17 Publications jobs in the United Kingdom
Publications Specialist
Posted today
Job Viewed
Job Description
Publications Specialist, London
Hybrid working (up to 50%)
Full-time or part-time (flexible)
Salary: circa. £47k with excellent benefits
Are you a brilliant Editor with strong project management skills and a flair for creating and delivering impactful content? We are looking for a Publications Specialist to take ownership of a diverse suite of publications and digital assets for a globally recognised mission-driven organisation. The role offers a competitive salary with excellent benefits and hybrid working (50% per month in beautiful Central London offices).
This is a brilliant opportunity for someone who thrives in a collaborative, purpose-driven environment and who is excited about taking ownership for a suite of impactful publications aimed at a b2b audience.
The successful candidate will:
- Lead the full lifecycle of print and digital publications, from concept through to delivery
- Write, edit, and proofread technical and awareness-raising content
- Manage external suppliers and stakeholders across design, print, and translation
- Oversee website updates and development projects to enhance the user experience and functionality
- Represent the organisation at international exhibitions and events
We are looking for a candidate with proven experience working on technical content as both an editor, and writer with an eagle eye for detail and strong project management skills. Experience in creating content for both print and digital is essential as well as proficiency with MS Office, Adobe InDesign and graphic design tools. Any experience or interest in the maritime, environmental or technical sectors would be an advantage.
This is an amazing opportunity to join an organisation who are making a real difference to the planet and this role offers the chance to contribute to their publishing efforts in a broad role where you will be able to write, edit, proofread and take real ownership of the final product. If this sounds like you, please get in touch!
Closing date: Midnight Sunday 31 August 2025.
Technical Publications Author
Posted 2 days ago
Job Viewed
Job Description
Technical Publications Author, Bournemouth, £50,000
Are you a detail-oriented technical writer with an engineering or aerospace background? Do you excel at turning complex technical information into clear, concise documentation for global manufacturers and engineers?
We’re hiring for a growing engineering firm in Bournemouth , renowned for its precision interior systems in aerospace. As a Technical Publications Author , you’ll produce high-quality manuals that support equipment installation, training, and maintenance.
This role suits a documentation specialist with experience in engineering or manufacturing, confident with regulatory standards and adept at cross-functional collaboration.
As Technical Publications Author, you’ll benefit from:
- £55,000 salary
- 25 days holiday (+ Bank Holidays)
- Health insurance and life assurance
- Onsite parking and cycle to work scheme
- Employee assistance programme
- The opportunity to work on high-profile certification projects
- Exposure to both UK and international programmes
- A technically progressive, collaborative engineering environment
As Technical Publications Author, your responsibilities will include:
- Creating and maintaining technical documents including CMMs, SBs, SILs , crew and maintenance training manuals
- Using industry-standard tools to format, illustrate and structure technical publications
- Ensuring documentation is delivered to OEM and industry specifications
- Collaborating with engineering, manufacturing, quality and customer support teams
- Working with regulatory frameworks and liaising with customer and certification stakeholders as needed
As Technical Publications Author, your experience will include:
- Prior experience authoring technical publications in an engineering or aerospace environment
- Proficiency with tools such as Adobe FrameMaker, IsoDraw, and Microsoft Office
- Experience with Simplified Technical English (ASD-STE100) and familiarity with iSpec 2200 (desirable)
- Strong written communication, time management and organisational skills
- A relevant engineering apprenticeship or technical qualification (degree desirable)
If you're looking to take your technical writing career to the next level in a specialist role where your precision and clarity make a real impact, apply today or speak with Amber at Rubicon for more details.
Technical Publications Author
Posted 2 days ago
Job Viewed
Job Description
Technical Publications Author, Bournemouth, £50,000
Are you a detail-oriented technical writer with an engineering or aerospace background? Do you excel at turning complex technical information into clear, concise documentation for global manufacturers and engineers?
