Technical Writer Jobs in Indianapolis, IN

Job Title: Technical Writer (no c2c) Industry: Pharmaceutical JOB DESCRIPTION: Theoris is looking for several Technical Writers for a long-term hybrid role in Indianapolis. The Technical Writer is responsible for developing and maintaining accurate, clear, and concise procedures, required tools, and resource documents. This role also ensures compliance with client standards and procedures by conducting quality checks of quality system documents and managing workflows and metadata in the document control system using Veeva QualityDocs. RESPONSIBILITIES: Ensure timely delivery of high-quality, error-free documents that meet international standards of written English. Develop and maintain accurate, clear, and concise procedures, required tools, and resource documents using appropriate technical writing standards, templates, and style guides. Correct errors in grammar, style, formatting, and syntax. Verify quality system architecture accuracy and ensure consistency of content within and between related documents. Coordinate with MQO Quality Systems on editing, quality checks, and data integrity reviews. Work with teams and stakeholders to ensure smooth and timely document development, escalating issues as needed. Facilitate the review/approval process for all documents, reconcile reviewer feedback, and address all issues. Exhibit flexibility in handling multiple document types. Participate in project teams as applicable. Manage key quality processes through QMS lifecycle management (e.g., periodic reviews) to ensure SEQS documents reflect current business processes and quality standards. Launch templates and manage document metadata. Ensure the accuracy and completeness of document control records, including revision histories, approvals, and related metadata. Track status, milestones, and associated documentation throughout the workflow. Influence or negotiate changes to timelines and content with other team members. REQUIREMENTS: Bachelor's degree (or equivalent work experience) in a scientific, health, communications, or technology-related field. Minimum of 5 years of experience in technical/medical writing. Experience using Veeva QualityDocs or other electronic document management systems (EDMS) is highly preferred. About Theoris: Our goal is to Fuel Your Career! As a Theoris team member, you join a culture based on people-centered values and an environment that fosters both personal and professional growth. We build long-term relationships with our clients and our consultants. With over 30 years of building strong relationships in the industry, we're uniquely positioned to make the right connections. This knowledge is used to find the right job placement. Our recruiting teams are experts dedicated to the information technology and engineering staffing space and are highly respected by our client base. Best-In-Class-Benefits We are in the people business; treating people right is our ONLY priority. Theoris Services consultants are full-time employees with full benefits, including: Robust Health Insurance 401(k) plan PTO accrual Paid holidays Excellent cash-based referral program

The Medical Technical Writer is responsible for supporting Medicines Quality Organization (MQO) Quality Systems team to deliver high quality documents in the Safety and Efficacy Quality System. The Technical Writer will support a pharmacovigilance initiative where new process maps have been created and document changes include new documents, retirement, and revisions within the pharmacovigilance system around surveillance and case management processes. This role works closely with the business process owners and the Quality System Sr. Principal. The Technical Writer is responsible for developing and maintaining accurate, clear, and concise procedures, required tools, and resource documents. The role is also responsible for quality checks of the quality system documents to ensure compliance with the client's standards and procedures. The role manages workflows and metadata in the document control system using Veeva QualityDocs. Job Responsibilities: 1. Quality Systems Document Management Ensure timely delivery of error-free, high-quality documents that meet international standards of written English: Develop and maintain accurate, clear, and concise procedures, required tools, and resource documents using appropriate technical writing standards, templates, and style guides. Correct errors in grammar, style, formatting, and syntax. Verify quality system architecture accuracy and consistency of content within and between related documents. 2. Document Control: Launch templates and manage document metadata. Support MQO Quality Systems with editing, Quality Checks and data integrity review. Ensure the accuracy and completeness of document control records, including document revision histories, revisions, approvals and related metadata. Track status, milestones & associated documentation throughout the workflow. General expectations: Maintain a strong customer focus. Communicate effectively. Manage activities efficiently and proactively to achieve timelines. Minimum Qualifications: Bachelor's degree in a relevant field, such as technical writing or life sciences 3+ years of experience in technical writing for procedures (pharmaceutical or biotech environment preferred) Writing GVP Documents Experience using Veeva QualityDocs or other electronic document management systems (EDMS) preferred Pharmacovigilance/ Surveillance experience Case processing/case management workflow

