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New Technology Manager


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Job Details

You will lead a highly engaged team of process and analytical experts, reporting directly to the Technology Director. The role is an exciting opportunity for a strategic professional and a leader who would like to make significant contribution to supply life-changing pharmaceuticals to patients.

The New technology team has the long-term perspective as their responsibility, together with support to the daily product flows as needed. The team is responsible for a strategic plan for the current and future products in the areas Tech Transfer, Yield Optimization, Quality, Business Performance, Robust Processes and Continuous Improvements.

The role is responsible for the process support lab, that is responsible for laboratory trouble shooting and validation studies as needed to ensure processes are maintained in cGMP. The role also has responsibilities with respect to providing product and quality oversight and SME input in production processes and biochemical analytical methods. This is achieved through establishing and growing strategic relationships across functions both within and above the Site, with a view to collaborating on improvement opportunities for both laboratory and product competitiveness and to improve performance, quality culture and efficiency.

The Technology organization consists of three teams, New Technology, Technical Services (direct product flow support) and Operational Excellence & Production Support (Lean/Six Sigma/Continuous Improvements and Deviation support), but at the site all managers work together in a united leadership team from all parts of the organization.

Your main responsibilities will involve:

+ Lead and develop a team of professionals in biotech and carbohydrate processes and analytics

+ Establish and constantly develop standard work procedures

+ Challenge current state and work on an Right First Time approach for the support functions

+ Product performance incl trends

+ Coach the expert function of tech transfer of analytical methods and production processes

+ Track performance of Continuous Improvements and Six sigma project

+ Continuously track trends in the industry to maintain and drive cGMP

+ Instill a good Quality Culture

+ Ensure the team works cross-functionally with manufacturing, QA, QC and other supporting functions, both within site, within Pfizer and within the industry

+ Effectively contribute to the development and execution of the site Leadership strategy as part of the Operational Leadership Team

+ Facilitate the establishment of objectives, activities and KPI's to drive continuous improvements

The role has accountability in own area for:

+ Personnel management and development

+ Financial management

+ Environment, Health and Safety

Your skills and qualifications will ideally include:

+ A Master degree in a Science or Pharmaceutical related discipline

+ Knowledge of global GMP and regulatory requirements

+ Experience in pharmaceutical manufacturing and/or development

+ Ability to develop highly effective teams

+ Ability to manage uncertainty and complexity

+ Preferably experience of working in a global environment

+ Fluent in written and spoken English

The closing deadline for applications is 7th Februrary 2018.

0 (Sweden)

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
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