We’re hiring for a growing engineering firm in Bournemouth , renowned for its precision interior systems in aerospace. As a Technical Publications Author , you’ll produce high-quality manuals that support equipment installation, training, and maintenance.
This role suits a documentation specialist with experience in engineering or manufacturing, confident with regulatory standards and adept at cross-functional collaboration.
As Technical Publications Author, you’ll benefit from:
- £55,000 salary
- 25 days holiday (+ Bank Holidays)
- Health insurance and life assurance
- Onsite parking and cycle to work scheme
- Employee assistance programme
- The opportunity to work on high-profile certification projects
- Exposure to both UK and international programmes
- A technically progressive, collaborative engineering environment
As Technical Publications Author, your responsibilities will include:
- Creating and maintaining technical documents including CMMs, SBs, SILs , crew and maintenance training manuals
- Using industry-standard tools to format, illustrate and structure technical publications
- Ensuring documentation is delivered to OEM and industry specifications
- Collaborating with engineering, manufacturing, quality and customer support teams
- Working with regulatory frameworks and liaising with customer and certification stakeholders as needed
As Technical Publications Author, your experience will include:
- Prior experience authoring technical publications in an engineering or aerospace environment
- Proficiency with tools such as Adobe FrameMaker, IsoDraw, and Microsoft Office
- Experience with Simplified Technical English (ASD-STE100) and familiarity with iSpec 2200 (desirable)
- Strong written communication, time management and organisational skills
- A relevant engineering apprenticeship or technical qualification (degree desirable)
If you're looking to take your technical writing career to the next level in a specialist role where your precision and clarity make a real impact, apply today or speak with Amber at Rubicon for more details.
Medical Writer - Publications
Posted today
Job Viewed
Job Description
It's not every day we have a chance to make the world a healthier place—but here, it’s our way of life. Idealistic? Maybe. Deeply pragmatic? Always. Real Chemistry is a global health innovation company that has carved out its space at the intersection between healthcare, marketing and communications, tech, and the people at the heart of it all. It’s with a great sense of purpose that we work together with brave health and wellness companies to create and inspire healthier, happier, and longer lives. It’s our passion. And if you’re still reading, we’re guessing it might be yours too. We are looking to add to our alchemic mix of more than 2,000 talented professionals. At Real Chemistry, we don’t just wish the world was healthier. We leverage tech, data and creativity to make it so. You in?
Real Chemistry is looking for a Medical Writer to join our growing team!
We believe that our work should be worthwhile and make a difference to the world. We set up our Medical Education Communications team to bring new energy to our sector. We are fearless in our pursuit of:
- Using science to help HCPs improve and prolong the lives of patients
- Putting ourselves in our clients’ shoes
- Being open to challenges and trying new things
- Achieving excellence, and persevering…even when it’s tough and we are afraid
- Doing our personal best – together as a team and as individuals – always!
What you’ll do:
- Use a range of resources to understand the underlying science and product strategy related to assigned projects
- Perform research to support assigned project work (KEE mapping, collating data from resources) and review literature and competitive information to continually expand understanding of brand/marketplace and emerging competitors
- Have an appreciation of commercial context and be able, with guidance, to assimilate commercial information for assigned therapeutic areas
- Demonstrate awareness of brand strategic objectives in written work
- Understand and adhere to the ABPI code of conduct under guidance of the senior team and following training
- Structure and develop various forms of scientific communications (e.g. manuscripts, posters, abstracts, slide decks, MSL material, , advisory board and symposia content and reports) annotate documents, perform data checks, and prepare reference packs
- Use existing, or quickly develop, relevant therapy area knowledge to ensure communication objectives are met on assigned projects (under supervision of senior editorial team)
- Adapt writing style to suit difference audiences (e.g. primary and secondary care physicians, nurses or patients) under the supervision of the senior team and direct manager
- Create, maintain and take ownership of assigned projects
- Adhere to quality control processes, including:
- Accurate referencing
- Data checking
- Proofreading
- Communicate relevant therapy area knowledge to the wider team to keep them up to date as needed