Milliman's Indianapolis Health consulting practice has created a Technical Writer & Editor, Life Sciences position for our growing Creative team. This role is responsible for creating content for target audiences within a highly regulated industry, ensuring the accuracy, clarity, and consistency of written content across various platforms. Responsibilities include writing, editing, and proofreading to correct grammatical, spelling, punctuation, and formatting errors, as well as creating documentation with a logical structure and consistent style, adhering to documentation standards, brand style guides, and industry best practices. The role involves collaborating with subject matter experts to align concepts and objectives with client goals and timelines. The selected candidate will work closely with graphic designers and the account team to enhance content quality and solicit feedback from users, support teams, and other stakeholders to continuously improve documentation. Additionally, they will use visuals, such as diagrams and charts, to enhance understanding of technical concepts and proficiently use documentation tools and technologies, such as content management systems, authoring tools, and collaboration platforms. Responsibilities Content Writing, Review and Editing: Author, edit and proofread articles, manuscripts, reports, web content, and other written materials Correct grammatical, spelling, punctuation, and formatting errors Ensure content adheres to the publication's style guide and editorial standards Proofreading: Conduct final proofreads of content before production to catch any remaining errors or inconsistencies Verify facts, data, and statistics to ensure accuracy Double check all QR codes and URLs for accuracy Collaboration: Work with subject matter experts, authors and other staff to resolve content-related questions or issues Provide constructive feedback to authors to help improve their writing skills Style and Tone Management: Ensure content maintains a consistent style and tone appropriate for the target audience Adapt content to meet specific guidelines for different platforms (e.g., print, web, social media) Content Formatting: Format content according to the brand's standards, including headings, subheadings, lists, and citations Ensure proper use of images, captions, and other multimedia elements Content Development: Interview key stakeholders as needed to gain insight and understanding to craft relevant and engaging content Enhance existing content to maximize clarity and audience engagement Overall Workload Allocation: 30% copywriting, 60% proofreading and editing marketing materials, 10% maintaining editorial center of excellence. Qualifications 3+ years of experience as a copywriter, copy editor, or in a similar content role Excellent command of the English language, including grammar, spelling, and punctuation Familiarity with various style guides (e.g., AP, Chicago, MLA) Strong attention to detail and the ability to spot errors quickly Proficiency in using word processing software and project management systems Strong organizational and time-management skills Ability to work independently and as part of a team Required Bachelor's degree in English, Journalism, Communications, or a related field Preferred Experience with SEO and digital content optimization Knowledge of additional languages Experience in Healthcare Communications or another highly regulated field The Team The Life Sciences consulting team is a group of 40+ individuals in the Indianapolis Health practice from varying backgrounds including actuaries, data analysts, pharmacists, and graphic designers. This group works primarily with pharmaceutical manufacturers by combining healthcare and payer knowledge, available data, analytic rigor, and industry experience to produce strategic and tactical insights for their clients. Location The person hired for this role will work in a dynamic, hybrid environment, with 2 to 3 days per week of on-site work required in our Indianapolis office on a weekly basis. Compensation The salary range for this role is $65,200 - $104,200, depending on a combination of factors, including, but not limited to, education, relevant work experience, qualifications, skills, certifications, location, etc. Benefits We offer a comprehensive benefits package designed to support employees' health, financial security, and well-being. Benefits include: Medical, Dental and Vision - Coverage for employees, dependents, and domestic partners. Employee Assistance Program (EAP) - Confidential support for personal and work-related challenges. 401(k) Plan - Includes a company matching program and profit-sharing contributions. Discretionary Bonus Program - Recognizing employee contributions. Flexible Spending Accounts (FSA) - Pre-tax savings for dependent care, transportation, and eligible medical expenses. Paid Time Off (PTO) - Begins accruing on the first day of work; Full-time employees accrue 15 days per year. Employees working less full-time accrue PTO on a prorated basis. Holidays - A minimum of 10 observed holidays per year. Family Building Benefits including Adoption and fertility assistance. Paid Parental Leave - Up to 12 weeks of paid leave for employees who meet eligibility criteria. Life Insurance & AD&D - 100% of premiums covered by Milliman. Short-Term and Long-Term Disability - Fully paid by Milliman. Who We Are Independent for 75 years, Milliman delivers market-leading services and solutions to clients worldwide. Today, we are helping companies take on some of the world's most critical and complex issues, including retirement funding and healthcare financing, risk management and regulatory compliance, data analytics and business transformation. Milliman invests in skills training and career development, and gives all employees access to a variety of learning and mentoring opportunities. Our growing number of Milliman Employee Resource Groups (ERG's) are employee-led communities that influence policy decisions, develop future leaders, and amplify the voices of their constituents. We encourage our employees to give back to their varied professions, including leadership in professional organizations. Please visit our web site (****************************************** to learn more about Milliman's commitments to our people, diversity and inclusion, social impact and sustainability. Through a team of professionals ranging from actuaries to clinicians, technology specialists to plan administrators, we offer unparalleled expertise in employee benefits, investment consulting, healthcare, life insurance and financial services, and property and casualty insurance. Equal Opportunity All qualified applicants will receive consideration for employment, without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. #LI-KM1#LI-HYBRID

Editor Up to $85K 25297 Pinnacle Partners is assisting our client in their search for an Editor to join their team in the Indianapolis, IN area. This successful resource will be responsible for content detailing and explaining commercial insurance policies. RESPONSIBILITIES: Edit and proofread content for accuracy and style Write new content based on customer needs requiring research Refine content ideas Ensure accuracy of content presented Research and stay up to date on trends and best practices REQUIREMENTS: 5+ years of experience with property and casualty commercial insurance Experience interpreting and understanding policy forms and documents Strong experience with Word, Outlook, and Excel Excellent writing and editing skills PREFERRED SKILLS: CPCU Designation AU and/or AINS Experience with casualty insurance TERMS: This is a direct hire opportunity with a salary up to $85K based on experience. They offer benefits including full medical, dental, and vision along with 401K and other soft benefits.

We are seeking a Technical Writer to support the sustaining engineering team on product support for quality defects within manufacturing. This role will be responsible for updating technical writing documents as changes are made to the manufacturing and process. You will play a crucial role in ensuring our commitment to quality within the manufacturing process. Responsibilities + Create, develop, write, and edit operational and instructional documents to support the end-users of company products. + Ensure that documents conform to existing department style guidelines as well as quality assurance and regulatory standards. + Collaborate cross-functionally to plan, research, develop, and prepare publication plans for each assigned project. + Assist in providing accurate cost and schedule estimates and manage the development and production of documents within budget on schedule. + Conduct interviews with technical staff and other functional groups to gather information for projects. + Manage the creation, review, update, and release of technical communication deliverables. + Provide rough drafts, sketches, and other appropriate inputs required by department illustrators to create illustrations and artwork for final documents. + Revise existing documents to support product changes. + Learn unfamiliar technical communication tools quickly and document complex technologies. + Work with appropriate team members to obtain translation and delivery schedule estimates. + Manage multiple projects simultaneously, prioritize work to satisfy multiple project teams, and seek assistance from colleagues as needed. Essential Skills + Bachelor's degree in engineering or related technical field. + 3+ years of experience in technical writing. + Familiarity with production processes for print documents and web-based publications, such as FrameMaker/Adobe Technical Communication Suite and Word. + Ability to adjust writing style and content according to audience needs, including clinicians/operators, technicians, and engineers. + Experience in medical writing and regulatory compliance. + Proficiency in document control, creation, change orders, and regulatory documents. Additional Skills & Qualifications + Excellent written and verbal communication skills. + Experience with content management systems and version control systems. + Ability to understand and explain complex technical concepts in a clear and concise manner. Work Environment This position operates within an onsite manufacturing and office environment. The work schedule includes being onsite 3 out of 5 days, specifically on Tuesday, Wednesday, and Thursday. The role supports manufacturing operations and involves collaboration with various teams. Pay and Benefits The pay range for this position is $25.00 - $35.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision- Critical Illness, Accident, and Hospital- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available- Life Insurance (Voluntary Life & AD&D for the employee and dependents)- Short and long-term disability- Health Spending Account (HSA)- Transportation benefits- Employee Assistance Program- Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a hybrid position in Indianapolis,IN. Application Deadline This position is anticipated to close on Mar 5, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Mindlance is a national recruiting company which partners with many of the leading employers in the Life Sciences, IT, and Financial Services sectors, feel free to check us out at ************************* Job Description Job Title: Technical Writer/Documentation Specialist Duration:- 1+ months Location: Indianapolis, IN, US Project Description: The Medicaid DW/DSS/BI will be a comprehensive, centralized-hybrid health and human services data warehouse with an open systems framework, containing leading integrated Commercial Off the Shelf (COTS) components, with wide-ranging business intelligence capabilities. This project will provide an environment that will be flexible enough to support any downstream analytical use of data. Under general supervision we are seeking to hire a Technical Writer/Documentation Specialist. The ideal candidate is someone with a technical writing background. The person holding this position will be responsible for writing various technical documents, documenting processes, and documenting and maintaining data lineage and the metadata repository. Basic Qualifications: - Must have 3 -5 yrs working experience as a Technical Writer/Documentation Metadata Coordinator/Specialist - 2yrs Data Analyst - 3yrs Technical Writing - 2yrs Data Warehouse Concepts knowledge Additional Information Thanks & Regards' Tanvi Kharbanda ************

