0 Ssa jobs in Swindon + 10 miles

GenO CSS Service Solution ArchitectStart your success story with GenO Oracle

At Oracle our mission is to help people see data in new ways, discover insights, and unlock endless possibilities. Organizations in all industries and of all sizes rely on Oracle to help them succeed. Learn how your work can have a truly global impact and influence the lives of billions of people every day: https://www.youtube.com/watch?v=yyUAPdt4VPE

GenOAre you passionate about changing lives through technology and driving innovation? Are you eager to learn, grow, and succeed in shaping your future? We’ll help you find your calling and kick-start an extraordinary career in a leading company as Oracle is.

Generation Oracle (GenO) is Oracle’s brand new career development initiative, focused on identifying and advancing early-in-career and returnship talent. GenO delivers learning, continuous development and clear, accessible career paths whilst offering the opportunity to influence and help steer our business into the future.

Join us as a Service Solution Architect Become an expert in Oracle Services Solutioning and put your passion for services, communication, knowledge management and professional practice development to work by playing a key role in the continual evolution of our world class community of Service Solution Architects.As part of the Customer Success Services programme, you will be a member of the international network of experts, who help our customers transform their businesses through optimal Oracle product and service solutions.

Job Description________________________________________What you'll do________________________________________Oracle Customer Success Services (CSS) is a services business unit within Oracle that establishes long-term enhanced support and managed service relationships with many of Oracle's largest customers. Click here for more information about CSS.CSS Service Solution Architect (SSA) play a key role in the continual evolution of our world class community of Service Solution Architects, assisting with community management, knowledge sharing, community communication and best practice collateral capture and creation. Each Associate will also be expected to become expert in a specific set of Oracle CSS service offerings, contribute to the creation of collateral and providing guidance to our Service Solution Architects and our sales force on those services.As an Service Solution Architect you will contribute to the continual evolution of our CSS EMEA Service Solution Architect community, assisting with community management, knowledge sharing, community communication and best practice collateral capture and creationProvide pre-sales service solution guidance to our Service Solution Architects and our sales force on specific service solutionsParticipate with our Service Solution Architects in the design, validation, and presentation of Oracle service solutionsParticipate in problem solving, with assistance and guidance, in understanding and applying company policies and procedures.Learn from experts from a wide network across Oracle’s EMEA and Global teamsUse Oracle internal tools, resources and network to learn and stay up to date with on innovation and leading technologiesContribute as a team member on projects together with Oracle experts and leadersConsult with the Service Solution Architect community to understand their requirements and provide that community with assistance, collateral and improvement initiativesLearn how to design compelling service solutions using Oracle leading technology and services innovation

What you'll bring________________________________________What we'll give you________________________________________Bachelor degree or up to 2 years relevant experience.Technical aptitude: You have an interest, understanding and curiosity in cloud technology and services conceptsFluency in English and local languageCommunication skills: You have an ability to collaborate and present concepts clearly.Innovation: You’re open to new ideas and challengesAgility: You’re a pro at embracing change. Your self-confidence helps you learn and adapt wherever you goDrive: You have a “roll-up-the-sleeves” and “get the job done” attitudeHigh energy: You’re optimistic, always eager to interact and influence peopleTeamwork: You’re a fantastic team player who also loves smashing individual goalsCritical thinking: You’re a natural strategist who can analyze situations, identify issues, and solve problems creativelyResilient and capable of working effectively under pressureStrong organization, negotiation and planning skillsLove & passion for customer success and world class IT servicesSignificant investment in your professional development and a social network of resources and thought leaders inside Oracle.Fun and flexible work for the ideal work-life balanceAn inspiring, inclusive, and multicultural community that values fresh perspectives. A buddy pro

Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so, our Biotechnology client is looking for individuals just like you!

The successful candidate will perform quality review to ensure documents authored by the Safety Surveillance and Aggregate Reports team or their vendors are of high quality and support process improvement.

This is a contract position offered initially on a 12 month contract basis working 37.5 hours a week Mon-Fri.