- Develop skills to confidently liaise with clients with appropriate support from more senior team members and respond promptly to client requests
- Actively participate in the briefing process for assigned work - interrogate the brief, and confirm understanding
- Ensure clarity on timelines, deadlines, and the availability of key people (reviewers)
- Prioritise workload accordingly and flag with account lead(s)/line manager at the earliest stage any potential barriers to successful project completion and suggests solutions
- Play a pivotal role within the editorial team, always leading by example and demonstrating knowledge of good practice/industry guidelines
- Recognise where your skills can be used to support colleagues in both the editorial and account handling teams
- Share insights and experiences with peers to support their professional development
- Seek feedback and proactively feeds back to improve individual and team performance
- Participate in the performance review process and deliver against your objectives
- Participate in the execution of established editorial deliverables, and understands the importance of adhering to project schedules, budgets and briefs
- Proactively clarify the number of hours available for each assigned project and key dates in project timeline and keeps the account team apprised of status on projects by providing timely and accurate communication
- Complete timesheets and expense claims accurately and on time
- Immerse yourself in the medical communications and pharma industries, clients' companies, and therapy areas
- Engage with every opportunity to establish an awareness of developments, innovations, and trends
- Seek opportunities to reflect these in project work and flags ideas to teams
This position is a perfect fit for you if:
- Our Company values – Best Together, Impact-Obsessed, Excellence Expected, Evolve Always and Accountability with an “I” – really speak to you.
- You are adaptable, resilient, and OK with adjusting your scope, responsibilities, and focus as we grow. When things change, so do we. We’re always evolving.
- You are proactive, driven, and resourceful with strong prioritization skills and a desire to dive into the data.
- You are highly organized self-starter, able to work independently and under tight deadlines.
What you should have:
- Experience in medical writing, ideally in an agency setting
- Understanding of GPP and ICMJE compliance as it relates to the development of publications
- Relevant degree (minimum of Masters, PhD preferred) PhD) in a science subject
- Possesses a solid scientific background and able to learn new therapeutic areas quickly and demonstrate this knowledge
- Possesses a good understanding of the clinical trials process and differences between Phase I-III; how trial data are presented; registrational trials and drug approval process
- Knowledge of the key statistical variables used in clinical trials (e.g. PFS, OS, safety data, relapse rate, etc.)
- Knowledge of measurement scales used in clinical trials (e.g. RECIST, EDSS, etc.) o Able to differentiate between strong and weak data
- Enthusiasm for learning and a keen eye for detail
- Demonstrates a clear, concise and accurate writing style, and:
- Understands the typical language which should and should not be used (comparisons, unverified claims etc.)
- Understand the processes involved in new business and terminology
- Demonstrate strong organisational, analytical, and interpersonal communication skills
- Independent thinker confident in taking ownership of assets and material development, but a team player who enjoys collaboration
- Professional presence, performs with a sense of urgency and with a client service orientation
- Has confidence to manage upward when required; able to communicate with managers when deadlines will not be met or when issues are foreseeable
- High energy, able to effectively operate in fast-paced, growing and evolving environment
- Good management of Microsoft Office tools (PowerPoint, Word, Excel) - particularly PowerPoint
Real Chemistry offers a comprehensive benefit program and perks, including a primary office location near in Moorgate, 25 days holiday, private medical insurance, dental insurance, pension contributions and a five-week sabbatical program. Other perks include health and wellness reimbursements, happy hours, and free healthy snacks to keep you running all day long. Learn more about our great benefits and perks at: .
*Notice: Real Chemistry and its affiliates' names are being misused by scammers through messaging services, fake websites, and apps. Do not share personal or financial information or make payments to any unverified sources claiming to be connected to Real Chemistry. We are working to stop these unauthorized activities and protect our community. Read more here .
Technical Publications Author
Posted today
Job Viewed
Job Description
Technical Publications Author, Bournemouth, £55,000
Are you a detail-oriented technical writer with an engineering or aerospace background? Do you excel at turning complex technical information into clear, concise documentation for global manufacturers and engineers?
