12 jobs found

General ManagerSolliciterenremote type: On-sitelocations: London, GBRtime type: Full timeposted on: Vandaag geplaatstjob requisition id: REQ523270 JLL empowers you to shape a brighter way .Our people at JLL are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients. We are committed to hiring the best, most talented people and empowering them to thrive, grow meaningful careers and to find a place where they belong. Whether you've got deep experience in commercial real estate, skilled trades or technology, or you're looking to apply your relevant experience to a new industry, join our team as we help shape a brighter way forward. General Manager Reporting into: Senior Facilities Manager (SFM),but will in many circumstances work closely with and take direction from OPLM. Direct Reports: Head of Engineering & Head of Operations Division: Property Management The Asset In 2019 the development of 20/22 Ropemaker Street in the City of London commenced with practical completion expected in Autumn 2023.The development comprises c. 425,000 sq ft, of grade A office, retail and SME space and is arranged over 27 storeys. This BREEAM 'outstanding' development will create a sustainable workspace of the highest standard including a stepped form that will create a series of extensive roof terraces to provide the occupiers with access to outside areas.Approximately 300,000 sq. ft of this development has been pre-let to Linklaters LLP as their new global headquarters. will commence their fit out in April 2024. A very close working relationship with the Ropemaker Management Team and Linklaters is essential and there are specific management protocols agreed with Linklaters.The self-contained SME area (comprising 5 units) will be the responsibility of the General Manager (GM) and the Ropemaker Management Team to operate.The building is designed to target BREEAM Outstanding and WELL Platinum certifications. The development manager is CO RE, the main contractor is Skanska, the architect is MAKEAt completion it is currently anticipated that the 22 Ropemaker Management Team will comprise four core team with outline plans showing that two additional roles may well be added to the Team later. What this job involves: JLL are appointed as Property Manager by the building owner, Great Elm Assets Limited (Client) by way of a Property Management Agreement (PMA) and they report directly to the owner's asset management advisor, Old Park Lane Management Limited (OPLM) GM will work with the JLL Property & Asset Management Team (JLL PAM Team) to ensure the JLL PMA scope is delivered to the highest possible standard.The GM role will be based at the building and will have key responsibility for delivery of all landlord operations to ensure that these services accord with the best practice standards as defined.The GM will be JLL's and the building owners' 'ambassador' and must maintain and promote the property's service delivery and position in the locality as best in class for occupiers to work in. In addition to working alongside the JLL PAM Team, the GM will have a close working relationship with OPLM's Head of Property Management, as well as senior representatives of the building tenants. Team Structure Reporting to the JLL SFM, the GM has line management responsibilities for senior members of the on-site and account specific Ropemaker FM team (as identified in the paragraph below). The GM will also be invited to work in several "virtual teams" with the client focused teams of JLL PAM (although it is accepted that the GM's primary role is to execute the core responsibilities and deliverables outlined in this job description and these will always take precedent over any 'virtual team' role)As mentioned above it is currently anticipated that at completion of the development, the 22 Ropemaker Management Team will comprise four core team (including the GM) with outline plans showing that two additional roles may well be added to the Team later. The Head of Engineering and Head of Operations will report directly to the GM. What your day to day would look like: Client Service To understand the Client's objective and instructions in relation to the property. To assist in Client reporting concerning all on-site rational issues and customer relations. Act as lead for the Client in all matters relating to the operation at the property to establish and enhance brand image Customer Experience Establish and manage a property strategy with a view to providing a high standard of customer service that enhances the customer experience and develops a property partnership community. Regularly meet with the occupier representatives to fully understand their wants and needs within the property. Manage the on-site service partner teams to ensure optimal customer satisfaction and minimise the downtime when service interruption occurs. Liaise with the Client to undertake periodic customer feedback sessions and respond to occupier feedback with a view to achieving positive outcomes and consistent high levels of customer satisfaction Operations Management Working with the JLL Design for Management Team take a lead role in mobilisation of the building from construction to operational i.e. undertaking all mobilisation tasks from before completion to a 'business as usual' state (in accordance with the JLL Mobilisation Plan and Budget which will be agreed from time to time with OPLM) Build, lead, develop and inspire the on-site 22 Ropemaker Management Team (both directly employed and sub-contracted) to deliver high standards of service at the property. Working with the JLL PAM Team ensure the JLL PMA scope is delivered and all SLAs and KPIs are met such that service excellence is delivered throughout all areas of on-site operations. To be responsible for the implementation of agreed best practice in accordance with the JLL PMA and JLL's Facilities Management Best Practice policies in the following areas: service charge financial management, information/communications, procurement, operations, repair & maintenance, social & environmental responsible management, customer experience and human resources (training and development) ensuring: standard systems and procedures; customer