You will oversee QC testing and support laboratory operations, ensuring compliance with GMP standards while managing projects and training staff. Your role includes investigating issues and implementing improvements to enhance quality and efficiency.
Anforderungen
- •Chemistry technician CFC or equivalent
- •Minimum 6 years’ experience
- •Proven process understanding
- •Continuous improvement experience
- •Safety, Quality, Result and Customer oriented
- •Basic speaker (A2) English level
- •Strong Team spirit
- •Leadership skills
- •Open minded and flexible
Deine Aufgaben
- •Perform end-to-end QC testing from reception to release.
- •Provide technical support to the laboratory manager.
- •Assist in achieving targeted objectives like planning adherence.
- •Investigate and manage laboratory deviations and CAPA.
- •Lead investigations into technical issues in the laboratory.
- •Manage analytical projects effectively.
- •Train technicians in QC analysis procedures.
- •Escalate issues to QC Managers as needed.
- •Suggest and implement continuous improvement actions.
- •Master and resolve analytical problems.
- •Act as subject matter expert for equipment.
- •Create SOPs and documentation for QC laboratories.
- •Ensure compliance with GMP standards and regulations.
- •Apply HSE rules in laboratory operations.
Original Beschreibung
# Raw Material Senior Analyst
**Switzerland - Nyon** | **Full time**
**Job Purpose:**
Perform all QC testing end to end, from reception to final disposition before release on time by appropriate methods while respecting Good Manufacturing Practices. Support resolution of technical issues in the laboratory. First contact in case of analytical issue in the laboratory.
**Key responsibilities:**
* Perform all QC testing end to end, from reception to release, including management of external testing.
* Technical back-up of the laboratory manager
* Be a support to reach objectives targeted such as planning adherence.
* Provide direct support to Investigate and Manage Laboratories, Deviations & CAPA and the resolution of technical issues in the laboratory. Act as Lead Investigator.
* Take in charge analytical projects
* Train other technicians to the QC analysis
* Escalates problems effectively to QC Managers
* Suggest and implement Continuous Improvement actions in accordance with site objectives: EHS, Quality and cost.
* Master the analytic problems
* Equipment SME
* Create SOPs and working documentation needed for QC laboratories
* Respect all GMP standards. GMP knowledge and experience to support the requirements expected by Swissmedic, European union agencies and other regulatory bodies to assure that our products meet all cGMP requirements together with our operations and documentation system.
* Know and apply HSE rules of Haleon
**Knowledge/Education Required:**
* Chemistry technician CFC or equivalent
* Minimum 6 years’ experience in a Pharmaceutical Environment.
* Proven process understanding (Pharma, GMP, investigation and method development)
* Continuous improvement experience (Lean, 5S, Problem Solving).
* Safety, Quality, Result and Customer oriented
* Basic speaker (A2) English level
* Strong Team spirit. Demonstrate exemplarity behaviours.
* Leadership skills
* Open minded and flexible
Haleon is an Equal Opportunity Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
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