We’re hiring for a growing engineering firm in Bournemouth , renowned for its precision interior systems in aerospace. As a Technical Publications Author , you’ll produce high-quality manuals that support equipment installation, training, and maintenance.
This role suits a documentation specialist with experience in engineering or manufacturing, confident with regulatory standards and adept at cross-functional collaboration.
As Technical Publications Author, you’ll benefit from:
- £55,000 salary
- 25 days holiday (+ Bank Holidays)
- Health insurance and life assurance
- Onsite parking and cycle to work scheme
- Employee assistance programme
- The opportunity to work on high-profile certification projects
- Exposure to both UK and international programmes
- A technically progressive, collaborative engineering environment
As Technical Publications Author, your responsibilities will include:
- Creating and maintaining technical documents including CMMs, SBs, SILs , crew and maintenance training manuals
- Using industry-standard tools to format, illustrate and structure technical publications
- Ensuring documentation is delivered to OEM and industry specifications
- Collaborating with engineering, manufacturing, quality and customer support teams
- Working with regulatory frameworks and liaising with customers and certification stakeholders as needed
As Technical Publications Author, your experience will include:
- Prior experience authoring technical publications in an engineering or aerospace environment
- Proficiency with tools such as Adobe FrameMaker, IsoDraw, and Microsoft Office
- Experience with Simplified Technical English (ASD-STE100) and familiarity with iSpec 2200 (desirable)
- Strong written communication, time management and organisational skills
- A relevant engineering apprenticeship or technical qualification (degree desirable)
If you're looking to take your technical writing career to the next level in a specialist role where your precision and clarity make a real impact, apply today or speak with Amber at Rubicon for more details.
Technical Publications Specialist
Posted today
Job Viewed
Job Description
Role: Aerospace Technical Publication Specialist
Type: Permanent/ Full-Time
Location: Derby, UK
Job Description:
Domain Consulting & Business Analysis
- Analyze complex client scenarios to identify business problems and assess the impact on operations.
- Facilitate business workshops to define project scope, identify process improvements, and gather requirements for IT solutions.
- Explore and implement AI and Gen AI technologies within solution designs to enhance efficiency.
- Document and re-engineer current (AS-IS) and future (TO-BE) business processes, ensuring alignment with organizational goals.
- Design business use cases, lead functional architecture discussions, and integrate various services for seamless solution delivery.
- Collaborate with Product Owners and business stakeholders to analyze requirements and prepare product backlog items.
- Create user stories, define acceptance criteria, and ensure clear communication between business stakeholders and the technology team through all project phases.
Sales Pursuits & Thought Leadership
- Support sales pursuits and market development activities in collaboration with the sales and account management teams.
- Contribute to thought leadership in industry solutions, partnerships, and publications.
- Participate in organizational initiatives, driving innovation and continuous improvement within the team.
Required Qualifications:
- Relevant experience in the Aerospace sector, with specific expertise in technical publications, supply chain, shopfloor operations, quality, or service/repairs domains.
- Experience in Technical Publication (TechPub) or related areas.
- Proven ability to lead business analysis and provide functional consulting in complex environments.
- Strong communication and stakeholder management skills, with the ability to engage effectively with both technical and non-technical teams.
- Hands-on experience in designing business processes, writing user stories, and defining functional requirements.
Preferred:
- Familiarity with design-thinking methodologies, including customer personas, customer journeys, and story maps.
- Experience with risk assessment, incident investigation, and continuous improvement methodologies such as Six Sigma.
- Knowledge of industry frameworks like APQC and SCOR.
- Experience in Agile software development and an understanding of the full software development lifecycle.
Education Requirements:
- Bachelor’s degree in Engineering, Science, or a related field.
