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Business Process Management Expert

SIRE Life Sciences®

Netherlands, zagranica

SIRE Life Sciences®

Business Process Management Expert

Location: Netherlands

SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!

THE COMPANY

Our client is a professional Pharmaceutical organization, based in Zuid-Holland Netherlands.

ROLE DESCRIPTION

The Business Process Management Expert (BPM Expert) is accountable for a larger section of the procedural framework and is responsible for ensuring that GxP and similar requirements are adequately described. The BPM expert has content knowledge of the area he/she is accountable for and works with partners form the business and other quality functions to ensure the process meets their requirements and aligns with their operations including the training development and roll-out.

The BPM expert is responsible for designing, improving and implementing projects related to business processes and the procedural framework for GxP, either as leader or key team member and has to implement a risk based methodology, both on the process as well as on the training side (role & risk based training plans).

RESPONSIBILITIES

Key tasks include (but not limited):

Process Alignment & Training Support:
1. The BPM expert will Lead or participate in improvement projects to describe the new desired state of processes for compliance. Gather and analyze metrics, CAPA and other performance data of the existing process, describe requirements and develop with the partners to be processes.
2. The BPM expert will oversee detailed process development, procedural document development, training development in collaboration with the responsible functions to ensure content and requirements of the design are fully transferred and implemented. Collaborate with responsible leaders to ensure planning is met, providing input to the functions in a matrix.
3. The BPM expert will collaborate with other BPM experts to plan and prioritize projects. Maintain relevant planning tools.
4. The BPM expert will create high level process maps in ARIS and provide sufficient detail to ensure all levels of the process can be worked out. Create detailed process flows for selected projects. Review detailed process flows and approve through agreed stage-gate and versioning approaches. Develop the associated training material and have it deployed to the relevant target audience applying a role risk based training methodology.
5. The BPM expert can lead or participate in the development of departmental processes and tools to improve own and departmental work.
6. The BPM expert will lead by example and ensure compliance systems are maintained and accurate (training plan, time registration, corporate compliance programs, etc).
7. The BPM expert will participate in partner organization leadership team meetings and individual meetings to ensure processes meet their requirements and keep them informed of progress.

Decision Making & Problem Solving:
Decisions made and problems solved will involve process and training development, working with various stakeholder groups both within BRQC and outside of BRQC, providing technical and content expertise to teams, reporting and summarizing to cluster leads and management.

REQUIREMENTS

Position Qualifications:
Master degree or BS/BA with minimum of 8 years’ experience in a medium to large scale matrix organization which includes applicable compliance related field and/or equivalent time and experience in a related R&D area is required. Requires knowledge of the drug development process, good knowledge of worldwide GxP compliance regulations, sound research and development practices, scientific and quality terminology, company quality assurance procedures and policies, and quality evaluation techniques as well as adult training development expertise.

Related Experience:
• Project Management Skillset
• Ability to interpret data to develop action plans to improve business;
• Must have strong personal leadership with demonstrated competency interfacing with all levels of the organization including senior leaders;
• Strong networking and relationship building skills;
• Ability to create an open and inviting environment;
• Embraces generational differences;
• Exceptional written and verbal communications skills;
• Ability to translate data into information and strategies into executable action plans;
• Ability to independently plan, organize, coordinate, manage and execute assigned tasks;
• Experience of quality related business processes and practices; experience of the overall drug development process is an asset.

OTHER

General Skills:
• Problem solver;
• Proactive strategic thinker;
• Strong leader and collaborator;
• Highly committed to quality;
• Flexible and persistent;
• Ability to independently plan, organize, co-ordinate, manage and execute assigned tasks;
• Excellent communicator and presenter, with excellent interpersonal skills and diplomacy;
• Excellent knowledge of English is required;
• Proficient in Microsoft Office applications;
• Stakeholder contacts are frequent and require excellent interpersonal skills and diplomacy.

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Rowin van der Zwaan.

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SIRE Life Sciences®

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