Writer Jobs in Valdosta, GA

(Must be local to the South Florida area OR open to relocating to South Florida) Who We Are: Happy V is one of sunny South Florida's fastest-growing, direct-to-consumer women's wellness brands. Founded in 2019 by necessity, our goal is to provide women with effective, high-quality, easy-to-use wellness products and informational content that covers the A-Z of women's health. Our A-players are results-driven creative thinkers who like to move fast, get the job done, and have fun doing it. If you love to roll up your sleeves, take on exciting new challenges daily, and drive massive growth… You should definitely keep reading. The Content Creator will be an integral part of the team to create new, fresh, digestible visual content on health and wellness topics. The ideal candidate will be skilled in content curation, script writing, and digital asset management, with a keen eye for identifying and amplifying authentic content that aligns with our brand. Please Note: If you're selected as a candidate, you will be required to do a small assignment. What You'll Be Doing: Assisting with content planning, balancing both brand and business objectives. Write compelling direct response copy, scripts, and storyboards for ads, IG Reels, and TikToks. Film and edit professional-quality content optimized for social media and digital campaigns. Collaborate with marketing to brainstorm and execute creative concepts, leveraging performance data to optimize content. Partner with the creative team to develop on-brand assets for social media and other platforms. Analyze content performance and iterate to enhance effectiveness. Stay updated on social media trends and experiment with new formats to engage audiences. Ensuring all user-generated content aligns with brand guidelines and messaging, obtaining necessary permissions and rights for use. Strategize for growth of engagement and following on Instagram, TikTok, and YouTube. Create fast, digestible visual content via mobile devices to turn educational or product information into social media content (TikTok, short-form videos, Reels, Stories, BTS.) Propose real-time content based on the latest social media trends and find relevant ways for the brand to participate in or leverage them through content. Assist in creating 360 campaigns to support overall brand strategy to support new product launches, influencer campaigns, events, and giveaways. Stay up to date with the latest social media trends, best practices, competitive tools, and marketing products. Support Senior Marketing Managers with influencer identification and UGC creators for content creation (evergreen and campaign-focused.) Qualifications: Must have 3+ years of experience in social media management, content creation, or a related role. Strong understanding of social media platforms (Instagram, YouTube, TikTok, etc.) and best practices. Experience ideating and managing still and video assets preferred Understanding of storytelling and what makes engaging content on social Ability to multitask Good with ideation and making ideas come to life Ability to work independently and collaboratively in a fast-paced environment Possess strong problem-solving skills In-depth understanding of relevant and upcoming social media platforms Excellent verbal, communication, and writing skills Must be an enthusiastic team player with outstanding organizational skills, time management, collaboration, and attention to detail Fluent in English (speak, read, and write) Experience in the women's wellness/supplement industry is a plus but not mandatory Passionate about women's wellness Benefits: Medical, Dental & Vision insurance 10 PTO days + 12 paid holidays Bi-Annual Performance Reviews WFH + Health and Wellness stipend Health and wellness stipend Continued education reimbursement Meals provided (in-office) Monthly Supplement Wellness Products Provided