service delivery standard systems and procedures standard documents and templates audit and inspection reduction of risk consistent high standards of service delivery (and their measurement) improved reporting to clients Inform the JLL PAM Team and Client of any occupier matters that may influence valuation/investment considerations including assistance in monitoring occupiers' compliance with covenants. In conjunction with the JLL PAM Team, ensure the financial management of the property, through the preparation of service charge budgets, the monitoring of agreed budgets to pre-defined cash limits, quarterly variance reporting and service charge reconciliation, is delivered to JLL accounting practices. To include the administration of non-recoverable budgets. To understand the principal terms of occupier leases as they affect the property management of the building and the Client's obligations to provide services including clarity on the extent of the common areas. Ensure that the procurement of all supplies and services at the property is undertaken in accordance with JLL's PMA and JLL's procurement policy to ensure the highest standards for the best value. Ensure high quality health and safety practices are maintained, in accordance with best practice guidelines from central support under the JLL's risk management programme and the RFM Ensure all aspects of the JLL PMA, Client's ESG requirements and JLL's 'Socially Responsible Management' programme is implemented in relation to environmental & sustainability policies. Be familiar with all heating, ventilating, mechanical and electrical equipment at the property and have a sound understanding of the purpose and general working of such equipment. Ensure maintenance contracts in place cover specification as defined within the O&M manual requirements and do not negate warranties/guarantees. Where required, work with appointed professional consultants Building Surveyors/Architects/Designers consultants as well as MEP, VT and Energy consultants.Sound like you? To apply you need to be/have: Role Requirements Excellent customer service skills and a track record of implementing successful customer orientated activities. Strong management experience gained within a high-profile Grade A commercial office environment Able to collaborate and partner where appropriate with the key stakeholders to deliver a high class environment reflective of the asset Able to represent the Client's and OPLM's, Great Elm Assets Limited's interests at meetings, events and within the Central London community Able to demonstrate a strong understanding of building design and base build management A proven track record in managing and motivating on-site operational management teams Experience of managing service charge budgets and major CAPEX projects Strong commercial acumen Strong commercial acumen and understanding of service charge management Strong leadership skills to build a team, effectively manage and motivate the team to achieve a high level of performance and to exceed targets Accountable and resilient Ability to work under pressure Demonstrate ability to support change related initiatives and to determine what expertise and resources are required to resolve problems quickly and efficiently. Ability to communicate at board room level and contribute to identification and evaluation of potential solutions to the problems based on the facts, assessment of risk and awareness of desired business objectives. Location: On-site -London . click apply for full job details

Principal Consultant in Product Lifecycle Management - Aerospace & Defence We believe in the power of ingenuity to build a positive human future. As strategies, technologies, and innovation collide, we create opportunity from complexity. Our teams of interdisciplinary experts combine innovative thinking and breakthrough technologies to progress further, faster. Our clients adapt and transform, and together we achieve enduring results. We are over 4,000 strategists, innovators, designers, consultants, digital experts, scientists, engineers, and technologists. And we have deep expertise in consumer and manufacturing, defence and security, energy and utilities, financial services, government and public services, health and life sciences, and transport. Our teams operate globally from offices across the UK, Ireland, US, Nordics, and Netherlands. PA. Bringing Ingenuity to Life. Hybrid working - our approach is to be in the office or on client site a minimum of 2-3 days per week. However, the actual time you spend and where you spend it will vary by role or assignment, including up to 5 days per week on a client site. Travel to client site will be necessary as and when the client requires Stuck in a rut, needing a new challenge? Our Systems Insights & Solutions team are looking for a Principal Consultant in Product Lifecycle Management (PLM) with experience in Aerospace & Defence or related discrete manufacturing industries. We believe that business value can be derived from PLM solutions when the correct application of end to end process thinking combines with enabling technology and the right transformation approach. As a Principal Consultant within Systems Insights and Solutions, you will take a leading role on projects that have a real impact on our clients' ability to deliver new products, delivering game changing solutions. This role will focus upon the delivery of PLM solutions supporting all phases of the product lifecycle, with primary focus on Digital Engineering: Product and Technology Portfolio Management Programme Delivery and Governance Multi Disciplinary Design and Optimisation Connected Verification and Certification Smart Manufacturing Optimised Sustainment and Availability We excel at working in complex environments to solve problems in collaboration with our clients. We often partner with vendors and other consultancies to bring the best team to address our clients' needs. Typical projects will include: Carrying out PLM diagnostic and development of business case Defining the business architecture / operating model, requirements and PLM solution blueprint Leading PLM Transformation initiatives Qualifications Essential qualifications