Tech Transfer Lead (Junior)

DPS Group Global; Dublin; On-site; EUR 65,000 - 95,000; Full time

Job summary

DPS Group Global in Ireland is seeking a Process Development Specialist to support NPI and lifecycle management changes for biologics drug product manufacturing within the global Process Development organization. The role includes moving to a new building with single-use end-to-end processes and syringe fillers.

You will lead product transfers from concept to PPQ, support validation activities, and ensure compliance with global regulatory requirements.

Qualifications

• Bachelor’s degree in science, engineering or equivalent with 2 years in commercial manufacturing or NPI, or Master’s degree with 1 year related experience, or Associate’s with 5 years.
• Strong technical writing skills.
• Knowledge of cGMPs and worldwide regulatory requirements.
• Excellent problem solving and communication skills.

Responsibilities

• Support and lead NPI from concept to PPQ and product filings.
• Own product transfer projects from initiation to regulatory approval.
• Provide solutions for trouble-shooting drug substance processing and parenteral filling.
• Develop process design and validation documentation for syringe filling and characterization.
• Collaborate across sites to ensure transfer and validation rules are followed.
• Participate in 24/7 support for projects as needed.

Skills

Process Development

NPI

Tech Transfer

cGMP

Education

Bachelor's degree in science/engineering

Master's degree (advantage)

Associate's degree + 5 years exp

Job description

This role will require the candidate to provide process development support primarily to new product introductions (NPI) and lifecycle management (LCM) changes. In addition, the candidate will be expected to provide technical support to biologics drug product manufacturing as part of the global Process Development organization. With the intention of moving to a new building construction that will house single use end to end processes and new syringe fillers.

Responsibilities would include the following:

• Support and/lead new product introductions to PM3 from concept to PPQ from a Process Development perspective and complete product filings.
• Be accountable for success of the product transfer project from initiation to the transfer, through line characterisation, engineering studies, process performance qualification and ultimately to regulatory approval.
• Provide solutions when trouble shooting drug substance freeze/thawing, formulation, filling syringes, inspection and transportation for parenteral products through the NPI or post-NPI phases.
• Provide process development knowledge for commercial drug product processing in specific areas such as sterile processing, process characterization, tech transfer and process validation, input on design for new parts of the facility where needed. Support commercial drug product manufacturing operations with technical evaluation of Change Control/NC/CAPA and technology transfer.

The position will report to Process Development Manager. Moderate international travel might be required during the course of the projects.

Key Responsibilities

• Development of documentation and process design for characterisation studies, engineering runs, electronic batch record creation, validation plans, process performance qualifications for syringe filling.
• Ensuring all aspects of activity within any given process validation adheres to required policies and procedures, including safety and training.
• Ensure that the site meets the quality requirements of its customers and applicable regulations (FDA, EU & international standards) with a full understanding of CMC business process related to technology transfer.
• Participate in process validation cross functional teams at the site to ensure adherence to required policies and procedures and be responsible to deliver against organizational goals and project milestones.
• Pre-approve and post-approve process validation protocols and assessments from a quality system documentation perspective.
• Actively communicates across functions and sites and is a strong collaborator with all the functional groups at the receiving site, sending site and corporate functions.
• Act as the responsible point contact from site for the transfer project for drug product teams and Global Operations Teams.
• Assist in the development of any existing validation program to ensure continued compliance to the necessary regulations and input to site validation guidance documents.
• Collate and report on relevant shipping and filter validation.
• Assist in deviation and exception resolution and root cause analysis.
• Contribute to product quality assessments and process flow documents.

Basic Qualifications

• Third level Bachelor’s degree in science, engineering or equivalent discipline with 2 years experience in a commercial manufacturing or NPI role OR Master’s degree & 1 years of directly related experience OR Associate’s degree & 5 years of directly related experience.
• Strong technical writing skills.
• Knowledge of cGMPs and other worldwide regulatory requirements.
• Problem solving ability and excellent oral and written communications skills.

Preferred Qualifications

• Experience in support of Commercial Protein Drug Product (DP) processing in specific areas such as sterile processing, process characterization, tech transfer (to commercial DP sites) or validation.
• Strong skills in applying fundamental engineering and scientific principles to the design, implementation and process validation of protein freeze-thawing, filtration, mixing, filling (PpK / batch homogeneity). Knowledge of protein biochemistry with regard to chemical and physical stability.
• Project management skills including the ability to manage multiple projects and evaluate project resource requirements
• Strong knowledge of Quality systems, Drug Product Manufacturing and Validation.
• Demonstrated ability in providing leadership to cross-functional teams to advance complex projects to completion. Excellent Communication skills are essential for this role.

The successful candidate will need to be prepared to participate in 24/7 support once or twice a quarter (depending on business needs) for approx. 1-2 weeks at a time. 35% shift rate applies.