Classic Collision is now hiring a Writer Trainee. Classic Collision was established in 1983 in Atlanta, Georgia with one single goal: To offer quality service to its customers with integrity and honesty. Be a part of a rapidly growing company whose mission is to put safety, quality, integrity, and heart into every vehicle we repair and customer we serve. Classic Collision offers competitive pay, benefits, and career advancement opportunities. Please come and join our team! Why Choose Classic Collision? Paid Weekly Continuous Training Supportive Team Culture Company match 401K Medical/Dental/Vision Paid Time Off - 6 Paid Holiday Rewarding Work Responsibilities Explain and educate customers on repair process on a high level, including insurance claim information and processes. Maintain a broad knowledge base of insurance partner requirements regarding authorizations, billing, and load level processes. Coordinate Rental Car /Tow companies to provide one-stop service to all customers. Ensure vehicles are delivered to customers once completed Responsible for customer communication throughout the repair process. Monitor DRP assignments, estimate/repair appointments and capture rates of assignments. Follow up on all DRP assignments present and past to maintain sales for the center. Secure proper payments Ensure all customer comfort items are always fresh and available for customers as well as maintaining the customer waiting area. Perform other administrative tasks and duties as required to successfully meet the needs of the business Assist in estimate and supplement writing Other duties as assigned Qualifications Must be at least 18 years of age. Previous experience in customer service, sales, or other related fields is preferred. Must have a valid driver's license and be eligible for coverage under company insurance policy. Effective communication (written and verbal) and interpersonal skills are required. Organization and multi-tasking skills, good time management, and the ability to adapt easily to fast-paced environment. Behaviors/Competencies Integrity-Respect and accountability at every level and every interaction Customer Service-Provide the highest level of customer service while building customer satisfaction and retention Innovation-Develops and displays innovative approaches and ideas to our business Teamwork-Contributes to building a positive team spirit and supports everyone's efforts to succeed Physical & Environmental While performing the duties of this job, the employee is regularly required to use hands, and is required to talk and hear. The employee is frequently required to stand, sit, and walk occasionally for long periods at a time. The employee may occasionally be required to reach with hands, arms and move objects up to 20 pounds. Specific vision abilities required by this job include close vision, peripheral vision, and the ability to adjust focus. In addition, abilities for assessing the accuracy, neatness and thoroughness of the work assigned are required. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential function. Classic Collision is an Equal Opportunity Employer As an equal opportunity employer, Classic Collision does not discriminate against any employee or candidate based on age, race, gender identity, gender expression, genetic information, national origin, physical or mental disability, protected veteran status, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by all applicable federal, state, and local laws. Reasonable Accommodations Classic Collision is an equal opportunity employer that is committed to working with and providing reasonable accommodations to individuals with disabilities. If you have a disability and you believe you need reasonable accommodation to search for a job opening or submit an online application, please e-mail or call . This email is listed exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. This job description is not a complete statement of all duties and responsibilities comprising the position.

Flexible Part-Time Hours (Approx. 15 hrs/week) $20 - $30 per hour (Based on experience) About Workforce Ready Now Workforce Ready Now is a professional coaching service that helps college students and recent graduates develop essential skills to secure internships and full-time jobs. Our services include resume building, networking, LinkedIn optimization, interview coaching, and confidence building. We also market students to potential hiring managers, bridging the gap between education and career success. Position Overview We are seeking a creative and skilled Social Media Content Creator to develop engaging photos and videos that promote our services across social media platforms. The ideal candidate understands our target audience-college students, recent graduates, and their parents-and can produce content that resonates with them. This is a part-time, flexible role (approx. 15 hours per week), requiring onsite work in Boca Raton for photography and video shoots. Key Responsibilities Develop high-quality photos and videos that align with our brand and messaging. Brainstorm and execute creative content ideas, including interactive videos, reels, and promotional materials. Edit and optimize content for social media platforms (Instagram, TikTok, LinkedIn, and Facebook). Collaborate on content strategy to enhance engagement and reach. Attend onsite shoots and capture authentic moments that showcase the impact of Workforce Ready Now. Stay updated on social media trends and best practices to keep content fresh and engaging. Qualifications & Requirements Experience in photography, videography, and social media content creation. Proficiency with editing tools such as Adobe Premiere Pro, Final Cut Pro, Photoshop, or similar software. Strong understanding of TikTok, Instagram Reels, and other social platforms. Ability to ideate, script, shoot, and edit high-quality, engaging content. Must be local to Boca Raton, FL, as onsite shooting is required. Ideal for a college or graduate student with relevant experience. Access to own camera, video equipment, and editing software. Self-motivated with a passion for storytelling and visual creativity. Why Join Workforce Ready Now? $20 - $30 per hour based on experience. Flexible schedule (approximately 15 hours per week). Creative freedom to bring fresh, engaging ideas to life. Make an impact by helping students and recent graduates succeed. Hands-on experience in content creation for a growing business.

