Process Validation/Technical Standards Specialist
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| Job Type | Contractor |
| Location | Dublin |
| Area | Dublin, Ireland |
| Sector | QualityRegulatory |
| Start Date | |
| Advertiser | Darcy Ainscough-Denton |
| Telephone | +353 1 574 6266 |
| Job Ref | 1002646 |
| Job Views | 474 |
- Description
- We have an exciting opportunity for our client, who are a leading biopharmaceutical company based in Dublin. The Process Validation & Technical Standards Individual Contributor will be responsible for developing Validation and Technical Standards and Guidelines for Process validation and technical transfer programs across the client’s internal and external manufacturing network. This individual will be a part of the Global Technical Operations team and will report to the Director of Validation and Technical Standards.
Why you should apply:
This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
What you will be doing:
Developing and maintaining Process Validation, continued process verification and other technical standards. This will ensure that technical guidelines are fit for purpose across multiple modalities and are updated as new modalities are introduced to the client’s pipeline. The role will also support the development of a Knowledge Management framework for the Global Technical Operations department
The role will also support internal and external sites as they build and execute Process validation and tech transfer strategy to support the client’s product pipeline.
The role will work across multiple functions and collaborate closely with Global Product Development, Site Technical Services, Site Validation teams, Quality and Regulatory functions to shape standards and guidelines that are compliant with current regulatory requirements and client standards.
Develop and support the implementation of scientifically sound, fit for purpose standards and procedures for process validation and other technical procedures based on current regulations, industry standards and industry practices.
Deliver associated training to the client’s colleagues.
Support the implementation of innovative and efficient approaches to validation and technical transfer by client internal and external sites incorporating science and risk-based approach.
Support the development and implementation of process validation plans and other validation documentation in collaboration with the validation and technical SME network.
Build strong cross functional working relationships with stakeholders (Quality, Development, Technical Services and CMOs) to ensure high quality deliverables meeting cGMP and the client’s validation requirements.
What you need to apply:
Minimum Bachelors’ degree in a scientific discipline (Biology, Biochemistry, Biotechnology, Chemistry), or related field.
A minimum of 6-8 years’ experience in the biopharmaceutical or pharmaceutical industry (Validation, Technical Services or Quality).
A minimum of 6 years’ direct experience in cGMP validation activities.
Widespread knowledge of Validation regulations, current validation and technical transfer industry practices, and experience of interpretation and application of guidelines and regulations.
Outstanding technical writing skills
Knowledge of biopharmaceutical Bulk Drug Substance (BDS) manufacturing and aseptic fill finish.
Proven active participation in industry and regulatory forums shaping validation practices and strategy.
Strong track record of working in a global and matrix environment and working cross functionally
