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
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:
- Conceives and designs, executes or evaluates, and interprets experimental strategies.
- Provides input to new processes to generate robust and reliable data.
- Ensures that studies are conducted in compliance with the respective protocol and applicable guidelines and regulations.
- Designs, monitors or conducts experimental strategies with general guidance from supervisor.
- Provides data analysis and interpretation and assesses impact of the data on the project.
- Keeps current in field of scientific expertise and areas relevant to their function.
- Monitors field of expertise, including literature and technology development, and communicates relevant observations.
- Represent the department on project teams under supervision of a senior scientific staff member.
- 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.
Job Requirements:
- Extensive experience in process development or manufacturing support within biotech, biopharma, or related industries.
- Strong ability to analyze and interpret complex process and experimental data to drive process understanding and optimization.
- Experience supporting process scale-up, technology transfer, and/or commercial manufacturing.
- Ability to integrate data from multiple sources (process, analytical, manufacturing) to develop actionable insights and recommendations.
- Strong track record of cross-functional collaboration (e.g., Manufacturing, Quality, Analytical, Regulatory).
- Experience working in a GMP-regulated environment, with deep understanding of data integrity and compliance requirements.
- Proficiency with scientific data analysis tools (e.g., JMP, Minitab, Excel or similar).
- Excellent technical communication skills, including writing reports, presenting data, and influencing stakeholders.
Education:
- Doctorate or master + 2 years of Scientific experience or Bachelors + 4 years of Scientific experience.
- Life Sciences or Engineering (statistics, mathematics, systems engineering, industrial engineering, computer science, or related field experience)
What We Do
Inteldot offers custom turn-key systems, systems integration, MES eBR configuration and integration solutions, business intelligence and analytics and technical staffing. We have been providing the Pharmaceutical, Manufacturing and Medical Device industries with services for a variety of applications since 2004
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