Medical Writer - Publications
Posted today
Job Viewed
Job Description
It's not every day we have a chance to make the world a healthier place—but here, it’s our way of life. Idealistic? Maybe. Deeply pragmatic? Always. Real Chemistry is a global health innovation company that has carved out its space at the intersection between healthcare, marketing and communications, tech, and the people at the heart of it all. It’s with a great sense of purpose that we work together with brave health and wellness companies to create and inspire healthier, happier, and longer lives. It’s our passion. And if you’re still reading, we’re guessing it might be yours too. We are looking to add to our alchemic mix of more than 2,000 talented professionals. At Real Chemistry, we don’t just wish the world was healthier. We leverage tech, data and creativity to make it so. You in?
Real Chemistry is looking for a Medical Writer to join our growing team!
We believe that our work should be worthwhile and make a difference to the world. We set up our Medical Education Communications team to bring new energy to our sector. We are fearless in our pursuit of:
- Using science to help HCPs improve and prolong the lives of patients
- Putting ourselves in our clients’ shoes
- Being open to challenges and trying new things
- Achieving excellence, and persevering…even when it’s tough and we are afraid
- Doing our personal best – together as a team and as individuals – always!
What you’ll do:
- Use a range of resources to understand the underlying science and product strategy related to assigned projects
- Perform research to support assigned project work (KEE mapping, collating data from resources) and review literature and competitive information to continually expand understanding of brand/marketplace and emerging competitors
- Have an appreciation of commercial context and be able, with guidance, to assimilate commercial information for assigned therapeutic areas
- Demonstrate awareness of brand strategic objectives in written work
- Understand and adhere to the ABPI code of conduct under guidance of the senior team and following training
- Structure and develop various forms of scientific communications (e.g. manuscripts, posters, abstracts, slide decks, MSL material, , advisory board and symposia content and reports) annotate documents, perform data checks, and prepare reference packs
- Use existing, or quickly develop, relevant therapy area knowledge to ensure communication objectives are met on assigned projects (under supervision of senior editorial team)
- Adapt writing style to suit difference audiences (e.g. primary and secondary care physicians, nurses or patients) under the supervision of the senior team and direct manager
- Create, maintain and take ownership of assigned projects
- Adhere to quality control processes, including:
- Accurate referencing
- Data checking
- Proofreading
- Communicate relevant therapy area knowledge to the wider team to keep them up to date as needed
- Develop skills to confidently liaise with clients with appropriate support from more senior team members and respond promptly to client requests
- Actively participate in the briefing process for assigned work - interrogate the brief, and confirm understanding
- Ensure clarity on timelines, deadlines, and the availability of key people (reviewers)
- Prioritise workload accordingly and flag with account lead(s)/line manager at the earliest stage any potential barriers to successful project completion and suggests solutions
- Play a pivotal role within the editorial team, always leading by example and demonstrating knowledge of good practice/industry guidelines
- Recognise where your skills can be used to support colleagues in both the editorial and account handling teams
- Share insights and experiences with peers to support their professional development
- Seek feedback and proactively feeds back to improve individual and team performance
- Participate in the performance review process and deliver against your objectives
- Participate in the execution of established editorial deliverables, and understands the importance of adhering to project schedules, budgets and briefs
- Proactively clarify the number of hours available for each assigned project and key dates in project timeline and keeps the account team apprised of status on projects by providing timely and accurate communication
- Complete timesheets and expense claims accurately and on time
- Immerse yourself in the medical communications and pharma industries, clients' companies, and therapy areas
- Engage with every opportunity to establish an awareness of developments, innovations, and trends
- Seek opportunities to reflect these in project work and flags ideas to teams
This position is a perfect fit for you if:
- Our Company values – Best Together, Impact-Obsessed, Excellence Expected, Evolve Always and Accountability with an “I” – really speak to you.
- You are adaptable, resilient, and OK with adjusting your scope, responsibilities, and focus as we grow. When things change, so do we. We’re always evolving.
- You are proactive, driven, and resourceful with strong prioritization skills and a desire to dive into the data.
- You are highly organized self-starter, able to work independently and under tight deadlines.
