Quality Control Specialist – Pharma & Biotech

Overview

Quality Control Specialist – Pharma & Biotech at Inova. Inova is a premier pharmaceutical consulting firm based in Switzerland, known for delivering cutting-edge solutions in the pharma industry. Our team specializes in guiding pharma companies through regulatory landscapes and ensuring the highest standards of product quality and safety. 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. Stakeholder 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 the provided form. Please include references and any relevant project details in your application. Job Category:

QC Job Type:

Full Time Job Location:

Romandie Seniority level

Mid-Senior level Employment type

Full-time Job function

Quality Assurance Industries Pharmaceutical Manufacturing

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