308 Ich Jobs - Page 10

Your work will include generating Tables, Listings, and Figures (TLFs) for analysis purposes. You will ensure adherence to ICH guidelines, Good Clinical Practices, and regulatory requirements. Supporting the Programming Lead, you may represent Statistical Programming in meetings with internal and external clients and cross-functional project teams. Additionally, you will mentor Statistical Programmers and external consulting resources, demonstrating a strong ability to integrate statistical concepts with SAS Programming efficiently and effectively. Independence is crucial in this role. Accountabilities Support development of technical programming specifications for SDTM, ADS or ADaM standards. Independently develop and/or validate programs that generate SDTM and analysis datasets based on Alexion or ADaM specifications. Support development and validate technical programming specifications for tables, listings, figures/graphs based on Protocol and SAP. Independently develop and validate programs that generate tables, listings, figures/graphs using Alexion specifications. Manage external vendors and contract programmers. Provide project progress updates of programming activities. Review, maintain, and approve protocol-specific documents as necessary. Provide guidance and mentoring to peer, junior-level Programmers and contract staff. Support project leadership ensuring that department standards are implemented in all studies. Contribute ideas and thoughts towards the optimization of standard operating procedures. Lead team meetings when appropriate. Any other activities as required. Essential Skills/Experience Minimum of 4 years of statistical programming experience in the Pharmaceutical, Biotechnology, or Contract Research Industry. Proven ability to: Develop and validate technical specifications and programs for safety and efficacy analysis datasets, tables, listings, and figures/graphs. Independently and collaboratively resolve problems Clearly communicate processes and standards with management and team members High competence in using SAS/Base, SAS/Macro, SAS/STAT. Knowledge of SAS/Graph, and SAS/SQL Knowledge and implementation of: SDTM and ADaM principles Relational Databases Good Clinical Practice principles Good Programming Practice principles 21CFR Part 11 Standards principles Integrated Summary Safety/Efficacy Analyses Safety data and Coding Dictionaries (MedDRA and WHODD) ICH eCTD format Integrated Summary Safety/Efficacy Analyses Desirable Skills/Experience Safety data and Coding Dictionaries (MedDRA and WHODD) ICH eCTD format

TASEC Limited is looking for Executive / Senior Executive - Quality to join our dynamic team and embark on a rewarding career journey. Assisting with the preparation of operating budgets, financial statements, and reports. Processing requisition and other business forms, checking account balances, and approving purchases. Advising other departments on best practices related to fiscal procedures. Managing account records, issuing invoices, and handling payments. Collaborating with internal departments to reconcile any accounting discrepancies. Analyzing financial data and assisting with audits, reviews, and tax preparations. Updating financial spreadsheets and reports with the latest available data. Reviewing existing financial policies and procedures to ensure regulatory compliance. Providing assistance with payroll administration. Keeping records and documenting financial processes.

Job ID/Reference Code INFSYS-NAUKRI-210549 Work Experience 3-5 Job Title Payments - GPP Responsibilities Global Pay Plus - Payments Technical and Professional Requirements: PaymentsISO-20022 standards SWIFT, SEPA, MT messages Preferred Skills: Banking->GPP Financial Services Domain->Payments->GPP Generic Skills: Banking Educational Requirements Bachelor of Engineering Service Line Infosys Quality Engineering * Location of posting is subject to business requirements

About The Role : Job Title Regulatory Control Support Compliance Surveillance - Analyst Corporate TitleAssociate LocationMumbai, India Role Description The Compliance Surveillance function at Deutsche Bank is a global function which focuses on the post-event detection of market manipulation, insider trading and other risks as defined by established DB standards and regulatory requirements. The focal point of our activities is the monitoring of communication, voice, and trade data. The successful candidate will join the Compliance Surveillance function in Deutsche India Private Limited. The role involves working closely with colleagues to support the Germany region. What we'll offer you As part of our flexible scheme, here are just some of the benefits that youll enjoy Best in class leave policy Gender neutral parental leaves 100% reimbursement under childcare assistance benefit (gender neutral) Sponsorship for Industry relevant certifications and education Employee Assistance Program for you and your family members Comprehensive Hospitalization Insurance for you and your dependents Accident and Term life Insurance Complementary Health screening for 35 yrs. and above Your key responsibilities Conduct daily surveillance - primarily on trade data - to detect potential breaches such as insider trading, market manipulative actions. Perform research and investigations within defined service levels to identify the reason for potential violations. Document research results and escalate violations and/or suspicious activity according to firm policy and regulatory requirements. Work with members of the broader Surveillance team (mostly the German Surveillance team) to identify, analyze, investigate, and resolve issues. Work on ad-hoc Surveillance tasks as needed. Your skills and experience Degree level preferably in finance or economics. Knowledge of Financial Markets and Financial Instruments and understanding of related risks (e.g., market abuse) as well as interest in financial news. At minimum two years of experience in Banking with exposure to Financial Instruments and / or Compliance. Fluent in spoken and written English. Being familiar with Mandarin or Cantonese is a plus. Strong attention to details, analytical skills and sound judgement. Team player with good communication skills with the ability to work independently. Proficiency in MS Office. How we'll support you Training and development to help you excel in your career Coaching and support from experts in your team A culture of continuous learning to aid progression A range of flexible benefits that you can tailor to suit your needs About us and our teams Please visit our company website for further information: https://www.db.com/company/company.htm We strive for a culture in which we are empowered to excel together every day. This includes acting responsibly, thinking commercially, taking initiative and working collaboratively. Together we share and celebrate the successes of our people. Together we are Deutsche Bank Group. We welcome applications from all people and promote a positive, fair and inclusive work environment.