Responsibilities:

• Perform QC Review of documents.
• Verify data in assigned documents against source documentation, including checking text against database outputs.
• Perform editorial and technical review for grammatical and stylistic consistency in line with the Style Guide and document templates. This includes reviewing format, internal linking, and external cross-referencing.
• Document QC findings so that appropriate actions can be taken by authors. Where needed, meet with the author to discuss findings and strategize the next steps (in case the error lies within the source document), including support with the development of preferred text.
• Document QC metrics for quality tracking.
• Review vendor authoring and QC as part of oversight activities.
• Support the creation of training material for new staff members and vendors on quality requirements.
• Support the preparation of aggregate report quality trends for discussion at regular team meetings.
• Assist with the development and maintenance of training materials and Job Aids.
• Assist with maintenance of SSA templates.
• Assist with SSA process improvement initiatives for quality documentation and technical tools/systems, including developing new templates.
• Represent the department, where appropriate, in cross-functional improvement initiatives.
• Perform general administrative tasks such as maintaining spreadsheets and communicating summaries and results with the relevant stakeholders.
• Provide support to other functions within SSA, which may include activities outside of QC review (e.g., vendor management, aggregate report processes, SharePoint maintenance, literature activities).

Experience and skills:

• Bachelor's Degree in biologic, natural science, or health care discipline.
• Advanced degree (PhD, MPH, NP, PharmD, etc.) preferred.
• Previous writing and editing experience, preferably in the pharmaceutical or biotech industry.
• Comfortable with medical concepts and terminology; familiar with the American Medical Association (AMA) Manual of Style.
• Familiar with pharmacovigilance and drug development, including knowledge of applicable clinical trial safety regulations and postmarketing safety regulations. Includes familiarity with case processing, expedited reporting rules, and safety database concepts.
• Ability to understand, interpret, analyse, and clearly present scientific and medical data in verbal and written format.
• Ability to interact collaboratively and effectively in a team environment.
• Strong organisational skills, including the ability to prioritise independently.
• Proficient and comfortable using Microsoft Office (in particular, Word, Excel, and PowerPoint) and SharePoint platforms.
• Familiar with Documentum-based systems.
• Knowledge of common safety database systems.

Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.

Candidates must be eligible to live and work in the UK.

For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.

Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so, our Biotechnology client is looking for individuals just like you!

The successful candidate will perform quality review to ensure documents authored by the Safety Surveillance and Aggregate Reports team or their vendors are of high quality and support process improvement.

This is a contract position offered initially on a 12 month contract basis working 37.5 hours a week Mon-Fri.

Responsibilities:

• Perform QC Review of documents.
• Verify data in assigned documents against source documentation, including checking text against database outputs.
• Perform editorial and technical review for grammatical and stylistic consistency in line with the Style Guide and document templates. This includes reviewing format, internal linking, and external cross-referencing.
• Document QC findings so that appropriate actions can be taken by authors. Where needed, meet with the author to discuss findings and strategize the next steps (in case the error lies within the source document), including support with the development of preferred text.
• Document QC metrics for quality tracking.
• Review vendor authoring and QC as part of oversight activities.
• Support the creation of training material for new staff members and vendors on quality requirements.
• Support the preparation of aggregate report quality trends for discussion at regular team meetings.
• Assist with the development and maintenance of training materials and Job Aids.
• Assist with maintenance of SSA templates.
• Assist with SSA process improvement initiatives for quality documentation and technical tools/systems, including developing new templates.
• Represent the department, where appropriate, in cross-functional improvement initiatives.
• Perform general administrative tasks such as maintaining spreadsheets and communicating summaries and results with the relevant stakeholders.
• Provide support to other functions within SSA, which may include activities outside of QC review (e.g., vendor management, aggregate report processes, SharePoint maintenance, literature activities).

Experience and skills:

• Bachelor's Degree in biologic, natural science, or health care discipline.
• Advanced degree (PhD, MPH, NP, PharmD, etc.) preferred.
• Previous writing and editing experience, preferably in the pharmaceutical or biotech industry.
• Comfortable with medical concepts and terminology; familiar with the American Medical Association (AMA) Manual of Style.
• Familiar with pharmacovigilance and drug development, including knowledge of applicable clinical trial safety regulations and postmarketing safety regulations. Includes familiarity with case processing, expedited reporting rules, and safety database concepts.
• Ability to understand, interpret, analyse, and clearly present scientific and medical data in verbal and written format.
• Ability to interact collaboratively and effectively in a team environment.
• Strong organisational skills, including the ability to prioritise independently.
• Proficient and comfortable using Microsoft Office (in particular, Word, Excel, and PowerPoint) and SharePoint platforms.
• Familiar with Documentum-based systems.
• Knowledge of common safety database systems.

Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.

Candidates must be eligible to live and work in the UK.

For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.

