Job Description

• Monitors equipment/instrument operating practices and conditions to minimize equipment down time, lower maintenance costs, reduce time to run project and repeat of work
• Monitors quality of the QC analysts and optimizes efficiency of the work
• Provides technical support including method transfer, suitability, and verification stability
• Provides troubleshooting support as needed
• Oversees execution of analytical testing including routine analysis, method transfer, or method verification as needed
• Ensures adherence to department, internal SOPs and other regulatory requirements
• Conducts OOT and OOS investigations with the QA dept
• Effectively communicates with clients and internal groups
• Participates in Quality audits as requested.
• Responsible for the selection, training and development, coaching/mentoring, engagement, retention and performance management of a high performing team to meet the current and evolving needs of the company

Requirements

•  Bachelor’s degree (Chemistry) required
• 5+ years of related pharmaceutical laboratory experience in a cGMP environment required
• 2+ years of supervisory experience required
• Prior experience in method development/validation and/or transfer/verification, protocols, and troubleshooting required
• Fluency in English language written and oral

The Company offers a challenging European environment with constant upgrade and competitive salary depending on candidate’s qualifications. In addition, a private health insurance coverage is provided.