Headquartered in suburban Atlanta, Georgia, Artivion, Inc. is a medical device company focused on developing simple, elegant solutions that address cardiac and vascular surgeons' most difficult challenges in treating patients with aortic diseases. Artivion has over 1,400 employees worldwide with sales representation in over 100 countries. The Company has manufacturing facilities located in Atlanta, Georgia, Austin, Texas and Hechingen, Germany. Additionally, it has sales and distribution offices in various countries throughout Europe, Asia, and South America. For additional information about Artivion, visit our website, www.artivion.com.
Position Overview:
Responsible for creating, editing, and managing high-quality scientific and regulatory documents that support the development, approval, and lifecycle management of medical devices. This role involves working cross-functionally with internal stakeholders-including Clinical, Regulatory, R&D, and Quality teams-to ensure timely and compliant documentation in line with global regulatory requirements. Manage assigned departmental project tasks/systems in principal areas or responsibilities identified below.
Responsibilities:
Writing regulatory documents supporting clinical deliverables for product lines.
Ensure product line compliance with US and International regulations and standards, as applicable to clinical regulatory requirements, including document preparation and submissions.
Coordinating deliverables for the CER, PMCF, and SSCP process for product lines.
Collaborate with Clinical, R&D, Quality, Regulatory, Risk Management, Field Assurance, and Marketing.
Effectively communicate timelines and assist teammates in keeping them.
Conduct literature reviews and write research summaries related to product lines.
Prepare product IFUs and assist with labeling and labeling changes (including receipt of applicable translations).
Collect, query, analyze, distribute and present clinical and pre-clinical data. Develop and maintain any applicable clinical research databases, as necessary.
Interface with technical representatives, regional managers, and research teams for the purpose of technical training and addressing customer questions/concerns.
Generate interim and final clinical study reports.
Communicate with customers and field staff regarding the planning of clinical trials, complaints, problems, and general correspondence.
Coordinate the execution of peer-reviewed projects (publications, posters, abstracts) and marketing literature.
Develop clinical protocols and/or investigational plans, informed consent forms, case report forms, handouts, SOPs, analyses, etc. as needed. Prepare status reports, as required.
Perform literature reviews and reference management using tools such as PubMed and EndNote.
Other assigned responsibilities (including previously identified tasks being performed at a higher level than one's current title).
Qualifications:
Education:
Bachelor's degree in life sciences, biomedical engineering, medical writing, or related field (advanced degree preferred: MS, PhD, PharmD, or MD).
Experience:
2-5 years of medical writing experience in the medical device, pharmaceutical, or healthcare industry.
Familiarity with regulatory documentation for medical devices and understanding of applicable regulations (EU MDR, FDA 510(k), etc.).
Skills:
Excellent written and verbal communication skills.
Strong attention to detail and organizational skills.
Ability to interpret complex scientific and clinical data.
Proficiency with Microsoft Office (Word, Excel, PowerPoint) and reference management software.
Preferred Qualifications:
Experience with Class II or III medical devices.
Familiarity with document management systems.
Knowledge of systematic literature review methodology.
Certification or training in medical writing (e.g., AMWA, EMWA) is a plus.
$64k-95k yearly est. 60d+ ago
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Medical Writer
Artivion, Inc.
Medical writer job in Kennesaw, GA
Headquartered in suburban Atlanta, Georgia, Artivion, Inc. is a medical device company focused on developing simple, elegant solutions that address cardiac and vascular surgeons' most difficult challenges in treating patients with aortic diseases. Artivion has over 1,400 employees worldwide with sales representation in over 100 countries. The Company has manufacturing facilities located in Atlanta, Georgia, Austin, Texas and Hechingen, Germany. Additionally, it has sales and distribution offices in various countries throughout Europe, Asia, and South America. For additional information about Artivion, visit our website, *****************
Position Overview:
Responsible for creating, editing, and managing high-quality scientific and regulatory documents that support the development, approval, and lifecycle management of medical devices. This role involves working cross-functionally with internal stakeholders-including Clinical, Regulatory, R&D, and Quality teams-to ensure timely and compliant documentation in line with global regulatory requirements. Manage assigned departmental project tasks/systems in principal areas or responsibilities identified below.
Responsibilities:
* Writing regulatory documents supporting clinical deliverables for product lines.
* Ensure product line compliance with US and International regulations and standards, as applicable to clinical regulatory requirements, including document preparation and submissions.
* Coordinating deliverables for the CER, PMCF, and SSCP process for product lines.
* Collaborate with Clinical, R&D, Quality, Regulatory, Risk Management, Field Assurance, and Marketing.
* Effectively communicate timelines and assist teammates in keeping them.
* Conduct literature reviews and write research summaries related to product lines.
* Prepare product IFUs and assist with labeling and labeling changes (including receipt of applicable translations).
* Collect, query, analyze, distribute and present clinical and pre-clinical data. Develop and maintain any applicable clinical research databases, as necessary.
* Interface with technical representatives, regional managers, and research teams for the purpose of technical training and addressing customer questions/concerns.
* Generate interim and final clinical study reports.
* Communicate with customers and field staff regarding the planning of clinical trials, complaints, problems, and general correspondence.
* Coordinate the execution of peer-reviewed projects (publications, posters, abstracts) and marketing literature.
* Develop clinical protocols and/or investigational plans, informed consent forms, case report forms, handouts, SOPs, analyses, etc. as needed. Prepare status reports, as required.
* Perform literature reviews and reference management using tools such as PubMed and EndNote.
* Other assigned responsibilities (including previously identified tasks being performed at a higher level than one's current title).
Qualifications:
Education:
* Bachelor's degree in life sciences, biomedical engineering, medical writing, or related field (advanced degree preferred: MS, PhD, PharmD, or MD).
Experience:
* 2-5 years of medical writing experience in the medical device, pharmaceutical, or healthcare industry.
* Familiarity with regulatory documentation for medical devices and understanding of applicable regulations (EU MDR, FDA 510(k), etc.).
Skills:
* Excellent written and verbal communication skills.
* Strong attention to detail and organizational skills.
* Ability to interpret complex scientific and clinical data.
* Proficiency with Microsoft Office (Word, Excel, PowerPoint) and reference management software.
Preferred Qualifications:
* Experience with Class II or III medical devices.
* Familiarity with document management systems.
* Knowledge of systematic literature review methodology.
* Certification or training in medical writing (e.g., AMWA, EMWA) is a plus.
$64k-95k yearly est. 60d+ ago
Senior Manager, Medical Writing
Edwards Lifesciences 4.6
Medical writer job in Atlanta, GA
Imagine how your ideas and expertise can change a patient's life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to increase access to pioneering technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize patient outcomes.
Aortic stenosis impacts millions of people globally, yet it often remains under-diagnosed and undertreated. Edwards' groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life-changing solution for patients by offering heart valve replacement without the need for open heart surgery. Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.
The Senior Manager, Medical Writing oversees medical writing projects and team operations in compliance with regulations, GCP, and SOPs. This role leads cross-functional collaboration, manages team performance and hiring, resolves operational issues, and builds strong relationships to drive change and share best practices while ensuring high-quality deliverables and exceptional client service.
