Senior Technical Services Engineer - Scale-Up & Process Innovation

Adare Pharma Solutions; Vandalia (OH); On-site; USD 90,000 - 120,000; Full time

Job summary

Adare Pharma Solutions in Vandalia, Ohio seeks a Senior Technical Services Engineer to support scale-up, technology transfer, and process development for commercial products. You will drive studies for bulk drug delivery, support optimization and troubleshooting, and contribute to lean manufacturing initiatives.

The role requires a BS/BA in a related field and 5–8 years of experience in pharma/manufacturing, with strong analytical and technical writing skills to produce protocols, validation

Qualifications

• BS/BA degree in biology, chemistry, engineering, or related field.
• 5–8 years of related pharmaceutical or manufacturing experience.
• Strong problem-solving and root-cause analysis skills.

Responsibilities

• Manage scale-up, technology transfer and process development for commercial products.
• Develop and execute studies related to bulk drug delivery and finished dosage forms per regulatory requirements.
• Support manufacturing through process optimization, troubleshooting, deviations, and investigations.
• Provide product impact assessments for deviations to QA and Regulatory Affairs.
• Technical writing: protocols, validation reports, batch records, deviations and investigations.
• Lead Lean Manufacturing and Operational Excellence initiatives within the facility.
• Operate and optimize pharmaceutical equipment and support cross-functional teams.
• Provide training and support to departments within Validation and Technical Services.

Education

BS/BA in Biology, Chemistry, Engineering

Tools

Microsoft Office

Visio

JMP

Job description

Adare Pharma Solutions in Vandalia, Ohio seeks a Senior Technical Services Engineer to support scale-up, technology transfer, and process development for commercial products. You will drive studies for bulk drug delivery, support optimization and troubleshooting, and contribute to lean manufacturing initiatives.

The role requires a BS/BA in a related field and 5–8 years of experience in pharma/manufacturing, with strong analytical and technical writing skills to produce protocols, validation