About The Role : Job TitleRegulatory Advisory Analyst Corporate TitleNCT LocationMumbai, India Role Description The CRM & PBCRO Regulatory Adherence at Deutsche Bank ensures a CRM-wide discipline for the assessment and analysis of consultations and new rules and regulations and is playing a key role in leading, supporting and validating regulatory driven changes initiatives impacting our credit systems and processes. Your role will primarily be focussed on global regulations impacting all international credit portfolios in Corporates & Investment Bank (CIB) as well as domestically in Germany (PB Germany) and in the International Private bank (IPB). Members of the team are located in Frankfurt, Bonn und Mumbai. This position is within Regulatory Adherence in Mumbai servicing global locations. What we'll offer you As part of our flexible scheme, here are just some of the benefits that youll enjoy, Best in class leave policy. Gender neutral parental leaves 100% reimbursement under childcare assistance benefit (gender neutral) Sponsorship for Industry relevant certifications and education Employee Assistance Program for you and your family members Comprehensive Hospitalization Insurance for you and your dependents Accident and Term life Insurance Complementary Health screening for 35 yrs. and above Your key responsibilities You are responsible for Regulatory Adherence activities along the regulatory life-cycle related to Credit Risk including tracking and review of incoming new rules & regulations and consultations affecting Credit Risk. You will support the performance of global impact assessments and tracking of potential gaps resulting in remediation- and corresponding project/ change activities, dependent on materiality of the regulations in conjunction with a Senior Analyst. You identify and analyse regulatory trends and supervisors priority topics and prepare bankwide advocacy work including project support in key regulatory initiatives (i.e. CRR; MaRisk) with corresponding change initiatives. You will support coordination and Senior Regulatory Leads in regulatory driven changes initiatives impacting our (IT) systems and processes as part of the adherence analysis and advocacy work, i.e. joining project teams and working groups to drive quality standards and control frameworks to meet new regulatory requirements. You will actively coordinate stakeholders feedback of the areas impacted including coordination of Subject Matter Experts in different credit areas. You are responsible for reporting tracking items, and preparation of Management presentations. Your skills and experience A Masters degree or the equivalent experience or qualifications Min 3yrs Background in a Risk function within the financial services industry. Credit risk management knowledge including experience in credit process and/or methodologies and/ or credit portfolio management appreciated Regulatory knowledge with focus on credit risk relevant or related regulations. Experience in project and change management with good analytical and conceptual skills with the ability to solve complex problems, develop innovative and structured solutions and ability to see the broader picture front-to-back and assess dependencies and interdependencies Very good communication and social skills with excellent client and service focus, as well as confidence in working with decision-makers from all levels of the organisation being a good team player Fluent in Microsoft Office tools Fluent in English How we'll support you Training and development to help you excel in your career. Coaching and support from experts in your team. A culture of continuous learning to aid progression. A range of flexible benefits that you can tailor to suit your needs.

About The Role : Job TitleBusiness Risk & Control Analyst LocationMumbai, India Role Description The team is part of the Team Business Risk & Controls (BRC). The PB BRC guards the Protect agenda by overseeing non-financial risks, conduct & control topics and regulatory changes. The team works across global PB franchise delivering complex key risk and control agenda, adding value for the Business to reduce complexity and enhance controls. The team works with cross-functional and global teams, collaborating with multiple stakeholders globally across the bank. About Deutsche Bank Deutsche Bank is the leading German bank with strong European roots and a global network. Were driving growth through our strong client franchise. Against a backdrop of increasing globalization in the world economy, Deutsche Bank is very well-positioned, with significant regional diversification and substantial revenue streams from all the major regions of the world. We serve our clients real economic needs in commercial banking, investment banking, private banking and asset management. We are investing heavily in digital technologies, prioritizing long term success over short-term gains, and serving society with ambition and integrity. All this means a career packed with opportunities to grow and the chance to shape the future of our clients. About the business division The Private Bank combines Deutsche Banks private clients business in Germany and its international business with private and commercial clients together with Wealth Management in a single division. In both the domestic German market and worldwide the Private Bank provides high-quality advice to ~20 million clients and a broad range of financial services in many countries ranging from day-to-day banking services right through to advisory services for sophisticated Private Banking and Wealth Management clients. In Italy, Spain, Belgium, and India the Private Bank offers its services to corporate clients as well as small and medium-sized enterprises. The Private Bank is a strong pillar of the Groupa modern bank that boasts capital markets and financing expertise, a strong global network, and modern digital services. What we'll offer you As part of our flexible scheme, here are just some of the benefits that youll enjoy Best in class leave policy Gender neutral parental leaves 100% reimbursement under child-care assistance benefit (gender neutral) Flexible working arrangements Sponsorship for Industry relevant certifications and education Employee Assistance Program for you and your family members Comprehensive Hospitalization Insurance for you and your dependents Accident and Term life Insurance Complementary Health screening for 35 yrs. and above Your key responsibilities Assist in designing and improving risk and control assessment processes in areas of responsibility Oversight/support in execution of non-financial risk topics including RCA topics Document and maintain various policies, manuals and internal procedures pertaining to non-Financial topics Support the production and delivery of monthly Non-Financial Risk materials, reports and MI at Global and Regional Level Develop subject matter expertise on non-financial risk and controls within the remit of the team Coordinate with a diverse set of stakeholders across 1LOD and 2LOD to help completion of NFR tasks and activities Support with implementation of new framework requirements wrt. to RCA process. Ensure that any sensitive issues are escalated promptly with sound analysis and recommendations Close cooperation with various BR&C stakeholders, primarily in Europe (focusGermany) Your skills and experience Education & Experience Strong knowledge of non-financial risks and controls Proven experience of working with risk and controls assessment processes Relevant experience in the Retail Banking / Private Banking sector or experience in financial services or consultancy (with Private Banking experience preferred but not essential) Experience working on small to medium scale projects within global environment. University degree Competencies Very strong analytical skills (quantitative and qualitative) Proficiency with Microsoft Office programs; e.g. Excel , Word and PowerPoint Ability to work in crunch situations Strong work ethic, commitment to excel and proven capacity to work effectively with limited supervision Strong communication (written and verbal) and relationship skills Ability to clearly articulate and present supported topics Excellent command of the English language (written and spoken skills) Personal Characteristics Proactive attitude and self-initiative Ability to think laterally. Strong Team Player skills as well as working independently Eagerness to learn and adapt to new situations and processes Delivery-focused, able to manage multiple deliverables to deadlines Flexibility with respect to new tasks and the ability to work diligently in stressful situations Ability to learn quickly Driven and able to handle day-to-day routine as well as cope with shifting priorities and changing responsibilities to meet needs and demands How we'll support you Training and development to help you excel in your career Flexible working to assist you balance your personal priorities Coaching and support from experts throughout the bank A culture of continuous learning to aid progression A range of flexible benefits that you can tailor to suit your needs About us and our teams Please visit our company website for further information: https://www.db.com/company/company.htm We strive for a culture in which we are empowered to excel together every day. This includes acting responsibly, thinking commercially, taking initiative and working collaboratively. Together we share and celebrate the successes of our people. Together we are Deutsche Bank Group. We welcome applications from all people and promote a positive, fair and inclusive work environment.

