Reckitt
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R&D PDM Senior Associate
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Reckitt We are Reckitt, home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. Research & Development: We're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. About The Role We are seeking a high-calibre individual with the necessary skill set to lead a team of scientists working on a cross-functional platform of projects spanning in-market R&D activities, regulatory technical support, troubleshooting and margin improvement programmes. Your responsibilities Acting as Subject Matter Expert (SME) for the end-to-end technology transfer of multiple OTC and VMS products, in partnership with Technical/Supply Ensuring Critical Process Parameters (CPP’s) and Critical Quality Attributes (CQA’s) are considered during early-stage technology transfer (TT1/2), providing input on supply equipment ordering, facility start-up and process transfer risk assessments Leading and managing a team of scientists to execute R&D laboratory start-up, maintenance and analytical method transfer activities, working in close partnership with R&D counterpart, QC and QA Establishing and overseeing the Wilson stability program to support technology transfer and commercialization of multiple OTC and VMS products, in partnership with QC/Supply Responsible for all R&D technical activities in the compliance programme under your remit, working closely with the technical project manager to ensure tasks are completed by you and your team on time to meet the transfer schedule Accountable for the delivery and execution of project work of your team Accountable for the KPIs / delivery of project milestones of your team Responsible for the development of your direct line reports Collaborate with cross-functional teams including Technical, Manufacturing, Quality, Regulatory, Procurement to ensure seamless product technology transfers into the Wilson site Foster a culture of safety, quality, and continuous improvement with the team Ensure all activities comply with relevant regulatory standards (e.g. FDA, cGMP) Can be counted on to consistently deliver performance targets An engaged and high performing individual, with the ability to motivate and develop their team Healthy, working relationship between cross-functional business partners The experience we're looking for Bachelor's degree in relevant scientific discipline (e.g. Chemistry, Pharmaceutical Science, Chemical Engineering, Biology, Biochemistry) Post graduate qualifications in further scientific disciplines would also be beneficial (i.e. PhD, or MSc, post-graduate diplomas (e.g. Pharmaceutical Quality by Design) The skills for success Required: Five+ years of related formulation and technology transfer experience in a regulated or technical industry (e.g. pharmaceuticals, manufacturing, healthcare) Experience leading or supporting technology transfer from R&D to manufacturing or site-to-site transfer projects Experience working with oral solid dosage (OSD) and liquid products (preferably OTC and/or VMS products) Strong knowledge of analytical testing equipment, techniques and method transfer requirements (proven experience strongly preferred) Proven experience in managing scientific teams and cross-functional projects Proficient in risk management processes and tools (e.g, FMEA) Proven ability to identify, assess and mitigate technical and regulatory risks Excellent project management, communication and leadership skills Ability to problem solve under pressure Strong technical writing skills Must be familiar with Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP), as well as FDA and ICH guidelines Proficient in Microsoft Project, Word, Excel and PowerPoint Preferred: Experience with laboratory start-up projects Experience with stability programs; including designing and managing stability studies per ICH guidelines Experience with data visualization tools (e.g., Power BI) Knowledge of Quality by Design (QbD) and Design of Experiment (DoE) What we offer With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. Salary ranges: USD $102,000.00 - $152,000.00 We recognize that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you.
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R&D PDM Senior Associate
role at
Reckitt We are Reckitt, home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. Research & Development: We're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. About The Role We are seeking a high-calibre individual with the necessary skill set to lead a team of scientists working on a cross-functional platform of projects spanning in-market R&D activities, regulatory technical support, troubleshooting and margin improvement programmes. Your responsibilities Acting as Subject Matter Expert (SME) for the end-to-end technology transfer of multiple OTC and VMS products, in partnership with Technical/Supply Ensuring Critical Process Parameters (CPP’s) and Critical Quality Attributes (CQA’s) are considered during early-stage technology transfer (TT1/2), providing input on supply equipment ordering, facility start-up and process transfer risk assessments Leading and managing a team of scientists to execute R&D laboratory start-up, maintenance and analytical method transfer activities, working in close partnership with R&D counterpart, QC and QA Establishing and overseeing the Wilson stability program to support technology transfer and commercialization of multiple OTC and VMS products, in partnership with QC/Supply Responsible for all R&D technical activities in the compliance programme under your remit, working closely with the technical project manager to ensure tasks are completed by you and your team on time to meet the transfer schedule Accountable for the delivery and execution of project work of your team Accountable for the KPIs / delivery of project milestones of your team Responsible for the development of your direct line reports Collaborate with cross-functional teams including Technical, Manufacturing, Quality, Regulatory, Procurement to ensure seamless product technology transfers into the Wilson site Foster a culture of safety, quality, and continuous improvement with the team Ensure all activities comply with relevant regulatory standards (e.g. FDA, cGMP) Can be counted on to consistently deliver performance targets An engaged and high performing individual, with the ability to motivate and develop their team Healthy, working relationship between cross-functional business partners The experience we're looking for Bachelor's degree in relevant scientific discipline (e.g. Chemistry, Pharmaceutical Science, Chemical Engineering, Biology, Biochemistry) Post graduate qualifications in further scientific disciplines would also be beneficial (i.e. PhD, or MSc, post-graduate diplomas (e.g. Pharmaceutical Quality by Design) The skills for success Required: Five+ years of related formulation and technology transfer experience in a regulated or technical industry (e.g. pharmaceuticals, manufacturing, healthcare) Experience leading or supporting technology transfer from R&D to manufacturing or site-to-site transfer projects Experience working with oral solid dosage (OSD) and liquid products (preferably OTC and/or VMS products) Strong knowledge of analytical testing equipment, techniques and method transfer requirements (proven experience strongly preferred) Proven experience in managing scientific teams and cross-functional projects Proficient in risk management processes and tools (e.g, FMEA) Proven ability to identify, assess and mitigate technical and regulatory risks Excellent project management, communication and leadership skills Ability to problem solve under pressure Strong technical writing skills Must be familiar with Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP), as well as FDA and ICH guidelines Proficient in Microsoft Project, Word, Excel and PowerPoint Preferred: Experience with laboratory start-up projects Experience with stability programs; including designing and managing stability studies per ICH guidelines Experience with data visualization tools (e.g., Power BI) Knowledge of Quality by Design (QbD) and Design of Experiment (DoE) What we offer With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. Salary ranges: USD $102,000.00 - $152,000.00 We recognize that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you.
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