Astro Studios, Inc.

PA Consulting is seeking a skilled technician to join the Prototyping Workshop, developing parts for multiple industries. You will program and machine components with CNC mills and lathes, while collaborating with engineers, scientists and designers to deliver innovative prototype solutions. The role offers training in a fast-paced environment, with opportunities to grow across prototyping equipment and contribute to diverse projects. Residency and security checks may apply in the UK.

Managing Consultant - C&M - Google Cloud (Technical Lead) You are pragmatic and already understand that building a platform is only part of what a cloud engineering entails. You can clearly communicate with both clients and peers, describing technical issues and solutions in both written and meeting/workshop contexts. You are a confident problem solver and troubleshooter. You are confident and generous in sharing your specialist knowledge, ideas and solutions. You know when a platform is "fit for purpose". You are constantly learning and able to make others better by consciously teaching and unconsciously inspiring. You are obsessed with ensuring PA's reputation and credibility is always regarded at a remarkably elevated level, and unafraid to initiate corrective actions should this not be at our desired level. As a GCP Technical Lead, you'll be a true subject matter expert for delivering ingenious solutions on the Google Cloud Platform. We'll be looking at you to set direction and take responsibility for successfully achieving an outcome or deliverable. You may have a team of people to support, leading a development team, or else you could be working across multiple teams, providing some centralised expertise necessary for a larger program of work. You'll have expertise in architecture and will feel comfortable leading higher level architectural discussions. Using your experience of the DevSecOps processes, it's likely you'll own the overall process across a team, or multiple teams, building strong principles and putting robust methods and patterns in place. You will be comfortable having conversations with the client regularly, being one of the main points of engagement between the client and the project. Coaching and mentoring the team will be important in the role. You'll play an active role in technical account management. As part of this role you will design ingenious GCP-enabled solutions and services for brilliant clients across industry sectors. You will learn and grow - PA will support you to further develop your specialisations and increase your GCP certifications. Expect a sleeves-up, fully associated, and immersive working week. All our people are client facing and empowered to fulfil the best outcome for their clients. Flexible working - We are guided by our client work and needs; however, you have autonomy to manage your time and diary to suit your work/life balance. Qualifications To be successful in this role, you will need to have knowledge of the following products and deep experience in one more of the categories: VPC networks and Service Perimeters BigQuery, Cloud SQL, Cloud Spanner and Firestore Data analytics services including Dataproc, Dataflow, Data Fusion and Cloud Composer Security controls, including Cloud IAM, PAM, VPC Service Controls and Security Command Centre Additionally you should have a sound understanding of the following Architectural principles: Event-driven architectures and message queues Relational and non-relational databases Development and/or scripting experience (e.g. Python, Node, Bash) Security best practices for access control, data protection and communications. In addition to the above, we would be thrilled if you also had: Knowledge of other cloud platforms Automation DevOps experience using Google tech like Cloud Build and open source tech like terraform 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. Benefits 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 for you and your family 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 other by any other range of human difference brought about by identity and experience. We welcome applications from underrepresented groups. 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 client site. Adjustments or accommodations - Should you need any adjustments or accommodations to the recruitment process, at either application or interview, please contact us

PA Consulting is seeking a Managing Consultant for the Energy & Utilities sector, focusing on design engineering and science. You will lead multidisciplinary teams to deliver high-impact scientific and engineering solutions across Carbon Capture, Sustainable Fuels, Electrification, and Water. You will drive business development, shape service propositions, and mentor team members within a collaborative, inclusive environment. Hybrid working with client-site collaboration is supported.

Managing Consultant - E&U - Design Engineering and Science Global Innovation and Technology Centre, Back Lane, Melbourn, Hertfordshire, SG8 6DP, United Kingdom, Melbourn SG8 6DP, GB 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. Why consider joining our Energy and Utilities community as a Design, Engineering and Science Managing Consultant? Join a team where you're trusted to shape your own path, manage your time, and influence real change for our clients and communities. Grow a flexible and unique career within a trust-based, inclusive environment that values excellence, innovation, and curiosity. Join other experts within our supportive and collaborative community through knowledge-sharing and peer-level support, coaching and mentoring What you can expect Be part of our management team, helping shape and launch new service propositions while driving strategic business growth in the Energy Transition Sector. Lead business development initiatives -building trusted client relationships, owning outcomes, and delivering innovative, high-impact solutions. Collaborate with clients as a respected advisor, accelerating the development and deployment of sustainable and negative emissions technologies. Lead multi-disciplinary teams delivering high-impact scientific and engineering solutions across Carbon Capture, Sustainable Fuels, Electrification, and Water. Support your team's growth through coaching, knowledge-sharing, and creating opportunities for them to thrive. Even if you don't meet every requirement below, feel free to still apply as we are often hiring for similar roles which your background might be better suited to. Significant experience leading complex science and/or engineering development and advisory services in the Energy Transition sector. Proven consulting and commercial experience, either within a consultancy or through equivalent internal advisory roles. Strong client relationship management and business development skills, with a track record of initiating and winning work. Experience in one or more of the following value chains: Carbon Capture, Sustainable Fuels, Electrification, or Water. An established network of senior decision-makers and potential clients across the Energy Transition sector. Additional information Please note that the interview stages may be subject to change based on the specific requirements of the role. Introductory Call with one of our senior Talent Acquisition partners to explore your background, the opportunity and PA. Round 1: 3x competency interviews, allowing you to meet different members of PA. Final Round Business plan presentation with PA leaders - you will be given guidance and time to prepare in advance. 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 for you and your family 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 other by any other range of human difference brought about by identity and experience. We welcome applications from underrepresented groups. 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 client site. 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 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

Astro Studios, Inc. is seeking an experienced Pharma Quality Specialist Consultant to join our Life Sciences consulting team. You will focus on GxP Quality Management System design, transformation, and implementation across the product lifecycle. This role requires a strong background in regulatory compliance with at least 8 years in pharmaceuticals. You will engage with clients to deliver impactful quality transformation initiatives, ensuring adherence to stringent GxP standards. The position offers hybrid working arrangements and various benefits including health perks, generous leave, and a pension scheme.

