About Us
Inova is a premier pharmaceutical consulting firm based in Switzerland, known for delivering cutting-edge solutions in the pharma industry. Our team of experts specializes in guiding pharma companies through complex regulatory landscapes and ensuring the highest standards of product quality and safety.
Job Description
The Quality Control Specialist at Inova plays a key role in overseeing laboratory operations, ensuring compliance with regulatory standards, and driving continuous improvement initiatives. This position focuses on maintaining and enhancing quality processes while collaborating with cross-functional teams to ensure optimal product control and operational efficiency.
Key Responsibilities
* Laboratory Oversight: Lead laboratory activities, ensuring compliance with GMP standards and national/international regulations. Serve as the subject matter expert (SME) for analytical methods and laboratory equipment.
* Process Improvement: Proactively identify and implement process enhancements in alignment with business needs. Drive operational excellence in laboratory functions, from troubleshooting to the introduction of new methods and equipment.
* Compliance and Quality Management: Ensure the laboratory is inspection-ready and compliant with quality standards. Oversee product-related deviations, CAPAs, and change control processes.
* Technical Support: Provide analytical support and manage equipment, including software administration and method development. Actively contribute to internal projects and cross-functional teams.
* takeholder Collaboration: Work closely with internal/external stakeholders to streamline processes and resolve issues. Maintain strong relationships with global and local quality teams to ensure alignment with strategic goals.
* Continuous Improvement: Drive initiatives focused on cost, time, quality, and safety improvements. Lead projects aimed at enhancing laboratory processes and product quality reviews.
Qualifications
* Bachelor’s or Master’s degree in Biochemistry, Chemistry, or a related field.
* 5+ years of experience in a quality control laboratory environment, preferably in the pharmaceutical or biotech industries.
* Expertise in analytical techniques such as HPLC, UPLC, Elisa, and microbiological assays.
* Strong knowledge of GMP regulations and quality management systems.
* Experience leading process improvements and handling deviations, CAPAs, and inspections.
* Proficiency in English; additional knowledge of French or German is a plus.
* Strong problem-solving skills, with the ability to lead projects and manage multiple tasks efficiently.
We Offer
* A competitive salary and benefits package.
* Opportunities for professional growth and development.
* A collaborative and inclusive work environment.
* Participation in cutting-edge projects in the pharma industry.
How to Apply
Interested candidates are invited to submit their CV using this form. Please include references and any relevant project details in your application.
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