Role Overview Responsible for qualification & calibration activities for defined instruments and equipment as per schedule & procedures with QMS. Illustrative Responsibilities Ensure that qualification & calibration activities are planned and executed within time frame defined by the procedure and equipments are released on time as per the pre-defined schedule. Responsible for coordinating with lab supervisors / system owners for handling of any non-conformances or escalations Handling of QMS related activities like, Change control, CAPA and Deviation with its effectiveness check. Responsible for quality compliance activities for laboratory instruments qualification and calibration. Summarize, review, and report the analytical Instruments qualification and calibration for further approval. Ensure a disciplined work environment to provide expertise to subordinates colleagues in the proper performance of laboratory procedures. Ensure on time GDP in technical function with right first time (RFT) approach. Responsible for ensuring team compliance to EHS, Quality & Business policies Any other work given by management from time to time. Quality & Compliance Responsible for following GMP/GLP/ GDP/EHS policies by self as well as the team Required skills Technical expertise in Analytical instruments qualification, calibration, protocol preparation and QMS. Build cohesive team valuing team spirit Able to anticipate the implications and consequences of situations and take appropriate actions in the interest of Client as well as Cal Scientific without compromising quality. Clear thoughts and effective and crisp communication. Job requirement M.Sc – specializing in Chemistry/ M. Pharma with proven experience of min. 7-8 yrs. in Instrument qualification and calibration. In depth experience in Chromatography (HPLC, UPLC, GC), Spectroscopy (MS, FTIR, UV), Thermal techniques (DSC, TGA) and Particle size measurements. Expertise in analytical instruments qualification and calibration, protocol preparation, CAPA, Investigations, Deviations (QMS) Good Knowledge of ICH guidelines and different global regulatory authorities.

What you will do Let’s do this. Let’s change the world. In this vital role you will play a key role in a regulatory submission content automation initiative which will modernize and digitize the regulatory submission process, positioning Amgen as a leader in regulatory innovation. The initiative maximizes pioneering technologies, including Generative AI, Structured Content Management, and integrated data to automate the creation, review, and approval of regulatory content. Role Description: We are seeking a highly skilled Software Engineer to join our team. You will contribute to the design, development, deployment and maintenance of complex software applications in a SAFe framework. You will collaborate closely with senior engineers, product managers, and multi-functional teams to deliver high-quality solutions that support content workflows, version control, and multi-platform delivery. This role will involve designing complex systems, optimizing content storage solutions, and integrating third-party services to deliver robust authoring platforms. Roles & Responsibilities: Write clean, efficient, and maintainable code for content authoring and management systems. Design, develop and deploy the structured content authoring system and its configurations. Build APIs and services to support content retrieval, storage, and rendering. Work on both front-end and back-end components of the authoring system, integrating user interfaces and configurations with back-end services. Fix and resolve technical issues. Assist with the ongoing maintenance of the system, including bug fixes, system upgrades, and enhancements. Participate in technical discussions, code and design reviews to help drive the architecture and implementation of new features. Create and maintain documentation on software architecture, design, and deployment. Stay updated with the latest trends and technologies in content authoring and management, and related fields. Work closely with product team, business team, and other collaborators. What we expect of you We are all different, yet we all use our unique contributions to serve patients. Basic Qualifications: Master’s degree and 1 to 3 years of experience in Computer Science Bachelor’s degree and 3 to 5 years of experience in Computer Science Diploma and 7 to 9 years of experience in Computer Science. Preferred Qualifications: Solid technical background, including understanding software development processes, databases, and cloud-based content systems. Proficiency in one or more programming languages such as Java, Python, or JavaScript and familiarity with API-driven content delivery. Experience working with databases (SQL/NoSQL). Experience with product backlog management (e.g., Jira) and collaboration tools. Good-to-Have Skills: Experience building and supporting GenAI solutions Experience with CI/CD pipelines, version control tools and working in an Agile environment. Understanding of international pharmaceutical regulatory submission guidelines and processes (eCTD, ICH, CDS, USPI etc.) Good communication skills, with the ability to convey complex technical concepts. Soft Skills: Excellent analytical and problem-solving skills. Strong verbal and written communication skills. Ability to work effectively with global, virtual teams. High degree of initiative and self-motivation. Ability to manage multiple priorities successfully. Team-oriented, with a focus on achieving team goals. Strong presentation and public speaking skills. What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.

Skill required: Com.Bkg- Commercial Real Estate - Real Estate Due Diligence Designation: Banking Advisory Senior Analyst Qualifications: BCom Years of Experience: 5 to 8 years What would you do? We help clients address quality and productivity issues, keep pace with customer expectations, navigate regulatory and operational pressures and ensure business sustainability by transforming their banking operations into an agile, resilient operating model.The Corporate banking /Wholesale banking team is responsible for helping clients and organizations processes trade finance transactions by providing superior service delivery to trade customers whilst safeguarding the bank from risks associated with this business.Identify and assess, prevent and mitigate and account to provide reasonable measures to adapt before executing an agreement in relation to the real estate and immovable property. Valuation of commercial real estate using software like Argus, extracting key information from lease agreements (including amendments) and rent rolls. What are we looking for? Team lead experience Roles and Responsibilities: In this role you are required to do analysis and solving of increasingly complex problems Your day to day interactions are with peers within Accenture You are likely to have some interaction with clients and/or Accenture management You will be given minimal instruction on daily work/tasks and a moderate level of instruction on new assignments Decisions that are made by you impact your own work and may impact the work of others In this role you would be an individual contributor and/or oversee a small work effort and/or team Please note that this role may require you to work in rotational shifts Qualifications BCom

