Senior QC Professional
Novo Nordisk
Are you driven by taking responsibility, setting direction, and ensuring high standards in Quality Control (QC) for both new and existing products? Do you have a passion for chemical analysis and a desire to lead the transformation of processes toward increased automation, digitalization, and optimization while maintaining a high level of compliance?If so, you could be the experienced QC Professional we are looking for. Apply now for a life-changing career!The position
As a Senior QC Professional, you will work in close collaboration with the QC chemists, laboratory technicians and QC Area Specialist to ensure that the analytical performance and equipment live up to industry standards, GMP and regulatory requirements (ICH guidelines, pharmacopeia, etc.)Your responsibilities will include:Serving as the method responsible chemist, ensuring alignment between product requirements and QC analyses.Approving and supporting delivery of analytical results within lead time, while supporting documentation preparation for customers and authorities.Leading the transfer and implementation of new analytical methods as well as new digital and automated solutions in current processes.Driving continuous improvement and optimization of processes, including systematic problem solving (SPS).Collaborating with stakeholders across the organization, participating in projects and facilitating audits and inspections.Working within GMP requirements, managing Change Requests, updating SOPs, and handling deviations, including OOS/OOT/OOE incidents, are integral aspects of the role.Qualifications
To succeed in this role, you have:A scientific academic degree such as cand. pharm., cand. scient., chemical engineer or similar; a Ph.D. in a relevant area could be an advantage.Experience from a GMP-regulated laboratory.Working experience as an analytical chemist with techniques such as HPLC, GC, titration and Spectrophotometer.Relevant LEAN experience from a comparable position or education, combined with a natural eye for upscaling work processes and reduce waste is an advantage.Strong communication skills and professionally proficient in both written and spoken Danish and English.Moreover, it will be considered an advantage if you have scientific experience within analytical work, impurity profiles and validation of QC methods.On a personal level, you are a team player with a solution-oriented mindset and a positive attitude. You bring strong analytical skills while maintaining a broad perspective. You thrive in a dynamic, collaborative environment with frequent interaction both within and outside the team. Meeting deadlines is important to you, and you excel at doing so. We value candidates who embrace change and proactively suggest new solutions, processes, and improvements. You are adaptable in a fast-paced setting where priorities can shift quickly. A good sense of humor and a strong drive for success are highly appreciated in our team culture.About the department
The QC department in AMSAT QC consists of 75 employees divided into 4 teams. You will be joining a team of 20 highly professional and motivated chemists, laboratory technicians, an operator, a student assistant and a GMP Coordinator. We perform a wide range of chemical drug product analysis, as well as mechanical injection tests on insulin pens. We work with many stakeholders across the organization and have a broad interface with other QC areas in Novo Nordisk.
Hillerød, Hovedstaden
Tue, 20 Aug 2024 22:24:25 GMT
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