopharmaceutical manufacturing environment.
• Understanding of protein science, formulation, and filling processes.
• Experience supporting deviations and investigations.

Responsibilities

• Designing and conducting strategies with guidance.
• Providing data analysis and impact assessments for projects.
• Developing new protocols and monitoring field of expertise.

Skills

Bilingual proficiency in Spanish and English

Technical writing skills

Project management skills

Data analysis and interpretation

Communication and presentation skills

Education

Doctorate or Masters + 2 years Scientific experience

Bachelors + 4 years Scientific experience

Educational background in Life Sciences or Engineering

Tools

Statistical analysis tools (e.g., JMP)

Job description

Inteldot has over 15 years in the life science industry with allocations across Puerto Rico, the United States, Europe, and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.

Administrative Shift - 8:00AM – 5:00PM

Description

To conceive, design, implement and execute specific scientific experiments, which contribute to the successful completion of goals and/or projects under general guidance of supervisor.

Responsibilities

• Designs, monitors, or conducts strategies with general guidance from the supervisor.
• Provides data analysis and interpretation and assesses the impact of the data on the project. Keeps current in technical expertise and areas relevant to their function.
• Monitors field of expertise, including literature and technology development, and communicates relevant observations.
• Develop and implement new and novel protocols to address specific issues.
• May represent the department on project teams under the supervision of a senior scientific staff member.
• May initiate productive collaborations within and outside of the department or company.
• Advises or assists others in experimental design and/or interpretation/diagnosis of data and implementing innovative remedies.
• Able to develop solutions to routine technical problems of limited scope.
• Comprehensive understanding of validation protocol execution requirements. In-depth knowledge of validation processes as applied to new equipment installations.

Job Requirements

• Relevant experience in a commercial biopharmaceutical manufacturing environment, preferably supporting formulation and aseptic filling operations.
• Understanding of protein science, formulation and filling processes.
• Experience with process monitoring, data trending, and statistical analysis tools (e.g., JMP)
• Experience supporting deviations, investigations, root cause analysis, and product impact assessments.
• Ability to provide manufacturing floor support in a fast-paced, 24/7 operation.
• Bilingual proficiency in Spanish and English (written and verbal).
• Strong technical writing skills with experience preparing documentation for regulatory audits.
• Excellent communication, presentation, problem-solving, project management skills and cross-functional collaboration skills.

Education

• Doctorate OR Masters + 2 years of Scientific experience OR Bachelors + 4 years of Scientific experience.
• Preferred: Educational background in Life Sciences or Engineering (Biochemistry, Chemical Engineering, etc.).