Collabera is ranked amongst the top 10 Information Technology (IT) staffing firms in the U.S., with more than $525 million in sales revenue and a global presence that represents approximately 12,000+ professionals across North America (U.S., Canada), Asia Pacific (India, Philippines, Singapore, Malaysia), and Europe (Ireland, Netherlands, Poland, United Kingdom). We support our clients with a strong recruitment model and a sincere commitment to their success, which is why more than 75% of our clients rank us amongst their top three staffing suppliers. Not only are we committed to meeting and exceeding our customer's needs, but also are committed to our employees' satisfaction as well. We believe our employees are the cornerstone of our success and we make every effort to ensure their satisfaction throughout their tenure with Collabera. As a result of these efforts, we have been recognized by Staffing Industry Analysts (SIA) as the “Best Staffing Firm to Work For” for five consecutive years since 2012. Collabera has over 50 offices across the globe with a presence in ten countries and provides staff augmentation, managed services and direct placement services to global 2000 corporations. For consultants and employees, Collabera offers an enriching experience that promotes career growth and lifelong learning. Visit ***************** to learn more about our latest job openings. Awards and Recognition --Staffing Industry Analysts: Best Staffing Firm to Work For (2016, 2015, 2014, 2013, 2012) --Staffing Industry Analysts: Largest U.S. Staffing Firms (2016, 2015, 2014, 2013) --Staffing Industry Analysts: Largest Minority Owned IT Staffing Firm in the US. Job Description A Fortune 500 manufacturing giant looking urgently for Technical Writer who write technical materials, such as equipment materials, appendices, or operating and maintenance instructions and will also be responsible for organizing, editing and maintaining technical records and files. NOTE: Recent graduates are also welcome to apply for this position ! Industry: Fortune 500 manufacturing giant Job Title: Technical Writer Location: Columbus, IN 47201 Key Responsibilities: · Organize material and complete writing assignment according to set standards regarding order, clarity, conciseness, style and terminology. · Maintain records and files of work and revisions. Would be owner of the needed documentation for things assigned to them as needed. · Confer with client to establish technical specifications and to determine subject material to be developed for publication. This is where the selected hires would be working with the SMEs on the content that needs to be capture for documentation purposes. Qualifications Required Education, Experience & Skills: · A Bachelors' degree is a requirement for this request. Manager is seeking this level of education as this helps confirm the level of dedication someone has in order to complete said degree as well as the maturity level of that candidate. · Minimum of 2 years' relative working experience in technical writing is required. · Basic knowledge of media production, communication and dissemination techniques and methods · Basic knowledge of principles and methods for curriculum and training design. · Basic knowledge of computer software, such as Adobe, JavaScript, Oracle, etc. Additional Information If you want to know more and apply, please connect with: Niraj Singh **************************** ************ ************************************************

Technical Writer needs 3+ years technical writing experience Technical Writer requires: Technical writing SOPs Analyze Training material Develop and Edits standard operating procedures, user tools, training materials, glossary content and global standards. Work with teams to document action plans to ensure SOP compliance, which includes writing and editing of documentation. Route documentation through review and approval processes in the document management system. Analyze existing documentation to ensure it is updated, reviewed, and maintained as appropriate with subject matter experts. Adhere to appropriate quality and verification-including SOPs and makes recommendations on system documentation. Organize existing and new documentation. If expertise in technical writing, then will need to coach and train the other document controllers on technical writing concepts and instruction. Suggest appropriate formatting for documentation. Serves as a point person for documentation advice and help

