field_job_employment_type

field_job_occupational_field_parents_all

job_organization_name

city

state

<h3>Job Description</h3>
Job Description
Limon's Road Service is currently accepting applications for a Qualified, Dependable Service writer with Heavy Duty, Medium Duty, Light Duty Truck and Trailer service experience
 
Requirements:
• 3+ year's experience • Assist in the day to day shop operations • Assist with invoicing and purchase orders • Inventory control • Customer communication skills
Company DescriptionFamily owned Commercial Fleet repair company. 
<h3>Company Description</h3>
Family owned Commercial Fleet repair company.

Service Writer Advisor

<h3>Job Description</h3>
Job Description
Service Advisor
Every service professional at a OPEN ROAD retail center must excel in listening,&nbsp;communicating and working efficiently to Open Road’s&nbsp;standards.&nbsp; Service Advisors help&nbsp;OPEN ROAD&nbsp;owners care for their cars and understand the value of maintaining their vehicles in accordance with&nbsp;factory guidelines. As a driver’s personal link to the Aftersales department, the&nbsp;Service Advisor establishes a critical and ongoing relationship with our clients.&nbsp; What You Do
<ul>
<li>Inspect vehicles and apply proper resources to accurately identify and verify clients’ service needs. Record them along with current vehicle and client information on the repair order.</li>
<li>Interact with customers to determine immediate&nbsp;service needs</li>
<li>Serve as a liaison between technicians and customers</li>
<li>Provide excellent customer service experience</li>
<li>Use a consultative approach to educate customers on&nbsp;services and products</li>
<li>Support&nbsp;center goals for service by generating:&nbsp;</li>
<li>High sales of services, parts, and accessories.</li>
<li>Repeat new vehicle sales by providing a premium Aftersales experience for each client.</li>
<li>Refer to service history, inspect vehicle, and recommend service to clients. Promote the sales of appropriate services, parts, and accessories by thoroughly understanding the product and associated service requirements.</li>
<li>Write and verify accurate repair orders and include supporting documentation.</li>
<li>Administer new and used vehicle warranty repairs in accordance with warranty specifications.</li>
<li>Ensure requested vehicle services are performed correctly upon completion by inspecting the vehicle prior to each service delivery.</li>
<li>Perform a consultative vehicle delivery with client when work is completed.</li>
<li>Supervise cleaning and preparation of new and used vehicles.</li>
<li>Build and maintain knowledge of&nbsp;products and services via on-the-job training and participation in educational and development programs.</li>
<li>Meet requirements of state and federal law for automobile repair and consumer protection.</li>
</ul>
Successful Attributes and Skills
<ul>
<li>Excellent communication skills and ability to be a team player</li>
<li>Ability to minimize and redirect customers frustrations</li>
<li>Technically knowledgeable, experienced, or trainable on product line</li>
<li>Outgoing and patient personality with good client relations ability</li>
<li>Professional appearance</li>
<li>Excellent communication capability</li>
<li>Strong organizational skills</li>
<li>1+ years of&nbsp;Service Advisor experience</li>
<li>Technical certification a plus</li>
<li>Manufacturer certifications a plus</li>
<li>Proven track record</li>
<li>Ability to supply CSI Reports and Productivity Reports</li>
</ul>
Open Road Auto Group owns and operates over twenty-five automotive facilities including seventeen dealerships throughout the New York/New Jersey metropolitan area. Currently, we are ranked as one of the largest automotive groups in the nation by Automotive News. We specialize in providing “in-demand” vehicles, both new and pre-owned, for our customers who have come to expect a “Five Star customer service experience”. With over 45 years of automotive experience, our mission is to remain one of the premier automobile retailers in the country, providing the best opportunities for our team members, customers and communities. We understand and acknowledge the importance of our customers and in doing so; we strive to develop a highly motivated, world-class, workforce that is committed to satisfying their needs. At Open Road we know our employees, and their achievements, drive our culture and success.
Our Total Compensation Rewards Program includes: &nbsp;
BASE PAY - Determined by competitive market pay rate for your job, your skills, experience and performance
BONUSES - Rewards achievement of specific business goals, in eligible positions
BENEFITS - Include wellness coverage, optional benefits, income protection, 401(k), purchase programs, such as:
<ul>
<li>Medical, Dental and Vision Plans</li>
<li>Vacation Time</li>
<li>Personal Time</li>
<li>Short and Long Term Disability</li>
<li>Life Insurance</li>
<li>401(k) Retirement Plan with employer match</li>
<li>Manufacturer Certifications</li>
<li>Leadership Training Programs</li>
<li>Vehicle Purchase Discounts</li>
<li>Wellness Initiatives</li>
<li>Volunteer Time</li>
</ul>
Powered by JazzHR
nfRJzMpAcN