**How you'll make an impact:**
+ Manage and oversee the work of small medical writing team to support clinical and regulatory submissions (e.g., clinical study reports, clinical evaluation reports) and may indirectly manage cross-functional or matrix teams as appropriate. Develop a robust talent development plan in alignment with functional growth strategies of the department
+ Identify risk, develop and lead in the implementation of strategies which may include negotiations with internal and external parties
+ Provide medical writing expertise and collaborate with cross functional teams including Regulatory Affairs, Biostatistics, R&D, QA and Marketing on clinical data reports and plans throughout product lifecycle
+ Manage activities with the accountability for successful completion of all deliverables. Identify risk, develop mitigation strategies, alternative solutions, resolve issues, action item follow up, etc. in collaboration with cross functional and/or matrix teams
+ Review and interpret study data analyses
+ Contribute to the generation of product life cycle plans (e.g., post-market surveillance).
**What you'll need (Required):**
+ Bachelor's Degree in in related field in related experience in medical writing and clinical data analysis or equivalent work experience based on Edwards criteria
+ Demonstrated track record in people management or equivalent work experience based on Edwards criteria
**What else we look for (Preferred):**
+ Master's Degree Experience working in a regulated industry or equivalent work experience based on Edwards criteria
+ Medical writing or regulatory certification or equivalent work experience based on Edwards criteria
+ Experience with Class III devices and CER development under MEDDEV rev. 4 and/or MDR preferred or equivalent work experience based on Edwards criteria
+ Experience working in a regulated industry or equivalent work experience based on Edwards criteria
+ Certification in related fields
+ Strong leadership in project and team management, including coaching and performance oversight.
+ Expertise in medical writing processes, regulatory requirements (FDA, EU MDR), GCP, and ICH guidelines.
+ Advanced knowledge of biomedical statistics, clinical literature review, and therapeutic/product operations.
+ Skilled in Microsoft Office Suite and publication/database tools (EndNote, Medline, PubMed).
+ Exceptional problem-solving, analytical, and communication skills; ability to influence and negotiate.
+ Familiarity with coronary interventional and structural heart environments.
+ Proven ability to develop metrics demonstrating medical writing value to the business.
+ Ability to thrive in a fast-paced, dynamic environment with strict attention to detail.
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California, the base pay range for this position is $142,000 to $201,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
**COVID Vaccination Requirement**
Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.
$142k-201k yearly 36d ago
Proposal Writer
Sharecare 4.4
Medical writer job in Atlanta, GA
Sharecare is the leading digital health company that helps people - no matter where they are in their health journey - unify and manage all their health in one place. Our comprehensive and data-driven virtual health platform is designed to help people, providers, employers, health plans, government organizations, and communities optimize individual and population-wide well-being by driving positive behavior change. Driven by our philosophy that we are all together better, at Sharecare, we are committed to supporting each individual through the lens of their personal health and making high-quality care more accessible and affordable for everyone. To learn more, visit ******************
Job Summary:
The Proposal Writer is responsible for developing a range of proposal content that meets proposal compliance and quality standards. The incumbent develops proposal content in coordination with the Proposal Manager and the proposal team.
Essential Job Functions:
Research, write, and edit persuasive and compliant proposal content that aligns with Sharecare's brand voice, value propositions, and solution differentiation
Partner cross-functionally with internal stakeholder groups (i.e., Sales, Product, Security, Legal, and Operations) to validate accuracy.
Ensure timely submission, formatting consistency, and adherence to brand and quality standards.
Translate complex health, wellness and technology concepts into clear, audience-specific messaging that demonstrates value and impact.
Leverage proposal management software (e.g., Loopio) to source, customize, and maintain reusable content that reflects current offerings and standards
Analyze RFP/RFI requirements and contribute to win strategy development.
Support the continuous improvement of the content library by identifying gaps, refreshing outdated material, and integrating feedback from past submissions.
Contribute to post-submission reviews and incorporate lessons learned to improve win rate and proposal quality.
Accept ownership for new and different responsibilities as business priorities shift, exploring and building opportunities to add value
Specific Skills/ Attributes:
Well organized, able to prioritize and re-prioritize work in a dynamic environment to meet changing business needs
Excellent written, oral, and verbal communication skills
Solid problem-solving skills
Lifelong learner, proactively seeks additional opportunities to expand knowledge
Results driven with disciplined follow-through and a focus on accuracy
Strong work ethic, excellent team player, and a "do what it takes" attitude
Demonstrated enthusiasm for intensive, deadline-driven, and high-profile role
Active listening and assessment skills with the ability to take complex technical information and translate information into compelling content
Ability to conceive the client need and write from their perspective
Qualifications:
A Bachelor's Degree in business, communications, English or related field, or equivalent experience. Experience in the healthcare industry is preferred.
Prior RFP/proposal writing experience 2 yrs. Plus 2-5 years' experience in a professional corporate or related environment.
Sharecare and its subsidiaries are Equal Opportunity Employers and E-Verify users. Qualified applicants will receive consideration for employment without regard to race, color, sex, national origin, sexual orientation, gender identity, religion, age, equal pay, disability, genetic information, protected veteran status, or other status protected under applicable law.
$67k-94k yearly est. Auto-Apply 10d ago
Principal Medical Writer / Senior Medical Writer - US - FSP
Parexel 4.5
Medical writer job in Atlanta, GA
The Senior MedicalWriter will research, create, and edit all documents associated with clinical research. Responsibilities also include: acting as primary client contact for medical writing projects, working with other Parexel departments and clients to set and meet internal/external deliverable timelines, project leadership, and training and support of junior medical writing staff.
**Key Accountabilities** :
**Author Clinical Documents**
+ Gather, review, analyze, and evaluate pertinent resources to prepare, develop, and finalize clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical document (CTD) clinical overviews and summaries, safety update/aggregate reports, and integrated summaries of safety and efficacy.
+ Revise document drafts based on the review comments from team members to ensure inclusion of all relevant input.
+ Follow required standard operating procedures (SOPs), templates, guidelines, regulations, client instructions and other processes, as applicable.
+ Perform literature searches/reviews as necessary to obtain background information and training for development of documents.
+ Review statistical analysis plans and mock statistical output to determine appropriateness of content/format for clinical writing.
**Quality Control**
+ Ensure that all work is complete and of high quality prior to team distribution or shipment to client.
+ Confirm data consistency and integrity across the document.
+ Prepare documents for publishing readiness, when applicable.
+ Ensure document structure, content, and style adheres to FDA/EMA or other appropriate regulatory guidelines, and comply with departmental, corporate or client SOPs and style guidelines, as applicable.
+ Provide suggested alternative content when contributors provide content that does not meet document needs.
+ Provide medical editing review of draft and final documents prepared by other writers before internal or external distribution. This includes both copyediting and content review.
**Document Project Management**
+ Act in the capacity of project manager/lead for medical writing projects, which may entail serving as the primary client contact, negotiating deliverable timelines, and resolving project-related issues. Project management of contractual and financial aspects may only be performed with the guidance of medical writing management.
+ Serve as the Medical Writing representative on assigned project teams and demonstrate document leadership: communicate content requirements, coordinate and conduct interdepartmental team review of draft and final documents, schedule and lead/facilitate authoring team meetings to agree on expectations, evaluate progress on tasks, identify issues and facilitate resolutions, manage/drive the timeline, and advance document development to approval, according to Parexel or client guidelines/SOPs. Distribute final documents to project team and client.
+ Identify any potential project challenges to departmental line management and project leader, including changes in project plan, timeline or out of scope requests, and suggest possible resolution options.
+ Attend or lead project team meetings as required. Mediate conflict or disagreement, as well as timeline delays, among team members by negotiating, compromising, and facilitating open exchange of ideas and opinions to come to a consensus.
