Technical Services / Manufacturing Science Scientist

Veg Group; Puerto Rico; On-site; USD 80,000 - 100,000; Full time

Job summary

Veg Group is seeking a Technical Services / Manufacturing Science Scientist in Puerto Rico. The ideal candidate will provide technical oversight and ensure compliance in spray dry and solid dosage manufacturing processes. With 5+ years of experience, you'll manage internal and external relationships while documenting compliance with cGMP regulations. Fluency in English and Spanish is essential, and you must be capable of supporting 24/7 operations across time zones. Join us in a collaborative environment focused on high ethical standards.

Qualifications

• 5+ years of hands-on working experience in spray dry, solid dosage manufacturing and packaging.
• Strong understanding of cGMP regulations and requirements.
• Ability to communicate and influence across diverse teams.

Responsibilities

• Provide technical oversight for spray dry and solid dosage manufacturing processes.
• Participate in resolution of manufacturing technical issues.
• Maintain compliant manufacturing processes and document process validation.

Skills

Technical writing capabilities

Communication skills

Project management expertise

Data management practices

Regulatory understanding

Fluency in English and Spanish

Education

Bachelor's degree in Chemistry, Pharmacy, or Engineering

Job description

Technical Services / Manufacturing Science Scientist

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position.

Scope and Responsibilities

• 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.
• 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.
• 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.
• Operate demonstrating a collaborative approach and positive attitude toward change.

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.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.