TSMS Scientist Dry EM

Validation & Engineering Group Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical Biotechnology Chemical Food and Medical Devices industries in the following areas: Laboratory Compliance Computer Engineering Project Management Validation and other services.

We are seeking an experienced professionals to support the Dry External Manufacturing (Dry-EM) Technical Services / Manufacturing Science organization. Selected candidates will provide technical leadership and scientific support for spray dry dispersion (SDD) solid oral dosage manufacturing technology transfer process validation continued process verification deviation investigations and manufacturing support activities performed by external manufacturing partners. The role requires strong technical expertise regulatory knowledge and the ability to collaborate with internal and external stakeholders to maintain compliant and reliable supply of pharmaceutical products.

• TS/MS Scientist - Dry EM

Description:

• 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.

Qualifications:

• Bachelors 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
• 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

At Validation & Engineering Group people always come first. We believe that when youre empowered to do your best work bold ideas thrive and real progress happens. This isnt just a job - its an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven supportive team.

Excited to build something meaningful together We look forward to hearing from you.

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.

Required Experience:

IC