QA Manufacturing Lead, Visp e/v/e/r/y/o/n/e
Department: Quality Assurance
Employment Type: Permanent employee
Schedule: Full-time
Seniority: Experienced
Location: Visp
ten23 health is a human-centric and sustainable strategic partner of choice for the pharmaceutical industry and biotech start-ups for the development, manufacture, and testing of tomorrow’s medicines. We support our clients in developing differentiated, stable, usable, and safe injectable treatments for patients.We are looking for a dedicated QA Manufacturing Lead to be our quality champion on the manufacturing shop floor. In this role, you will play a critical part in maintaining Good Manufacturing Practices (GMPs), ensuring that every product meets our rigorous quality standards.Your responsibilites will include,
1. Real-Time Shop Floor Oversight
- Perform on-the-floor quality assurance support during manufacturing, cleaning, and environmental monitoring operations.
- Monitor adherence to GMP practices during critical manufacturing steps (e.g., line clearance, material dispensing, equipment setup).
- Witness and verify critical process steps, in-process controls (IPCs), and reconciliations.
- Perform and document line clearances before manufacturing operations.
- Review manufacturing processes in real time for compliance with approved batch records and SOPs.
- Ensure proper material handling, labeling, and segregation during production.
- Identify and report deviations or abnormal events on the shop floor.
- Support or lead immediate impact assessment and documentation of on-the-floor deviations.
- Ensure timely escalation and coordination with QA and production leadership for resolution.
- Review completed batch manufacturing records for accuracy, completeness, and compliance.
- Ensure timely corrections to documentation issues and assist operators in proper GMP documentation practices.
- Verify logbooks, equipment use records, and cleaning records on the shop floor.
- Observe and assess interventions during aseptic operations for compliance with aseptic technique and contamination control.
- Support environmental monitoring activities, gowning practices, and cleanroom behavior compliance.
- Conduct routine walkthroughs and spot checks to assess compliance with housekeeping, gowning, and other GMP standards.
- Participate in internal audits and regulatory inspections as needed, providing on-the-floor knowledge and documentation.
- Provide on-the-job coaching and GMP guidance to operators and technicians.
- Reinforce good documentation practices (GDP) and quality culture.
- Provide input into root cause analysis based on first-hand observations.
- Support implementation and follow-up of corrective and preventive actions directly related to shop floor findings.
- A strong background in quality assurance within a pharmaceutical or regulated manufacturing environment, with a solid understanding of GMP (Good Manufacturing Practices).
- Good understanding of aseptic process and its core requirements
- Excellent communication and coaching skills to effectively guide production teams and reinforce a culture of quality.
- The ability to make sound decisions and manage deviations in a fast-paced setting.
- A collaborative spirit and a genuine passion for ensuring compliance and product integrity.
We offer a dynamic environment where you can contribute meaningfully, collaborate with exceptional minds, and unlock your full potential.
Here's what sets ten23 apart:
- A valuable and impactful career development opportunity in an inspiring environment
- Flexible working arrangements and environment with an open culture and diverse workforce
- The opportunity to work with and learn from highly qualified and experienced employees
- Our learning and self-developing culture offers a wide range of training options
- Competitive pension fund plan, annual bonus, and other financial and non-financial benefit
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