and experience PLM Leadership: 10+ years of PLM experience, working with the major PLM vendors to design and deploy their solutions. Experience working with Siemens solutions will be an advantage. Technical Expertise: Deep hands on expertise in core PLM processes, such as BOM management, change/config, variant/options management, CAD/CAE integration, ALM/requirements trace, maintenance and through life support. Business acumen. Experience in shaping business cases and implementation roadmaps for investment in PLM solutions. Ability to hold executive level conversations to build alignment on a PLM transformation vision. Prior consulting experience. Ability to manage client stakeholders, and all aspects of the consulting engagement lifecycle. Desirable qualifications and experience: Degree in engineering or related subject. Standards & Frameworks: Proficiency in ISO/IEC/IEEE 15288, TOGAF, EIA 649, STEP/PLCS awareness, AS9145, ISO 9001/27001. Understanding of defence export control constraints. Industry Experience: Experience and knowledge of key working practices in Defence, or other discrete manufacturing industries. We know the skill gap and 'somewhat need to tick every box' can get in the way of meeting brilliant candidates, so please don't hesitate to apply - we'd love to hear from you. Apply today by completing our online application Please be aware that some of our UK roles at PA Consulting require a UK security clearance. All PA people are required to undergo background checks and to achieve the Baseline Personnel Security Standard however, some UK roles also require higher levels of National Security Vetting, where applicants must have at least 5 years of continuous residency in the UK. We therefore ask that you only apply if you meet the residency requirements (i.e. you are a British citizen or have been resident in the UK for the past 5 years), as this is the prerequisite for a security clearance. If you're unsure about your eligibility, we encourage you to review the UK Government's guidance on security vetting before applying. Additional information Life At PA encompasses our peoples' experience at PA. It's about how we enrich peoples' working lives by giving them access to unique people and growth opportunities and purpose led meaningful work. Our purpose guides how we work with our clients and our teams, and support our communities, to deliver insight and impact, solving the world's most complex challenges. We're focused on building a workplace that values human difference and diverse mindsets, and a culture of inclusion and equality that unlocks the potential in our people so everyone can be their best self. We are dedicated to supporting the physical, emotional, social and financial well being of our people. Check out some of our extensive benefits: Health and lifestyle perks accompanying private healthcare 25 days annual leave (plus a bonus half day on Christmas Eve) with the opportunity to buy 5 additional days Generous company pension scheme Opportunity to get involved with community and charity based initiatives Annual performance based bonus PA share ownership Tax efficient benefits (cycle to work, give as you earn) We're committed to advancing equality. We recruit, retain, reward and develop our people based solely on their abilities and contributions and without reference to their age, background, disability, genetic information, parental or family status, religion or belief, race, ethnicity, nationality, sex, sexual orientation, gender identity (or expression), political belief, veteran status, or any other range of human difference brought about by identity and experience. We welcome applications from underrepresented groups. Adjustments or accommodations - Should you need any adjustments or accommodations to the recruitment process, at either application or interview, please contact us on

We believe in the power of ingenuity to build a positive human future. As strategies, technologies, and innovation collide, we create opportunity from complexity. Our teams of interdisciplinary experts combine innovative thinking and breakthrough technologies to progress further, faster. Our clients adapt and transform, and together we achieve enduring results. We are over 4,000 strategists, innovators, designers, consultants, digital experts, scientists, engineers, and technologists. And we have deep expertise in consumer and manufacturing, defence and security, energy and utilities, financial services, government and public services, health and life sciences, and transport. Our teams operate globally from offices across the UK, Ireland, US, Nordics, and Netherlands. PA. Bringing Ingenuity to Life. Hybrid working - our approach is to be in the office or on client site a minimum of 2 days per week. However, the actual time you spend and where you spend it will vary by role or assignment, including up to 5 days per week on a client site. This role can be based in our London Victoria or Melbourn offices Our Life Sciences teams work with leading pharmaceutical, biotechnology and healthcare organisations to strengthen quality, compliance and operational excellence across the product lifecycle - from early research through to commercial supply. We are seeking an experienced Pharma Quality Specialist Consultant to join our Life Sciences consulting team, specialising in GxP Quality Management System (QMS) design, transformation and implementation. In this role, you will advise clients across pharmaceutical, biotechnology and related life sciences environments, supporting compliance with GMP, GDP, GCP and GLP requirements. You will lead and deliver quality transformation initiatives, combining strong hands on expertise with a pragmatic, client focused consulting approach. What you'll do You'll work across a diverse portfolio of client engagements, applying your quality expertise to deliver tangible impact. Your work will include: QMS design and process transformation Leading the design and implementation of GxP compliant QMS across R&D, manufacturing, clinical and distribution environments. Conducting process mapping and gap assessments, and supporting the rollout of new or enhanced systems aligned to global regulatory