Copywriter/Content Writer for Reframe App About Us: Reframe is the #1 leading app dedicated to alcohol reduction, offering personalized support, resources, and a supportive community to help individuals achieve their goals of mindful drinking and healthier habits. Our mission is to empower users to take control of their relationship with alcohol and live their best lives. Position Overview: We're looking for a skilled and creative copywriter to embody the voice of Reframe across our app and digital platforms. You'll be at the forefront of developing compelling, engaging, and impactful messaging that aligns with our brand and resonates with our audience. This role is ideal for someone who thrives in a fast-paced environment, loves storytelling, and has a strong grasp of effective communication strategies. Key Responsibilities: Craft clear, persuasive, and on-brand copy for in-app content, push notifications, email campaigns, social media, and marketing materials. Collaborate with marketing, product, and design teams to develop creative concepts and impactful messaging strategies. Maintain consistency in brand voice, tone, and style across all communications. Research alcohol-related topics, gather user feedback, and monitor industry trends to inform content development. Stay current with best practices in copywriting, digital marketing, and user experience to continuously enhance our messaging. Requirements: Proven experience as a copywriter, ideally in health, wellness, or lifestyle industries. Strong writing and editing skills, with a keen eye for detail and grammar. Ability to transform complex ideas into clear, concise, and compelling copy that drives engagement. Solid understanding of brand voice, tone, and messaging strategies. Collaborative team player who can adapt to feedback and work cross-functionally. Familiarity with digital marketing channels, including social media, email, and app notifications. Preferred Qualifications: Experience working with mobile apps or digital health platforms. Knowledge of behavioral psychology, behavior change theory or neuroscience. Personal experience or interest in alcohol reduction or mindful drinking. Bachelor's degree in a related field. Benefits: Health insurance Opportunity to make a meaningful impact on people's lives. Competitive salary based on experience. Flexible work environment. Access to a supportive and collaborative team. Opportunities for professional development and growth.

Our client, a well known pharmaceutical manufacturer is urgently looking to hire a Technical Writer ON SITE in Athens, GA! ** This is a 9+ month contract to hire on W2 offering a full benefits package ** Required Skills & Experience Bachelors degree or higher 4+ years of experience Must have experience with pharma technical writing Working knowledge of Change Controls (Comet, Salesforce, Truevault) GMP facility / environment exp and knowledge Experience in validations Job Responsibilities Produces complex technical written communications used for projects assigned to department. Projects may include marketing tools, technical manuals, and presentations. Prepares work to be accomplished by reviewing delivery schedules and prioritizing work, gathering, organizing and analyzing technical information from various relevant sources. Verifies facts and clarifies information as needed. Develops, writes, edits and proofs complex assignments for various internal customers. Ensures Company publications meet established standards of style and format. Reviews photographs, drawings, sketches, diagrams, and charts selected for specific publications to ensure relevance to content. Generates and reviews text for nontechnical documents upon request. Serves as editing consultant to other staff. Suggests format, layout and graphics for materials reviewed. Reviews published materials and recommends revisions or changes in scope, format, and content. Produces rough draft of revised versions. Mentors less experienced employees by providing guidance and input on work assignments. Reviews drafts for adherence to business standards. Investigates and resolves customer complaints and concerns. Responds to complicated inquiries.

PLEASE READ BEFORE APPLYING Due to a high number of rejections, only applicants location in the USA with a valid work permit unable to travel for in person interview will be considered. ALL APPLICANTS BASED OUTSIDE THE USA WILL BE AUTOMATICALLY REJECTED. Company: 24/7 Mindset Location: 404w main st Apopka, FL 32712 Employment Type: Full-Time (Monday to Friday, 8:00 AM - 5:00 PM) Position Overview: We are seeking a creative and motivated Content Creator/Videographer who will be responsible for producing high-quality video content on-site. You will collaborate with the Marketing Director, following direction to ensure the content aligns with the company's vision and client goals. Some travel may be required for on-location shoots. Key Responsibilities: Video Creation: Produce professional, high-quality videos that align with the company's vision and brand identity. On-Site Production: Travel to locations as needed for video shoots and capture engaging footage. Collaboration: Work closely with the Marketing Director to ensure content meets specific guidelines and objectives. Social Media Trends: Stay up-to-date with social media video trends and create content optimized for various platforms. Requirements: Proven experience in videography and video editing. Strong knowledge of social media platforms (LinkedIn, Instagram, etc.) and video trends. Proficiency in video editing software (Adobe Premiere Pro, Final Cut Pro,Cap cut, Captions etc.). Ability to work independently, follow direction, and maintain a positive attitude. Willingness to travel for shoots and adapt to new challenges. Why Join Us: Opportunity for Growth: Advance your career with opportunities for development within the company. Creative Freedom: Bring your creative ideas to life and make an impact through video. Collaborative Environment: Work closely with a supportive team and the Marketing Director. If you're passionate about video content creation and ready to help businesses thrive, apply now to join the 24/7 Mindset Team!