We have been retained by a reputed Pharmaceutical Consulting firm working in the area of GMP, Global Regulatory Affairs & Product Development to hire a "Consultant - Regulatory Affairs" to be based at their HO located at Navi Mumbai. Details of the position are mentioned below: Company: Our Client is a reputed Pharmaceutical Consulting firm working in the area of GMP, Global Regulatory Affairs & Product Development. They have their head office in Mumbai and subsidiaries in Europe, Singapore, Australia and Malaysia. They have been providing high quality & credible consulting services to the Pharmaceutical Industry in India and internationally. They have a young and committed team of GMP and Regulatory Experts. Role & responsibilities: The person will be responsible for Regulatory consulting services at the firm. The responsibilities of this position include, but are not limited to, the following: Ownership for assigned regulatory projects including dossier writing, submissions, approval tracking, query resolution across Developed markets (UK, Australia, EU and US) and Emerging markets Ensure regulatory compliance, accuracy, timely completion, version control & adherence to internal SOPs Providing strategic input to the Management and Partners on regulatory projects Keep abreast of new developments in regulations across all critical health authorities Experience & Qualifications Regulatory affairs experience in small molecules for a minimum of 3-8 years is mandatory Must be well versed with ICH CTD guidelines and other regulatory guidelines from developed markets (US, EU, UK etc). Must have hands-on experience in regulatory submissions pertaining to generics/ small molecules (m1-m5 CTD writing for EU, Australia and other markets) CEP/ DMF/ ASMF filing with a good knowledge of EDQM requirements would be advantage. Experience in biologics/ biosimilar filings will be an added benefit. Computer and technical skills (including eCTD software knowledge) Strong & Flawless communication skills. Accuracy and attention to detail. Those of you whose profile matches the above mentioned description and would like to apply for this position shall forward their updated CV to sudhirvinayak@gmail.com In case of a query, please feel free to speak to the undersigned: Sudhir Vinayak, Director, Pharma Placements Inc. Mobile: 98202 34987 / 81307 24980

We have been retained by a reputed Pharmaceutical Consulting firm working in the area of GMP, Global Regulatory Affairs & Product Development to hire a "Junior GMP Consultant - QC & QA" to be based at their HO located at Navi Mumbai. Details of the position are mentioned below: Company: Our Client is a reputed Pharmaceutical Consulting firm working in the area of GMP, Global Regulatory Affairs & Product Development. They have their head office in Mumbai and subsidiaries in Europe, Singapore, Australia and Malaysia. They have been providing high quality & credible consulting services to the Pharmaceutical Industry in India and internationally. They have a young and committed team of GMP and Regulatory Experts. Role & responsibilities: Adequate experience and well versed with Quality Control and Quality Assurance systems and procedures in accordance to regulatory standards. Hands on experience in handling HPLC, GC, UV, FTIR, etc., worked on LIMS, audit trail, CSV , familiarity with GMP, GLP, EUGMP and ICH guidelines, Should have exposure working in formulations like oral solids dosage form (OSD), injectables, etc. Experience: Min 5-10 years experience in quality control & Quality Assurance in pharmaceutical industry. Knowledge & Skills Candidate should have exposure working in QC/QA laboratory in Regulated companies. Well versed with Quality Management systems/procedures Thorough knowledge of testing Raw materials, finished product, Packing materials and handling of key instrumentation like HPLC (auto sampler), GC, dissolution testing. Well versed with QC systems & procedures, audit trail review of HPLC, GC and have knowledge of computer system validation related to QC instruments. Familiarity with GMP, GLP, EUGMP and ICH guidelines. Familiar with stability management and calibration Well versed in carrying out Analytical Method validation/verification, Analytical tech transfers. Fluency in English and good communication written and verbal. Job responsibility: 1)To assist project lead in reviewing the QC systems, documentation and practices for client. 2) Participate in Supplier audits at various sites 3) Maintaining GMP data base and preparation of SOPs 4) Ready to do extensive travelling to visit Client sites and supplier audits (domestic & international) Preferred candidate: Candidates based only in Mumbai/Navi Mumbai will be preferred. 6. Qualifications: Education: A masters degree in Pharmaceutical Sciences or a master's degree in Analytical Chemistry Skills and Competencies: Strong analytical and problem-solving skills. Attention to detail and accuracy in testing and documentation. Proficient in the use of laboratory equipment and software. Those of you whose profile matches the above mentioned description and would like to apply for this position shall forward their updated CV to sudhirvinayak@gmail.com In case of a query, please feel free to speak to the undersigned: Sudhir Vinayak, Director, Pharma Placements Inc. Mobile: 98202 34987 / 81307 24980

Skill required: Com.Bkg- Commercial Real Estate - Real Estate Due Diligence Designation: Banking Advisory Associate Qualifications: BCom/Any Graduation Years of Experience: 1 to 3 years What would you do? We help clients address quality and productivity issues, keep pace with customer expectations, navigate regulatory and operational pressures and ensure business sustainability by transforming their banking operations into an agile, resilient operating model.The Corporate banking /Wholesale banking team is responsible for helping clients and organizations processes trade finance transactions by providing superior service delivery to trade customers whilst safeguarding the bank from risks associated with this business.Identify and assess, prevent and mitigate and account to provide reasonable measures to adapt before executing an agreement in relation to the real estate and immovable property. Valuation of commercial real estate using software like Argus, extracting key information from lease agreements (including amendments) and rent rolls. What are we looking for? ** Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your expected interactions are within your own team and direct supervisor You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments The decisions that you make would impact your own work You will be an individual contributor as a part of a team, with a predetermined, focused scope of work Please note that this role may require you to work in rotational shifts Qualifications BCom,Any Graduation

Accountabilities Act as a resource on regulatory matters with regard to product changes. Collaborate to prepare and organize forums and gatherings with government officials to exchange ideas and information on business activities and potential legislation that may affect the organization. Help ensure that the organizations interests are represented and protected in legislative proceedings and in the development of market rules and procedures. Participate as part of a team to develop and maintain policies and programs to ensure awareness of government legislation and regulatory issues that affect the organization. Independently solve moderately complex issues with minimal supervision, while escalating more complex issues to appropriate staff. Other duties as assigned Qualifications Minimum Qualifications Bachelors degree in a related field or equivalent experience Minimum requirement of 3 years of relevant work experience with Public offices liaising in the Government departments of Andhra Pradesh. Preferred Qualifications Overall 7-12 years experience in a Govt Liaising role Certification in public law and proven experience of working on approvals, legislations in forums with Government officials in a manufacturing environment . Willingness to be based in a manufacturing site at Krishnapatnam Previous experience of working in close coordination with plant officials on Government related issues of the plant .