standards (including GMP, GDP, GCP, GLP, FDA 21 CFR 210/211, EU GMP/EudraLex, ICH Q7/Q10). Authoring, reviewing and maintaining quality policies, standards, SOPs, forms and controlled documentation, enabling sustainable compliance and operational excellence. Supporting effective change management, embedding best practices through close collaboration with quality, technical and business teams. Computer system validation and data integrity Leading and advising on computer system validation (CSV) activities within GxP environments. Supporting the development of validation strategies, protocols, test scripts and data integrity controls in line with global regulatory expectations. Supplier quality and audit support Applying hands on experience in supplier qualification, evaluation and audit activities (internal and external). Interpreting audit findings and supporting CAPA development, supplier improvement initiatives and ongoing risk mitigation activities. Regulatory systems implementation Leading the implementation and optimisation of Regulatory Information Management (RIM) systems to improve submission tracking, data integrity and global regulatory oversight. Supporting Product Lifecycle Management (PLM) system implementations to enable end to end control of product data, changes and documentation across development phases. Working closely with client IT, regulatory and quality teams to tailor solutions that are practical, scalable and compliant. Regulatory and Qualified Person (QP) support Acting as a subject matter expert on GxP regulations and inspection readiness. Acting as, or supporting, a Qualified Person (QP) for product certification and release, where appropriate. Client and stakeholder engagement Building trusted relationships with clients, quality leaders, business stakeholders and regulators. Translating complex regulatory expectations into clear, practical process improvements. Leading and facilitating cross functional collaboration to deliver successful QMS and regulatory initiatives. Qualifications We're looking for a quality professional with strong consulting instincts and the confidence to operate in complex, regulated environments. You'll ideally bring: Management Consultancy experience highly desirable A scientific or technical background (life sciences, pharmaceutical sciences, quality or a related discipline). Typically 8+ years' experience within pharmaceuticals, biotechnology or life sciences, with a strong track record in GxP QMS transformation and implementation. Extensive experience drafting and managing quality documentation, including SOPs, standards, policies, forms and templates. Strong knowledge of global GxP regulatory frameworks, including FDA, EU GMP/EudraLex, MHRA, EMA and ICH guidance. Hands on experience with supplier qualification, audits, CAPA and compliance management. Experience of RIM and PLM system implementation in regulated environments (highly desirable). Knowledge of computer system validation and data integrity principles. Excellent problem solving, communication and stakeholder management skills. QP status is highly desirable but not essential. Experience with ISO 13485 and combination product environments would be advantageous but is not required. We know the skill-gap and 'somewhat need to tick every box' can get in the way of meeting brilliant candidates, so please don't hesitate to apply - we'd love to hear from you. Please be aware that some of our UK roles at PA Consulting require a UK security clearance. All PA people are required to undergo background checks and to achieve the Baseline Personnel Security Standard however, some UK roles also require higher levels of National Security Vetting, where applicants must have at least 5 years of continuous residency in the UK. We therefore ask that you only apply if you meet the residency requirements (i.e. you are a British citizen or have been resident in the UK for the past 5 years), as this is the prerequisite for a security clearance. If you're unsure about your eligibility, we encourage you to review the UK Government's guidance on security vetting before applying. Additional information Life At PA encompasses our peoples' experience at PA. It's about how we enrich peoples' working lives by giving them access to unique people and growth opportunities and purpose led meaningful work. Our purpose guides how we work with our clients and our teams, and support our communities, to deliver insight and impact, solving the world's most complex challenges. We're focused on building a workplace that values human difference and diverse mindsets, and a culture of inclusion and equality that unlocks the potential in our people so everyone can be their best self. We are dedicated to supporting the physical, emotional, social and financial well-being of our people. Check out some of our extensive benefits: Health and lifestyle perks accompanying private healthcare 25 days annual leave (plus a bonus half day on Christmas Eve) with the opportunity to buy 5 additional days Generous company pension scheme Opportunity to get involved with community and charity-based initiatives Annual performance-based bonus PA share ownership Tax efficient benefits (cycle to work, give as you earn) We're committed to advancing equality.We recruit, retain, reward and develop our people based solely on their abilities and contributions and without reference to their age, background, disability, genetic information, parental or family status, religion or belief, race, ethnicity, nationality, sex, sexual orientation, gender identity (or expression), political belief, veteran status, or any other range of human difference brought about by identity and experience. We welcome applications from underrepresented groups. Adjustments or accommodations - Should you need any adjustments or accommodations to the recruitment process, at either application or interview, please contact us on