Quantfury is a fintech company that develops and supports the Quantfury global brokerage, with a monthly trading volume above 15 billion dollars. Quantfury is seeking an experienced Financial Content Writer to cover the latest developments in capital markets. The ideal candidate is a skilled writer with a track record of covering public companies, capable of producing unique, timely, and informative content across a wide range of topics from company earnings to interest rates. This presents an exciting opportunity for individuals seeking a dynamic work environment. The successful candidate will be based onsite at Quantfury's vibrant Miami office, fostering a collaborative and engaging atmosphere. Responsibilities: Monitor and follow data from capital markets including company earnings, global economic data, and industry trends. Analyze developments in the US and abroad to generate a steady pipeline of interesting topics and new stories. Write and publish articles with strong attention to detail and minimal editing required. Required Qualifications: Extensive knowledge of and experience in covering capital markets. Strong professional writing portfolio; experience with a major publication or newswire is a plus. Familiarity with economics, financial markets, and business trends. Ability to write clean, well-organized, and accurate copy. Experience with publishing and editing tools, including WordPress. Fluency in Spanish is preferred. What we have to offer... Competitive salaries, often better than industry, for comparable roles; Daily premium lunch catering, and keeping the office stacked with fruits and snacks; Comprehensive health benefits plan that kicks in after 90 days of successful employment, including access to exclusive employee discounts; Bonus and incentive programs

Custom software lacks comprehensive documentation, creating challenges in understanding code functionality, business rules, and database structures. To address this, we aim to hire a technical writer to document the software systematically. This documentation will include technical/white papers for designated code modules, processes, business rules, table structures, and data dictionaries. ________________________________________ Project Objectives 1. Provide clear, comprehensive documentation for the custom software. 2. Facilitate knowledge transfer and ease onboarding for new team members. 3. Enable efficient troubleshooting and software maintenance. 4. Standardize and centralize all documentation for future scalability. ________________________________________ Scope of Work 1. Module-Level Documentation o Breakdown of all designated code modules. o Description of functionality and interdependencies. 2. Process Documentation o Overview of software workflows. o Step-by-step explanation of key processes. 3. Business Rules o Comprehensive list of business rules embedded in the code. o Explanation of how rules are applied and their impact on processes. 4. Database Documentation o Table structures, including field definitions and data types. o Entity-relationship diagrams (ERDs) to illustrate relationships. 5. Data Dictionary o Definitions of all database fields and their usage. o Index of terms and acronyms used across the software. ________________________________________ Approach and Methodology 1. Preparation o Conduct initial meetings with IT and development teams to identify key areas requiring documentation. o Create an inventory of modules, processes, and database structures to be documented. 2. Technical Writer Onboarding o Provide the technical writer with access to software, code repositories, and SMEs (Subject Matter Experts). o Share existing documentation and relevant materials. 3. Documentation Development o Follow a structured process: 1. Review code and system behavior. 2. Interview SMEs for additional context. 3. Draft documentation and validate accuracy with the development team. o Use templates for consistency across all documents. 4. Validation and Review o Iterative review process involving IT leadership and SMEs. o Update documentation based on feedback. 5. Finalization and Handoff o Compile all documents into a central repository. o Provide training to IT staff on accessing and maintaining documentation. ________________________________________ Deliverables 1. Technical/White Papers for all designated code modules. 2. Comprehensive process documentation. 3. Business rules documentation. 4. Database structure documentation, including ERDs. 5. Data dictionary with field definitions and usage. ________________________________________ Timeline Phase Duration Milestone Preparation 2 weeks Find consultant, and setup working area. Technical Writer Onboarding 1 week Access and knowledge transfer Documentation Development 10 weeks Drafting and reviews Validation and Review 4 weeks Feedback incorporation Finalization and Handoff 2 weeks Document repository setup Total Project Duration 19 weeks ________________________________________ Resources Needed 1. Personnel o Technical writer with experience in software documentation. o SMEs from the IT and development teams. o Project manager to oversee the documentation effort. 2. Tools o Documentation software (e.g., Confluence, Microsoft Word, Team, or SharePoint). o Diagramming tools (e.g., Lucidchart or Visio) for ERDs and workflows. 3. Access o Code repositories and development environment. o Existing documentation and technical notes. ________________________________________ Budget Considerations 1. Salary or contract fees for the technical writer. 2. Licenses for documentation and diagramming tools. 3. SME time allocation for interviews and reviews. All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

