Senior Quality Specialist (100%)
Quick Summary
Quality Ownership & Purpose: You ensure robust quality control and quality assurance for sorbent materials and related QC processes in a dynamic scale‑up environment, delivering compliant, inspection‑ready outcomes and reliable product decisions within the QC scope.
Quality Ownership & Purpose: You ensure robust quality control and quality assurance for sorbent materials and related QC processes in a dynamic scale‑up environment, delivering compliant, inspection‑ready outcomes and reliable product decisions within the QC scope.
Quality Control Execution: You plan and coordinate QC campaigns for sorbents and related materials, and you oversee measurements to meet workload and timelines. You review and approve QC data within defined QC specifications and testing standards and maintain inspection‑ready documentation and records in SAP QM and linked systems.
Quality Assurance Ownership: You manage deviations and change controls arising from QC activities and QC‑owned processes, ensuring accurate root‑cause analysis with preventive actions. You are responsible for method validation activities, ensuring accuracy and timely execution, and you prepare/support audits on QC topics, including supplier‑related evidence and follow‑ups.
QC Process Improvement & Risk Management: You identify bottlenecks across QC processes and documentation as well as data handling, release workflows and handoffs, apply risk‑based thinking to propose and implement lean improvements that reduce rework, cycle time and compliance risk, and contribute to the implementation and maintenance of LIMS and SAP QM.
Interfaces & Collaboration: You act as the QC technical interface to suppliers and manufacturers, support Procurement with commercial and contractual topics, and support the Product Owner on applications and operations discussions while aligning timelines and QC deliverables with plant requirements.
Decision Rights: You decide on QC record content quality and investigation strategy to ensure compliance with SOPs and QC standards. You recommend corrective and preventive actions (CAPA) and risk mitigations to approvers, as well as QC metrics and reporting routines aligned with the Product Owner and Operations, and escalate issues that could affect product quality, compliance, or delivery timing to the line manager.
Location & Eligibility
Listing Details
- First seen
- May 5, 2026
- Last seen
- May 7, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 51%
- Scored at
- May 6, 2026
Signal breakdown
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