Our Life Sciences teams work with leading pharmaceutical, biotechnology and healthcare organisations to strengthen quality, compliance and operational excellence across the product lifecycle - from early research through to commercial supply. Hybrid working / location Hybrid working - our approach is to be in the office or on client site a minimum of 2 days per week. However, the actual time you spend and where you spend it will vary by role or assignment, including up to 5 days per week on a client site. This role can be based in our London Victoria or Melbourn offices We are seeking an experienced Pharma Quality Specialist Consultant to join our Life Sciences consulting team, specialising in GxP Quality Management System (QMS) design, transformation and implementation. In this role, you will advise clients across pharmaceutical, biotechnology and related life sciences environments, supporting compliance with GMP, GDP, GCP and GLP requirements. You will lead and deliver quality transformation initiatives, combining strong hands on expertise with a pragmatic, client focused consulting approach. What you'll do QMS design and process transformation Leading the design and implementation of GxP compliant QMS across R&D, manufacturing, clinical and distribution environments. Conducting process mapping and gap assessments, and supporting the rollout of new or enhanced systems aligned to global regulatory standards (including GMP, GDP, GCP, GLP, FDA 21 CFR 210/211, EU GMP/EudraLex, ICH Q7/Q10). Authoring, reviewing and maintaining quality policies, standards, SOPs, forms and controlled documentation, enabling sustainable compliance and operational excellence. Supporting effective change management, embedding best practices through close collaboration with quality, technical and business teams. Computer system validation and data integrity Leading and advising on computer system validation (CSV) activities within GxP environments. Supporting the development of validation strategies, protocols, test scripts and data integrity controls in line with global regulatory expectations. Supplier quality and audit support Applying hands on experience in supplier qualification, evaluation and audit activities (internal and external). Interpreting audit findings and supporting CAPA development, supplier improvement initiatives and ongoing risk mitigation activities. Regulatory systems implementation Leading the implementation and optimisation of Regulatory Information Management (RIM) systems to improve submission tracking, data integrity and global regulatory oversight. Supporting Product Lifecycle Management (PLM) system implementations to enable end to end control of product data, changes and documentation across development phases. Working closely with client IT, regulatory and quality teams to tailor solutions that are practical, scalable and compliant. Regulatory and Qualified Person (QP) support Acting as a subject matter expert on GxP regulations and inspection readiness. Acting as, or supporting, a Qualified Person (QP) for product certification and release, where appropriate. Client and stakeholder engagement Building trusted relationships with clients, quality leaders, business stakeholders and regulators. Translating complex regulatory expectations into clear, practical process improvements. Leading and facilitating cross functional collaboration to deliver successful QMS and regulatory initiatives. Qualifications We're looking for a quality professional with strong consulting instincts and the confidence to operate in complex, regulated environments. You'll ideally bring: Management Consultancy experience highly desirable A scientific or technical background (life sciences, pharmaceutical sciences, quality or a related discipline). Typically 8+ years' experience within pharmaceuticals, biotechnology or life sciences, with a strong track record in GxP QMS transformation and implementation. Extensive experience drafting and managing quality documentation, including SOPs, standards, policies, forms and templates. Strong knowledge of global GxP regulatory frameworks, including FDA, EU GMP/EudraLex, MHRA, EMA and ICH guidance. Hands on experience with supplier qualification, audits, CAPA and compliance management. Experience of RIM and PLM system implementation in regulated environments (highly desirable). Knowledge of computer system validation and data integrity principles. Excellent problem solving, communication and stakeholder management skills. QP status is highly desirable but not essential. Experience with ISO 13485 and combination product environments would be advantageous but is not required. Benefits Health and lifestyle perks accompanying private healthcare 25 days annual leave (plus a bonus half day on Christmas Eve) with the opportunity to buy 5 additional days Generous company pension scheme Opportunity to get involved with community and charity based initiatives Annual performance based bonus PA share ownership Tax efficient benefits (cycle to work, give as you earn) Equal Opportunity Statement We're committed to advancing equality. We recruit, retain, reward and develop our people based solely on their abilities and contributions and without reference to their age, background, disability, genetic information, parental or family status, religion or belief, race, ethnicity, nationality, sex, sexual orientation, gender identity (or expression), political belief, veteran status, or any other range of human difference brought about by identity and experience. We welcome applications from underrepresented groups. Security Clearance and Eligibility Please be aware that some of our UK roles at PA Consulting require a UK security clearance. All PA people are required to undergo background checks and to achieve the Baseline Personnel Security Standard; some UK roles also require higher levels of National Security Vetting, where applicants must have at least 5 years of continuous residency in the UK. We therefore ask that you only apply if you meet the residency requirements (i.e., you are a British citizen or have been resident in the UK for the past 5 years), as this is the prerequisite for a security clearance. If you're unsure about your eligibility, we encourage you to review the UK Government's guidance on security vetting before applying. Accommodations Adjustments or accommodations - Should you need any adjustments or accommodations to the recruitment process, at either application or interview, please contact us .