Group Purpose Global Regulatory Policy and Intelligence engages regulators, industry and professional associations, and patient advocates externally and subject matter experts across Amgen to advance important Regulatory policy issues aligned with Amgen’s goals and priorities. Regulatory Intelligence for the GRAAS organization enables fast, efficient global filings by effectively monitoring, analyzing, and communicating regulatory requirements to regulatory strategy leads and others involved in the delivery of regulatory submissions and approvals. Coordination of change management activities in response to major changes in regulation also falls within the remit of this organization. Job Summary Performs monitoring and analysis of the global regulatory landscape according to defined plans and priorities and delivers agreed regulatory intelligence outputs. The Technology Systems Manager will be responsible for creating, developing, and maintaining a comprehensive databases and systems to facilitate optimizing data resource platforms and systems to collect and disseminate relevant regulatory information to internal stakeholders, ensuring timely awareness and compliance. The ideal candidate will have a strong background in system analysis/administration, regulatory affairs and intelligence. Key Activities Facilitates and supports the tools and platforms utilized to prepare regulatory intelligence outputs that guide the successful development, submission and approval of Amgen products worldwide. Uses internal and external contacts, tools and systems to gather regulatory intelligence Applies professional skills and experience with advanced tools to summarize and contextualize regulatory intelligence information and identify trends in agency feedback Effectively communicates regulatory requirements to Regulatory Affairs staff Continually seeks opportunities to improve the usefulness of regulatory intelligence outputs and the effectiveness of tools and systems. Works with limited supervision according to predefined regulatory intelligence workplans Applies tools and systems to deliver agreed intelligence objectives Communicates progress and escalates issues impacting delivery of intelligence outputs Provides suggestions for improvement of processes, systems and tools employed within the function. Knowledge and Skills Basic: Regulatory intelligence monitoring, analyzing, and interpreting global regulatory developments to ensure compliance and inform strategic decision-making. Knowledge of regulatory agency guidelines and procedures (major and non-major markets) Knowledge of regulatory intelligence systems and platforms Understanding and application of aspects of global and local regulatory process Project management skills Presentation and interpersonal communication skills Preferred: Global Regulatory Intelligence monitoring experience Education and Experience (basic) Doctorate degree, OR Master’s degree and 3 years of directly related experience. OR Bachelor’s degree and 5 years of directly related experience, OR Associate’s degree and 10 years of directly related experience Education and Experience (preferred) A bachelor's degree in life sciences or a related field; advanced degrees may be preferred. A minimum of 5 years of experience in regulatory affairs, with at least 3 years in a regulatory intelligence role within the pharmaceutical, biotechnology, or medical device industries. In-depth knowledge of global regulatory frameworks and guidelines, such as those from the FDA, EMA, and other health authorities. Strong analytical and problem-solving skills, with the ability to interpret complex regulatory information and provide actionable insights. Excellent communication skills, both written and verbal, to effectively present information to diverse audiences. Proficiency with regulatory intelligence databases and software tools.

- Must have good knowledge of Regulatory Submissions and Research - Must be familiarity with chemical industry specific regulations and guidelines. - Prepare and submit regulatory documents, such as INDs, NDAs, and MAAs, to regulatory agencies Required Candidate profile - Ensure company products with relevant regulatory requirements such as USFDA, FDA, EMA, and local regulations. - Stay up-to-date with changing regulatory requirement to internal stakeholders.

Role & responsibilities Keen Knowledge on Regulatory guidelines for finished product registration. Dossier compilation as per guidelines. Compilation and review the product dossiers for submission in CTD, ACTD . Gap analysis of the dossier and addressing the gaps before submission to MOH. Handling the customer and MOH queries . Life cycle management of the product. Development report, scale up report , specification, COA, stability protocol and Process validation protocol. Documents review (Specification, STP, Analytical method validations, Development report and validation reports, BMR, BPR, PVP/R and stability). Post approval experience to file the applicable variations timely. Knowledge on EAEU, ICH and EMEA guidelines. Re-registration (Renewal) procedures. Administrative documents requirements (COPP, Mfg. License and Import License) . Registration information management system updates on regular basis.

Position Summary: The Senior Medical Writer (MW) will be responsible for leading the development of high-quality and on-time clinical study documents. Specific responsibilities include clinical document planning, writing, editing/formatting, and performing QC review. Develops documents in compliance with Precision MW Style Guide, Precision SOPs, applicable regulatory guidelines (ie, ICH, FDA, GCP) and eCTD requirements. The successful candidate has a clear understanding of content requirements for key clinical documents based on regulatory requirements for all phases of development and will complete MW activities with impeccable attention to detail. Essential functions of the job include but are not limited to: Planning, writing, editing, formatting, and QC review of timely and high-quality clinical documents including clinical study protocols, IBs, ICF templates, DSURs, CSRs, CSR patient narratives with a clear understanding of content requirements based on regulatory guidances Ensures smooth and effective document management from start to finish (ie, from template to final, approved version) in collaboration with Sponsor, external vendors, and/or internal Precision project teams/departments Ability to independently formulate key messages from clinical study data Ability to author complex content using knowledge/skills and understanding of processes Ability to communicate clearly and concisely both in writing and verbally with internal and client teams Contributes to the development and maintenance of medical writing processes, SOPs, templates, and work instructions for key documents Excellent problem-solving skills, performing literature-based research to support writing activities Qualifications: Minimum Required: BS degree or equivalent in a scientific or medical discipline with relevant writing expertise 5+ years of experience as a medical writer in the sponsor and/or CRO setting Other Required: Proficiency with Microsoft Windows, Teams, Word, Excel, Adobe Acrobat, and PowerPoint Clear understanding of applicable regulations (eg, ICH, FDA, GCP), clinical trial transparency requirements (ie, EudraCT, CT.gov), and eCTD requirements for all phases of development Impeccable attention to detail and ability to complete writing assignments in a timely manner Ability to work effectively in a fast-paced environment with multiple high priority projects with no instruction on routine work and minimal instruction on new assignments Preferred: Advanced degree (MS/PhD) Oncology and/or rare disease experience (especially protocol and CSR development.

