# Technical Services / Manufacturing Science (TS/MS) Scientist

> BioPharma Consulting JAD Group · Carolina, Puerto Rico · Contract · Posted 2026-10-14

**Workplace:** on_site

## Description

Under limited supervision the Technical Services / Manufacturing Science (TS/MS) Scientist – Dry External Manufacturing will performe the following tasks and duties:

-   Provide technical oversight for spray dry, solid dosage manufacturing and packaging processes, leveraging a strong technical foundation and previous experience supporting these processes.
-   Participate in resolution of technical issues, including those related to control strategy and manufacturing.
-   Possess excellent technical writing capabilities, including authoring of deviations and change controls.
-   Participating in root cause investigations to support Corrective Actions and Preventive Actions (CAPA) closure Activities within the expected timeline.
-   Employ excellent communication skills to manage internal and external relationships with external partners, site management, and cross-functional teams.
-   Build and maintain relationships with development and central technical organizations.
-   Ensure that manufacturing processes are compliant, capable, in control, and maintained in a validated or qualified state.
-   Understand, justify, and document the state of process validation with data that evaluates the capability of the manufacturing process to meet its stated purpose.
-   Maintain processes in a state of compliance with US and global regulations, including cGMPs and applicable global regulatory manufacturing guidance.
-   Support ongoing manufacturing at External Partners through process monitoring, issue response, and process improvements where necessary.
-   Support technical transfer and validation activities to external partners manufacturing and packaging sites by review technical transfer documentation, participate in process qualifications activities and support validation campaigns.
-   Work cross-functionally within the site and other functions to deliver on technical objectives.
-   Some flexibility may be required to support 24/7 operations and issue resolutions with external partners across different time zones.

## Requirements

-   Bachelor's degree (minimum) in scientific disciplines of Chemistry, Pharmacy, or Engineering.
-   5+ years of demonstrated hands-on working experience and proficiency with spray dry, solid dosage manufacturing and packaging.
-   Working knowledge of regulatory expectations (cGMPs and applicable global regulatory guidance).
-   Strong understanding of regulatory requirements and their application in a manufacturing environment.
-   Proficient in data management practices across manufacturing and packaging operations.
-   Proven ability to effectively communicate and influence across diverse technical and business teams.
-   Demonstrated project management expertise with a track record of coordinating and executing multifaceted projects.
-   Demonstrates adaptability, a collaborative mindset, and a positive attitude toward change.
-   Available to support 24/7 operations and issue resolutions across multiple time zones as needed.
-   Fluent in English and Spanish, with the ability to communicate effectively across diverse teams and stakeholders.

**Must have:**

-   Experience supporting External Manufacturing Organizations (CMOs).
-   Spray Dry Dispersion (SDD) experience.
-   Oral Solid Dosage manufacturing experience.
-   Technology Transfer experience.
-   GMP regulatory inspection support experience.
-   TrackWise experience.
-   SAP experience.
-   Statistical analysis experience.
-   FDA regulated manufacturing experience

## Benefits

-   Work Schedule: Monday-Friday (core business hours) but to support 24/7 Operation as needed (Shift Support May require support outside normal business hours)
-   Contract: 6 Months (with possible extension)

## Apply

[Apply at BioPharma Consulting JAD Group](https://apply.workable.com/biopharma-consulting-jad-group/j/9954391E1F/apply)

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