Our Life Sciences teams work with leading pharmaceutical, biotechnology and healthcare organisations to strengthen quality, compliance and operational excellence across the product lifecycle - from early research through to commercial supply. Hybrid working / location Hybrid working - our approach is to be in the office or on client site a minimum of 2 days per week. However, the actual time you spend and where you spend it will vary by role or assignment, including up to 5 days per week on a client site. This role can be based in our London Victoria or Melbourn offices We are seeking an experienced Pharma Quality Specialist Consultant to join our Life Sciences consulting team, specialising in GxP Quality Management System (QMS) design, transformation and implementation. In this role, you will advise clients across pharmaceutical, biotechnology and related life sciences environments, supporting compliance with GMP, GDP, GCP and GLP requirements. You will lead and deliver quality transformation initiatives, combining strong hands on expertise with a pragmatic, client focused consulting approach. What you'll do QMS design and process transformation Leading the design and implementation of GxP compliant QMS across R&D, manufacturing, clinical and distribution environments. Conducting process mapping and gap assessments, and supporting the rollout of new or enhanced systems aligned to global regulatory standards (including GMP, GDP, GCP, GLP, FDA 21 CFR 210/211, EU GMP/EudraLex, ICH Q7/Q10). Authoring, reviewing and maintaining quality policies, standards, SOPs, forms and controlled documentation, enabling sustainable compliance and operational excellence. Supporting effective change management, embedding best practices through close collaboration with quality, technical and business teams. Computer system validation and data integrity Leading and advising on computer system validation (CSV) activities within GxP environments. Supporting the development of validation strategies, protocols, test scripts and data integrity controls in line with global regulatory expectations. Supplier quality and audit support Applying hands on experience in supplier qualification, evaluation and audit activities (internal and external). Interpreting audit findings and supporting CAPA development, supplier improvement initiatives and ongoing risk mitigation activities. Regulatory systems implementation Leading the implementation and optimisation of Regulatory Information Management (RIM) systems to improve submission tracking, data integrity and global regulatory oversight. Supporting Product Lifecycle Management (PLM) system implementations to enable end to end control of product data, changes and documentation across development phases. Working closely with client IT, regulatory and quality teams to tailor solutions that are practical, scalable and compliant. Regulatory and Qualified Person (QP) support Acting as a subject matter expert on GxP regulations and inspection readiness. Acting as, or supporting, a Qualified Person (QP) for product certification and release, where appropriate. Client and stakeholder engagement Building trusted relationships with clients, quality leaders, business stakeholders and regulators. Translating complex regulatory expectations into clear, practical process improvements. Leading and facilitating cross functional collaboration to deliver successful QMS and regulatory initiatives. Qualifications We're looking for a quality professional with strong consulting instincts and the confidence to operate in complex, regulated environments. You'll ideally bring: Management Consultancy experience highly desirable A scientific or technical background (life sciences, pharmaceutical sciences, quality or a related discipline). Typically 8+ years' experience within pharmaceuticals, biotechnology or life sciences, with a strong track record in GxP QMS transformation and implementation. Extensive experience drafting and managing quality documentation, including SOPs, standards, policies, forms and templates. Strong knowledge of global GxP regulatory frameworks, including FDA, EU GMP/EudraLex, MHRA, EMA and ICH guidance. Hands on experience with supplier qualification, audits, CAPA and compliance management. Experience of RIM and PLM system implementation in regulated environments (highly desirable). Knowledge of computer system validation and data integrity principles. Excellent problem solving, communication and stakeholder management skills. QP status is highly desirable but not essential. Experience with ISO 13485 and combination product environments would be advantageous but is not required. Benefits Health and lifestyle perks accompanying private healthcare 25 days annual leave (plus a bonus half day on Christmas Eve) with the opportunity to buy 5 additional days Generous company pension scheme Opportunity to get involved with community and charity based initiatives Annual performance based bonus PA share ownership Tax efficient benefits (cycle to work, give as you earn) Equal Opportunity Statement We're committed to advancing equality. We recruit, retain, reward and develop our people based solely on their abilities and contributions and without reference to their age, background, disability, genetic