Service Advisor / Writer

<h3>Job Description</h3>
Job Description
Service Advisor
Kinnaman’s Auto Repair – Cartersville, GA
Kinnaman’s Auto Repair is a locally owned, family-operated automotive repair shop committed to honesty, quality repairs, and long-term customer relationships. We are currently seeking a motivated Service Writer / Service Advisor to join our growing team.
This position is critical to our success. The Service Writer serves as the primary point of contact for our customers and is responsible for selling recommended services and repairs based on technician inspections and the customer’s needs, goals, and priorities—while delivering an outstanding customer experience.
Salary Range: $41,600 - $52,000
Benefits: Health, Vision, Dental
PTO: 7 Major Holidays, Sick and Personal
Key Responsibilities
Primary Responsibilities
<ul>
<li>Present and sell recommended maintenance and repair services using Kinnaman’s Auto Repair guidelines and best practices</li>
<li>Clearly explain technician findings and repair options in a way customers can understand</li>
<li>Build trust and long-term relationships through honest, professional communication</li>
<li>Manage customer expectations regarding timelines, pricing, and vehicle needs</li>
<li>Daily scheduled follow up with customers to keep them informed of the status of repairs</li>
</ul>
Secondary Responsibilities
<ul>
<li>Greet and assist customers in person, over the phone, and via email</li>
<li>Answer customer questions and address concerns professionally</li>
<li>Create estimates and invoices using company systems and procedures</li>
<li>Assist with parts ordering, returns, and repair dispatching using company systems and procedures</li>
<li>Support daily shop workflow to ensure smooth and efficient operation</li>
</ul>
Additional Duties
<ul>
<li>Checking customers in and out</li>
<li>Picking up parts IF needed</li>
<li>Light cleaning or other tasks needed to maintain shop flow and customer experience</li>
</ul>
Minimum Qualifications
<ul>
<li>Sales Experience: Minimum of 1 year of sales experience in any industry or a demonstrated ability to sell</li>
<li>Organization &amp; Focus: Ability to stay organized and complete tasks in a fast-paced environment with frequent interruptions</li>
<li>Computer Skills:
<ul>
<li>Working knowledge of Windows-based computers</li>
<li>Ability to type or dictate at least 30 words per minute</li>
<li>Comfortable using email, word processing, and basic spreadsheet programs</li>
</ul>
</li>
<li>Communication Skills:
<ul>
<li>Fluent in English, both verbal and written</li>
<li>Comfortable speaking with customers by phone and in person</li>
</ul>
</li>
<li>Math Skills:
<ul>
<li>Ability to perform basic math using a calculator</li>
</ul>
</li>
</ul>
Physical Requirements
<ul>
<li>Ability to get in and out of various vehicles without assistance</li>
<li>Ability to safely drive a motor vehicle with passengers (valid driver’s license required)</li>
</ul>
Why Work at Kinnaman’s Auto Repair?
<ul>
<li>Family-owned, community-focused business</li>
<li>Positive, team-oriented work environment</li>
<li>Stable, full-time position</li>
<li>Opportunity to grow in sales, customer service, and automotive knowledge</li>
<li>Competitive pay based on experience and performance</li>
</ul>
Apply today if you enjoy helping people, thrive in a fast-paced environment, and want to be part of a shop that values integrity, teamwork, and customer relationships.
 #hc215114

Service Writer/Advisor

<h3>Job Description</h3>
Job Description
We have an immediate opportunity for a Technical Proposal Writer that has Federal Government proposal writing experience. This is a part-time position. Anticipated hours are 15 to 20 hours weekly. Duration of position is January to mid-March.
Primary Responsibilities:
<ul>
<li>Previous experience with analyzing procurement documents to understand requirements in addition to the Federal Government’s evaluation criteria and compliance rules</li>
<li>Ability to daft and edit proposals, including technical responses</li>
<li>Work as Subject Matter Expert to conceive, document, articulate, and write winning solutions in alignment with proposal requirements</li>
<li>Responsible for supporting written responses to technical, management, past performance, staffing plans and transition sections</li>
<li>Experience and ability to understand RFP requirements and respond with compliant and compelling solutions</li>
<li>Work as part of a collaborative team to clearly articulate solution and strategy approach to performing the work, experience, win themes, and discriminators</li>
<li>Effectively communicate and employ interviewing skills to gather needed information from internal and external personnel to support writing activities</li>
<li>Ability to write clear, compliant, completing, persuasive, proposal text</li>
<li>Ability to develop and implement process improvements to help improve proposal quality</li>
</ul>
Desired Qualifications:
<ul>
<li>Three plus years of experience working as a proposal writer responding to Federal Government solicitations required</li>
<li>Evidence of successful track record of high quality, high scoring proposals</li>
<li>Demonstrated success writing and leading technical, management, transition, staffing, and/or corporate experience and past performance volumes for complex efforts</li>
<li>Excellent writing and communication skills along with organizational and time management skills</li>
<li>Proficiency with Microsoft Word, Excel, and PowerPoint</li>
<li>Candidate must be available for the duration of position from RFP release through submission</li>
</ul>
Upon a conditional job offer, a drug test and background check will be required.
Compensation based on experience.
(Technical Writer, Federal Government Proposal Writing, SME, RFP, Microsoft Suite)
Company DescriptionAbout us: 347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>. 
<h3>Company Description</h3>
About us:\r\n\r\n347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>.