What you should have:
- Experience in medical writing, ideally in an agency setting
- Understanding of GPP and ICMJE compliance as it relates to the development of publications
- Relevant degree (minimum of Masters, PhD preferred) PhD) in a science subject
- Possesses a solid scientific background and able to learn new therapeutic areas quickly and demonstrate this knowledge
- Possesses a good understanding of the clinical trials process and differences between Phase I-III; how trial data are presented; registrational trials and drug approval process
- Knowledge of the key statistical variables used in clinical trials (e.g. PFS, OS, safety data, relapse rate, etc.)
- Knowledge of measurement scales used in clinical trials (e.g. RECIST, EDSS, etc.) o Able to differentiate between strong and weak data
- Enthusiasm for learning and a keen eye for detail
- Demonstrates a clear, concise and accurate writing style, and:
- Understands the typical language which should and should not be used (comparisons, unverified claims etc.)
- Understand the processes involved in new business and terminology
- Demonstrate strong organisational, analytical, and interpersonal communication skills
- Independent thinker confident in taking ownership of assets and material development, but a team player who enjoys collaboration
- Professional presence, performs with a sense of urgency and with a client service orientation
- Has confidence to manage upward when required; able to communicate with managers when deadlines will not be met or when issues are foreseeable
- High energy, able to effectively operate in fast-paced, growing and evolving environment
- Good management of Microsoft Office tools (PowerPoint, Word, Excel) - particularly PowerPoint
Real Chemistry offers a comprehensive benefit program and perks, including a primary office location near in Moorgate, 25 days holiday, private medical insurance, dental insurance, pension contributions and a five-week sabbatical program. Other perks include health and wellness reimbursements, happy hours, and free healthy snacks to keep you running all day long. Learn more about our great benefits and perks at: .
*Notice: Real Chemistry and its affiliates' names are being misused by scammers through messaging services, fake websites, and apps. Do not share personal or financial information or make payments to any unverified sources claiming to be connected to Real Chemistry. We are working to stop these unauthorized activities and protect our community. Read more here .
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Associate Director, Global Publications

Posted 18 days ago
Job Viewed
Job Description
Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
**Job Description**
**Associate Director, Global Publications**
We are seeking a highly motivated individual to join us as Associate Director, Global Publications within Kite Global Medical Affairs. You will partner with internal and external subject matter experts and investigators to execute the publication strategy for key publication tactics including congress abstracts, presentations, and manuscripts in Cell Therapy. You will apply good publication practices and help lead adherence to established publication processes and industry guidelines. This position will report to the Senior Director, Global Publications.
**Responsibilities**
+ Work with the Senior Director, Global Publications to help lead cross-functional, Global Publication Planning Team (GPPT) strategy in alignment with early- and late-stage subject matter experts, cross-functional teams, and alliance partners to create strategic annual publication plans and publish high-impact scientific and medical data
+ Work cross-functionally with subject matter experts across all data-generating functions (including, but not limited to, Clinical Development, Biometrics, Translational Medicine, Real World Evidence, Health Economics and Outcomes Research) to execute on tactics consistent with inline and pipeline strategy
+ Publications will be in the field of cell therapy primarily in hematological malignancies - therapeutic areas may include lymphoma, leukemia, and multiple myeloma
+ Work independently to prioritize, execute, review, and edit key tactics consisting of congress abstracts and presentations and peer-reviewed manuscripts
+ Establish and maintain effective intellectual partnerships with internal collaborators, external scientific and medical external authors and healthcare professionals (HCPs), and alliance partners
+ Travel to scientific conferences as needed
+ Guide and oversee publication vendors, and manage publications budgets
**Basic Qualifications**
Advanced degree (Pharm D, MD, PhD) and significant experience in biotech/pharmaceutical industry or medical communications agency experience with focus on scientific/medical publications
**Preferred Qualifications**
+ Experience in publications within the biotech/pharmaceutical industry, including experience in hematology/oncology and/or cell therapy
+ Excellent interpersonal, negotiation, communication, and collaborative skills with individuals, groups, and senior management
+ Ability to write/edit scientific manuscripts, posters, and abstracts with a medically strategic mindset
+ Working knowledge of Medical Affairs, Clinical Development, Legal, and Intellectual Property functions
+ Ability to lead and work across multi-disciplinary groups and to lead decision-making discussions
+ Knowledge of and compliance with all relevant guidelines (GPP3, ICMJE), laws, industry standard best practices, and corporate policies
+ Ability to work under challenging deadlines with key stakeholders
+ Up to 15% travel including weekends
**Equal Employment Opportunity (EEO)**
It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual's gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.