See Yourself at Telix We are seeking an experienced Technical (CMC) Writer in Regulatory Affairs. This position offers a unique opportunity to contribute to the achievement of Telix's strategic goals by leading and driving the technical (CMC) regulatory writing to accelerate the development of diagnostic and therapeutic assets in areas of high unmet medical need. This role will lead the preparation of the quality/CMC sections of the regulatory module 3 dossier and associated information in agency briefing books using internal manufacturing and quality source documentation. The Technical Regulatory Writer will identify, engage, and project manage the work of contract technical writers as required. Key Accountabilities: Lead the compilation, writing, and editing of high-quality module 3 documents. Develop and update pertinent SOPs, processes, templates, style guides, and manuals, as needed. Maintain working knowledge of the Telix development pipeline. Prepare, review, and edit regulatory submission documents (e.g., INDs, NDAs, BLAs, CTDs). Ensure all documents comply with regulatory guidelines, company standards, and industry best practices. Lead and manage multiple regulatory technical writing projects simultaneously, ensuring timely delivery of high-quality documents. Coordinate with cross-functional teams to gather necessary information and resolve any issues that arise during the document development process. Conduct thorough reviews of documents for accuracy, consistency, and clarity as needed. Work closely with clinical development teams, including clinical operations, regulatory affairs, biostatistics, physicians, and medical affairs, to ensure alignment and accuracy of clinical documents. Provide medical writing expertise and support to project teams, contributing to strategic planning and decision-making. Mentor and train junior medical writers, providing guidance and support to enhance their skills and career development, along with oversight to external contractors. Stay current with industry trends, guidelines, and best practices, and share knowledge with the team. Support regulatory submissions by preparing high-quality documentation and addressing health authority comments and queries. Ensure compliance with regulatory requirements and timelines for all submission-related activities. Education and Experience: Bachelor's degree in a scientific or related field required; MS or PhD preferred. 5+ years' overall experience in technical/CMC writing, 2+ years within Regulatory CMC required Experience overseeing and mentoring contractors and junior team members strongly preferred Strong understanding of drug development, drug substance and drug product manufacturing, regulations (CFR, FDA, EMA, and ICH guidelines), and scientific principles. Experience and proficiency with document templates, document toolbars and proper version control. Strong project management skills. Organized and self-motivated. Strong attention to detail. Key Capabilities: Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills

Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer a wide range of delivery systems including pre-filled syringes, liquid/lyophilized vials, diluents for reconstitution, powder-filled vials and sterile crystallization. Our product types include biologics and small molecules, cytotoxics, highly potent compounds, diluents for reconstitution and vaccines - which are all directly injected into patients worldwide. As such, there is a strong emphasis on quality and continuous improvement at Simtra. We hold ourselves to the highest quality and regulatory standards. While our primary focus is cGMP manufacturing, we offer many support services including formulation and development, lyophilization optimization, global regulatory support and secondary packaging. Our teams are driven to help clients scale, innovate and bring life-changing medicines to patients worldwide. Why join Team Simtra? Because we: Make it HAPPEN - We bring a growth mindset to every opportunity, developing new skillsets and exceeding our expectations and those of our customers. Make it TOGETHER - We work as one, respecting each voice and tapping into our unique strengths across teams-so we can solve problems in new ways. Make it RIGHT - We hold ourselves to a high standard of excellence, fulfilling our commitments to the customer, their patients, and our team members. Make it COUNT - We take pride in our day-to-day work, knowing the impact we make - taking on challenges big and small to improve patient health. This role: The Manufacturing Technical Writer is responsible for performing site Non-Conformance Report (NCR) and Significant SNCRs investigations, utilizing investigative tools, identifying the root cause(s), documenting the results and processing the relevant records in the corporate Trackwise system, collaborating with impacted departments to determine appropriate corrective or preventive actions and related effectiveness criteria. Personnel filling this role will be the primary investigator for the NCR and SNCRs for the entire Bloomington facility. This candidate will sit onsite at the Bloomington facility and report to the Sr. Manager, Technical Services. The responsibilities: Develop the scope and devise an approach for assigned investigations Determine the Define/Measure/Analyze (problem-solving technique) elements of the investigation by utilizing investigation tools Identify cross-functional team members and assemble the investigation team Confirm corrections/containment identified based on the investigation results Determine the appropriate data sources to be evaluated for the investigation and obtain the required data Investigate the root cause(s) of the issue and document the investigation results Ensure the Investigation record is maintained with current and accurate information throughout its lifecycle Collaborate with Action Owner/CAPA (Corrective Action and Preventive Action) Owner to develop the Action Plan/Effectiveness Plan Present in Quality Review Board (QRB) stages (initiation and closure for SNCRs) Manage multiple investigations at any given time Responsible for speaking to client auditors and regulatory authorities to explain investigations Required qualifications: BS degree required, preferably in a science or technical area or equivalent experience 2+ years technical writing experience, preferably in pharmaceutical industry Knowledge of applicable CAPA procedures, specifications, regulations and standards Microsoft Office Suite (Word, Excel, PowerPoint, and Outlook) intermediate proficiency Goal-setting, prioritize, organization, attention to detail, and time management skills Critical & creative thinking and problem-solving skills Ability to use logic and scientific principles to reach conclusions when presented with ambiguous data Strong oral and written communication skills Ability to demonstrate strong leadership skills Knowledge of FDA regulations and application of Good Manufacturing Practices (GMP) Ability to utilize enterprise software systems (Trackwise) Physical / safety requirements: Duties will require overtime work, including nights and weekends on occasion Ability to gown in C/D gowning area In return, you'll be eligible for [1]: Day One Benefits Medical & Dental Coverage Flexible Spending Accounts Life and AD&D Insurance Supplemental Life Insurance Spouse Life Insurance Child Life Insurance Short and Long-Term Disability Insurance 401(k) Retirement Savings Plan with Company Match Time Off Program Paid Holidays Paid Time Off Paid Parental Leave and more Adoption Reimbursement Program Education Assistance Program Employee Assistance Program Community and Volunteer Service Program Additional Benefits Voluntary Insurance Benefits Vision Coverage Accident Critical Illness Hospital Indemnity Insurance Identity Theft Protection Legal and more Onsite Campus Amenities Workout Facility Cafeteria Credit Union [1] Current benefit offerings are in effect through 12/31/25 Disclaimer This job description is intended to provide the minimum knowledge, skills and abilities necessary to perform the job. It may not be inclusive of all the duties and responsibilities of the job. Simtra reserves the right to make modifications based on business requirements. Equal Employment Opportunity Simtra is proud to be an equal opportunity employer. Simtra evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. Data Privacy To learn more about Simtra's approach to data privacy, please review the Simtra Recruitment Platform Global Privacy Policy: **********************************

Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer a wide range of delivery systems including pre-filled syringes, liquid/lyophilized vials, diluents for reconstitution, powder-filled vials and sterile crystallization. Our product types include biologics and small molecules, cytotoxics, highly potent compounds, diluents for reconstitution and vaccines - which are all directly injected into patients worldwide. As such, there is a strong emphasis on quality and continuous improvement at Simtra. We hold ourselves to the highest quality and regulatory standards. While our primary focus is cGMP manufacturing, we offer many support services including formulation and development, lyophilization optimization, global regulatory support and secondary packaging. Our teams are driven to help clients scale, innovate and bring life-changing medicines to patients worldwide. Why join Team Simtra? Because we: Make it HAPPEN - We bring a growth mindset to every opportunity, developing new skillsets and exceeding our expectations and those of our customers. Make it TOGETHER - We work as one, respecting each voice and tapping into our unique strengths across teams-so we can solve problems in new ways. Make it RIGHT - We hold ourselves to a high standard of excellence, fulfilling our commitments to the customer, their patients, and our team members. Make it COUNT - We take pride in our day-to-day work, knowing the impact we make - taking on challenges big and small to improve patient health. This role: The Manufacturing Technical Writer is responsible for performing site Non-Conformance Report (NCR) and Significant SNCRs investigations, utilizing investigative tools, identifying the root cause(s), documenting the results and processing the relevant records in the corporate Trackwise system, collaborating with impacted departments to determine appropriate corrective or preventive actions and related effectiveness criteria. Personnel filling this role will be the primary investigator for the NCR and SNCRs for the entire Bloomington facility. This candidate will sit onsite at the Bloomington facility and report to the Sr. Manager, Technical Services. The responsibilities: Develop the scope and devise an approach for assigned investigations Determine the Define/Measure/Analyze (problem-solving technique) elements of the investigation by utilizing investigation tools Identify cross-functional team members and assemble the investigation team Confirm corrections/containment identified based on the investigation results Determine the appropriate data sources to be evaluated for the investigation and obtain the required data Investigate the root cause(s) of the issue and document the investigation results Ensure the Investigation record is maintained with current and accurate information throughout its lifecycle Collaborate with Action Owner/CAPA (Corrective Action and Preventive Action) Owner to develop the Action Plan/Effectiveness Plan Present in Quality Review Board (QRB) stages (initiation and closure for SNCRs) Manage multiple investigations at any given time Responsible for speaking to client auditors and regulatory authorities to explain investigations Required qualifications: BS degree required, preferably in a science or technical area or equivalent experience 2+ years technical writing experience, preferably in pharmaceutical industry Knowledge of applicable CAPA procedures, specifications, regulations and standards Microsoft Office Suite (Word, Excel, PowerPoint, and Outlook) intermediate proficiency Goal-setting, prioritize, organization, attention to detail, and time management skills Critical & creative thinking and problem-solving skills Ability to use logic and scientific principles to reach conclusions when presented with ambiguous data Strong oral and written communication skills Ability to demonstrate strong leadership skills Knowledge of FDA regulations and application of Good Manufacturing Practices (GMP) Ability to utilize enterprise software systems (Trackwise) Physical / safety requirements: Duties will require overtime work, including nights and weekends on occasion Ability to gown in C/D gowning area In return, you'll be eligible for [1]: Day One Benefits Medical & Dental Coverage Flexible Spending Accounts Life and AD&D Insurance Supplemental Life Insurance Spouse Life Insurance Child Life Insurance Short and Long-Term Disability Insurance 401(k) Retirement Savings Plan with Company Match Time Off Program Paid Holidays Paid Time Off Paid Parental Leave and more Adoption Reimbursement Program Education Assistance Program Employee Assistance Program Community and Volunteer Service Program Additional Benefits Voluntary Insurance Benefits Vision Coverage Accident Critical Illness Hospital Indemnity Insurance Identity Theft Protection Legal and more Onsite Campus Amenities Workout Facility Cafeteria Credit Union [1] Current benefit offerings are in effect through 12/31/25 Disclaimer This job description is intended to provide the minimum knowledge, skills and abilities necessary to perform the job. It may not be inclusive of all the duties and responsibilities of the job. Simtra reserves the right to make modifications based on business requirements. Equal Employment Opportunity Simtra is proud to be an equal opportunity employer. Simtra evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. Data Privacy To learn more about Simtra's approach to data privacy, please review the Simtra Recruitment Platform Global Privacy Policy: **********************************

Onebridge, a Marlabs Company, is an AI and data analytics consulting firm that strives to improve outcomes for the people we serve through data and technology. We have served some of the largest healthcare, life sciences, manufacturing, financial services, and government entities in the U.S. since 2005. We have an exciting opportunity for a highly skilled Technical Content Writer to join an innovative and dynamic group of professionals at a company rated among the top “Best Places to Work” in Indianapolis since 2015. Open to Full Time or Contract. Technical Content Writer | About you As a Technical Content Writer, you will be responsible for crafting clear, engaging content that transforms complex Data and AI topics into accessible, compelling materials. You will excel at creating white papers, case studies, and other collateral that effectively highlight our expertise. You will work closely with internal teams to ensure the accuracy and relevance of your content, tailoring your writing for both technical and business audiences. Ultimately, your work will drive action and support Onebridge's mission to deliver innovative solutions in the Data and AI space. Technical Content Writer | Day-to-day Develop clear, concise, and engaging content focused on Data Management, AI, Analytics, and related consulting services. Create high-quality written materials, including white papers, case studies, blog posts, and client-facing documents to support business development and marketing. Collaborate with internal teams (subject matter experts, marketing, and sales) to gather insights and ensure an accurate representation of Onebridge's services and value propositions. Maintain and evolve Onebridge's voice and tone, ensuring consistency across all content and materials. Stay informed on industry trends in Data, AI, and technology to produce relevant and innovative content. Tailor content for different audiences, from executives and business leaders to technical teams, ensuring clarity and impact. Technical Content Writer | Skills & Experience 7+ years of experience in content writing, with a focus on Data, AI, or technology. Proven ability to create high-quality technical content, including white papers, case studies, blog posts, and other business collateral. Strong understanding of Data, AI, and analytics, with the ability to communicate complex topics in a clear and engaging way. Experience collaborating with cross-functional teams to develop content that aligns with business goals and objectives. Exceptional written and verbal communication skills, with a keen attention to detail. Experience writing for industries such as healthcare, financial services, manufacturing, or logistics, and familiarity with AI consulting services and related technologies. A Best Place to Work in Indiana, since 2015.

