Tech Transfer (Junior)

DPS Group Global; Dún Laoghaire-Rathdown; On-site; EUR 70,000 - 95,000; Full time

Benefits offered by this job

Shift premium (35%)]

Job summary

DPS Group Global is seeking a qualified process development professional to support NPI introductions and lifecycle changes for biologics drug product manufacturing in the EMEA region.

The role involves ensuring successful product transfer through engineering studies, process performance qualification, and regulatory alignment, with a focus on sterile processing, fill-finish, and technology transfer. 35% shift premium may apply.

Qualifications

• Bachelor's or higher degree in science, engineering or related field with relevant experience.
• Strong technical writing skills and understanding of cGMPs and regulatory requirements.
• Experience in process development for biologics or pharma manufacturing is preferred.
• Ability to manage multiple projects and communicate across functions.

Responsibilities

• Provide process development support for NPI and lifecycle changes.
• Lead or support tech transfer and validation activities from concept through regulatory approval.
• Support sterile processing, fill-finish, and related manufacturing operations with technical evaluation of Change Control/NC/CAPA.

Skills

Process development

NPI

Tech transfer

CMC

Regulatory awareness

Education

Bachelor's degree in science/engineering

Master's degree in science/engineering

Associates degree in related field

Job description

Overview

The 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.

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 Bachelors degree in science, engineering or equivalent discipline with 2 years experience in a commercial manufacturing or NPI role OR Masters degree & 1 years of directly related experience OR Associates 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.