EXPIRED – Business Analyst Enterprise Recipe Management / ro-220

Location
CH-Kaiseraugst
Start
asap
End
30.06.2022
Workload
100 %
All-in / Hour
please ask us
Total Hours
952h

Deadline:

Deadline
EXPIRED

 

EXPIRED – Business Analyst Enterprise Recipe Management / ro-220

Location
CH-Kaiseraugst
Workload
100 %

Start

asap

End

30.06.2022

DEADLINE

Deadline
EXPIRED

  • CH-Kaiseraugst
  • CH-Kaiseraugstasap30.06.2022100 % 952hplease ask usDeadline
    EXPIRED

For our customer located in Basel/Switzerland we are currently looking for a: Business Analyst (m/f/x)

  • Location: 4303 Kaiseraugst
  • Branch: pharma
  • Duration: 6 months +

General Information:

  • Start date: ASAP/ 17.01.2022
  • latest Start Date: 01.02.2022
  • End date: 30.06.2022
  • Extension: possible
  • Workplace: Kaiseraugst
  • Workload: 100%
  • Team: 3 local people and several virtual teams
  • Remote/Home Office: currently yes, on-site work required
  • Travel: currently no, max. up to 25%
  • Department: PT IX Chapter Business Analysis Process (FP)

Tasks & Responsibilities

We are looking for a Business Analyst located at Kaiseraugst to work for PT Informatics, the Informatics supporting Pharma Global Technical Operations. The Business Analyst will support the Enterprise Recipe Management project.

  • Performs typical Business Analysis activities and creates deliverables as per company standards within a squad / project like URS / User Stories, Functional Specifications / Acceptance Criteria as well as contributing to other project documents such as Business Cases and Project Charters
  • Main contact and escalation point for the sites to the project
  • Work closely with Site Implementation Leads to understand the needs of each of the sites in scope
  • Accountable to highlight site specific risks, assumptions, issues and dependencies (specifically such with local processes / systems) to the Rollout Squad Lead
  • Together with Site Implementation Leads ensures the template rollout approach is adopted and adjusted to match local needs
  • Supports Rollout Lead in improving the template rollout approach, as well as identifying and sharing lessons-learnt and best practices between site implementations
  • Help identifying equipment and substance master data required for site
  • Analyze and (together with OCM expert) address required business process changes; keep track that these changes indeed get implemented
  • Facilitate (virtual) workshops with teams on site to identify and address the process changes
  • Support sites in adapting to a standardized manufacturing process and nomenclature
  • Help to identify workarounds / where possible processes changes to mitigate gaps in the application
  • Support Site Implementation Lead or present themselves to senior leaders and line managers to get them to buy into our goals and support us in introducing the change to their teams
  • Work closely with Rollout Squad Lead for the rollout planning and ensuring that administrative tasks related to the go-live get carried out (e.g. collection of user lists, coordination of training slots etc.)

Must Haves

We are looking for a candidate who has min. 5 years of experience in Manufacturing in a pharmaceutical environment with GMP experience. In addition the candidate should have worked as Business Analyst previously for at least 2-3 years.

  • Min. Bachelor degree in Computer Science or any related area or equivalent work experience
  • Min. 3-5 years of experience in IT or OT related to the pharmaceutical environment (GxP compliant area) working as a Business Analyst
  • Min. 5-7 years of experience manufacturing of drug substances and ideally drug products
  • Experience with MES, LIMS and related ISA95 production systems
  • Business analysis and business process modelling experience
  • Fluent in English (written and spoken)
  • Experience working in a global, virtual team with people across all management levels
  • Excellent communication skills
  • Facilitation of (virtual) workshops

Nice to Haves

  • Organizational Change Management experience is a plus
  • Fluent in German (written and spoken)
  • ISA S88 / S95 knowledge
  • Experience with global / multi-site manufacturing projects
  • internal project methodology

Did we catch your interest?

The SimplyVision-Team is looking forward to receive your application (Word file is highly appreciated).

Kindly be informed that our customer is located in Switzerland. Therefore only applications from candidates within the EU or candidates holding Swiss work permission are required.

Preferred Interview Dates

  • asap after halting date

Tagged as: change management, GxP, LIMS, MES, process modelling

Files must be less than 5 MB.
Allowed file types: txt rtf pdf doc docx.
If not - no problem - we'll organize one.
More optional Information about your way of finding us
You agree that your data will be used to process your request. Further information and revocation instructions can be found in the privacy policy.


