TS/MS Scientist - Spray Dry and Solid Dose External Manufacturing

Biopharma-Consulting-Jad-Group; Carolina (PR); On-site; USD 90,000 - 130,000; Part time

Job summary

Biopharma-Consulting-Jad-Group is seeking a technical owner to oversee spray dry, solid dose and packaging operations at external manufacturing partners in Carolina, Puerto Rico. You will troubleshoot, lead tech transfers and keep processes validated and in control.

Responsibilities include authoring deviations, change controls, supporting qualification and validation campaigns, and monitoring process capability with statistics to support GMP inspections and regulatory readiness.

Qualifications

• 5+ years hands-on with spray dry dispersion, solid dose manufacturing and packaging.
• CMO / external manufacturing support and technology transfer.
• GMP inspection support; FDA-regulated manufacturing.
• TrackWise, SAP and statistical analysis.
• Fluent English and Spanish.

Responsibilities

• Provide technical oversight of spray dry, OSD and packaging processes at CMOs.
• Author deviations and change controls; lead root-cause investigations to on-time CAPA closure.
• Support tech transfer, process qualification and validation campaigns.
• Monitor process capability with statistics; support GMP inspections.

Skills

Spray dry dispersion

Solid dose manufacturing

Packaging processes

Tech transfer

GMP inspections

Bilingual English/Spanish

Education

Bachelor's degree in Chemistry, Pharmacy or Engineering

Tools

TrackWise

SAP

Statistical analysis

Job description

Be the technical owner for spray dry, solid dose and packaging processes run at external manufacturing partners (CMOs) for a global pharmaceutical company in Carolina, Puerto Rico. You will troubleshoot, investigate, lead tech transfers and keep the processes validated and in control.

What you'll do

• Provide technical oversight of spray dry, OSD and packaging processes at CMOs.
• Author deviations and change controls; lead root-cause investigations to on-time CAPA closure.
• Support tech transfer, process qualification and validation campaigns.
• Monitor process capability with statistics; support GMP inspections.

• Bachelor's degree in Chemistry, Pharmacy or Engineering.
• 5+ years hands-on with spray dry dispersion, solid dose manufacturing and packaging.
• CMO / external manufacturing support and technology transfer.
• GMP inspection support; FDA-regulated manufacturing.
• TrackWise, SAP and statistical analysis.
• Fluent English and Spanish.

• Contract: 6 months, with possible extension (LLC / corp-to-corp)
• Shift: Monday–Friday core hours, with 24/7 support as needed across time zones
• Start: Immediate