Technical Proposal Writer

<h3>Job Description</h3>
Job Description
We have an immediate opportunity for a Proposal Writer that has Federal Government proposal writing experience. This is a part-time position. Anticipated hours are 15 to 20 hours weekly. Duration of position is January to mid-March.
Primary Responsibilities:
<ul>
<li>Previous experience with analyzing procurement documents to understand requirements in addition to the Federal Government’s evaluation criteria and compliance rules</li>
<li>Ability to daft and edit proposals, including technical responses</li>
<li>Work as Subject Matter Expert to conceive, document, articulate, and write winning solutions in alignment with proposal requirements</li>
<li>Responsible for supporting written responses to technical, management, past performance, staffing plans and transition sections</li>
<li>Experience and ability to understand RFP requirements and respond with compliant and compelling solutions</li>
<li>Work as part of a collaborative team to clearly articulate solution and strategy approach to performing the work, experience, win themes, and discriminators</li>
<li>Effectively communicate and employ interviewing skills to gather needed information from internal and external personnel to support writing activities</li>
<li>Ability to write clear, compliant, completing, persuasive, proposal text</li>
<li>Ability to develop and implement process improvements to help improve proposal quality</li>
</ul>
Desired Qualifications:
<ul>
<li>Three plus years of experience working as a proposal writer responding to Federal Government solicitations required</li>
<li>Evidence of successful track record of high quality, high scoring proposals</li>
<li>Demonstrated success writing and leading technical, management, transition, staffing, and/or corporate experience and past performance volumes for complex efforts</li>
<li>Excellent writing and communication skills along with organizational and time management skills</li>
<li>Proficiency with Microsoft Word, Excel, and PowerPoint</li>
<li>Candidate must be available for the duration of position from RFP release through submission</li>
</ul>
Upon a conditional job offer, a drug test and background check will be required.
Compensation based on experience.
(Technical Writer, Federal Government Proposal Writing, SME, RFP, Microsoft Suite)
Company DescriptionAbout us: 347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>. 
<h3>Company Description</h3>
About us:\r\n\r\n347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>.

<h3>Job Description</h3>
The Senior Technical Writer will be responsible for authoring, reviewing, and maintaining high-quality CMC and GMP documentation to support development, manufacturing, testing, and regulatory submissions for radiopharmaceutical products. This role is heavily focused on analytical methods, validation protocols/reports, batch records, and product development reports, ensuring that all documentation is scientifically sound, inspection-ready, and aligned with applicable regulatory and quality standards (e.g., GMP, ICH, FDA, EMA).
 
The ideal candidate combines strong technical understanding of radiopharmaceuticals or sterile drug products with excellent writing, data interpretation, and cross-functional collaboration skills.
 
&nbsp;Key Responsibilities
1. Technical Document Authoring &amp; Review
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Draft, edit, and finalize technical documents including, but not limited to:
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Analytical method development and validation protocols/reports
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Equipment qualification and validation protocols/reports
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Master batch records (MBRs) and associated controlled forms
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Product development reports, technical summaries, and investigation reports
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Stability protocols and reports
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Specifications and test methods for raw materials, intermediates, and finished radiopharmaceutical products
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Ensure documents are clear, concise, scientifically accurate, and consistent with internal templates and style guides.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Translate complex technical data and experimental outcomes into well-structured, comprehensible documents for both technical and regulatory audiences.
 
