Process Development Scientist- 35933

CIS International LLC; Juncos (PR); On-site; USD 85,000 - 120,000; Full time

Job summary

CIS International LLC in Juncos, Puerto Rico, seeks a highly qualified scientist to conceive, design, implement and execute scientific experiments under supervision. You will interpret data, ensure compliance with protocols, and contribute to robust, license-ready results.

The role emphasizes innovation, collaboration with teams, and leadership development. Ideal candidates hold a Doctorate or Master’s with significant lab experience, proficiency with AI tools, and strong communication skills in

Qualifications

• Doctorate or Master’s with 2+ years scientific experience required.
• Bachelor’s with 4+ years scientific experience accepted.
• Experience using laboratory equipment and instruments required.
• Strong manual dexterity and problem-solving skills required.
• Proficiency with AI tools to support research and workflow.

Responsibilities

• Conceives and designs, executes or evaluates, and interprets experimental strategies.
• Provides input to new processes to generate robust and reliable data.
• Ensures studies comply with protocols and applicable guidelines and regulations.
• Develops and implements new protocols to address issues.
• Authors scientific reports, summary documents, and regulatory submissions.

Skills

Advanced scientific analysis

Troubleshooting

Organization

Multi-tasking

Verbal communication

Written communication

AI tools proficiency

Education

Doctorate

Master’s + 2 years experience

Bachelor’s + 4 years experience

Tools

Calipers

Microscopes

Analytical balances

Job description

SUMMARY

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.

FUNCTIONS

• 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.
• May introduce advanced scientific methods.
• Develops and implements new and novel protocols to address specific issues.
• May represent the department on project teams under 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.
• Independently authors scientific reports, summary documents, complex regulatory documents, invention disclosure submissions and/or patents.
• Participates in external scientific community.
• May assume lead role in department-wide support efforts such as safety, recruiting and committees.
• May develop supervisory and mentoring skills.
• Develops and follows timelines for completing project team work.

EDUCATION

• Doctorate orMaster’s + 2 years of Scientific experience.
• Bachelors + 4 years of Scientific experience.

PREFERRED QUALIFICATIONS

• Experience preparing syringes and vials with cosmetic, particle, or solution defects for developmental studies, equipment characterization, training activities, and commercial equipment setup.
• Experience using laboratory equipment and instruments, including calipers, microscopes, and analytical balances.
• Strong manual dexterity, creativity, and practical problem-solving skills, with the ability to develop and create defects in glass containers.
• Strong creative mindset and exceptional fine motor skills, with the ability to handle, cut, shape, and craft miniature items with precision, including preparing particles and creating defects for laboratory studies
• Ability to develop, introduce, or improve defect-creation methods for laboratory use.
• Ability to evaluate defects and other conditions in primary containers.
• Knowledge of aseptic techniques, 5S, Lean Manufacturing, and visual manual inspection techniques.
• Ability to manage projects of limited scope under general direction.
• Ability to motivate and support the work of others.
• Innovative, resourceful approach to developing methods for creating cosmetic defects in vials and syringes.
• Proficiency with AI tools to support research, information organization, and workflow improvement, using sound judgment and following applicable company requirements.
• Strong organizational and multitasking skills, including experience coordinating projects and working with other departments.
• Ability to work in a fast-paced environment and prioritize competing tasks.
• Excellent interpersonal and communication skills, with the ability to work effectively with internal and external customers.
• Highly motivated, charismatic, and approachable team player who actively supports colleagues, stays engaged, and contributes positively to team activities and shared goals.

SKILLS

• Advanced scientific analysis and troubleshooting skills.Advanced laboratory work skills.
• Ability to motivate and/or supervise the activities of others.
• Must be well organized, have multi-task project experience, and be able to communicate and work well with other departments.
• Must have demonstrated skills and competencies in the following areas: Verbal communication, Written communication including technical writing skills, negotiation and conflict resolution. Analytical problem solving Project management.
• Ability to be flexible and manage change.
• Computer literacy (Windows environment: Word, Excel, Power Point).
• Skills requiring the application of scientific theory.
• Creative skills in the design and performance of scientific experiments and interpretation of results.
• Strong knowledge of cGMP
• Fully bilingual (English/Spanish).

WORK METHODOLOGY

• Full on site job in Juncos, PR
• Full time job
• Expected project duration: 6months for the first contractwith a high possibility of extension based on performance and budget.
• Administrative Shift(weekends and overtime may also be required).
• Expected hiring date: November 2026