Material Planning Analyst (Senior) job in Solothurn, Switzerland

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First Name*

Last Name*

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Phone Number*

Country*

Are you an employer or a jobseeker?*

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First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

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Are you an employer or a jobseeker?*

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Job type: Contract

Discipline: Good Manufacturing Practice (GMP)

Location: Switzerland

This vacancy has now expired. Please see similar roles below...

Proclinical is seeking a dedicated Materials Planning Specialist to support manufacturing planning for clinical and commercial programs. You will collaborate with various departments to resolve raw material issues, manage inventory levels, and ensure smooth delivery processes. Your role will involve lifecycle management of Master Data and ensuring efficient data flow in production planning and manufacturing systems.

Responsibilities:

Plan and control raw materials inventory, including demand forecasting, safety stock management, and expiry reporting.
Revise and maintain Standard Operating Procedures (SOPs), Bills of Materials (BOMs), and other production-related documents.
Support new item creation and Master Data enrichment.
Review vendor change notifications and facilitate cross-functional discussions to manage inventory impacts.
Assist in tech transfers and maintain manufacturing bills of materials.
Analyze data for quarterly expired and obsolete reports and discuss findings with the planning team.
Participate in site leadership meetings and escalate issues as needed.
Perform additional duties as required by business needs.

Key Skills and Requirements:

Bachelor's degree in Chemical/Biochemical Engineering, Supply Chain Management, or related field, or equivalent experience.
Experience in supply chain management within a GMP-regulated industry.
Strong analytical skills and ability to drive process improvements.
Proficient in communication across departments and management.
Knowledge of manufacturing systems such as Oracle, Trackwise, and others.
Understanding of QA and cGMP principles.
Technical writing skills and proficiency in Microsoft Office.

If you are having difficulty in applying or if you have any questions, please contact Ashley Bennett at a.bennett@proclinical.com.

Apply Now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

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