Title: Pharmaceutical Quality Technical Writer Duration: 8 months Pay Rate: $43.76/an hr. on W2 Work Authorization: US Citizens and GC Holders only This role involves producing complex technical written communications for various projects, such as marketing tools, technical manuals, and presentations. The individual will review delivery schedules, prioritize tasks, gather and analyze technical information, and ensure that company publications meet established standards. Additionally, the role may involve participating in projects providing input on project parameters and timelines and recommending methods for optimal results. Responsibilities: Prepares work to be accomplished by reviewing delivery schedules and prioritizing work, gathering, organizing and analyzing technical information from various relevant sources. Verifies facts and clarifies information as needed. Develops, writes, edits and proofs complex assignments for various internal customers. Ensures Company publications meet established standards of style and format. Reviews photographs, drawings, sketches, diagrams, and charts selected for specific publications to ensure relevance to content. Generates and reviews text for nontechnical documents upon request. Serves as editing consultant to other staff. Suggests format, layout and graphics for materials reviewed. Recommends revisions or changes in scope, format, and content for reviewed published materials. Produces rough draft of revised versions. Mentors less experienced employees by providing guidance and input on work assignments. Reviews drafts for adherence to business standards. Investigates and resolves customer complaints and concerns. Responds to complicated inquiries. Participates in or leads projects as assigned. Provides input into project parameters and timelines. Makes recommendations on method and materials for optimum results. Qualifications: University/Bachelor's degree or equivalent Previous experience in the pharmaceutical industry is required Requires 3+ years of pharmaceutical quality assurance work experience Must be proficient with MS Office applications

Immediate need for a talented Pharmaceutical Technical Writer. This is a 08+ Months Contract to possible extension opportunity with long-term potential and is located in Athens, GA (Onsite). Please review the job description below and contact me ASAP if you are interested. Job ID:25-64067 Pay Range: $40 - $43.50/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location). Key Responsibilities: Produces complex technical written communications used for projects assigned to department. Projects may include marketing tools, technical manuals, and presentations. May participate in special projects. Prepares work to be accomplished by reviewing delivery schedules and prioritizing work, gathering, organizing and analyzing technical information from various relevant sources. Verifies facts and clarifies information as needed. Develops, writes, edits and proofs complex assignments for various internal customers. Ensures Company publications meet established standards of style and format. Reviews photographs, drawings, sketches, diagrams, and charts selected for specific publications to ensure relevance to content. Generates and reviews text for nontechnical documents upon request. Serves as editing consultant to other staff. Suggests format, layout and graphics for materials reviewed. Reviews published materials and recommends revisions or changes in scope, format, and content. Produces rough draft of revised versions. Mentors less experienced employees by providing guidance and input on work assignments. Reviews drafts for adherence to business standards. Investigates and resolves customer complaints and concerns. Responds to complicated inquiries. Participates in or leads projects as assigned. Provides input into project parameters and timelines. Makes recommendations on method and materials for optimum results. Key Requirements and Technology Experience: Key Skills: Experience in validations ,Experience with writing protocols, Working knowledge of Change Controls (Comet, Salesforce, Truevault), Must have at least 4 years of exp. Technical Writing experience a must. Generally Requires 4-6 Years Work Experience . University/Bachelors Degree or Equivalent. Notes from HM: Role will be Onsite Possible Title: Pharmaceutical Technical Writer Bachelor's degree required Should have GMP facility / environment exp and knowledge Resolving non-conformances (nice to have) Project exp is ideal Experience in validations Experience with writing protocols Working knowledge of Change Controls (Comet, Salesforce, Truevault) Must be able to communicate clearly Must have at least 4 years of exp- Technical Writing experience a must- Should be Proficient in MS Office Should be comfortable with working with Stakeholders to get work done and to get communications out . Our client is a leading Healthcare Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration. Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. By applying to our jobs you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here.