You can apply to this job and others using your online resume. Click the link below to submit your online resume and email your application to this employer.

  • CH-Kaiseraugst
  • CH-Kaiseraugstasap30.06.2022100 % 952hplease ask usDeadline
    EXPIRED

For our customer located in Basel/Switzerland we are currently looking for a: Business Analyst (m/f/x)

  • Location: 4303 Kaiseraugst
  • Branch: pharma
  • Duration: 6 months +

General Information:

  • Start date: ASAP/ 17.01.2022
  • latest Start Date: 01.02.2022
  • End date: 30.06.2022
  • Extension: possible
  • Workplace: Kaiseraugst
  • Workload: 100%
  • Team: 3 local people and several virtual teams
  • Remote/Home Office: currently yes, on-site work required
  • Travel: currently no, max. up to 25%
  • Department: PT IX Chapter Business Analysis Process (FP)

Tasks & Responsibilities

We are looking for a Business Analyst located at Kaiseraugst to work for PT Informatics, the Informatics supporting Pharma Global Technical Operations. The Business Analyst will support the Enterprise Recipe Management project.

  • Performs typical Business Analysis activities and creates deliverables as per company standards within a squad / project like URS / User Stories, Functional Specifications / Acceptance Criteria as well as contributing to other project documents such as Business Cases and Project Charters
  • Main contact and escalation point for the sites to the project
  • Work closely with Site Implementation Leads to understand the needs of each of the sites in scope
  • Accountable to highlight site specific risks, assumptions, issues and dependencies (specifically such with local processes / systems) to the Rollout Squad Lead
  • Together with Site Implementation Leads ensures the template rollout approach is adopted and adjusted to match local needs
  • Supports Rollout Lead in improving the template rollout approach, as well as identifying and sharing lessons-learnt and best practices between site implementations
  • Help identifying equipment and substance master data required for site
  • Analyze and (together with OCM expert) address required business process changes; keep track that these changes indeed get implemented
  • Facilitate (virtual) workshops with teams on site to identify and address the process changes
  • Support sites in adapting to a standardized manufacturing process and nomenclature
  • Help to identify workarounds / where possible processes changes to mitigate gaps in the application
  • Support Site Implementation Lead or present themselves to senior leaders and line managers to get them to buy into our goals and support us in introducing the change to their teams
  • Work closely with Rollout Squad Lead for the rollout planning and ensuring that administrative tasks related to the go-live get carried out (e.g. collection of user lists, coordination of training slots etc.)

Must Haves

We are looking for a candidate who has min. 5 years of experience in Manufacturing in a pharmaceutical environment with GMP experience. In addition the candidate should have worked as Business Analyst previously for at least 2-3 years.

  • Min. Bachelor degree in Computer Science or any related area or equivalent work experience
  • Min. 3-5 years of experience in IT or OT related to the pharmaceutical environment (GxP compliant area) working as a Business Analyst
  • Min. 5-7 years of experience manufacturing of drug substances and ideally drug products
  • Experience with MES, LIMS and related ISA95 production systems
  • Business analysis and business process modelling experience
  • Fluent in English (written and spoken)
  • Experience working in a global, virtual team with people across all management levels
  • Excellent communication skills
  • Facilitation of (virtual) workshops

Nice to Haves

  • Organizational Change Management experience is a plus
  • Fluent in German (written and spoken)
  • ISA S88 / S95 knowledge
  • Experience with global / multi-site manufacturing projects
  • internal project methodology

Did we catch your interest?

The SimplyVision-Team is looking forward to receive your application (Word file is highly appreciated).

Kindly be informed that our customer is located in Switzerland. Therefore only applications from candidates within the EU or candidates holding Swiss work permission are required.

Preferred Interview Dates

  • asap after halting date

Tagged as: change management, GxP, LIMS, MES, process modelling

Files must be less than 5 MB.
Allowed file types: txt rtf pdf doc docx.
If not - no problem - we'll organize one.
More optional Information about your way of finding us
You agree that your data will be used to process your request. Further information and revocation instructions can be found in the privacy policy.


You can apply to this job and others using your online resume. Click the link below to submit your online resume and email your application to this employer.

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