+ Supervise collection of documentation by Medical Writing Support Coordinator, Document Specialist, and/or Associate MedicalWriter for assembly of project files and client deliverables. Ensure appropriate filing of project documentation with assistance from the Medical Writing Support Coordinator.
+ Build and maintain collaborative relationships with teams/clients for an efficient, productive, and professional working relationship.
**Training/ Compliance**
+ Attend and complete mandatory, corporate, project-specific, and departmental training as required.
+ Keep abreast of professional information and technology through workshops and conferences (when approved), and assure appropriate transfer of that information to the department.
+ Assist in the training/mentoring of new staff as well as less experienced departmental members.
**General**
+ Attend departmental and company meetings as necessary.
+ Comply with departmental procedures and requirements, such as completion of project assignment and workload trackers on the applicable software platform.
+ When requested, assist management with preparation of resourcing estimates for potential new medical writing projects, or review request for proposal packages to determine content and appropriateness of materials required for development of clinical documents.
+ Initiate and participate in departmental or interdepartmental process improvement and training initiatives, including development of departmental SOPs, templates, and general guidelines for clinical documentation and workflow procedures.
**Skills:**
+ Excellent interpersonal, verbal, and written communication skills.
+ Ability to consistently produce documents of high quality.
+ Demonstrates attention to details and proactivity.
+ Ability to understand all necessary steps in a project, plan ahead, and identify critical paths.
+ A flexible attitude with respect to work assignments and new learning; readily adapts to changes.
+ Ability to efficiently manage time spent on tasks and proactively identify deficiency. Manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail, e.g., organizational skills.
+ Competent working in a matrix environment and values the importance of teamwork. Possesses team leadership skills and cross-cultural sensitivity.
+ Ability to negotiate on behalf of medical writing to ensure resources, timelines and expectations are aligned.
+ Understands and satisfies client needs.
+ Gains trust and establish a connection with the client beyond one's project, to gain repeat business and/or to widen existing scope and services.
+ Provides departmental expertise and perspectives to promote prospective business opportunities; provide Parexel colleagues with pertinent information to formalize a sound business strategy.
**Knowledge and Experience** :
+ Demonstrated understanding of clinical research, the drug development process, and industry guidelines and regulations, e.g., ICH-GCP.
+ Extensive clinical/scientific writing skills.
+ Scientific background essential; writing experience includes multiple clinical documents: study reports, study protocols, or CTD documents or similar.
+ Advanced word processing skills, including MS Office (expertise in Word); software and systems knowledge or ability to learn and adapt to various IT systems: document management systems, collaborative authoring (e.g., SharePoint), and file conversion and databases (Excel).
+ Fluent in written and spoken English with appropriate attention to phraseology, grammar, and punctuation.
+ If required to perform translation work and quality control of documents written in non-English language, proficiency in relevant language is a prerequisite
**Education:**
+ Bachelor's degree in Life Sciences/Health Related Sciences or equivalent.
\#LI-CF1
\#LI-REMOTE
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
$68k-99k yearly est. 35d ago
GDI - Technical Proposal Writer
Oracle 4.6
Medical writer job in Atlanta, GA
This role is ideal for someone who: + Is a meticulous reader and writer with a drive to learn about cloud technology at a national scale. + Can interpret expert input to craft proposal content that is informative _and_ persuasive. + Takes pride in the writing they produce and is always looking for ways to hone their craft.
+ Possesses knowledge and experience with any of public cloud providers including Oracle, Amazon Web Services (AWS), Azure or Google (GCP) architecture, tools, and cloud methodologies.
As a Technical Proposal Writer, you will be responsible for:
+ Writing technical proposals for US federal government customers seeking Oracle Cloud services and task order solutions.
+ Capturing and organizing content and knowledge from subject matter experts across Oracle and presenting it in clear, compliant, compelling format for technical and non-technical audiences.
+ Understanding, identifying, and documenting client requirements and driving compliance with those requirements across internal response teams.
+ Becoming an internal expert on Oracle GDI's proposal process.
+ Actively identify team process enhancements and work with team members to implement them.
+ Support response teams in online and in-person efforts to ensure the written components of the proposals are compelling and aligned.
+ Managing multiple versions of documents across separate systems, including maintaining current working documents throughout the proposal drafting process.
+ Employing superior written and verbal communication skills with attention to grammar, formatting, term consistency, and adherence to Oracle writing practices.
**EXPERIENCE**
**_Required_**
+ Minimum of four years' experience working in industry as a technical writer.
**_Desired_**
+ Minimum of six years' experience working in industry as a technical writer.
**EDUCATION AND CERTIFICATIONS**
**_Required_**
+ Bachelor's degree, any discipline.
**_Desired_**
+ APMP Foundation Level Certification or higher.
**Security Clearance:**
+ Candidates will need to be able to obtain and maintain a Secret / Top-Secret Security Clearance to work with the US Federal government _This is a remote position with the candidate willing to travel to the Reston, VA Office a few times quarterly._
**Responsibilities**
Responsible for participating in customer engagements to collaboratively design and implement solutions. Displays product/application understanding through more customized presentation demonstrations to customers and at conferences and events. May work directly with customers to gather requirements, develop architectures and translates business needs into solutions. Implements solutions and ensures successful deployments through code development and scripting. Supports customer from Proof of Concept (POC) through production deployment of services via resource configuration, planning, and customer education/training. Creates and distributes technical assets (white papers, solution code, blog posts, and video demonstrations). Serves as a technical point of contact for customers and sales on technical cloud solutions and customer success. Further builds business and technical acumen.
Disclaimer:
**Certain US customer or client-facing roles may be required to comply with applicable requirements, such as immunization and occupational health mandates.**
**Range and benefit information provided in this posting are specific to the stated locations only**
US: Hiring Range in USD from $37.88 to $60.63 per hour; from: $78,800 to $126,100 per annum. May be eligible for equity. Eligible for commission with an estimated pay mix of 70/30.
Oracle maintains broad salary ranges for its roles in order to account for variations in knowledge, skills, experience, market conditions and locations, as well as reflect Oracle's differing products, industries and lines of business.
Candidates are typically placed into the range based on the preceding factors as well as internal peer equity.
Oracle US offers a comprehensive benefits package which includes the following:
1. Medical, dental, and vision insurance, including expert medical opinion
2. Short term disability and long term disability
3. Life insurance and AD&D
4. Supplemental life insurance (Employee/Spouse/Child)
5. Health care and dependent care Flexible Spending Accounts
6. Pre-tax commuter and parking benefits
7. 401(k) Savings and Investment Plan with company match
8. Paid time off: Flexible Vacation is provided to all eligible employees assigned to a salaried (non-overtime eligible) position. Accrued Vacation is provided to all other employees eligible for vacation benefits. For employees working at least 35 hours per week, the vacation accrual rate is 13 days annually for the first three years of employment and 18 days annually for subsequent years of employment. Vacation accrual is prorated for employees working between 20 and 34 hours per week. Employees working fewer than 20 hours per week are not eligible for vacation.
9. 11 paid holidays
10. Paid sick leave: 72 hours of paid sick leave upon date of hire. Refreshes each calendar year. Unused balance will carry over each year up to a maximum cap of 112 hours.
11. Paid parental leave
12. Adoption assistance
13. Employee Stock Purchase Plan
14. Financial planning and group legal
15. Voluntary benefits including auto, homeowner and pet insurance
The role will generally accept applications for at least three calendar days from the posting date or as long as the job remains posted.