• Managing permanent and temporary works designs for live projects and tenders.
• Managing the design process, with a focus on buildability and efficiency, to ensure the optimum solution is reached
• Development of Design Deliverables schedule in co-ordination with the designers
• Liaising with tender and project teams to ensure design is developed in line with expectations
• Ensuring a design programme is prepared and agreed with each designer
• Incorporating the design programme into the main programme
• Meeting with designers on a regular basis to ensure the design is developing as planned
• Monitoring progress of the design and works and updating the programme as necessary
• Ensuring the design is managed in accordance with the relevant quality procedures
• Ensuring Principal Designer duties are fulfilled for pre-construction operations under the CDM Regulations
• Providing design input as required for tender submissions
• Liaising with clients, designers, subcontractors, suppliers and third parties as appropriate
• Providing technical input and advice as required for live projects and tenders
• Providing input into programmes where required, including tender, design, construction and Variation / Compensation Event programmes
• Coordinating the design of temporary works and where appropriate design elements of temporary works
• Undertaking a review of design drawings and raising technical queries accordingly
• Providing construction methodology input and incorporating in the programme where required
• Managing the flow of information from the design team and advising the project team of any impact on progress and programme
• Providing necessary information to the Procurement Department to enable the procurement of materials and subcontractors
• Preparing handover documents
• Introducing improvements and innovations where appropriate

Trainee Safety Engineer

Overview

Stirling Dynamics is recruiting trainee safety engineers to join our Systems & Safety team.

Due to expanding project needs, Stirling Dynamics have an exciting opportunity for multiple talented engineers who are looking for new opportunities to develop and grow their skills towards a career in safety. We have created a Safety Engineer training programme designed for engineers who have some experience within Systems Engineering and are looking to change specialisms.

The successful engineers will be part of Stirling’s Systems & Safety team and will work on a variety of projects related to the next generation marine and aerospace applications. The role offers a unique opportunity to receive targeted training (internally and externally provided) across many aspects of systems safety, covering the full development life-cycle.

The role provides opportunities to work across all stages of the design cycle from concept phase through to certification, giving the candidate a broad range of experience to support them in the development of their career. The role gives a unique opportunity to work on varied projects such as, commercial aviation and submarines, through to the development of designs within the new areas of aircraft electrification and urban air mobility including eVTOL aircraft.

The successful candidate must have a keen interest in safety. The ideal candidate would be someone who has 2-3 years of systems engineering experience but would like to adjust their career path towards safety specifically.

The Safety Engineers will be predominantly based in our Bristol office with occasional travel to our clients’ sites as required. As part of our commitment to flexibility, employees can work part of the week from home.

As the successful candidates will need to be able to support marine projects, they must be eligible to obtain SC clearance.

Responsibilities

The Safety Engineer role will suit engineers looking to diversify their experience and work within a team responsible for guiding safety programme requirements, creating evidence and deliverables to support product safety argument generation and offering expert safety consultancy services to our business and our customers on multiple and varied projects.

Training will be provided by members of Stirling’s Systems & Safety team, which will focus on recognised safety methodologies/techniques, and Stirling’s business-related safety requirements/experience such as:

• ARP4761A & ARP4754A
• FHA (Functional Hazard Analysis)
• FTA (Fault Tree Analysis)
• Common Cause Analysis – Particular Risk, Common Mode & Zonal Safety Assessment
• FMEA (Failure Mode Effect Analysis), FMES (Failure Mode Effect Summary)
• Hardware & Software safety
• Route to certification

The successful candidate will also attend an external training course to supplement the internal learning.

The candidate will broaden their wider engineering skills by working in multi-disciplinary teams, engaging with customers, and helping contribute to the business’ internal safety techniques and processes.

The candidate must have a keen interest in safety methods and processes, a willingness to learn and strong interpersonal skills.

Candidates will have the following responsibilities upon completion of the training programme:

• Guiding safety programme requirements for our business’ or our customers products/equipment/systems
• Contribute to a variety of different analyses methods/techniques (FHA, PSSA/SSA, FTA, FMEA, PRA etc.) as part of the safety process
• Work with experienced colleagues to develop evidence and deliverables demonstrating the safety credentials of the system/equipment under design or modification for our own products and/or for our customers.

Qualifications

Candidates will ideally be degree qualified (or equivalent), in a related discipline preferably Aerospace Engineering, Mechanical Engineering, Physics, Electrical Engineering, Mathematics or a similar course with high technical content.

Skills

Systems Engineering:

• Aerospace industry experience (civil/military aviation, CS-23, CS-27, CS-25 certification)
• Defence/Marine industry experience (CADMID life-cycle)

PERSONAL CHARACTERISTICS

• Confidentiality
• Flexible, can-do approach
• Ability to deal with multiple conflicting requests
• Professional attitude
• Self-motivated to see tasks through to successful completion

Desired Skills

Training will be provided but any