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

Astro Studios, Inc. is seeking an experienced Pharma Quality Specialist Consultant in Melbourn to join their Life Sciences consulting team. The role focuses on GxP Quality Management System design, transformation, and implementation. The successful candidate will lead compliance initiatives for clients in pharmaceutical and biotech sectors, requiring strong knowledge of global regulatory frameworks and 8+ years of relevant experience. This position involves hybrid working, with a minimum of 2 days in the office or on client site.

Astro Studios, Inc. is seeking an experienced Pharma Quality Specialist Consultant in Melbourn to join their Life Sciences consulting team. The role focuses on GxP Quality Management System design, transformation, and implementation. The successful candidate will lead compliance initiatives for clients in pharmaceutical and biotech sectors, requiring strong knowledge of global regulatory frameworks and 8+ years of relevant experience. This position involves hybrid working, with a minimum of 2 days in the office or on client site.

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 .

Astro Studios, Inc. is seeking a Principal Consultant for Product Lifecycle Management (PLM). This role focuses on delivering PLM solutions in the Aerospace & Defence sector, emphasizing digital engineering. The ideal candidate will have over 10 years of PLM experience, lead transformation initiatives, and engage with clients on complex projects. The position offers a hybrid working model requiring 2-3 days in the office or client site. Join us to make a significant impact through innovative PLM solutions.

Astro Studios, Inc. is looking for a Principal Consultant in Product Lifecycle Management (PLM) based in Manchester, UK. The role is focused on delivering PLM solutions across product lifecycles, emphasizing Digital Engineering methodologies, and requires over 10 years of relevant experience. The position offers a hybrid working environment, with 2-3 days in the office or on client sites, and includes health perks, generous leave, and a pension scheme.

Medical Device Regulatory and Quality Consultant We are seeking a highly skilled consultant with experience in medical device and/or combination product Quality and Regulatory processes to join our Healthcare & Life Sciences (HLS) consulting team. This role focuses on advising clients on the regulatory, Quality and compliance aspects of medical devices, through a strong understanding of regulatory and quality requirements for medical devices, software as a medical device (SaMD), and/or combination products. The ideal candidate will have experience leading complex technical projects, integrating multidisciplinary expertise, and ensuring regulatory and quality compliance in innovative MedTech and pharmaceutical product developments. Key Responsibilities Regulatory & Quality Compliance for Medical Devices and Combination Products Provide expertise on global regulatory requirements for medical devices and combination products ensuring compliance with FDA, EMA, MHRA, MDR/IVDR, and ISO standards. Guide processes for hardware, software, and AI-driven medical device development to ensure compliance with applicable regulatory standards and guidance, including ISO 13485, ISO 14971, IEC 62304, and related standards and guidance for AI-driven medical technologies. Advise cross functional teams of designers, mechanical, electrical, software and usability engineers on requirements and best practices for regulatory and quality compliance. Ensure requirements traceability from user needs through design, development, verification, and validation. Lead risk management activities in accordance with ISO 14971, ensuring safety and efficacy through robust design and process controls. Develop and optimise clients' Quality Management Systems (QMS) to streamline compliance and lifecycle management. Stakeholder & Client Engagement Work closely with clients' R&D teams, business stakeholders, and notified bodies to align project goals with industry requirements. Facilitate cross functional collaboration, ensuring smooth integration between engineering, quality, and regulatory disciplines. Translate complex technical and regulatory requirements into actionable development strategies for medical technologies. Flexible working - you have autonomy to manage your time and diary to suit your work/life balance. Qualifications The ideal candidate will have: A technical background in Engineering (systems, biomedical, mechanical, electrical, software, or related field) or Applied Science (physics, chemistry, biology, materials science, etc.). Demonstrated prior direct experience in the design, development, or testing of medical devices and/or combination products. At least five years' experience in MedTech, pharmaceuticals, or life sciences, with a strong track record in regulated product development. Deep expertise in regulatory frameworks (FDA, EMA, MDR/IVDR, ISO 13485, IEC 62304, ISO 14971, GAMP, 21 CFR 4/820). Proven ability to work cross functionally with engineering, quality, and regulatory teams, contributing practical insights from previous technical roles. Strong problem solving skills, troubleshooting expertise and the ability to drive technical decision making in a highly regulated environment ensuring alignment with business and regulatory needs. Ability to manage multiple concurrent projects. Benefits Health and lifestyle perks accompanying private healthcare for you and your family. 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 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 by any other range of human difference brought about by identity and experience. We are on a journey towards ensuring our workforce is diverse at all levels and that our firm is representative of the world around us. 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.

Astro Studios, Inc. is looking for a Medical Device Regulatory and Quality Consultant to join our dynamic Healthcare & Life Sciences consulting team in Melbourn, UK. This role involves providing regulatory and quality compliance expertise for medical devices and combination products. Candidates should have at least five years of experience in the MedTech field, a technical background, and a strong understanding of regulations. Benefits include private healthcare, generous leave, and a pension scheme.

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

Astro Studios, Inc. is seeking a Principal Consultant in Product Lifecycle Management to lead crucial projects in Aerospace & Defence. This role focuses on delivering PLM solutions from inception to completion, with a strong emphasis on Digital Engineering. The successful candidate will possess over 10 years of PLM experience, showcasing technical expertise in core PLM processes and excellent business acumen. The work model is hybrid, requiring office presence 2-3 days per week.

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