Career Level - IC2
**About Us**
As a world leader in cloud solutions, Oracle uses tomorrow's technology to tackle today's challenges. We've partnered with industry-leaders in almost every sector-and continue to thrive after 40+ years of change by operating with integrity.
We know that true innovation starts when everyone is empowered to contribute. That's why we're committed to growing an inclusive workforce that promotes opportunities for all.
Oracle careers open the door to global opportunities where work-life balance flourishes. We offer competitive benefits based on parity and consistency and support our people with flexible medical, life insurance, and retirement options. We also encourage employees to give back to their communities through our volunteer programs.
We're committed to including people with disabilities at all stages of the employment process. If you require accessibility assistance or accommodation for a disability at any point, let us know by emailing accommodation-request_************* or by calling *************** in the United States.
Oracle is an Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability and protected veterans' status, or any other characteristic protected by law. Oracle will consider for employment qualified applicants with arrest and conviction records pursuant to applicable law.
$78.8k-126.1k yearly 4d ago
Senior Technical Writer
Contact Government Services, LLC
Medical writer job in Atlanta, GA
Job DescriptionSenior Technical WriterEmployment Type: Full-Time, ExperiencedDepartment: Technology Support CGS is seeking an experienced Senior Technical Writer to provide consultative, analytical, and documentation support for a large Federal agency initiative.
CGS brings motivated, highly skilled, and creative people together to solve the government's most dynamic problems with cutting-edge technology. To carry out our mission, we are seeking candidates who are excited to contribute to government innovation, appreciate collaboration, and can anticipate the needs of others. Here at CGS, we offer an environment in which our employees feel supported, and we encourage professional growth through various learning opportunities.
Skills and attributes for success:- Drafting and development of technical documentation related to a variety of projects in the IT space.- Work closely with project stakeholders to establish technical processes and procedures.- Document projects through the SDLC.- Provide status reports for multiple ongoing projects and related documentation efforts.- Assist with both user and admin level documentation.
Qualifications:- Excellent writing and Communication skills.- 5+ years experience with development of technical documentation.- 3+ years experience with development of user documentation.- Fluency with industry standard technical summary and reporting techniques including Agile project management methodology.- Ability to produce quality work independently or in a group setting.- Experience with MS Office Suite including Visio.- Willingness and ability to pass background check/security screening.
Ideally, you will also have:- Familiarity with Business Intelligence/Analysis applications.- Experience with Government software development policies and procedures.- Client facing communication experience.- Federal Agency issued security clearance.
Our Commitment:Contact Government Services (CGS) strives to simplify and enhance government bureaucracy through the optimization of human, technical, and financial resources. We combine cutting-edge technology with world-class personnel to deliver customized solutions that fit our client's specific needs. We are committed to solving the most challenging and dynamic problems.
For the past seven years, we've been growing our government-contracting portfolio, and along the way, we've created valuable partnerships by demonstrating a commitment to honesty, professionalism, and quality work.
Here at CGS we value honesty through hard work and self-awareness, professionalism in all we do, and to deliver the best quality to our consumers mending those relations for years to come.
We care about our employees. Therefore, we offer a comprehensive benefits package.- Health, Dental, and Vision- Life Insurance- 401k- Flexible Spending Account (Health, Dependent Care, and Commuter)- Paid Time Off and Observance of State/Federal Holidays
Contact Government Services, LLC is an Equal Opportunity Employer. Applicants will be considered without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Join our team and become part of government innovation!
Explore additional job opportunities with CGS on our Job Board:**************************************** more information about CGS please visit: ************************** or contact: Email: *******************
#CJ
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
$62k-86k yearly est. Easy Apply 2d ago
Proposal & Communication Writer
Retail and Dining Positions
Medical writer job in Atlanta, GA
The Proposal and Communications Writer will be a highly skilled team member within the company's Business Development division supporting the business growth and organizational visibility through compelling written content. This role is responsible for contributing to the successful and persuasive submittals to airport retail and restaurant concessions Requests For Proposals (RFPs), along with broader corporate communications, to ensure our voice is clear, consistent, and impactful in our proposal responses and across all channels.
This collaborative role will engage with local and corporate teams to develop story lines, facts, and creatively strategic directions that will most effectively align our organization's successes, capabilities and offerings to the client's interests and needs. Our submitted proposals act as unique pitches for new business within the company's retail and dining divisions. With the workload being a balance of technical writing as well as creative writing and research, the ideal candidate will have a passion for excellent communication skills, and the ability to turn complex information into persuasive, compelling narratives.
About the company: Paradies Lagardère is an award-winning airport concessionaire operating more than 720 national, local, and proprietary retail stores and restaurants in more than 90 airports across North America. It's headquartered in the Vinings, Georgia, a suburb of Atlanta. This position will work out of the Atlanta office.
DUTIES AND RESPONSIBILITIES:
Proposals:
Read and translate incoming requests for proposals (RFPs, RFIs, and RFQs) and contribute to the win theme and strategy
Participate in kick-off meetings, strategy sessions and proposal project planning
Collaborate with subject matter experts and business development teams to craft clear, persuasive, and compliant narratives
Conduct research as necessary related to national or local brands, community initiatives, philanthropic efforts and more.
Review and customize RFP responses from the proposal content library; adapt recurring content for each individual opportunity while creating new content specific to that individual RFP
Lead the development and writing of proposal responses (RFPs, RFIs, and RFQs), ensuring alignment with client requirements and company messaging
Ensure responses follow brand style and tone guidelines as well as coach SMEs as needed
Edit and format technical content for clarity, tone, and impact Verify that responses address key customer hot buttons and win themes
Write or review additional RFP response documents and attachments including RFP cover letters and executive summaries
Partner with design teams to ensure written and visual elements align
Incorporate feedback from proposal review sessions; Proofread all content for accuracy, compliance, and proper spelling and grammar.
Assist with proposal knowledge management and retention of content for future use
Communications:
Build, manage and maintain the company's content libraries, templates, and style guides for proposal and marketing materials
As requested, write and edit internal and external communications such as press releases, blog articles, newsletters and award submissions
Uphold brand voice, tone, and messaging consistency across all platforms
POSITION QUALIFICATIONS:
Bachelor's degree in Communications, English, Marketing, Journalism, or related field.
5-7 years of experience in proposal writing, business development communications, or technical writing
Strong understanding of RFP processes and compliance-driven writing
Excellent research, storytelling, editing, and proofreading skills
Experience working in a fast-paced environment and ability to balance multiple deadlines while maintaining attention to detail
Experience working with cross-functional teams
Proficiency in MS Office and familiarity with content management tools; Adobe Creative Suite a plus.
Flexible and adaptable to changing priorities and deadlines
Self-motivated and able to work independently with minimal supervision
Flexible and adaptable to changing priorities and deadlines.
or with startups is a plus.
At EY, we're all in to shape your future with confidence. We'll help you succeed in a globally connected powerhouse of diverse teams and take your career wherever you want it to go. Join EY and help to build a better working world.
**Job Title: Endpoint Security Senior Technical Writer**
**Job Description:**
We are looking for a dedicated and skilled Senior Technical Writer to join our cybersecurity team. The ideal candidate will be responsible for creating, maintaining, and enhancing documentation that supports the planning, implementation, and operational readiness of multiple endpoint security initiatives. This role requires exceptional writing skills, a strong understanding of cybersecurity concepts, and the ability to collaborate closely with technical subject matter experts to produce clear, accurate, and standardized documentation.