Position: Head of Analytical Development and Lead (ADL) Location: Rajkot Job Overview: The Head of Analytical Development and Lead (ADL) will be responsible for overseeing the analytical method development, validation, and transfer processes within the pharmaceutical industry. This role involves leading a team of analysts, ensuring that analytical methods for drug substances, intermediates, and raw materials are developed and validated in compliance with regulatory guidelines. The ADL Head will also provide technical expertise in troubleshooting, optimizing methods, and ensuring adherence to GMP, ICH, and other relevant standards. Key Responsibilities: Leadership & Team Management Lead and manage the Analytical Development team, providing guidance, mentorship, and performance management to ensure continuous team development. Foster a collaborative and high-performance culture to achieve departmental and organizational goals. Ensure proper training and development opportunities for team members, ensuring alignment with regulatory standards and industry best practices. Method Development & Validation Develop, validate, and transfer analytical methods for drug substances, intermediates, and raw materials, ensuring alignment with regulatory guidelines (e.g., ICH, GMP). Optimize analytical methods for improved accuracy, precision, and efficiency. Prepare validation protocols and lead the execution of validation studies, ensuring proper documentation and reporting of results. Generate and maintain comprehensive validation reports for regulatory submissions and internal purposes. Regulatory Compliance & Troubleshooting Ensure all analytical methods are developed and validated according to regulatory guidelines (e.g., ICH, GMP). Review and respond to regulatory queries related to analytical methods and data. Troubleshoot analytical issues, identifying root causes and implementing corrective actions to address any problems encountered during method development or validation. Support the preparation of responses to regulatory queries, ensuring compliance with relevant standards. Collaboration & Cross-Functional Support Collaborate with R&D, Regulatory Affairs, Process Development, and Manufacturing teams to support product development and lifecycle management. Provide technical support for technology transfer activities, ensuring smooth transition of analytical methods from development to commercial manufacturing. Work closely with cross-functional teams to ensure analytical methods meet product development timelines and regulatory requirements. Continuous Improvement Lead efforts to improve existing analytical methods and optimize laboratory processes. Implement best practices and continuous improvement initiatives in analytical development to increase efficiency, reduce costs, and improve the quality of the final product. Stay up-to-date with the latest developments and technologies in the field of analytical chemistry and pharmaceutical sciences. Key Skills and Competencies: In-depth knowledge of analytical techniques such as HPLC, GC-HS, UV-Vis, FTIR, and other instrument testing . Expertise in analytical method development, validation, and transfer for drug substances, intermediates, and raw materials. Familiarity with regulatory guidelines and standards , including ICH and GMP . Strong troubleshooting skills, with the ability to identify root causes of analytical issues and resolve them effectively. Experience with deviation management , change control , OOS (Out of Specification) , incident handling , and CAPA (Corrective and Preventive Action) processes. Proficiency in SOP preparation and ensuring compliance with internal and regulatory standards. Excellent project management skills , with the ability to prioritize and manage multiple tasks simultaneously. Strong collaboration skills , with the ability to work cross-functionally with R&D, Regulatory Affairs, Process Development, and Manufacturing teams. Qualifications: Educational Qualification: M.Sc. or B.Pharm or equivalent in Chemistry, Analytical Chemistry, Pharmaceutical Sciences , or a related scientific discipline. Experience: Minimum 8+ years of experience in analytical method development, validation, and transfer in the pharmaceutical industry. Regulatory Knowledge: In-depth understanding of regulatory guidelines (e.g., ICH, GMP) and experience in responding to regulatory queries . Industry Experience: Significant experience in the pharmaceutical industry , specifically in analytical development for drug substances, intermediates, and raw materials. Preferred Skills: Knowledge of advanced analytical techniques and emerging technologies in the pharmaceutical industry. Familiarity with regulatory submissions , including DMF (Drug Master File) , and experience with regulatory inspections . Previous experience in technology transfer activities in a GMP-compliant environment.

About Paytm: Paytm is India's leading mobile payments and financial services distribution company. Pioneer of the mobile QR payments revolution in India, Paytm builds technologies that help small businesses with payments and commerce. Paytms mission is to serve half a billion Indians and bring them to the mainstream economy with the help of technology. About the Team: The Compliance department has five areas of responsibilityidentification, prevention, monitoring and detection, resolution, and advisory for the entity with respect to regulations/ laws, and is part of the enterprise compliance group at Paytm. About the role: This role will focus on advising business and overseeing compliance-related matters in the company. The role entails advising in terms of the relevant regulatory expectations to the respective business units and ensuring timely monitoring and detection of compliance-related issues. Expectations/ Requirements: 1) Oversee and monitor adherence to applicable laws and regulations in the domains of digital lending, offline payments aggregators, BBPS, and UPI TPAP segments. 2) Provide informed compliance opinions to the internal stakeholders on the applicability of regulatory laws and guidelines. 3) Assess compliance and regulatory risks associated with business activities and ensure effective risk management strategies are in place. 4) Collaborate closely and creatively with cross-functional teams to guide the seamless implementation of regulatory guidelines and compliance requirements. 5) Manage audits and ensure timely, accurate responses to regulatory/ third-party inquiries and inspections. 6) Interpret policies, procedures, and compliance requirements while influencing and collaborating with professionals across all organizational levels. Lead and mentor the compliance team to achieve organizational compliance objectives effectively. 7) Ensure effective assessment of control design and maintenance of compliance framework, training on the regulatory guidelines/ laws and conduct risks, and effective communication of compliance expectations across the organization. 8) Prepare and present clear, concise compliance reports to the management, report to various committees of the board, ensure timely escalations to the Leadership team on incidents of compliance breaches and recommend corrective actions. Superpowers/ Skills that will help you succeed in this role: 1) 15+ years experience in the Compliance team of any NBFC/ Bank/ FinTech organizations. 2) Effective interpersonal skills to communicate and coordinate complex issues and projects with diverse levels of management. 3) Conversant with NPCI and RBI regulations and compliances apart from in depth knowledge of management of compliance function. 4) Knowledge of RBI rules and regulations for digital loan disbursement, repayments, offline payment products, operational knowledge of UPI TPAP and BBPS would be an added advantage. 5) Ability and willingness to independently manage all compliance-related functions and activities. Proactive and strategic approach in addressing compliance challenges, ensuring seamless alignment with regulatory expectations and organizational objectives. Education : Must be a Qualified CA/ CS /MBA Graduate or an LLB/ LLM is highly preferred.