The Clinical Evaluations Specialist is responsible for managing regulatory documentation related to clinical evaluations, particularly for Medical Device Regulation (MDR) remediation and Post Production Risk Reviews (PPRRs). This role requires strong expertise in clinical literature reviews, regulatory writing, and post-market surveillance activities to support the life cycle management of medical devices. The specialist will serve as a primary point of contact for clinical project leads and collaborate closely with cross-functional teams, including Regulatory Affairs, Quality Assurance, and Clinical Development. Key Responsibilities: Regulatory Documentation & Clinical Evaluation: Author, revise, and update clinical documents for MDR remediation and PPRRs. Conduct systematic literature reviews and clinical data appraisals in alignment with EU MDR, MEDDEV 2.7/1 Rev. 4, and FDA guidance. Review and summarize large clinical documents such as literature reports, clinical research protocols, and templates. Assist in the development and maintenance of Clinical Evaluation Reports (CERs), Post-Market Clinical Follow-up (PMCF) Plans and Reports, and risk-benefit analyses. Support regulatory submissions by ensuring all clinical documentation meets scientific and regulatory standards. Life Cycle Management & Risk Assessment: Act as clinical contact for Life Cycle Management (LCM) and Post Production Life Cycle Management (PPLCM) activities. Provide clinical functional review and expertise on assigned projects, ensuring compliance with global regulatory requirements. Process Improvement & Compliance: Monitor evolving EU MDR, FDA, and ISO 14155 regulations to ensure compliance with clinical evaluation processes. Develop and improve standard operating procedures (SOPs) related to clinical regulatory documentation. Track and analyze quality metrics related to clinical evaluations and risk reviews. Required Qualifications: Master's or Ph.D. in Vision Science, Biomedical Engineering, Life Sciences, or related field. Foreign-trained ophthalmologists are encouraged to apply. Proficiency in European Medical Device Regulations (MDR), particularly in clinical evaluations and post-market surveillance. Experience in writing and reviewing clinical evaluation reports (CERs), literature reviews, and clinical risk assessments. Strong background in regulatory compliance, medical writing, and scientific research methodologies. Proficient in Microsoft Office Suite and regulatory documentation software. Strong communication and writing skills. Preferred Qualifications: Experience in eye care/ophthalmology is highly preferred. Experience in conducting systematic literature reviews and regulatory risk analysis. Knowledge of clinical trial registries, biostatistics, and regulatory intelligence. Certification in Regulatory Affairs (RAC), Medical Writing (AMWA, EMWA), or a related field.

IntePros is seeking a dedicated Technical Writer/Publisher for a global leader in biopharmaceuticals. The ideal candidate will collaborate with subject matter experts (SMEs) to create clear, concise, and user-friendly documentation while ensuring accuracy and compliance with industry standards. Job Summary: As a Technical Writer, you will be responsible for creating, editing, and maintaining clear, concise, and accurate documentation for various departments, including R&D, manufacturing, quality assurance, and regulatory compliance. You will collaborate with scientists, engineers, and subject matter experts to translate complex information into user-friendly materials, ensuring compliance with industry standards and company policies. Primary Responsibilities: Work closely with SMEs to gather and interpret technical information. Develop and edit various types of documents including qualification documents, qualification plans, test plans, test cases, acceptance criteria, test reports, change control documents, user guides, manuals, API documentation, and other technical content. Maintain and update existing documentation to reflect product updates and changes. Ensure consistency in style, tone, and terminology across all documentation. Conduct document reviews with stakeholders and incorporate feedback. Apply version control and documentation management best practices. Required Qualifications: 3-5 years of experience in technical writing, preferably in the biotechnology or life sciences field. Strong technical writing and editing skills with the ability to explain complex concepts clearly. Experience with documentation tools such as Microsoft Word, Google Docs, and SharePoint. Proficiency in Jira, Confluence, and Veeva (preferred). Experience with Microsoft Visio or similar tools for creating diagrams and flowcharts. Familiarity with collaboration tools such as Slack or Microsoft Teams. Understanding of Agile methodologies and iterative documentation processes. Ability to interact with SMEs, developers, and product managers to produce high-quality documentation. Preferred / Nice to Have: Previous experience writing and routing documentation in Veeva. Experience with style guides, internal documentation best practices, and product training materials. Background in biotechnology, pharmaceuticals, or healthcare-related industries is a plus.

Produces complex technical written communications used for projects assigned to department. Projects may include marketing tools, technical manuals, and presentations. May participate in special projects. Duties & Responsibilities: Prepares work to be accomplished by reviewing delivery schedules and prioritizing work, gathering, organizing and analyzing technical information from various relevant sources. Verifies facts and clarifies information as needed. Develops, writes, edits and proofs complex assignments for various internal customers. Ensures Company publications meet established standards of style and format. Reviews photographs, drawings, sketches, diagrams, and charts selected for specific publications to ensure relevance to content. Generates and reviews text for nontechnical documents upon request. Serves as editing consultant to other staff. Suggests format, layout and graphics for materials reviewed. Reviews published materials and recommends revisions or changes in scope, format, and content. Produces rough draft of revised versions. Mentors less experienced employees by providing guidance and input on work assignments. Reviews drafts for adherence to business standards. Investigates and resolves customer complaints and concerns. Responds to complicated inquiries. Participates in or leads projects as assigned. Provides input into project parameters and timelines. Makes recommendations on method and materials for optimum results. Work Experience: Generally Requires 4-6 Years Work Experience Education Required: University/Bachelors Degree or Equivalent

