Lead Sterile Parenteral Drug Product Tech Transfer Scientist

LSC, Life Science Consultants; Dublin; On-site; EUR 85,000 - 120,000; Full time

Job summary

LSC, Life Science Consultants, invites applications for a Senior Scientist - Sterile Drug Product Technology Transfer position for a 12-month contract in Dublin. You will join a cutting-edge biopharma manufacturing environment, supporting sterile drug product transfer and critical quality control operations.

The role requires at least 6 years’ experience in pharma/biotech, with expertise in parenteral operations, aseptic processing, regulatory knowledge (EU GMP and FDA CFR), and a focus on

Qualifications

• Experience in parenteral operations including aseptic processing and fill-finish.
• Strong knowledge of EU GMP and FDA CFR guidelines.
• Proven track record of technology transfer and scale-up for commercial drug products.
• Familiarity with DoE, QbD, and QRM concepts in pharma manufacturing.

Responsibilities

• Support technology transfer of biologics drug products for sterile facilities.
• Contribute to aseptic manufacturing activities: equipment prep, filling, and visual inspection.
• Lead/Support materials workstreams and qualification activities for new materials and components.
• Assist lifecycle biologic parenteral product transfers and establish process parameters.

Skills

Parenteral operations

Aseptic processing

Sterilisation

Sterile filtration

Isolator technology

Lyophilisation

Fill-finish operations

Regulatory knowledge EU GMP & FDA CFR

Technology transfer

Quality by Design (QbD)

Quality Risk Management (QRM)

Job description

LSC, Life Science Consultants, invites applications for a Senior Scientist - Sterile Drug Product Technology Transfer position for a 12-month contract in Dublin. You will join a cutting-edge biopharma manufacturing environment, supporting sterile drug product transfer and critical quality control operations.

The role requires at least 6 years’ experience in pharma/biotech, with expertise in parenteral operations, aseptic processing, regulatory knowledge (EU GMP and FDA CFR), and a focus on