2. GMP &amp; Regulatory Compliance
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Ensure all documentation complies with GMP, ICH guidelines, and relevant regional regulations (e.g., FDA, EMA) for radiopharmaceuticals and sterile products.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Incorporate appropriate data integrity and 21 CFR Part 11 principles into documentation practices.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Support the preparation of CMC sections of regulatory submissions (e.g., IND/CTA, NDA/MAA, DMFs) by providing high-quality source documents and summaries.
 
3. Cross-Functional Collaboration
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Work closely with Analytical Development, Product Development, Manufacturing, Quality Control, Quality Assurance, and Regulatory Affairs to gather data and technical content.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Facilitate document review cycles, consolidating and addressing comments from multiple stakeholders.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Participate in project meetings to understand technical strategies, timelines, and document needs.
 
4. Document Control &amp; Lifecycle Management
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Prepare documents in alignment with document control procedures and manage revisions through the electronic quality management system (eQMS or DMS).
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Own the lifecycle of key documents, ensuring timely updates following process changes, validation activities, or regulatory feedback.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Support preparation for audits and inspections by ensuring documentation is complete, organized, and readily retrievable.
 
5. Continuous Improvement
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Contribute to the development and refinement of templates, style guides, and best practices for technical documentation.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Provide guidance and mentoring to junior writers or subject matter experts (SMEs) on effective technical writing and documentation standards.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Identify opportunities to streamline documentation processes and improve consistency and quality.
 
Qualifications
 
Required:
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Bachelor’s or Master’s degree in Chemistry, Pharmaceutical Sciences, Chemical Engineering, Radiopharmacy, or a related scientific discipline.
 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;5–8+ years of experience in technical writing within the pharmaceutical, biotech, or radiopharmaceutical industry, preferably in a GMP environment.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Demonstrated experience authoring analytical method validation protocols/reports, batch records, and other CMC/GMP documentation.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Strong understanding of GMP, ICH Q guidelines, and regulatory expectations for sterile injectable or radiopharmaceutical products.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Proven ability to interpret analytical and process data and present it clearly in written form.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Excellent written and verbal communication skills in English, with strong attention to detail, organization, and consistency.
 
Preferred:
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Experience in radiopharmaceuticals, nuclear medicine, or other short-lived isotope-based products.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Familiarity with aseptic processing, cleanroom operations, and QC testing relevant to radiopharmaceuticals (e.g., sterility, endotoxin, radionuclidic purity, radiochemical purity).
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Experience contributing to CMC sections for regulatory submissions (IND/CTA, NDA/MAA, ANDA, or equivalent).
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Proficiency with electronic document management systems (eQMS/DMS) and standard office tools (Word, Excel, PowerPoint).
 
 
Key Competencies
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Strong scientific and technical literacy, with the ability to quickly understand new processes and analytical methods.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Exceptional technical writing and editing skills, with a focus on clarity, structure, and data integrity.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;High level of ownership, accountability, and ability to manage multiple documents and deadlines in parallel.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Collaborative mindset with the ability to work effectively across multi-disciplinary teams.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Detail-oriented, quality-focused, and comfortable working in a regulated environment.

Senior Technical Writer

<h3>Job Description</h3>
Principle duties and responsibilities
 
Provide content strategy to ensure relevant content is delivered contextually
 
<ul>
<li>Collaborate on a content roadmap and conduct content audits</li>
<li>Establish and maintain operational processes and procedures for managing content requests and delivery</li>
<li>Lead content governance and implementation of best practices at an enterprise level</li>
<li>Work with product stakeholders and bring them along as you provide content to ensure messaging is optimized and successful</li>
<li>Coach and mentor others on content strategy best practices</li>
<li>Create documentation based on user groups to understand the tone and voice -</li>
<li>Artifacts you will deliver scripts content strategy knowledge base articles and content embedded within the product All youll need for success</li>
</ul>
 
Minimum qualifications -education and prior job experience
 
<ul>
<li>Bachelors degree in English journalism technical writing or equivalent experience / training</li>
<li>5 years creating and executing digital content strategy across multiple channels</li>
<li>Extensive experience planning for and developing useful usable content including instructional text error and confirmation message taxonomy and SEO</li>
</ul>
 
Preferred qualifications - education and prior job experience
 
<ul>
<li>Masters degree in English journalism or technical writing</li>
<li>Experience using a content management or knowledge management system and agent-facing applications</li>
<li>Experience with technical projects involving AI / machine learning</li>
<li>Travel industry experience</li>
</ul>
Skills licenses and certifications
 
Superior writing editing and proofreading skills:
 