A very well known, top, national Not for Profit (youth) is seeking to hire a Grants Specialist for their Miami (Coconut Grove) facility. Our client is an international, multi-billion dollar Not for Profit organization. This Not for profit offers an outstanding benefits package, upward career mobility, strong retirement plan, many corporate perks, good work life balance, and a fun filled, activity driven, high energy corporate culture. Position Title: Grant Specialist Location: Miami, Florida (Coconut Grove Area) Salary: $50,000 Technical Skill Set Required: Responsible for revenue targets, developing, and enhancing partnerships with other funders, and achieving desired impact within the community Responsible for researching, preparing, submitting, and managing grant proposals/reports that support agency goals and meet funder guidelines and criteria Responsible for the monthly, quarterly, or annual reporting requirements for assigned grants Support the development of donor applications and reports, as well as ensuring donor compliance and quality control Contribute to the development and revision of funding proposals, budgets, and donor reports Be updated on donor priorities and track and share relevant calls for proposals Contribute to continuously improve internal grant management systems Job Requirements: To qualify, candidates must have: Minimum of 1 year of Not for Profit Experience Minimum of 1 year of Grant Analyst / Grant Specialist experience Associates Degree For immediate consideration, please forward resume ASAP to Matthew Deering at Ascendo Resources: mdeering@ascendore.com *E-mails and resumes received will remain highly confidential and will not be released to anyone.

Job Details SBC Lakeland - Lakeland, FL AutomotiveDescription Do you have have experience in the collision field and want to further your career? SBC Lakeland is looking for a Body Shop writer to join our family! As a part of Myers Auto Group, SBC Lakeland's vision is to redefine the automotive experience one relationship at a time. We are looking for career-minded, highly motivated individuals to join our team. We provide training, a performance-based pay package, comprehensive benefits (medical, dental, vision, life and short-term disability, PTO, 401(k) with company match, associate discounts and more) and the opportunity to excel in a supportive environment. Qualifications Essential job functions and qualifications Some knowledge and experience with basic estimating and collision center operations. At least basic knowledge with CCC One estimating platform or Mitchell Connect. The ability to examine a collision repair at final delivery and work with the team to complete an excellent repair and customer experience. Ability to source and use of OEM specific repair procedures to accurately write a complete repair estimate. Ability to explain and negotiate required repair operations to both customers and insurance adjusters. Ability to work with the insurance company to ensure proper repairs and procedures are being done along with the correct dollar figures being accounted for. Detail oriented Manage time efficiently Team player Insight into automotive systems and repair techniques (manufacturing, paint finishes). Upbeat and positive personality Active listening skills Ability to provide excellent guest service Strong communication skills Ability to build relationships with team members and guests Valid driver's license DFWP/EOE

Required Qualifications Must be a current UNF student . This position requires a strong understanding of the foundational principles of journalism and storytelling, a firm understanding of the legal/ethical issues of newsgathering, good leadership, interpersonal and communication skills. The position requires at least one semester of experience working at a student media outlet. See Spinnaker Media Advisory Board bylaws for additional requirements. Must be continuously enrolled at UNF for the duration of the position and not be on academic probation or suspension as defined by the most recent University of North Florida course catalog. Preferred Qualifications N/A

will operate on a remote, contractual basis. Are you an experienced blogger with a knack for cutting through the fat and extracting the beating heart of a story in a flash? Oh, and do you have a passion for everything related to productivity? XDA is seeking a Productivity Author to cover the latest and most relevant PC productivity updates and releases in a fast-paced, collaborative environment. The XDA team is dedicated to staying ahead of the curve, continuously sourcing the latest in computing news, sharing tips, tutorials, and videos, while reviewing devices, apps, and games. Job Responsibilities Ability to contribute reliably and consistency (features, buying guides, tutorials, and news) under tight deadlines. Willing to input work into our in-house CMS, as well as find and format images, according to our guidelines. Stay up-to-date with the latest PC hardware, product releases, and software updates. Coordinate with the editorial team for assignments and feedback. Application Requirements CV Cover Letter (tell us why you want to write for us!) 2-3 tech articles you've written that demonstrate your writing abilities Applicants must have a self-starter attitude and possess the following requirements: Relevant experience in writing and editing in the English language. Ability to think analytically; applauding or criticizing aspects of the news source. In-depth knowledge and extensive experience with productivity apps and tools. The XDA hiring team will reach out to applicants who align well with our needs. Please note that only applications with relevant writing samples will be reviewed.

