Senior Manager, Biologics Manufacturing Technical Support

Scorpion Therapeutics; Hampton (NJ); On-site; USD 140,000 - 190,000; Full time

Job summary

Scorpion Therapeutics seeks a Senior Manager, Biologics Manufacturing Technical Support to oversee technology transfer, process validation, and manufacturing support for biologics. You will lead scale-up activities, manage CDMO batch data analysis, and investigate deviations and OOS/OOT issues, serving as person-in-plant when needed.

You will collaborate with manufacturing sciences, quality, and analytical groups to ensure successful tech transfer, process validation, and continuous process

Qualifications

• Bachelor's degree in Life Sciences, Engineering, or related field.
• 6+ years in biotech/pharma manufacturing.
• 3+ years working with biologics CDMOs.
• Experience with late-phase biologics programs.
• Strong data analysis skills.
• Ability to travel 30%.

Responsibilities

• Oversee technology transfer, process validation, and manufacturing support for biologics.
• Lead scale-up activities and CDMO batch data analysis.
• Investigate deviations and OOS/OOT issues.
• Serve as person-in-plant when needed.
• Collaborate with cross-functional teams to ensure successful tech transfer and continuous process verification.

Skills

Data analysis

Education

Bachelor's in Life Sciences, Engineering, or related field

Tools

JMP

Minitab

Job description

Role: Senior Manager, Biologics Manufacturing Technical Support, oversees technology transfer, process validation, and manufacturing support for biologics. Responsibilities include leading scale-up activities, managing CDMO batch data analysis, investigating deviations and OOS/OOT issues, and serving as person-in-plant when needed. The role collaborates with cross-functional teams such as manufacturing sciences, quality, and analytical groups to ensure successful tech transfer, process validation, and continuous process verification.

Qualifications

• Bachelor's in Life Sciences, Engineering, or related field
• 6+ years in biotech/pharma manufacturing
• 3+ years working with biologics CDMOs
• experience with late-phase biologics programs
• strong data analysis skills
• ability to travel 30%

High Value

• biologics manufacturing
• process validation
• CDMO oversight
• late-phase biologics
• GxP adherence
• statistical data analysis tools (JMP/Minitab)
• cross-functional collaboration

Work Setup: not specified.