**Key Responsibilities:**
1. **Documentation Development:**
1. Develop, revise, and maintain high-quality documentation for cybersecurity technologies, processes, and workflows.
2. Create standard operating procedures (SOPs), implementation guides, engineering runbooks, and architectural overviews.
3. Produce documentation for system requirements, architecture designs, and operational readiness for new and existing solutions.
2. **Content Accuracy & Compliance:**
1. Ensure all documentation reflects current tools, configurations, and organizational standards.
2. Support documentation needs for compliance audits, risk assessments, and onboarding materials.
3. Align outputs with established documentation templates and governance frameworks.
3. **Collaboration & Knowledge Transfer:**
1. Work closely with cybersecurity SMEs, engineering teams, and operations to gather technical details and translate them into clear, user-friendly content.
2. Facilitate knowledge continuity by creating materials that enable smooth handoffs between teams.
4. **Continuous Improvement:**
1. Identify gaps in existing documentation and propose enhancements.
2. Stay informed on cybersecurity trends and incorporate best practices into documentation processes.
**Qualifications:**
+ Strong technical writing skills with demonstrated ability to create clear, concise, and user-focused documentation.
+ Experience in cybersecurity or IT infrastructure environments, with familiarity in topics such as endpoint protection, SIEM, identity management, and cloud security.
+ Proficiency in documenting system requirements, architecture diagrams, SOPs, and implementation guides for technical audiences.
+ Excellent interviewing and collaboration skills to work with subject matter experts, engineers, and project stakeholders.
+ Familiarity with documentation tools and platforms, such as Confluence, SharePoint, Google Workspace, or equivalent.
+ Ability to interpret and standardize technical content, applying consistent tone, structure, and formatting across documents.
+ Understanding of documentation standards and style guides
+ Version control and change tracking awareness, including using tools like Git, document repositories, or structured file naming/versioning systems.
+ Experience in the utility sector, with an understanding of industry-specific terminology, operations, or regulatory environments.
+ Experience developing documentation specific to cybersecurity technologies used to protect systems within the utility vertical.
+ Experience in creating secure configuration and hardening guides for technologies used in utility environments (e.g., Windows, Linux, firewalls, etc.)
+ Familiarity with cybersecurity frameworks and standards, including NIST 800-53, NIST Cybersecurity Framework (CSF), ISA/IEC 62443, or ISO/IEC 27001.
+ Experience documenting critical infrastructure protection strategies, including risk assessments and vulnerability management programs.
+ Understanding of cybersecurity standards and ability to translate compliance and regulatory language into practical documentation.
**What we offer you**
At EY, we'll develop you with future-focused skills and equip you with world-class experiences. We'll empower you in a flexible environment, and fuel you and your extraordinary talents in a diverse and inclusive culture of globally connected teams. Learn more .
+ We offer a comprehensive compensation and benefits package where you'll be rewarded based on your performance and recognized for the value you bring to the business. The base salary range for this job in all geographic locations in the US is $77,500 to $140,900. The base salary range for New York City Metro Area, Washington State and California (excluding Sacramento) is $92,900 to $160,500. Individual salaries within those ranges are determined through a wide variety of factors including but not limited to education, experience, knowledge, skills and geography. In addition, our Total Rewards package includes medical and dental coverage, pension and 401(k) plans, and a wide range of paid time off options.
+ Join us in our team-led and leader-enabled hybrid model. Our expectation is for most people in external, client serving roles to work together in person 40-60% of the time over the course of an engagement, project or year.
+ Under our flexible vacation policy, you'll decide how much vacation time you need based on your own personal circumstances. You'll also be granted time off for designated EY Paid Holidays, Winter/Summer breaks, Personal/Family Care, and other leaves of absence when needed to support your physical, financial, and emotional well-being.
**Are you ready to shape your future with confidence? Apply today.**
EY accepts applications for this position on an on-going basis.
For those living in California, please click here for additional information.
EY focuses on high-ethical standards and integrity among its employees and expects all candidates to demonstrate these qualities.
**EY | Building a better working world**
EY is building a better working world by creating new value for clients, people, society and the planet, while building trust in capital markets.
Enabled by data, AI and advanced technology, EY teams help clients shape the future with confidence and develop answers for the most pressing issues of today and tomorrow.
EY teams work across a full spectrum of services in assurance, consulting, tax, strategy and transactions. Fueled by sector insights, a globally connected, multi-disciplinary network and diverse ecosystem partners, EY teams can provide services in more than 150 countries and territories.
EY provides equal employment opportunities to applicants and employees without regard to race, color, religion, age, sex, sexual orientation, gender identity/expression, pregnancy, genetic information, national origin, protected veteran status, disability status, or any other legally protected basis, including arrest and conviction records, in accordance with applicable law.
EY is committed to providing reasonable accommodation to qualified individuals with disabilities including veterans with disabilities. If you have a disability and either need assistance applying online or need to request an accommodation during any part of the application process, please call 1-800-EY-HELP3, select Option 2 for candidate related inquiries, then select Option 1 for candidate queries and finally select Option 2 for candidates with an inquiry which will route you to EY's Talent Shared Services Team (TSS) or email the TSS at ************************** .
$92.9k-160.5k yearly 8d ago
Proposal Writer
The EDH 3.3
Medical writer job in Atlanta, GA
EDH is a currently looking to identify a Proposal Writer, for one of our clients in the Atlanta, Georgia area.
Producing high-quality, effective, proposals is an integral part of Business Development process. This position will support multiple proposals simultaneously at different stages in their production. Our work is focused heavily on federal government customers and municipal government. The candidate will work closely with Program Managers and technical subject matter experts to plan, develop, and complete responses to, RFPs, RFQs and RFIs. The successful candidate will be comfortable working with senior management, communicating with customers/partners, and providing leadership related to proposal process execution.
Job Duties
Develops proposal by assembling information including project nature, objectives/outcomes/deliverables, implementation, methods, timetable, staffing, budget, standards of performance, and evaluation; writing, revising, and editing drafts including executive summaries, conclusions, and organization credentials.
Ensure the content matches the RFP, and include standard or approved proposal language for legal sections according to company policy.
Gathers proposal information by identifying sources of information; coordinating submissions and collections; identifying and communicating risks associated with proposals.
Determines proposal concept by identifying and clarifying opportunities and needs; studying requests for proposal (RFPs); attending strategy meetings.
Study and outline the requirements of proposal with the expectations of the client and the team in mind.
\Meets proposal deadline by establishing priorities and target dates for information gathering, writing, review, and approval; entering and monitoring tracking data; coordinating requirements with contributors; contributing proposal status information to review meetings; transmitting proposals.
Prepares presentation by evaluating text, graphics, and binding; coordinating printing.
Maintains quality results by using templates; following proposal-writing standards including readability, consistency, and tone; maintaining proposal support databases
Obtains approvals by reviewing proposal with key providers and project managers.
Improves proposal-writing results by evaluating and re-designing processes, approach, coordination, and boilerplate; implementing changes.
Updates job knowledge by participating in educational opportunities; maintaining personal networks.
Accomplishes organization goals by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments.
Qualifications:
Management, Marketing or comparable Degree.
Professional document formatting and editing expertise using a variety of tools (MS Word, Excel, PPT, Visio).
Interest and desire to write high quality creative business documents with the ability to effectively communicate concepts for specific target audiences.
Demonstrated ability to quickly understand technical concepts
Excellent written and verbal communication skills.
