Senior Technical Transfer Specialist - Tucson, United States - Dawar Consulting

Description

Job DescriptionOur client, a world leader in diagnostics and life sciences, is looking for a Senior Technical Transfer SpecialistKindly have a look at the details below and let us know if you are interested

Job Title :

Senior Technical Transfer Specialist Job Duration:
Long Term Contract(Possibility Of Extension)

Location:

Tucson, AZCompany Benefits include:

• Healthcare (Medical, Dental, & Vision)
• Paid Sick leave
• 401k (with 2% employer match)The Senior Technical Transfer Specialist is the overall coordinator between Operations and the Development, Regulatory and Project team at Roche while launching of new Assays, Reagents and Bulk materials used in tissue diagnostic tests. This position is responsible for ensuring that all Operations needs are met from a manufacturability, quality, cost and schedule perspective. The application of program management skills, process engineering, lean manufacturing principles and sound scientific rigor are essential to ensure that new Assays, Reagents and Bulk materials are introduced into the existing manufacturing processes. This position ensures that the requirements for a minimum viable product are met within Operations and clearly communicates project risks and proposes gap closure plans to eliminate these risks. This position will also support, as needed, the transfer of products from site to site or site to supplier within the US to other US or international sites.

Responsibilities:

• Define, understand and communicate manufacturing best practices at the site and communicate minimum requirements to the core project team to ensure manufacturability and scalability of Assays, Reagents and Bulks used in tissue diagnostics
• Be the Global Operations project focal and ensure that all Operations stakeholders (Manufacturing, Process Engineering, Validation Engineering, Functional Leads, Quality, Validation, Planning, Purchasing, Procurement and Label Control) needs are understood and communicated through the transfer process
• Actively establish and refine Technology Transfer standard work to continuously improve the transfer process. Actively seeks out, creates and implements new ways to drastically simplify our ways of working within the team
• Define, lead and execute Validation protocols utilizing Good Manufacturing Processes (GMP) and standards for transferred products. Actively define and improve Validation standard work in coordination with the site Validations team to ensure uniformity across the organization.
• Actively demonstrates project management techniques at an expect level to plan, track and ensure timely completion of transfer projects
• Utilizes expertise in site manufacturing processes to promote, train and improve GMP within the site to ensure transfer activity is successful from cost, quality and delivery perspective
• Troubleshooting problems. Participates in transfer planning and process updates.

Prepares and delivers presentations of project results to others; presents data to larger and more diverse audiencesKnowledge, Skills and Abilities:

• Demonstrates potential for technical proficiency, scientific creativity, collaboration with others, and independent thought
• Strong understanding of assay, bulk and reagent manufacturing processes and design and the ability to apply scientific method as it relates to production
• Advanced technical writing skills to produce reports and documents
• Ability to apply 6 Sigma and Lean Manufacturing Methods during the development phase
• Ability to utilize systems such as SAP and ETQ - PreferredIf interested, please send us your updated resume at