The Senior Associate, Clinical Trial Submission Management, will help ensure the technical compliance of our Clinical Trial submissions via the smooth compliant flow of information between all functional areas, internal and external to GRAAS, local offices, external partners and regulatory authorities. This vital role is assigned to one or more Amgen products under development to ensure clinical trial application approvals in the EU, delivering technical compliance with EU Clinical Trial Regulation No.536/2014 for every clinical trial submission dossier through close internal cross-functional collaboration. Roles & Responsibilities: Support assembly of the submission package and supportive documentation for regulatory deliverables, for the management of clinical trials Be the operational driver for Clinical Trial Submissions and notifications in the state-of-the-art regulatory document management system and maintain tracking systems. Be the critical technical coordinator for Clinical Trial Submissions and notifications through the EMA CTIS system, performing accurate and timely input of data and documents into the EMA Clinical Trial Information System for Clinical Trial Applications, Modifications and Notifications. Be the Single Point of Contact for incoming EMA CTIS notifications and alerts through daily monitoring and swift dispatching of incoming requests to cross functional teams. Be responsible for reviewing and triaging of Requests for Information from Health Authorities through CTIS to relevant cross functional teams. Ensure Requests for Information are tracked within the document management system. Recipient of notification of compliant events from Amgen Clinical Trial Registry System for input into CTIS within regulation timelines. Ensure efficient and timely data entry and communication of submissions to key process stakeholders. Submitting Clinical Trial Results to CTIS through the Marketing Authorisation Holder Access. Support Sponsor High Level Administrator within CTIS with access requests. Act as Subject Matter Expert for CTIS providing intelligence and expertise on technical submission requirements and system processes. Assist with definition, development, and implementation of processes to meet the evolving CTIS needs. Escalates, informs and resolves any issues that may impact submission process or timelines within CTIS. Build effective relationships and communication paths across local and functional organizations. Enable efficiencies and seamless execution across the EU region countries Required Knowledge and Skills: Advanced technical and project management skills, demonstrated experience working in teams Advanced knowledge of the regulations and regulatory guidance applicable to EU Clinical Trial Applications Advanced knowledge of the submission and maintenance of EU Clinical Trial Applications Preferred Knowledge and Skills: Advanced knowledge of Veeva Vault RIM, Expertise in the regulations and regulatory guidance applicable to global Clinical Trial and Marketing Applications Proven experience of working with clinical trial applications under CTR Basic Education and Experience: Master’s degree and 1-2 years of directly related experience OR Bachelor’s degree and 2-3 years of directly related experience OR Associate’s degree and 3-5 years of directly related experience OR High school diploma / GED and 5+ years of directly related experience Preferred Education and Experience: Practical experience with CTIS system

The Regulatory Data & Systems Senior Associate will be responsible for interpreting and executing business requirements, based on a combination of industry best practice and Amgen regulatory processes. This role involves optimizing complex data systems supporting the health authority submission process, while ensuring compliance with regulatory regulations and guidance. The ideal candidate will have a strong background in system analysis and data science/AI in a regulated industry. Roles & Responsibilities: Data Administration/AI: Optimize and maintain the organization's complex data models, ensuring they are integrated, efficient, and compliant with regulatory requirements. Regulatory Business Analysis: Interpret and implement regulatory requirements, ensuring all systems and processes adhere to relevant regulatory requirements and industry best practices. Project Coordination Assist in planning, tracking, and executing departmental projects and initiatives. Stakeholder Communication: Liaise with internal and external stakeholders to ensure timely and accurate communication regarding regulatory requirements and system updates. Required Knowledge and Skills: Strong interpersonal and teamwork skills, with the ability to interact with business users, technical IT groups, project managers, senior management, outsourced service providers, and vendors. 5+ years' experience as a business analyst, with command of business analysis techniques & tools, as well as SDLC & agile systems development methodologies. Excellent oral and written communication skills; able to organize and present ideas in a convincing and compelling manner. Ability to operate effectively in a matrix environment; team player yet able to work independently with minimal direction. Familiarity with GxP requirements and systems validation. Life Sciences, Biotech or pharmaceutical industry experience. Preferred Knowledge and Skills: Advanced knowledge of Veeva Vault Familiarity with global regulatory processes and standards. Proficiency in Agile methodologies, including Scrum or Kanban, to enhance collaboration, efficiency, and adaptability within an Agile work environment. Basic Education and Experience: Bachelor’s degree and 2 years of directly related experience Associate’s degree and 6 years of directly related experience High school diploma / GED and 8 years of directly related experience Preferred Education and Experience: Practical experience with regulatory data standards, such as IDMP 5+ years’ experience in data management, machine learning, or related fields

What you will do Prepare clinical regulatory documents for public disclosure, including anonymization of personal data and redaction of commercially confidential information Work closely with cross-functional stakeholders to define redaction strategy, lead review and approval, ensure submission readiness, and hand off for timely submission or posting Ensure consistent quality across documents, ensure submission readiness, and hand off for timely submission or posting Communicate with team members to resolve problems and escalate issues Record and maintain written redaction strategy for the study and product Support trend analysis and process improvement What we expect of you Master’s degree and 1 to 3 years of relevant experience OR Bachelor’s degree and 3 to 5 years of relevant experience OR Diploma and 7 to 9 years of relevant experience Minimum of 2 years experience in preparing regulatory documents for public disclosure Familiarity with clinical research and clinical regulatory documents Knowledge of clinical trial disclosure regulations, guidelines, and best practices Basic Qualifications: Experience understanding and interpreting data/information and its practical application Self-motivated with developed skills in multi-tasking, attention to detail, and follow-through Ability to follow controlled processes Excellent spoken and written English Ability to negotiate and influence Project management skills, including ability to prioritize work in order to meet required deadlines Problem solving ability EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