<ul>
<li>You understand the importance of clearly and concisely communicating for digital channels.</li>
<li>A proven track record of collaboration across product and UX teams:</li>
<li>You can translate complex concepts into easy-to-understand interactive experiences.</li>
<li>A passion for creating great digital user experiences with actionable knowledge of the digital landscape:</li>
<li>Keeping up with industry and user trends emerging technologies and best practices and trends is fun for you.</li>
<li>You're able to influence decision makers.</li>
<li>A passionate advocacy for effective user-friendly communication</li>
<li>You can talk about the importance of consistent messaging across multiple channels and make a case for a strategic approach to content delivery.</li>
<li>Collaborate with multiple stake holder groups to gain alignment and input related to content needs.</li>
</ul>

UX Content Writer

<h3>Job Description</h3>
Job Description
 About Us
At cGMP Consulting, we specialize in providing expert validation, qualification, and compliance services to the life sciences industry. Our team works with clients to ensure their facilities, equipment, and processes meet regulatory standards, enabling the safe and efficient production of pharmaceuticals. cGMP Consulting is based in Lake Forest, IL. This position will be located in&nbsp;Worcester, MA.
Position Summary
cGMP Consulting, Inc. is seeking technical writers who would support engineers of all experience levels to provide technical support/ documentation to Engineering and Validation teams with a focus on change management and SOP updates for a variety of on-going projects in the pharmaceutical industry. Knowledge and application of the CFR’s and cGMP’s is preferred.
The ideal candidate for this job is resourceful, independent, organized, and capable of working in a fast-paced environment. Assuring a steady and accurate completion of the workload on time is key to success in this position.
Responsibilities
<ul>
<li>Author and revise SOPs, Work Instructions, and controlled documents to ensure clarity, compliance, and alignment with current Good Manufacturing Practices (cGMP), regulatory requirements (e.g., 21 CFR Part 11, EU Annex 11), and internal quality standards.</li>
<li>Translate change control records into clear procedural updates by collaborating with QA, Validation, Manufacturing, and Engineering to interpret change requests and accurately reflect them in controlled documentation.</li>
<li>Manage document lifecycle in electronic document management systems (EDMS) such as Veeva Vault, MasterControl, or Documentum, ensuring version control and audit readiness.</li>
<li>Participate in cross-functional change control meetings, including Change Control Board (CCB) or Quality Review Board (QRB) sessions, to gather context, clarify scope, and align on documentation impacts.</li>
<li>Conduct impact assessments for procedural changes, evaluating how proposed changes affect existing SOPs, training materials, and regulatory filings, and identifying required updates.</li>
<li>Ensure traceability and compliance in documentation updates by maintaining clear linkage between change control records, risk assessments (e.g., PFMEA), and revised documents.</li>
<li>Support training deployment for revised procedures by collaborating with Learning &amp; Development to ensure timely training assignment and completion tracking for impacted personnel.</li>
<li>Standardize documentation practices across departments, promoting consistency in formatting, terminology, and structure in line with internal style guides and regulatory expectations.</li>
<li>Prepare documentation for internal audits and regulatory inspections, and respond to document-related queries and CAPAs to support audit readiness.</li>
<li>Drive continuous improvement in documentation processes by identifying inefficiencies in SOP workflows and proposing enhancements to improve clarity, usability, and compliance.</li>
</ul>
Requirements
<ul>
<li>Bachelors’ degree in Engineering, Science, or a related field of study.&nbsp;</li>
<li>0-2 years’ experience in a GMP manufacturing environment.&nbsp;</li>
<li>Experience in technical writing including drafting standard operating procedures, protocols, and/or reports is preferred.&nbsp;</li>
<li>Familiar with regulatory (FDA) requirements.&nbsp;</li>
<li>Business minor or coursework is strongly encouraged.&nbsp;</li>
<li>Advanced critical thinking and technical writing skills.</li>
<li>Strong organizational, communication, and interpersonal skills.&nbsp;</li>
</ul>
Compensation and Benefits&nbsp;
<ul>
<li>Expected pay range per year: $65,000-$85,000 USD&nbsp;</li>
<li>Expected benefits include: Medical, Dental, Vision, PTO, 401K&nbsp;</li>
</ul>
Disclaimer&nbsp;
The duties and responsibilities described are not a comprehensive list and additional tasks may be assigned to the employee from time to time; or the scope of the job may change as necessitated by business demands. All duties and responsibilities are subject to possible modification to reasonably accommodate individuals with disabilities. The requirements listed are the minimum levels of knowledge, skills, or abilities necessary to perform this job successfully. The company is an Equal Opportunity Employer, drug-free workplace, and complies with ADA regulations as applicable.&nbsp;
Powered by JazzHR
JveuJpJVSA

24,104 Writer Jobs