Dry External Manufacturing Scientist, TS/MS (External Partners)

BioPharma Consulting JAD Group; Carolina (PR); On-site; USD 120,000 - 180,000; Full time

Job summary

BioPharma Consulting JAD Group is seeking a TS/MS Scientist to oversee spray dry and solid dosage manufacturing with external partners. You will ensure regulatory compliance, drive process validation, and coordinate cross-functional teams to maintain controlled, validated processes.

The role requires 5+ years of hands-on experience, excellent technical writing, and ability to work across time zones. Shift flexibility and a contract of 6 months are possible, with potential extension.

Qualifications

• Bachelor's degree in Chemistry, Pharmacy or Engineering.
• 5+ years of hands-on spray dry, solid dosage manufacturing and packaging experience.
• Working knowledge of cGMPs and global regulatory guidance.
• Strong communication across technical and business teams.
• Proven project management experience coordinating multifaceted projects.
• Ability to support 24/7 operations across time zones.

Responsibilities

• Provide technical oversight for spray dry, solid dosage manufacturing and packaging processes.
• Resolve technical issues related to control strategy and manufacturing.
• Author deviations and change controls with strong technical writing.
• Contribute to root cause investigations for CAPA closures.
• Manage external partner relationships and cross-functional teams.
• Support technology transfer and validation activities with external sites.

Skills

Spray dry

Solid dosage manufacturing

Cross-functional collaboration

Regulatory compliance

Project management

Data management

Bilingual English/Spanish

Education

Bachelor's degree in Chemistry/Pharmacy/Engineering

Tools

SAP

TrackWise

MS Office

Job description

BioPharma Consulting JAD Group is seeking a TS/MS Scientist to oversee spray dry and solid dosage manufacturing with external partners. You will ensure regulatory compliance, drive process validation, and coordinate cross-functional teams to maintain controlled, validated processes.

The role requires 5+ years of hands-on experience, excellent technical writing, and ability to work across time zones. Shift flexibility and a contract of 6 months are possible, with potential extension.