Graphic Design Skills
Technical Documentation
Layout Skills
Problem Solving
Deadline-Oriented
Process Improvement
Coordination, Strategic Planning
Market Knowledge
$50k-71k yearly est. 60d+ ago
Proposal & Communication Writer
The Paradies Shops 4.2
Medical writer job in Atlanta, GA
The Proposal and Communications Writer will be a highly skilled team member within the company's Business Development division supporting the business growth and organizational visibility through compelling written content. This role is responsible for contributing to the successful and persuasive submittals to airport retail and restaurant concessions Requests For Proposals (RFPs), along with broader corporate communications, to ensure our voice is clear, consistent, and impactful in our proposal responses and across all channels.
This collaborative role will engage with local and corporate teams to develop story lines, facts, and creatively strategic directions that will most effectively align our organization's successes, capabilities and offerings to the client's interests and needs. Our submitted proposals act as unique pitches for new business within the company's retail and dining divisions. With the workload being a balance of technical writing as well as creative writing and research, the ideal candidate will have a passion for excellent communication skills, and the ability to turn complex information into persuasive, compelling narratives.
About the company: Paradies Lagardère is an award-winning airport concessionaire operating more than 720 national, local, and proprietary retail stores and restaurants in more than 90 airports across North America. It's headquartered in the Vinings, Georgia, a suburb of Atlanta. This position will work out of the Atlanta office.
DUTIES AND RESPONSIBILITIES:
Proposals:
* Read and translate incoming requests for proposals (RFPs, RFIs, and RFQs) and contribute to the win theme and strategy
* Participate in kick-off meetings, strategy sessions and proposal project planning
* Collaborate with subject matter experts and business development teams to craft clear, persuasive, and compliant narratives
* Conduct research as necessary related to national or local brands, community initiatives, philanthropic efforts and more.
* Review and customize RFP responses from the proposal content library; adapt recurring content for each individual opportunity while creating new content specific to that individual RFP
* Lead the development and writing of proposal responses (RFPs, RFIs, and RFQs), ensuring alignment with client requirements and company messaging
* Ensure responses follow brand style and tone guidelines as well as coach SMEs as needed
* Edit and format technical content for clarity, tone, and impact Verify that responses address key customer hot buttons and win themes
* Write or review additional RFP response documents and attachments including RFP cover letters and executive summaries
* Partner with design teams to ensure written and visual elements align
* Incorporate feedback from proposal review sessions; Proofread all content for accuracy, compliance, and proper spelling and grammar.
* Assist with proposal knowledge management and retention of content for future use
Communications:
* Build, manage and maintain the company's content libraries, templates, and style guides for proposal and marketing materials
* As requested, write and edit internal and external communications such as press releases, blog articles, newsletters and award submissions
* Uphold brand voice, tone, and messaging consistency across all platforms
POSITION QUALIFICATIONS:
* Bachelor's degree in Communications, English, Marketing, Journalism, or related field.
* 5-7 years of experience in proposal writing, business development communications, or technical writing
* Strong understanding of RFP processes and compliance-driven writing
* Excellent research, storytelling, editing, and proofreading skills
* Experience working in a fast-paced environment and ability to balance multiple deadlines while maintaining attention to detail
* Experience working with cross-functional teams
* Proficiency in MS Office and familiarity with content management tools; Adobe Creative Suite a plus.
* Flexible and adaptable to changing priorities and deadlines
* Self-motivated and able to work independently with minimal supervision
* Flexible and adaptable to changing priorities and deadlines.
* or with startups is a plus.
$49k-74k yearly est. 32d ago
Grants Management Specialist
Morehouse College Portal 4.2
Medical writer job in Atlanta, GA
The Post-Award Grant Management Specialist is responsible for the financial and administrative management of federal, state, and private grants after awards have been received. This role ensures compliance with sponsor requirements and institutional policies, provides timely reporting, and supports faculty and staff with the effective stewardship of awarded funds.
Physical Demands
Sitting and standing for extended periods of time. Occasional walking as required.
Required Qualifications
Minimum of Bachelor's degree required. Minimum of 4 years of related experience required. Knowledge of and experience in obtaining grants/contracts from federal/state/private agencies. Strong software and computer skills. Excellent oral and written communication skills.
$42k-49k yearly est. 60d+ ago
Proposal Writer (Government Contracting)
Certified Technical Experts
Medical writer job in Peachtree City, GA
Full-time, Part-time, Contract Description
Company: Certified Technical Experts, Inc. (CTE) Department: Business Development / Proposals
Certified Technical Experts, Inc. (CTE) is seeking a detail-oriented and experienced Proposal Writer to support the development of high-quality, compliant, and compelling proposals for federal, state, and local government opportunities. The Proposal Writer will play a critical role in coordinating inputs from subject matter experts, ensuring compliance with solicitation requirements, and producing clear, persuasive content that positions CTE for successful contract awards.
This position requires strong writing skills, knowledge of the government procurement process, and the ability to work under tight deadlines in a fast-paced environment.
Key ResponsibilitiesProposal Development
Review and analyze RFPs, RFIs, RFQs, and other solicitations to extract requirements and ensure compliance.
Write, edit, and format proposal sections including technical, management, staffing, and past performance narratives.
Collaborate with business development, contracts, IT, and subject matter experts to gather necessary input and tailor content to agency priorities.
Compliance and Quality Assurance
Develop and maintain compliance matrices to ensure all solicitation requirements are addressed.
Edit and proofread proposals for clarity, consistency, and accuracy.
Ensure proposals align with CTE branding, messaging, and win themes.
Coordination and Collaboration
Work closely with Proposal Manager, Capture Managers, and leadership to translate strategies into compelling written responses.
Participate in proposal reviews (Pink/Red Teams) and incorporate feedback.
Support the development of graphics, charts, and other visuals to enhance proposal readability.
Documentation and Templates
Maintain a library of boilerplate content, resumes, and past performance references.
Contribute to continuous improvement of proposal templates, style guides, and processes.
Support knowledge management efforts by capturing reusable proposal content.
Requirements Qualifications and Experience
Experience: Minimum of 3-5 years writing proposals for government contracting (federal, state, or local).
Knowledge: Familiarity with federal procurement processes, FAR/DFARS, and small business programs.
Skills:
Exceptional writing, editing, and proofreading skills.
Ability to translate technical inputs into clear, customer-focused narratives.
Strong organizational skills and ability to meet strict deadlines.
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and Adobe Acrobat; experience with proposal management tools is a plus.
Education: Bachelor's degree in English, Communications, Technical Writing, Business, or related field.
About CTE
Certified Technical Experts, Inc. (CTE) is a SBA-certified Small Disadvantaged Business (SDB) and minority-owned firm with nearly two decades of experience supporting federal, state, and local government agencies. We specialize in cybersecurity, IT services, systems engineering, cloud solutions, business services, and staffing. With certifications including ISO 9001:2015, ISO 27001:2013, and CMMI SVC Level 3, CTE delivers innovative, compliant, and mission-focused solutions that empower government clients to achieve success.
$52k-81k yearly est. 60d+ ago
Proposal Writer (54895)
Ats Family
Medical writer job in Marietta, GA
Applied Technical Services, LLC (“ATS” or the “Company”) is a leading provider of critical testing, inspection, certification, and compliance services. The Company serves clients across a diverse set of large and stable end markets including manufacturing, power generation, aerospace, medical, and defense. ATS was founded in 1967 and is headquartered in Marietta, GA. Today the Company employs nearly 2,100 team members in over 95 locations across the United States.