information, parental or family status, religion or belief, race, ethnicity, nationality, sex, sexual orientation, gender identity (or expression), political belief, veteran status, or any other range of human difference brought about by identity and experience. We welcome applications from underrepresented groups. Security Clearance and Eligibility Please be aware that some of our UK roles at PA Consulting require a UK security clearance. All PA people are required to undergo background checks and to achieve the Baseline Personnel Security Standard; some UK roles also require higher levels of National Security Vetting, where applicants must have at least 5 years of continuous residency in the UK. We therefore ask that you only apply if you meet the residency requirements (i.e., you are a British citizen or have been resident in the UK for the past 5 years), as this is the prerequisite for a security clearance. If you're unsure about your eligibility, we encourage you to review the UK Government's guidance on security vetting before applying. Accommodations Adjustments or accommodations - Should you need any adjustments or accommodations to the recruitment process, at either application or interview, please contact us .

Principal Consultant in Product Lifecycle Management - Aerospace & Defence Our Systems Insights & Solutions team are looking for a Principal Consultant in Product Lifecycle Management (PLM) with experience in Aerospace & Defence or related discrete manufacturing industries. We believe that business value can be derived from PLM solutions when the correct application of end to end process thinking combines with enabling technology and the right transformation approach. As a Principal Consultant within Systems Insights and Solutions, you will take a leading role on projects that have a real impact on our clients' ability to deliver new products, delivering game changing solutions. This role will focus upon the delivery of PLM solutions supporting all phases of the product lifecycle, with primary focus on Digital Engineering: Product and Technology Portfolio Management Programme Delivery and Governance Multi Disciplinary Design and Optimisation Connected Verification and Certification Smart Manufacturing Optimised Sustainment and Availability Typical projects will include: Carrying out PLM diagnostic and development of business case Defining the business architecture / operating model, requirements and PLM solution blueprint Leading PLM Transformation initiatives Working Conditions Hybrid working - we favor a mix of office and client site presence; a minimum of 2-3 days per week in the office or on client sites, with up to 5 days per week on a client site depending on the assignment. Travel to client sites will be necessary as and when the client requires. Qualifications Essential qualifications and experience PLM Leadership: 10+ years of PLM experience, working with the major PLM vendors to design and deploy their solutions. Experience with Siemens solutions will be an advantage. Technical Expertise: Deep hands on expertise in core PLM processes, such as BOM management, change/config, variant/options management, CAD/CAE integration, ALM/requirements trace, maintenance and through life support. Business acumen: Experience in shaping business cases and implementation roadmaps for investment in PLM solutions. Ability to hold executive level conversations to build alignment on a PLM transformation vision. Prior consulting experience: Ability to manage client stakeholders, and all aspects of the consulting engagement lifecycle. Desirable qualifications and experience: Standards & Frameworks: Proficiency in ISO/IEC/IEEE 15288, TOGAF, EIA 649, STEP/PLCS awareness, AS9145, ISO 9001/27001. Understanding of defence export control constraints. Industry Experience: Experience and knowledge of key working practices in Defence, or other discrete manufacturing industries. We know the skill gap and 'somewhat need to tick every box' can get in the way of meeting brilliant candidates, so please don't hesitate to apply - we'd love to hear from you. Please be aware that some of our UK roles at PA Consulting require a UK security clearance. All PA people are required to undergo background checks and to achieve the Baseline Personnel Security Standard; some UK roles also require higher levels of National Security Vetting, where applicants must have at least 5 years of continuous residency in the UK. We therefore ask that you only apply if you meet the residency requirements (i.e. you are a British citizen or have been resident in the UK for the past 5 years), as this is the prerequisite for a security clearance. If you're unsure about your eligibility, we encourage you to review the UK Government's guidance on security vetting before applying. Benefits Health and lifestyle perks accompanying private healthcare 25 days annual leave (plus a bonus half day on Christmas Eve) with the opportunity to buy 5 additional days Generous company pension scheme Opportunity to get involved with community and charity based initiatives Annual performance based bonus PA share ownership Tax efficient benefits (cycle to work, give as you earn) Equal Opportunity Employer We're committed to advancing equality. We recruit, retain, reward and develop our people based solely on their abilities and contributions and without reference to their age, background, disability, genetic information, parental or family status, religion or belief, race, ethnicity, nationality, sex, sexual orientation, gender identity (or expression), political belief, veteran status, or any other range of human difference brought about by identity and experience. We welcome applications from underrepresented groups. Adjustments or accommodations - Should you need any adjustments or accommodations to the recruitment process, at either application or interview, please contact us on

