{"id":5990,"date":"2026-05-08T12:58:01","date_gmt":"2026-05-08T10:58:01","guid":{"rendered":"https:\/\/www.itcag.com\/de\/jobs\/quality-control-project-lead-8052\/"},"modified":"2026-05-08T12:58:01","modified_gmt":"2026-05-08T10:58:01","slug":"quality-control-project-lead-5990","status":"publish","type":"wpbb_job","link":"https:\/\/www.itcag.com\/de\/jobs\/quality-control-project-lead-5990\/","title":{"rendered":"Quality Control Project Lead"},"content":{"rendered":"

Quality Control Project Lead Laboratory Technician \/GMP \/ cGMP\/ Quality Control \/ Analytical Chemistry\/ LIMS \/ English<\/strong><\/p>\n

Project: <\/strong>
For our customer a big pharmaceutical company in Basel we are looking for a highly qualified
Quality Control Project Lead<\/p>\n

Background:<\/strong>
Global Technical Development (PTD) is an organization of over two thousand people globally that are integral for the mission of Roche to develop meaningful medicines for patients. Therefore, PTD actively collaborates and develops creative technical solutions to bridge early- stage, late-stage and commercial product needs. The mandate of the group is to reliably deliver the pipeline and supply quality products to patients. The group excels in its work through innovation, teamwork, dedication, and mutual respect and contributes every single day, continuously improving what it does. Synthetic Molecules Technical Development (PTDC) brings a broad range of experience across drug substance (DS), drug product (DP), analytical sciences and Manufacturing Science & Technology (MS&T), and collaborates closely with key partners in the departments Research and Early Development (pRED \/ gRED), Small and Large Molecules (PTC, PTB), PTD and MS&T across our manufacturing network. This position on offer is located in Analytical Development Synthetic Molecules within Pharma Technical Development.<\/p>\n

Analytical Development is responsible for the development of resource and cost efficient analytical methods for all materials used during drug manufacturing using state of the art methodologies such as e.g. High-performance liquid chromatography (HPLC), Gas Chromatography (GC), Ion Chromatography (IC), Mass Spectrometry (MS), and others. The ultimate goal of our work is a robust control strategy to release
pharmaceutical products for clinical trials, and finally for commercial supply. The QC-Section within the Analytical Development Department is responsible for the Release of Materials based on the GMP compliant execution of Analyses of Inprocess controls, raw materials, intermediates, APIs and Drug products.<\/p>\n

The Perfect Candidate:<\/strong>
The perfect candidate has a Master’s degree (or higher) in Organic Chemistry, Analytical Chemistry, or Pharmacy, at least 3 years of professional experience in Quality Control, and very good GMP knowledge.<\/p>\n

Tasks & Responsibilities: <\/strong>
* Work in a modern quality control organization in compliance with cGMP regulations.
* Cooperation with internal and\/or external partners of Analytical Development
* Active participation in shaping the working methods of the analytical group
* Comprehensive analytical support for supply plants for API and drug product for clinical use
* Critical evaluation of own work results
* Support the analytical group by fulfilling cross-laboratory tasks and project tasks (e.g.reference standard management, CSV business process owner of analytical applications)
* Implementing and fully complying with relevant Roche policies, procedures, and standards in the areas of safety, health, and environmental protection
* Ensuring that laboratory employees are informed of all relevant SHE requirements and their implementation
* Ensuring an appropriate GMP standard in the laboratory
* Scientific and regulatory documentation of the work done<\/p>\n

Must Haves: <\/strong>
* Bachelor’s or Master’s degree in Natural Sciences OR a Laboratory Technician with 10+ years of high-level GMP experience
* 3-5 years of professional industry experience with a core focus on Analytical Chemistry
* Practical experience working under cGMP regulations is required
* Proficiency in laboratory-specific software (e.g., Waters Empower, Metrohm Tiamo, or Labware LIMS)
* English (Fluent\/Mandatory). German language skills are considered a significant advantage<\/p>\n

Nice to haves: <\/strong>
* Roche Experience
* Experience in roles such as Lab Head, Analytical Project Manager, or equivalent.<\/p>\n

Reference Nr.: 924939SDA<\/strong>
Role: Quality Control Project Lead<\/strong>
Industrie: Medical<\/strong>
Workplace: Basel <\/strong>
Pensum: 100%<\/strong>
Start: ASAP(01.08.20260<\/strong>
Duration : 12 months<\/strong>
Deadline :18.05.2026<\/strong><\/p>\n

If you are interested in this position, please send us your complete dossier. If this position does not fit your profile and you wish to be considered for another position directly, you can also send us your dossier via this ad or to jobs[at]itcag[dot]com.
Contact us for more information about our company, our positions or our attractive Payroll-Only programme: +41 41 760 77 01.<\/p>\n

About us: ITech Consult is an ISO 9001:2015 certified Swiss company with offices in Germany and Ireland. ITech Consult specialises in the placement of highly qualified candidates for recruitment in the fields of IT, Life Science & Engineering.
We offer staff leasing & payroll services. For our candidates this is free of charge, also for Payroll we do not charge you any additional fees.<\/p>\n

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