Our purpose is to create a safe and reliable world and our mission is to deliver assurance through precise technical and professional services.
The Position:
Proposal Writer specializing in developing, organizing, and producing professional quality proposals and client submissions while partnering closely with business development and the ATS Operations Team within the Consulting and Design division. This position coordinates and tracks proposals and ensures the highest quality in all proposal materials within our suite of design, inspection, testing solutions. This multifaceted role demands a blend of strategic thinking, technical understanding, and persuasive writing.
Responsibilities:
Conduct thorough needs analysis and project scope assessments to create accurate and compelling proposals
Collaborate with customers, sales team, and ATS Operations Managers to ensure proposals align with codes and industry standards
Participate in virtual client meetings and incorporate visuals (graphics, photos) to strengthen proposal messaging.
Engage in pricing strategy discussions with sales and operations teams
Manage priorities to meet strict deadlines
Coordinate the full lifecycle of pre-qualifications, tenders, and proposals (RFPs, RFIs, RFQs)
Draft, edit, and proofread proposal materials, including project profiles, resumes, and bid-specific content
Maintain a library of standard proposal content and administer collected information
Monitor bid portals and notifications to identify new opportunities
Track multiple concurrent proposals with short turnaround times
Utilize Microsoft Dynamics CRM to document customer opportunities and sales data
Revise proposals based on feedback and ensure consistency with company standards
Research clients, prospects, markets, competitors, and industry trends to inform business development strategies
Qualifications
Required Experience and Skills:
Bachelor's degree in engineering, communication, marketing, or related field; or equivalent experience
Minimum 3 years of experience in proposal writing, business development, or marketing within construction, engineering, property management, or safety industries
Strong technical writing and editing skills
Proficiency in Adobe, Microsoft Office Suite, and CRM tools
Exceptional verbal and written communication skills
Ability to manage multiple tasks and meet deadlines with precision
Strategic planning skills and high motivation to deliver exceptional outcomes
Understanding of building envelope services and related terminology (preferred)
Additional requirements:
Previous exposure to proposal writing is highly desirable
Strong organizational skills and attention to detail
Ability to work collaboratively with cross-functional teams
Comfortable conducting research and presenting information in a professional manner
Work Conditions:
Fast-paced environment with multiple concurrent deadlines
Requires participation in virtual meetings and occasional coordination across different time zones
Standard office setting with typical physical requirements:
Ability to sit for extended periods
Frequent use of computer and office equipment
Occasional lifting of up to 20 lbs
Ability to bend, reach, and carry light office materials as needed
U.S. Persons Only:
A requirement of this position is access to information that is subject to U.S. export controls under the U.S. International Traffic in Arms Regulations (“ITAR”). Accordingly, the company will consider only “U.S. Persons” for this position. A “U.S. Person” includes (a) U.S. citizens or nationals; (b) U.S. lawful permanent residents (i.e., “green card” holders); (c) persons granted refugee status; or (d) persons granted asylum in the United States. This information is collected solely for purposes of complying with U.S. export control requirements and will not be used to unlawfully discriminate in the hiring process.
Equal Employment Opportunity Statement
Applied Technical Services is an Equal Opportunity and Affirmative Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability unrelated to ability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, order of protection status, protected veteran or military status, or an unfavorable discharge from military service, and other categories protected by federal, state or local law.
Stratfield is seeking a Technical Writer/Trainer to join our client as they stand up a new distribution center that will utilize advanced automation equipment integrated with their Manhattan Warehouse solution. This individual will create clear, easy-to-follow documentation, SOPs, skills matrices, and training curriculum for the new distribution center and participate in training programs.
Experience with industrial automation and Integrated Work Systems (IWS) is highly desired. Candidates who have set up training programs within manufacturing environments will stand out.
This is a 6-month contract position that will be mostly remote, with occasional onsite work and minimal travel. Preferred location: Atlanta. Sponsorship is not available for this position.
Responsibilities:
Write and update SOPs and training curriculum for systems within the distribution center.
Maintain documentation ensuring accuracy and compliance with client standards.
Develop and participate in training programs for new team members.
Capture and preserve expert knowledge from experienced team members.
Update documentation for new automation systems and features.
Qualifications:
Bachelor's degree in Technical Communication, Engineering, Journalism, or related field.
Technical writing experience in manufacturing or industrial settings.
Training experience within a manufacturing environment is a strong plus.
Familiarity with Lean Manufacturing, IWS, or similar methods highly preferred.
Understanding of automation systems is desired.
Proficiency with Microsoft Office Suite and technical writing tools.
Strong writing and editing skills with attention to detail.
Ability to simplify complex technical information for diverse audiences.
Excellent collaboration and communication skills.
Ability to work independently and proactively seek information.
Willingness to travel if necessary.
What We Offer:
Competitive salary and benefits package.
Opportunities for professional growth and development.
Health insurance and retirement plans
A dynamic and inclusive work environment.
About Stratfield
We started Stratfield Consulting with the belief that companies are looking for a more reliable consulting firm to deliver an expanding list of projects. We believe that Better People combined with Better Tools will lead to Better Projects. Our objective is to be the most trusted consulting firm for our clients. We are very careful about the people that we invite into the firm.
Check out some of our Project Spotlights!
$45k-62k yearly est. 8d ago
Proposal Writer (54895)
Applied Technical Services 3.7
Medical writer job in Marietta, GA
Applied Technical Services, LLC ("ATS" or the "Company") is a leading provider of critical testing, inspection, certification, and compliance services. The Company serves clients across a diverse set of large and stable end markets including manufacturing, power generation, aerospace, medical, and defense. ATS was founded in 1967 and is headquartered in Marietta, GA. Today the Company employs nearly 2,100 team members in over 95 locations across the United States.
Our purpose is to create a safe and reliable world and our mission is to deliver assurance through precise technical and professional services.
The Position:
Proposal Writer specializing in developing, organizing, and producing professional quality proposals and client submissions while partnering closely with business development and the ATS Operations Team within the Consulting and Design division. This position coordinates and tracks proposals and ensures the highest quality in all proposal materials within our suite of design, inspection, testing solutions. This multifaceted role demands a blend of strategic thinking, technical understanding, and persuasive writing.
Responsibilities:
* Conduct thorough needs analysis and project scope assessments to create accurate and compelling proposals
* Collaborate with customers, sales team, and ATS Operations Managers to ensure proposals align with codes and industry standards
* Participate in virtual client meetings and incorporate visuals (graphics, photos) to strengthen proposal messaging.
* Engage in pricing strategy discussions with sales and operations teams
* Manage priorities to meet strict deadlines
* Coordinate the full lifecycle of pre-qualifications, tenders, and proposals (RFPs, RFIs, RFQs)
* Draft, edit, and proofread proposal materials, including project profiles, resumes, and bid-specific content
* Maintain a library of standard proposal content and administer collected information
* Monitor bid portals and notifications to identify new opportunities
* Track multiple concurrent proposals with short turnaround times
* Utilize Microsoft Dynamics CRM to document customer opportunities and sales data
* Revise proposals based on feedback and ensure consistency with company standards
* Research clients, prospects, markets, competitors, and industry trends to inform business development strategies
$51k-72k yearly est. 29d ago
Grant Writer for Profit
Careperks
Medical writer job in Tucker, GA
We are seeking an experienced and motivated Grant Writer to join our team at CarePerks LLC in Tucker, GA. This position will be responsible for researching, writing, and submitting grant proposals to various funding sources in order to secure financial support for our for-profit organization.
