Process Development Scientist (Downstream)
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| Job Type | Contractor |
| Location | Dublin |
| Area | Dublin, Ireland |
| Sector | Operations & Manufacturing |
| Start Date | |
| Advertiser | Darcy Ainscough-Denton |
| Telephone | +353 1 574 6266 |
| Job Ref | 1003016 |
| Job Views | 399 |
- Description
- Team Horizon is seeking a Process Development Scientist (Downstream) on an initial 12-month contract for our client who are a biopharmaceutical leader globally. The role will be based in the Dublin site and will be responsible for supporting the cGMP manufacture of biological bulk drug substance (BDS) at the facility. The Technical Specialist will provide processing expertise to support the technology transfer, process validation and routine commercial manufacturing for Downstream manufacturing.
Why you should apply:
This is a challenging opportunity and a chance to work in a diverse team with a great mix of people. Joining our client means joining a team that you can truly learn from.
Employees are encouraged to develop their skills to meet the demands of an ever-changing work environment, providing them with opportunities to achieve personal and professional goals that will make them valued contributors throughout their careers.
What you will be doing:
The Technical Specialist will be responsible for providing support for technology transfer of new/existing drug substance (DS) manufacturing processes to the Dublin facility, and will be required to work in close collaboration with Process Development, DS Process Sending unit, Operations, Engineering, Supply Chain, Quality, Quality Control, Regulatory and other involved departments to ensure successful facility startup and process qualification.
The position is accountable for timely completion of technical transfer related milestones, with particular emphasis on new product introduction, Process Owner for downstream unit operations, Process Validation (PPQ), Process Monitoring, Risk Assessment (using QRM tools), and building strategies / SME capability.
Downstream: to include buffer preparation, purification and viral reduction steps including chromatography, ultrafiltration viral reduction filtration and viral inactivation technologies and DS formulation and bulk fill.
To author and review process transfer documentation, gap assessments, technical protocols and reports, and process validation documentation, strategy documents.
To identify requirements for laboratory studies to support process fit, decisions or process transfer, and to liaise closely with Global Process Development to oversee the design and execution of studies.
To support the introduction of new raw materials and consumables through the generation of materials lists, Bills of Materials, material specifications and outline testing requirements.
To work closely with colleagues in Quality, Supply Chain and Manufacturing Operations to ensure availability and release of materials to meet technology transfer and routine manufacturing timelines.
To identify and implement process improvements, e.g. yield, cycle time reduction.
To generate documentation protocols and lead the execution of plant supporting studies and technical studies on the manufacturing floor at commercial scale.
May be required to work periodically out of normal business hours (temporary shift working) during periods of engineering and validation batch execution and provide on-call support to manufacturing.
To provide on the floor support for troubleshooting processing issues and to lead manufacturing investigations into process deviations and resolution.
Lead any key process changes using change control system.
Adherence to highest standards for Compliance (Quality and Safety), implement corporate standards and liaise effectively with global groups and provide technical support during audits.
Ensure compliance with site EHS policy, cGMP and other business regulations and participate in risk assessments, audits, and incident investigations.
To author and review common technical document (CTD) sections and reports for regulatory agency submissions.
To serve as a subject-matter expert (SME) on technology transfer and process support during regulatory agency inspections.
Any other duties as assigned.
What you need to apply:
Minimum 5+ years’ experience in Technical Services / Process Development / Manufacturing Support in a biological bulk drug substance manufacturing organization.
Technical and operational knowledge of multiple unit operations in downstream processing.
Comprehensive understanding of cGMP requirements for biopharmaceutical manufacturing.
Good interpersonal skills coupled with demonstrated ability to effectively work in a matrix organization, and in local group settings.
Ability to present and defend technical and scientific approaches in both written and verbal form.
Ability to drive for results independently and adapt to rapidly changing priorities.
Experience of Technology Transfer activities is advantageous.
Knowledge or experience of start-up or systems would be ideal.
Detail orientated.
Technical writing competency.
Experience of authoring CMC sections of regulatory submissions.
B.Sc. in Biochemistry, Biology, Chemistry or equivalent, or B.Eng. Process or Chemical Engineering.
M.Sc. or other postgraduate qualification in Biochemistry, Biology, Chemistry or equivalent, or B.Eng. Process or Chemical Engineering.
