Drug Product Expert
il y a 3 semaines
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Looking for skilled professionals within Life Sciences | Talent Acquisition Specialist at Jefferson WellsDrug Product Expert
Your responsibilities?
- Senior expert in clinical DP development accountable for leading and running assigned project work packages, ranging from clinical formulation orientation work for FIH study up to commercial registration and launch for the development pipeline and as part of the life cycle management of commercial brands.
- Contribute to project sub-team (DS, DP or analytical) as senior SME representing own area of expertise and actively contributing to the elaboration of project strategy.
- To drive development (internal or external) of innovative formulations and manufacturing processes for the supply of bulk clinical trial material for development pipeline projects.
- To identify scientifically the best formulation and process for accelerated, standard and enabling clinical formulations by designing, planning, performing, interpreting and reporting results of experiments in time to influence strategic project decisions and recommend next steps.
- To ensure process robustness, validation and transfer of NCEs and Lifecycle management of mature product manufacturing process and technologies to commercial launch site.
- To perform clinical formulation orientation work in collaboration with Non-Clinical Formulation Lead to transition the project from Product Material Orientation (PMO) team to DP dev. team.
- Manage CLO/CRO/CMO activities, including selection, negotiation and implementation of appropriate agreements in cooperation with Outsourcing representative.
- Contribute to setting and delivering departmental goals & priorities.
- Subject matter expert and trusted partner in a specific area of DS, DP or Analytical function working according to appropriate standards for quality (GMP, GSP and GLP), ethics, health, safety, environment, protection and IT; leading functional initiatives to ensure continuous improvement.
- Contribute to DS, DP or Analytical project sub-team to the elaborate project DS, DP or analytical strategies by proactively sharing plans, information, data and conclusions and taking full responsibility for all designated tasks associated with own area of expertise.
- Autonomously coordinate and manage technical activities for assigned work packages internally and/or externally to required quality, timeline and budget eg. DS/DP clinical campaigns, DS & DP process optimization, analytical method development & validation, stability program, route evaluation, form selection, material characterization, …
- Design experiments/trials and studies in accordance with Operating Model to support projects DS, DP or analytical development in an autonomous manner.
- Evaluate and interpret data with different degree of complexity, draw relevant conclusions; openly collaborate with laboratory technicians and scientists to deliver activities for assigned work package; perform complex tasks without having established procedures.
- Work according to appropriate standards following the principles of Quality by Design (QbD).
- Autonomously write high quality source documents including experiment plans, protocols and reports according to data integrity requirements to enable regulatory filing. Support department with the review of protocols and reports from other SMEs.
- Lead the transfer of know how to other departments or external contractors, including troubleshooting and on-site training.
- Champion the use of the operating model to ensure the right experiments/work packages are executed at the right time fully utilizing the strategy/guideline documents that will be embedded in the operating model. Leading implementation of the “how of the operating model”.
- Closely collaborate with other SMEs within PS, our client community across functions and organizations to ensure delivery of cross-functional technical activities to quality time and to develop patient centric solutions.
- Support DS, DP or analytical PL with by providing resource and timelines for specific activities
- Uses technical and regulatory knowledge to anticipate HA expectations and identify risks
- Proactively communicate risks and deviations from forecasted plans to DS, DP or analytical PL and sub-team members.
- Take an active role for area of expertise in audits and interactions with Health Authorities and inspection as required.
- Collaborate, support and provide scientific mentoring/coaching for laboratory scientists and less experienced SMEs in execution of experimental work.
- Contribute to departmental goals & priorities in a collaborative manner using knowledge of our client’s organizational systems and structures.
- Contributes to setting the sciences and technology strategy direction of the department as it relates to own area of expertise.
- Maintain an up-to-date knowledge of own area of expertise to be recognized as a technical expert within own function and across PS
- To develop proactively creative and efficient solutions for IP protection of Drug Product and manufacturing processes.
- As an expert contribute to scientific publications, present at conferences and represent area of expertise on industry boards and through academic collaborations.
Your profile?
- You have a Scientific Master’s degree (Ph.D is an asset)
- You are fluent in English and French
- Use scientific expertise to design technical experiments independently/autonomously in order to resolve complex problems
- Problem solving mindset and proven ability to critically interpret results, build new experimental hypotheses, and take calculated risks and smart decisions. Coaches and encourages team members to adopt risk-based approach to own activities.
- Demonstrated ability to collaborate effectively across teams within and beyond own department
- Proactive, self-motivated and independent working style and able to manage own activities independently/autonomously to drive smart decisions
- Significant project management abilities needed to coordinate/manage activities internally/externally and to forecast resources and timelines
- Proven and recognized technical expertise in a specific area of DS, DP or analytical development
- Show interest in learning about area outside own expertise, projects, platforms, technologies and regulations to influence own work and department
- Up to date knowledge of GMP and regulatory requirements within area of expertise.
- Excellent communication and presentation skills with the ability to convey information in a clear and concise manner to write clear instructions, protocol and reports
Our offer?
Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way. You’re interested in this job? We kindly invite you to apply or send me your CV, lena.palmeri@jeffersonwells.be
Seniority level- Associate
- Full-time
- Science
- Industries: Pharmaceutical Manufacturing
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