The Grant Writer will work closely with the executive team to identify funding opportunities that align with CarePerks LLC's mission and goals. The ideal candidate will have strong writing and research skills, attention to detail, and the ability to meet deadlines.
Responsibilities:
Conduct research to identify potential grant opportunities
Write and submit compelling grant proposals
Manage grant application process and deadlines
Collaborate with team members to gather necessary information for proposals
Maintain accurate records of grant submissions and outcomes
Qualifications:
Bachelor's degree in English, Communications, or related field
Proven experience as a Grant Writer in a for-profit setting
Excellent writing and editing skills
Strong research abilities
Ability to work independently and as part of a team
If you are a talented Grant Writer looking to make a difference in the for-profit sector, we want to hear from you! Join CarePerks LLC and help us continue to provide valuable services to our community.
About Us:
CarePerks LLC is a leading provider of employee benefits and wellness programs for businesses of all sizes. We offer a wide range of services to help organizations improve employee satisfaction and retention. Our mission is to create healthy and happy workplaces through innovative solutions and personalized support. Learn more about us at careperksllc.com.
$42k-61k yearly est. 60d+ ago
News Writer (Part-Time) - WSB TV
Cox Media Group 4.7
Medical writer job in Atlanta, GA
Job Title: News Writer (Part-Time) - WSB TV
WSB TV Atlanta is looking for a News Writer to join our team! The Writer will write clear, concise and easy to understand stories with value clearly conveyed. Writers use process language in scripts with a focus on the latest information available to avoid newscasts and stories feeling repetitive or old.
Essential Duties and Responsibilities
Write stories in all formats, conveying the value in the lead line or first ten seconds of the script
Regularly showcase and execute process language
Coordinate with producers on assigned scripts to execute the direction and vision of each story
Maximize use of graphics and pre-production to make the newscast clear and easy to understand
Consistently integrate references/pushes to our digital and social media platforms
Work with production team to ensure that ideas can be executed with robotic cameras and control room automation system
Use all resources possible to get the newest and best information into stories
Contribute story ideas
Attend editorial meetings if they fall within your regular shift and as time allows
Learn to produce newscasts and fill-in produce as needed
Available to have a flexible schedule, that allows to fill-in, as needed, with advance notice
Minimum Qualifications
Must be well read on current affairs and have a wide-range working knowledge and understanding of general interest subjects
Preferred Qualifications
Previous work in a television newsroom, newspaper, or digital publishing organization preferred
Bachelor's degree (B. A.) from four-year College or university in Journalism or Communications preferred
About Cox Media Group
CMG Media Corporation (d/b/a Cox Media Group) is an industry-leading media company with unparalleled brands, award-winning content, and exceptional team members. CMG provides valuable local and national journalism and entertainment content to the people and communities it serves. The company's businesses encompass 14 high-quality, market-leading television brands in 9 markets; 45 top-performing radio stations delivering multiple genres of content in 9 markets; and numerous streaming and digital platforms. CMG's TV portfolio includes multiple primary affiliates of ABC, CBS, FOX, NBC, Telemundo and MyNetworkTV, as well as several valuable news and independent stations. For more information about CMG, visit *********************
Req #: 2024 #LI-Onsite
$49k-57k yearly est. 26d ago
Senior Technical Writer
Contact Government Services, LLC
Medical writer job in Atlanta, GA
Senior Technical WriterEmployment Type: Full-Time, ExperiencedDepartment: Technology Support CGS is seeking an experienced Senior Technical Writer to provide consultative, analytical, and documentation support for a large Federal agency initiative. CGS brings motivated, highly skilled, and creative people together to solve the government's most dynamic problems with cutting-edge technology. To carry out our mission, we are seeking candidates who are excited to contribute to government innovation, appreciate collaboration, and can anticipate the needs of others. Here at CGS, we offer an environment in which our employees feel supported, and we encourage professional growth through various learning opportunities.
Skills and attributes for success:- Drafting and development of technical documentation related to a variety of projects in the IT space.- Work closely with project stakeholders to establish technical processes and procedures.- Document projects through the SDLC.- Provide status reports for multiple ongoing projects and related documentation efforts.- Assist with both user and admin level documentation.
Qualifications:- Excellent writing and Communication skills.- 5+ years experience with development of technical documentation.- 3+ years experience with development of user documentation.- Fluency with industry standard technical summary and reporting techniques including Agile project management methodology.- Ability to produce quality work independently or in a group setting.- Experience with MS Office Suite including Visio.- Willingness and ability to pass background check/security screening.
Ideally, you will also have:- Familiarity with Business Intelligence/Analysis applications.- Experience with Government software development policies and procedures.- Client facing communication experience.- Federal Agency issued security clearance.
Our Commitment:Contact Government Services (CGS) strives to simplify and enhance government bureaucracy through the optimization of human, technical, and financial resources. We combine cutting-edge technology with world-class personnel to deliver customized solutions that fit our client's specific needs. We are committed to solving the most challenging and dynamic problems.
For the past seven years, we've been growing our government-contracting portfolio, and along the way, we've created valuable partnerships by demonstrating a commitment to honesty, professionalism, and quality work.
Here at CGS we value honesty through hard work and self-awareness, professionalism in all we do, and to deliver the best quality to our consumers mending those relations for years to come.
We care about our employees. Therefore, we offer a comprehensive benefits package.- Health, Dental, and Vision- Life Insurance- 401k- Flexible Spending Account (Health, Dependent Care, and Commuter)- Paid Time Off and Observance of State/Federal Holidays
Contact Government Services, LLC is an Equal Opportunity Employer. Applicants will be considered without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Join our team and become part of government innovation!
Explore additional job opportunities with CGS on our Job Board:**************************************** more information about CGS please visit: ************************** or contact: Email: *******************
#CJ
$62k-86k yearly est. Auto-Apply 60d+ ago
Grant Specialist: post-award
Morehouse College Portal 4.2
Medical writer job in Atlanta, GA
The grant specialist is responsible for administering the post-award process at Morehouse College, ensuring that agency-required reports are submitted in a timely manner, and coordinating the closeout of federal grants to the college.. Additional duties include facilitating the issuance and monitoring of sub-awards, providing grant administration training for faculty and staff, assisting with internal and external audits of grants and other sponsored programs, and ensuring the integrity of internal grants controls. The individual who occupies this role will represent Morehouse in grant-related matters with outside funding sources, administer database management activities concerning Morehouse grants and contracts activity, assist with the preparation of reports, and collaborate with other Morehouse College offices to manage and administer federal grants.
Physical Demands
This is an in-person position and the grant specialist will be expected to report to the office during normal business hours. Additionally, the successful candidate must be able to walk across the campus, sit and stand for extended periods of time, and posses a level of dexterity of hands and fingers needed to operate a computer keyboard. They must also be able to read small font on printed on digital media, and lift up to 50 lb. Occasionally, the grant specialist may need to work outside of business hours to meet critical deadlines.
Required Qualifications
Bachelor's degree 2+ years of related experience Knowledge of and experience in obtaining grants/contracts from federal/state/private agencies Knowledge of Uniform Guidance Working knowledge of MS Office Suite, Adobe Acrobat, Google Forms Excellent oral and written communication skills
Preferred Qualifications
Experience working in a college or non-profit setting Research Administrator Certification - CRA
How much does a medical writer earn in Atlanta, GA?
The average medical writer in Atlanta, GA earns between $53,000 and $115,000 annually. This compares to the national average medical writer range of $63,000 to $137,000.