Baker Tilly is a leading advisory, tax and assurance firm, providing clients with a genuine coast-to-coast and global advantage in major regions of the U.S. and in many of the world's leading financial centers - New York, London, San Francisco, Los Angeles, Chicago and Boston. Baker Tilly Advisory Group, LP and Baker Tilly US, LLP (Baker Tilly) provide professional services through an alternative practice structure in accordance with the AICPA Code of Professional Conduct and applicable laws, regulations and professional standards. Baker Tilly US, LLP is a licensed independent CPA firm that provides attest services to its clients. Baker Tilly Advisory Group, LP and its subsidiary entities provide tax and business advisory services to their clients. Baker Tilly Advisory Group, LP and its subsidiary entities are not licensed CPA firms. Baker Tilly Advisory Group, LP and Baker Tilly US, LLP, trading as Baker Tilly, are independent members of Baker Tilly International, a worldwide network of independent accounting and business advisory firms in 141 territories, with 43,000 professionals and a combined worldwide revenue of $5.2 billion. Visit bakertilly.com or join the conversation on LinkedIn, Facebook and Instagram. Please discuss the work location status with your Baker Tilly talent acquisition professional to understand the requirements for an opportunity you are exploring. Baker Tilly is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability or protected veteran status, gender identity, sexual orientation, or any other legally protected basis, in accordance with applicable federal, state or local law. Any unsolicited resumes submitted through our website or to Baker Tilly Advisory Group, LP, employee e-mail accounts are considered property of Baker Tilly Advisory Group, LP, and are not subject to payment of agency fees. In order to be an authorized recruitment agency ("search firm") for Baker Tilly Advisory Group, LP, there must be a formal written agreement in place and the agency must be invited, by Baker Tilly's Talent Attraction team, to submit candidates for review via our applicant tracking system. Job Description: Responsibilities Baker Tilly is seeking a dynamic and resourceful Special Advisor Consultant to join our Public Sector Recon team on a part-time, as-needed basis. The ideal candidate will bring a wealth of experience and expertise in the CPA and consulting industry, specifically supporting governmental clients such as municipalities, counties, schools, libraries, utilities, and other special units with duties related to compliance, operations and reporting. This role requires limited travel, presentation of information both in writing and in person, and ability to work effectively with larger project groups. Responsibilities Provide consulting services to governmental clients on a part-time, as-needed basis. Support and advise on various client projects, ensuring the highest level of service and expertise - client projects could include help with GAAP complications and accounting services. Travel to client locations as required for project needs. Prepare and deliver clear, concise findings, presentations and written reports. Collaborate with larger project teams, providing specialized knowledge and insights. Utilize Microsoft products effectively to manage and present data and information. Document and analyze processes, internal controls, and workflow in order to identify opportunities for improvement. Perform research into best practices, operational polices, and organizational design. Interview clients to better understand processes and to recommend improvements. Qualifications Bachelor's degree required; Master of Public Administration (MPA), Certified Public Accountant (CPA), or Master of Business Administration (MBA) highly desired. Extensive experience in the CPA and consulting industry, with a focus on governmental clients. Strong proficiency with Microsoft products (Word, Excel, PowerPoint, Outlook). Exceptional communication skills, both written and verbal. Proven ability to be resourceful and adapt to various project needs and environments. Demonstrated experience in presenting information clearly and effectively to diverse audiences. .A strong work ethic and willingness to take on a variety of roles and levels of responsibility in a dynamic and entrepreneurial setting. Three (3) years or more prior experience in a government organization a plus (state government, municipality, utility, k-12 schools,etc.). Ability to travel as needed Skills and Attributes: Highly resourceful with strong problem-solving capabilities. Excellent organizational and time management skills. Ability to work independently and as part of a team. Strong analytical and critical thinking skills. Ability to manage projects and meet deadlines. Additional Information The compensation range for this role is $35.00 to $68.25. Actual compensation is influenced by a variety of factors including but not limited to skills, experience, qualifications, and geographic location.

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Its a simple route driver job and company will be providing the car. Job Description Job Details: Produce system documentation from the content provided by subject-matter experts (SMEs). Assist SMEs in creating quality documentation by providing guidance on format. Supports and/or contributes to the design, development, and delivery of end user training and/or procedures. Revise documents to support the resolution of incidents (Trouble Tickets) within committed service levels. Revise documents in support of the execution of change requests in compliance with local change control procedures. Operate with a quality mindset (capable, in control, compliant, and continuously improving). Primary Position Responsibilities (major or daily tasks): Documenting business and IT processes and systems. This resource must have the ability to quickly comprehend complex business processes and IT terminology in order to participate in technical discussions and walk away with a clear understanding of what was discussed and be able to document that understanding. Requirements / have to haves not listed elsewhere: This resource must have the ability to quickly comprehend complex business processes and IT terminology in order to participate in technical discussions and walk away with a clear understanding of what was discussed and be able to document that understanding. The individual must have strong communication and writing skills. Qualifications Requirements / have to haves not listed elsewhere: This resource must have the ability to quickly comprehend complex business processes and IT terminology in order to participate in technical discussions and walk away with a clear understanding of what was discussed and be able to document that understanding. The individual must have strong communication and writing skills. Additional Information All your information will be kept confidential according to EEO guidelines.

