Apply to Process Development Scientist- 35588

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 or Master’s + 2 years of Scientific experience.
Bachelors + 4 years of Scientific experience.

PREFERRED QUALIFICATIONS:

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.

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: 4 months for the first contract with a high possibility of extension based on performance and budget.
Work schedule: 8:00 am to 5:00 pm (admin shift). However, staff will support a 24/7 formulation and filling operations, and irregular shifts, including extended hours (12 hrs.), nights, weekends, or holidays may be required based on business needs.
Expected hiring date: August 2026