Principal Consultant in Product Lifecycle Management - Aerospace & Defence Our Systems Insights & Solutions team are looking for a Principal Consultant in Product Lifecycle Management (PLM) with experience in Aerospace & Defence or related discrete manufacturing industries. We believe that business value can be derived from PLM solutions when the correct application of end to end process thinking combines with enabling technology and the right transformation approach. As a Principal Consultant within Systems Insights and Solutions, you will take a leading role on projects that have a real impact on our clients' ability to deliver new products, delivering game changing solutions. This role will focus upon the delivery of PLM solutions supporting all phases of the product lifecycle, with primary focus on Digital Engineering: Product and Technology Portfolio Management Programme Delivery and Governance Multi Disciplinary Design and Optimisation Connected Verification and Certification Smart Manufacturing Optimised Sustainment and Availability Typical projects will include: Carrying out PLM diagnostic and development of business case Defining the business architecture / operating model, requirements and PLM solution blueprint Leading PLM Transformation initiatives Working Conditions Hybrid working - we favor a mix of office and client site presence; a minimum of 2-3 days per week in the office or on client sites, with up to 5 days per week on a client site depending on the assignment. Travel to client sites will be necessary as and when the client requires. Qualifications Essential qualifications and experience PLM Leadership: 10+ years of PLM experience, working with the major PLM vendors to design and deploy their solutions. Experience with Siemens solutions will be an advantage. Technical Expertise: Deep hands on expertise in core PLM processes, such as BOM management, change/config, variant/options management, CAD/CAE integration, ALM/requirements trace, maintenance and through life support. Business acumen: Experience in shaping business cases and implementation roadmaps for investment in PLM solutions. Ability to hold executive level conversations to build alignment on a PLM transformation vision. Prior consulting experience: Ability to manage client stakeholders, and all aspects of the consulting engagement lifecycle. Desirable qualifications and experience: Standards & Frameworks: Proficiency in ISO/IEC/IEEE 15288, TOGAF, EIA 649, STEP/PLCS awareness, AS9145, ISO 9001/27001. Understanding of defence export control constraints. Industry Experience: Experience and knowledge of key working practices in Defence, or other discrete manufacturing industries. We know the skill gap and 'somewhat need to tick every box' can get in the way of meeting brilliant candidates, so please don't hesitate to apply - we'd love to hear from you. Please be aware that some of our UK roles at PA Consulting require a UK security clearance. All PA people are required to undergo background checks and to achieve the Baseline Personnel Security Standard; some UK roles also require higher levels of National Security Vetting, where applicants must have at least 5 years of continuous residency in the UK. We therefore ask that you only apply if you meet the residency requirements (i.e. you are a British citizen or have been resident in the UK for the past 5 years), as this is the prerequisite for a security clearance. If you're unsure about your eligibility, we encourage you to review the UK Government's guidance on security vetting before applying. Benefits Health and lifestyle perks accompanying private healthcare 25 days annual leave (plus a bonus half day on Christmas Eve) with the opportunity to buy 5 additional days Generous company pension scheme Opportunity to get involved with community and charity based initiatives Annual performance based bonus PA share ownership Tax efficient benefits (cycle to work, give as you earn) Equal Opportunity Employer We're committed to advancing equality. We recruit, retain, reward and develop our people based solely on their abilities and contributions and without reference to their age, background, disability, genetic information, parental or family status, religion or belief, race, ethnicity, nationality, sex, sexual orientation, gender identity (or expression), political belief, veteran status, or any other range of human difference brought about by identity and experience. We welcome applications from underrepresented groups. Adjustments or accommodations - Should you need any adjustments or accommodations to the recruitment process, at either application or interview, please contact us on