Job Title: Technical WriterJob Description We are seeking a Technical Writer to support the sustaining engineering team on product support for quality defects within manufacturing. This role will be responsible for updating technical writing documents as changes are made to the manufacturing and process. You will play a crucial role in ensuring our commitment to quality within the manufacturing process. Responsibilities + Create, develop, write, and edit operational and instructional documents to support the end-users of company products. + Ensure that documents conform to existing department style guidelines as well as quality assurance and regulatory standards. + Collaborate cross-functionally to plan, research, develop, and prepare publication plans for each assigned project. + Assist in providing accurate cost and schedule estimates and manage the development and production of documents within budget on schedule. + Conduct interviews with technical staff and other functional groups to gather information for projects. + Manage the creation, review, update, and release of technical communication deliverables. + Provide rough drafts, sketches, and other appropriate inputs required by department illustrators to create illustrations and artwork for final documents. + Revise existing documents to support product changes. + Learn unfamiliar technical communication tools quickly and document complex technologies. + Work with appropriate team members to obtain translation and delivery schedule estimates. + Manage multiple projects simultaneously, prioritize work to satisfy multiple project teams, and seek assistance from colleagues as needed. Essential Skills + Bachelor's degree in engineering or related technical field. + 3+ years of experience in technical writing. + Familiarity with production processes for print documents and web-based publications, such as FrameMaker/Adobe Technical Communication Suite and Word. + Ability to adjust writing style and content according to audience needs, including clinicians/operators, technicians, and engineers. + Experience in medical writing and regulatory compliance. + Proficiency in document control, creation, change orders, and regulatory documents. Additional Skills & Qualifications + Excellent written and verbal communication skills. + Experience with content management systems and version control systems. + Ability to understand and explain complex technical concepts in a clear and concise manner. Work Environment This position operates within an onsite manufacturing and office environment. The work schedule includes being onsite 3 out of 5 days, specifically on Tuesday, Wednesday, and Thursday. The role supports manufacturing operations and involves collaboration with various teams. Pay and Benefits The pay range for this position is $25.00 - $35.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision- Critical Illness, Accident, and Hospital- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available- Life Insurance (Voluntary Life & AD&D for the employee and dependents)- Short and long-term disability- Health Spending Account (HSA)- Transportation benefits- Employee Assistance Program- Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a hybrid position in Shelbyville,IN. Application Deadline This position is anticipated to close on Feb 28, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Collabera is ranked amongst the top 10 Information Technology (IT) staffing firms in the U.S., with more than $525 million in sales revenue and a global presence that represents approximately 12,000+ professionals across North America (U.S., Canada), Asia Pacific (India, Philippines, Singapore, Malaysia), and Europe (Ireland, Netherlands, Poland, United Kingdom). We support our clients with a strong recruitment model and a sincere commitment to their success, which is why more than 75% of our clients rank us amongst their top three staffing suppliers. Not only are we committed to meeting and exceeding our customer's needs, but also are committed to our employees' satisfaction as well. We believe our employees are the cornerstone of our success and we make every effort to ensure their satisfaction throughout their tenure with Collabera. As a result of these efforts, we have been recognized by Staffing Industry Analysts (SIA) as the “Best Staffing Firm to Work For” for five consecutive years since 2012. Collabera has over 50 offices across the globe with a presence in ten countries and provides staff augmentation, managed services and direct placement services to global 2000 corporations. For consultants and employees, Collabera offers an enriching experience that promotes career growth and lifelong learning. Visit ***************** to learn more about our latest job openings. Awards and Recognition --Staffing Industry Analysts: Best Staffing Firm to Work For (2016, 2015, 2014, 2013, 2012) --Staffing Industry Analysts: Largest U.S. Staffing Firms (2016, 2015, 2014, 2013) --Staffing Industry Analysts: Largest Minority Owned IT Staffing Firm in the US. Job Description A Fortune 500 manufacturing giant looking urgently for Technical Writer who write technical materials, such as equipment materials, appendices, or operating and maintenance instructions and will also be responsible for organizing, editing and maintaining technical records and files. Industry: Fortune 500 manufacturing giant Job Title: Technical Writer Location: Columbus, IN 47201 Key Responsibilities: · Organize material and complete writing assignment according to set standards regarding order, clarity, conciseness, style and terminology. · Maintain records and files of work and revisions. Would be owner of the needed documentation for things assigned to them as needed. · Confer with client to establish technical specifications and to determine subject material to be developed for publication. This is where the selected hires would be working with the SMEs on the content that needs to be capture for documentation purposes. Qualifications Required Education, Experience & Skills: · A Bachelors' degree is a requirement for this request. Manager is seeking this level of education as this helps confirm the level of dedication someone has in order to complete said degree as well as the maturity level of that candidate. · Minimum of 2 years' relative working experience in technical writing is required. · Basic knowledge of media production, communication and dissemination techniques and methods · Basic knowledge of principles and methods for curriculum and training design. · Basic knowledge of computer software, such as Adobe, JavaScript, Oracle, etc. Additional Information If you want to know more and apply, please connect with: Niraj Singh **************************** ************ ************************************************

Technical Writer needs 5+ years experience. Pharma, medica device industry Technical Writer requires: Technical writing Documentation SOPs Pharma medical device industry Develop and edits standard operating procedures, user tools, training materials, glossary content and global standards. Work with teams to document action plans to ensure SOP compliance, which includes writing and editing of documentation. Route documentation through review and approval processes in the document management system. Analyze existing documentation to ensure it is updated, reviewed, and maintained as appropriate with subject matter experts. Adhere to appropriate quality and verification-including SOPs and makes recommendations on system documentation. Organize existing and new documentation. Coach and train the other document controllers on technical writing concepts and instruction. S Suggest appropriate formatting for documentation. Serves as a point person for documentation advice and help. Reports status of documentation deliverables