**For Current Gilead Employees and Contractors:**
Please apply via the Internal Career Opportunities portal in Workday.
Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.
Content Creation Specialist
Posted today
Job Viewed
Job Description
Content Creation Specialist
Telford Outskirts
£25k - £30k plus excellent benefits
Own transport is essential due to location.
Content Creation Specialist
Our prestigious client is seeking a motivated Content Creation Specialist with strong creative flair, proven campaign management skills, and the ability to deliver engaging, results-driven content. Reporting to the Creative Manager, you’ll work closely with marketers and creatives to create compelling social strategies that drive performance.
Key Skills & Experience
- Minimum 2 years’ proven experience managing social media campaigns. li>Creative flair with the ability to independently create engaging content across TikTok, Instagram, Meta, LinkedIn, and YouTube.
- Strong copywriting skills with excellent attention to detail and brand consistency.
- Confident in creating Instagram Reels and TikTok content.
- Solid understanding of social media analytics and reporting (Meta Analytics, GA4, Tag Manager, SEMrush an advantage).
- Proficiency in Microsoft Office, including PowerPoint for reporting.
- Excellent time management, organisation, and multitasking abilities.
- Strong communication and client relationship skills.
Responsibilities
- Develop and deliver audience-focused social strategies aligned with client objectives.
- Manage campaigns across multiple platforms, ensuring measurable performance and impact.
- Produce creative, high-quality social content—written, visual, and video. < i>Write engaging copy for social, email, and web, ensuring clarity, tone, and accuracy.
- Monitor, analyse, and report on campaign performance, providing insights and recommendations.
- Maintain strong client relationships and deliver outstanding service.
To apply for this role please contact Sarah Dyehouse at Anderson Scott .
Content Creation Specialist
Posted today
Job Viewed
Job Description
Content Creation Specialist
Telford Outskirts
£25k - £30k plus excellent benefits
Own transport is essential due to location.
Content Creation Specialist
Our prestigious client is seeking a motivated Content Creation Specialist with strong creative flair, proven campaign management skills, and the ability to deliver engaging, results-driven content. Reporting to the Creative Manager, you’ll work closely with marketers and creatives to create compelling social strategies that drive performance.
Key Skills & Experience
- Minimum 2 years’ proven experience managing social media campaigns. li>Creative flair with the ability to independently create engaging content across TikTok, Instagram, Meta, LinkedIn, and YouTube.
- Strong copywriting skills with excellent attention to detail and brand consistency.
- Confident in creating Instagram Reels and TikTok content.
- Solid understanding of social media analytics and reporting (Meta Analytics, GA4, Tag Manager, SEMrush an advantage).
- Proficiency in Microsoft Office, including PowerPoint for reporting.
- Excellent time management, organisation, and multitasking abilities.
- Strong communication and client relationship skills.
Responsibilities
- Develop and deliver audience-focused social strategies aligned with client objectives.
- Manage campaigns across multiple platforms, ensuring measurable performance and impact.
- Produce creative, high-quality social content—written, visual, and video. < i>Write engaging copy for social, email, and web, ensuring clarity, tone, and accuracy.
- Monitor, analyse, and report on campaign performance, providing insights and recommendations.
- Maintain strong client relationships and deliver outstanding service.
To apply for this role please contact Sarah Dyehouse at Anderson Scott .