# Process Development Scientist

> BioPharma Consulting JAD Group · Juncos, Puerto Rico · Contract · Posted 2026-05-21

**Workplace:** on_site

## 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.

**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 teamwork.

**COMPETENCIES/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 solvingProject 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).

## Requirements

-   Doctorate degree in Sciences OR
-   Master’s degree in sciences and 2 years of directly related experience experience OR
-   Bachelor’s degree and 4 years of directly related experience experience.

**Preferred Qualifications**

-   Background in sciences
-   Experience in Regulated Industry
-   Proficient in creating and executing validation and qualification documentation
-   Provide support to vision inspection qualification and characterizations
-   Requires excellent communication skills with suppliers and other sites
-   A Plus: Knowledge in automated vision inspection systems
-   A Plus: Knowledgeable in CSV. Support CQV documentation and execution

## Benefits

-   Administrative Shift
-   6-month contract

## Apply

[Apply at BioPharma Consulting JAD Group](https://apply.workable.com/biopharma-consulting-jad-group/j/CF964CBA68/apply)

---
Powered by [Workable](https://www.workable.com)