Baker Tilly is a leading advisory, tax and assurance firm, providing clients with a genuine coast-to-coast and global advantage in major regions of the U.S. and in many of the world's leading financial centers - New York, London, San Francisco, Los Angeles, Chicago and Boston. Baker Tilly Advisory Group, LP and Baker Tilly US, LLP (Baker Tilly) provide professional services through an alternative practice structure in accordance with the AICPA Code of Professional Conduct and applicable laws, regulations and professional standards. Baker Tilly US, LLP is a licensed independent CPA firm that provides attest services to its clients. Baker Tilly Advisory Group, LP and its subsidiary entities provide tax and business advisory services to their clients. Baker Tilly Advisory Group, LP and its subsidiary entities are not licensed CPA firms. Baker Tilly Advisory Group, LP and Baker Tilly US, LLP, trading as Baker Tilly, are independent members of Baker Tilly International, a worldwide network of independent accounting and business advisory firms in 141 territories, with 43,000 professionals and a combined worldwide revenue of $5.2 billion. Visit bakertilly.com or join the conversation on LinkedIn, Facebook and Instagram. Please discuss the work location status with your Baker Tilly talent acquisition professional to understand the requirements for an opportunity you are exploring. Baker Tilly is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability or protected veteran status, gender identity, sexual orientation, or any other legally protected basis, in accordance with applicable federal, state or local law. Any unsolicited resumes submitted through our website or to Baker Tilly Advisory Group, LP, employee e-mail accounts are considered property of Baker Tilly Advisory Group, LP, and are not subject to payment of agency fees. In order to be an authorized recruitment agency ("search firm") for Baker Tilly Advisory Group, LP, there must be a formal written agreement in place and the agency must be invited, by Baker Tilly's Talent Attraction team, to submit candidates for review via our applicant tracking system. Job Description: Responsibilities Baker Tilly is seeking a dynamic and resourceful Special Advisor Consultant to join our Public Sector Recon team on a part-time, as-needed basis. The ideal candidate will bring a wealth of experience and expertise in the CPA and consulting industry, specifically supporting governmental clients such as municipalities, counties, schools, libraries, utilities, and other special units with duties related to compliance, operations and reporting. This role requires limited travel, presentation of information both in writing and in person, and ability to work effectively with larger project groups. Responsibilities * Provide consulting services to governmental clients on a part-time, as-needed basis. * Support and advise on various client projects, ensuring the highest level of service and expertise - client projects could include help with GAAP complications and accounting services. * Travel to client locations as required for project needs. * Prepare and deliver clear, concise findings, presentations and written reports. * Collaborate with larger project teams, providing specialized knowledge and insights. * Utilize Microsoft products effectively to manage and present data and information. * Document and analyze processes, internal controls, and workflow in order to identify opportunities for improvement. * Perform research into best practices, operational polices, and organizational design. * Interview clients to better understand processes and to recommend improvements. Qualifications * Bachelor's degree required; Master of Public Administration (MPA), Certified Public Accountant (CPA), or Master of Business Administration (MBA) highly desired. * Extensive experience in the CPA and consulting industry, with a focus on governmental clients. * Strong proficiency with Microsoft products (Word, Excel, PowerPoint, Outlook). * Exceptional communication skills, both written and verbal. * Proven ability to be resourceful and adapt to various project needs and environments. * Demonstrated experience in presenting information clearly and effectively to diverse audiences. * .A strong work ethic and willingness to take on a variety of roles and levels of responsibility in a dynamic and entrepreneurial setting. * Three (3) years or more prior experience in a government organization a plus (state government, municipality, utility, k-12 schools,etc.). * Ability to travel as needed Skills and Attributes: * Highly resourceful with strong problem-solving capabilities. * Excellent organizational and time management skills. * Ability to work independently and as part of a team. * Strong analytical and critical thinking skills. * Ability to manage projects and meet deadlines. Additional Information The compensation range for this role is $35.00 to $68.25. Actual compensation is influenced by a variety of factors including but not limited to skills, experience, qualifications, and geographic location.

Established in 1991, Collabera has been a leader in IT staffing for over 22 years and is one of the largest diversity IT staffing firms in the industry. As a half a billion dollar IT company, with more than 9,000 professionals across 30+ offices, Collabera offers comprehensive, cost-effective IT staffing & IT Services. We provide services to Fortune 500 and mid-size companies to meet their talent needs with high quality IT resources through Staff Augmentation, Global Talent Management, Value Added Services through CLASS (Competency Leveraged Advanced Staffing & Solutions) Permanent Placement Services and Vendor Management Programs. Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence. Collabera offers a full range of benefits to its employees including paid vacations, holidays, personal days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance, Disability Insurance. Job Description Job Title: Technical Writer I Duration: 6 month (High possibility of extension) Position Summary: • Develops high-quality information/documentation for Cummins applications. Key responsibilities for this position will include the following: • Develop/maintain design documentation and information provided by subject matter experts in the engineering and service functions. • Integrate relevant information into well written text instructions, functional descriptions, and operation and service procedures with illustrating graphics. • Develop and manage a resource plan, project schedule and work plan for multiple and complex projects. • Maintain and communicate status for all active projects. • Assist in maintaining a departmental schedule and resource assignments as projects and organizational priorities shift. • Lead improvement activities that reduce translation cost and complexity and improve content quality. • Develop the framework to publish, update and maintain the documentation in a manner that is easy to consume and share. • Assist / coach Technical Writers with project schedule development and execution. • Audit Content Developers information for content quality and accuracy. • Resolve day-to-day service information problems and customer inquiries. • Maintain the library of product support information as products change. • Write for re-use using XML authoring system. • Write effectively with translations in mind. • Develop and maintain up to date work procedures. Qualifications • College, university or equivalent technical experience is required. • Intermediate level of relevant experience required. Additional information from the manager: • This position falls under the Product Activity Group for Client. The need driving this position is that this is a growing group and they need more help. If someone does well in this role, they could be considered for a full-time opportunity. • Selected candidate will be assigned to 2 current applications to manage. They will be responsible for updates, version control and publishing of those apps. As new applications come in to the group, some of those may also be assigned to that person to manage. Additional Information To set-up an Interview. Please contact Himanshu Prajapat Contact # ************ Email- himanshu.prajapat(@)collabera.com