Grindley Williams Engineering (GWE) in Lakeland, Florida is growing their team! This Report Writer I role is full-time, W2 employment. The writing team assists the Professional Engineers in the completion of documentation of a site visit by producing an initial draft report. The Report Writer I enhances the effectiveness of the forensic department by utilizing templates and field notes to draft comprehensive engineering reports on behalf of the Professional Engineers. DUTIES AND RESPONSIBILITIES: • Very strong attention to detail and command of the English language is essential • Utilizes the company templates, style guides, and proprietary software to draft comprehensive engineering reports on behalf of Professional Engineers • Collaborates with office team members, professional engineers, and field staff • Researches, documents, and collects the required background information for reports • Summarizes documents and information provided by client • Maintains quality assurance and control standards • Additional tasks as assigned The Mission and Vision of Grindley Williams Engineering provide the foundation for the work performed by our employees. 1. Principal: Trusted partner for our clients and community. 2. Provides: Diversified menu of engineering services that serve our clients' needs. 3. Emphasis: Education, responsiveness, clarity, and value. 4. Ensures: Public safety, health, and welfare. 5. Commitment: Individually and collectively, we are steadfast to the team and its purpose by adding value, strength, and beauty to the built environment. Benefits: Employee-only medical, dental, and vision plans that cost the employee $0 in premiums/payroll deductions You will be eligible for health insurance benefits plans and retirement plans available to full-time employees Entry into Medical, Dental, Vision, Life Insurance and Disability Plans is on the 1st day of the month following hire date. Entry into the company's 401(k) plan is on the 1st of the month after 6 months of employment with a 4% auto-enroll unless the employee opts out. Company match is up to 4%. You will be eligible for PTO (Paid Time Off) accruals for the first 5 years of employment at 4.62 hours per pay period, up to 120 hours (3 weeks) per year Up to seven paid holidays annually

Title: Key Account Excellence Investigation Writer Job Purpose: Investigation Writer is responsible for the initiation, investigation and completion of process deviations related to our Key Accounts. They identify and investigate process deviations to find the cause, assess impact, and implement corrective and preventive actions to prevent recurrence. Technical Writer perform all Effectiveness Checks requires for the associated written investigation. Investigation Writer is expected to work in a cGXP environment, have working knowledge of cGxP processes, the ability to manage multiple ongoing projects concurrently and conflict resolution skills, a strong technical writing capability, be action oriented, and be compliant minded while performing investigation. Main Duties and Responsibilities: Act as an Issue Reporter, Lead Investigator and provide a high-Quality standard to the investigation within the systems and CIR (Client Investigation Report) to Key Account defined scope. Able to report within the systems and make sure all information are accurate Conduct detailed and structured investigations through data collection, collaboration, interviews and analysis to determine root causes. Write Investigation reports and summaries clearly and promptly to ensure Key Account and Marken timelines are met, and information is accurately conveyed. Work with the functional areas to identify the root cause and determine appropriate preventive and corrective action to prevent recurrence. Perform all Effectiveness checks required for the associated investigations written. Lead and support prompt investigations are performed in compliance with Marken's procedures and Client's requirements documentation. Issue escalation and mitigation, work with Key Account Excellence Team members to identify trends on investigations. Participate actively in all meetings to update management, peers, sites on current deviations Act as a method SME (Senior Matter Expert) for root cause analysis tools and general problem-solving techniques. Requirements: Knowledge of Good Manufacturing Practice, Good Storage Practice and Good Distribution Practice guidelines. Previous experience in Technical Writer, Customer Services or quality management with an eye for details. Knowledge of local regulations. Six Sigma certified preferred. Strong written and verbal communication skills are required. Ability to read and comprehend complex subjects. Organized, methodical and efficient approach to work. Strong typing and computer skills, including efficiency using Microsoft Office Suite (Word, Excel, PowerPoint). Fluent in English Ability to work in a fast-paced, high workload environment, and balance multiple projects and objectives for timely event closure. Collaboration skills, with the ability to troubleshoot and problem solve in a cross-functional team setting. Marken is a wholly owned subsidiary of UPS and is a critical part of UPS Healthcare. Marken offers a state-of-the-art GMP-compliant depot network and logistic hubs for clinical drug product storage and distribution worldwide and supports cell and gene therapy logistics services from clinical to commercial, while maintaining the leading position for Direct-to-Patient and Home Healthcare services, biological sample shipments and biological kit production. Moving Our World Forward by Delivering What Matters.