Role: Data Acquisition Lead (FSP) Duration: Contract Location: Remote Work timing: IST or UK Hours Job Description: - Serve as the subject matter expert for the planning, set-up, and acquisition of external clinical data at the study level and manage study start up, conduct and close out activities. - Create external data transfer agreements, ensuring external clinical trial data are in alignment with company Standards and specifications to support data integration, analysis, and reporting. - Help and advice in setting up infrastructure for external data, to flow into company Clinical data pipelines. - Responsible for validation of all 3rd Party Data generated in clinical trial into company Clinical Data pipelines. - Develop strong and productive working relationships with key stakeholders like Clinical Data Management, Clinical Data Engineering, Standards and other Study Execution Team members. - Participate in preparing function for submission readiness and may represent Clinical Trial Tools & Technologies (CT3) group in a formal inspection or audit. - Representing company in interactions with key external partners as part of company CT3 3rd Party Data Acquisition team. - Responsible for timely submission and on-going maintenance of study related 3rd Party Data Acquisition documentation in TMF. - Follow procedural documents and participating in reviewing and updating documents to make sure they are reflective of industry standards and regulatory requirements and include optimal processes. - Liaise with and reviewing work delivered by external partners (e.g. laboratories, eCOA providers, technology providers, etc.) performing services on behalf of company. - Escalate issues to CT3 leadership appropriately. Technical/Functional Expertise: - Working knowledge and understanding of FDA and ICH regulations and industry standards and quality control principles. - Experience with all phases of drug development. - Solid Experience in handling Clinical data acquisition and management from external/3rd Party vendors. - May lead study level negotiation and agreement for data transfer or integration on behalf of company. - Should be able to function collaboratively (with some guidance) with all levels of employees , moderate supervision required. - Knowledge on FTP tools like GlobalScape, Clinical platforms like Veeva CDMS, Elluminate and Veeva TMF will be a plus. Thanks & Regards: Abhinav Krishna Srivastava Mob : +91- 9667680709 FCS Software Solutions Ltd. Email: asrivastava@fcsltd.com

We are seeking a skilled PADER Aggregate Report Specialist with expertise in drafting, reviewing, and submitting PADER reports in compliance with regulatory requirements. Key Responsibilities: Draft PADER aggregate reports as per the aggregate reporting schedule. Prepare line listings and tabulations for inclusion in the PADER report. Develop and maintain the PADER report calendar and schedule. Coordinate and resolve queries with cross-functional teams before finalizing line listings, addressing any issues identified in draft cases. Communicate with cross-functional teams to obtain required inputs and resolve queries efficiently. Archive all PADER-related information in the designated shared drive. Submit PADER documents and reports within specified timelines, ensuring compliance with internal and regulatory submission requirements. Prepare and review SOPs and work instructions in alignment with ICH-GCP, GVP modules, and FDA guidelines. Provide training to junior associates on PADER report preparation and processes. Support client audits and regulatory authority inspections as needed. Experience Required: 4-6 years of experience in aggregate report preparation for quality control roles. 3-4 years of experience in aggregate report drafting roles. Educational Qualifications: M.Pharm or Pharm.D candidates are preferred.

About The Role : Job TitlePrincipal Auditor Corporate TitleAVP LocationMumbai, India Role Description Overview As a global function of approximately 850 team members, Group Audit (GA) is the bank's 'Third Line of Defence' acting as an independent and forward-looking challenger and adviser to Senior Management. We are also strongly relied upon by local regulators. We closely partner and collaborate with all Group business and infrastructure areas. This includes the Investment Bank, Corporate Bank and International Private Bank businesses, and Technology, Anti-Financial Crime, Compliance, Risk, Finance and Operations infrastructure functions. A diverse and inclusive culture is at the core of our team dynamic, with strong corporate and ethical governance as a driving philosophy. New joiners are supported with a structured and comprehensive career programme. What we'll offer you As part of our flexible scheme, here are just some of the benefits that youll enjoy, Best in class leave policy. Gender neutral parental leaves 100% reimbursement under childcare assistance benefit (gender neutral) Sponsorship for Industry relevant certifications and education Employee Assistance Program for you and your family members Comprehensive Hospitalization Insurance for you and your dependents Accident and Term life Insurance Complementary Health screening for 35 yrs. and above Your key responsibilities The Senior Principal Auditor is responsible for working with the Validations Principal Audit Manager (PAM) on the Validation book of work. The core responsibilities of the role are: Assess finding validations by conducting walkthroughs, identify risks and controls, define test plan, and conclude on the test plan. Be able to assess exceptions materiality and conclude. Keep abreast of regulatory and audit related developments in the industry and ensure effective communication to enhance regulatory knowledge throughout the wider GA team. Act as a role model by being proactive and support the team and broader department. Escalate key emerging risks to senior management through the appropriate forums such as ad hoc communications, monthly/quarterly control reports, and management meetings. Build strategic relationships internally and externally to enhance the departments performance and maximize stakeholder support for the department. Support the PAMby regularly reporting on the status of the validation coverage and timely escalate any delays or coverage gaps, if required Your skills and experience Bachelor's degree in Accounting, Finance or related discipline. Advanced Degree (e.g., Masters, Juris Doctor) and professional certification (e.g., CPA, CIA, CAMS, CFE, etc.) preferred. In depth experience of working in an audit function within the financial services industry, with strong experience of leading audits or finding validations within a fast-paced business environment. Good knowledge of regulatory requirements, and a thorough understanding of the risk and control environment within the financial services industry. Demonstrated experience in proactively building meaningful relationships. Excellent verbal and written communication skills, with the ability to articulate complex issues/data simply and clearly. How we'll support you Training and development to help you excel in your career. Coaching and support from experts in your team. A culture of continuous learning to aid progression. A range of flexible benefits that you can tailor to suit your needs. About us and our teams Please visit our company website for further information: https://www.db.com/company/company.htm We strive for a culture in which we are empowered to excel together every day. This includes acting responsibly, thinking commercially, taking initiative and working collaboratively. Together we share and celebrate the successes of our people. Together we are Deutsche Bank Group. We welcome applications from all people and promote a positive, fair and inclusive work environment.