R&d Documentation Specialist Ii

il y a 4 semaines


Wavre, Belgique Ansys Temps plein

Ansys is the global leader in engineering simulation, helping the world's most innovative companies deliver radically better products to their customers. By offering the best and broadest portfolio of engineering simulation software, Ansys helps companies solve the most complex design challenges and engineer products limited only by imagination.

**Summary / Role Purpose**

The R&D Documentation Specialist II (M/F/d) creates a variety of Ansys documentation deliverables. They determine the best way to organize and deliver information, write and revise supporting content for products, and review content for technical accuracy, consistency, and style. This role requires effective planning, scheduling, research, writing, and editing skills. The R&D Documentation Specialist II (M/F/d) works with development teams, keeping informed of product development activities to determine the need for new documentation as well as revisions, corrections, and changes in previously released materials.

**Key Duties and Responsibilities**
- Determines audience needs to create user documentation, tutorials, microcopy/user interface copy, and videos for Ansys products
- Updates and revises previously released documentation
- Acquires enhanced knowledge about both Ansys products and Ansys documentation tools, processes, and procedures
- Works under some supervision

**Minimum Education/Certification Requirements and Experience**
- BS in Technical Writing, Technical Communication, Computer Science, English/Linguistics, Journalism, or Engineering with 2 years’ experience or MS
- Fluency in English, along with excellent written and spoken communication skills
- Ability to gather and analyze technical and product information from various sources, paying close attention to detail
- Capacity to develop user-centric documentation ensuring a high level of quality, consistency, and accuracy
- Comfort in managing multiple tasks and priorities simultaneously in a fast-paced, deadline-driven, geographically diverse environment
- This position does not qualify for immigration sponsorship

**Preferred Qualifications and Skills**
- Familiarity with Ansys products
- Familiarity with the concepts of documentation authoring, common project management software, version control, and structured documentation, as well as build tools, oXygen, DITA, XML, Git, Camtasia, DocBook, user-centered design processes, and agile development methodologies, familiarity with Modeling Languages such as UML or SysML
- Experience determining the best method in which to present information and then creating the appropriate output(s), such as topic-based help, videos, tutorials, graphics, and interactive learning systems

**CULTURE AND VALUES**
Culture and values are incredibly important to Ansys. They inform us of who we are, of how we act. Values aren't posters hanging on a wall or about trite or glib slogans. They aren't about rules and regulations. They can't just be handed down the organization. They are shared beliefs - guideposts that we all follow when we're facing a challenge or a decision. Our values tell us how we live our lives; how we approach our jobs. Our values are crucial for fostering a culture of winning for our company:

- Customer focus
- Results and Accountability
- Innovation
- Transparency and Integrity
- Mastery
- Inclusiveness
- Sense of urgency
- Collaboration and Teamwork

**WORKING AT ANSYS**
At Ansys, you will find yourself among the sharpest minds and most visionary of leaders, collectively aiming to change the world with innovative technology and remarkable solutions. With the prestigious reputation in servicing well-known, world-class companies, standards at Ansys are high, met by those willing to rise to the occasion and meet those challenges head-on. Because at Ansys, it’s about the learning, the discovery and the collaboration. It’s about the “what’s next” as much as the “mission accomplished”. It’s about the melding of disciplined intellect with strategic direction and results that have, can and will impact real people in real ways, forged within a working environment built on respect, autonomy and ethics.

At Ansys, you will find yourself among those eager to drive the world towards the next best thing with hands planted firmly on the wheel.
Our team is passionate about pushing the limits of world-class simulation technology so our customers can turn their design concepts into successful, innovative products faster and at lower cost. As a measure of our success in attaining these goals, Ansys has been recognized as one of the world's most innovative companies by prestigious publications such as Bloomberg Businessweek and FORTUNE magazines.

Ansys is an S&P 500 company and a component of the NASDAQ-100.

Ansys is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disabilit



  • Wavre, Belgique RHEA Group Temps plein

    Are you looking for a new opportunity in a fast-moving global company with a family feel? A job where you could have an impact? We are looking for a Document Management Specialist to work at RHEA Group’s headquarters in Wavre, Belgium. The Document Management Specialist (EDMS Administrator) is an experienced document control administrator who is...


  • Wavre, Wallonie, Belgique RHEA Group Temps plein

    Are you looking for a new opportunity in a fast-moving global company with a family feel? A job where you could have an impact?We are looking for a Document Management Specialist to work at RHEA Group's headquarters in Wavre, Belgium.The Document Management Specialist (EDMS Administrator) is an experienced document control administrator who is responsible...


  • Wavre, Belgique GSK Temps plein

    **Site Name**: Belgium-Wavre **Posted Date**: Aug 2 2023 The purpose of the job is to partner with Business counterparts to guide them towards documentation and training excellence through continuous improvement and transformation projects. The role has a key strategic relevance for the partnership with the Business and to raise the culture of...


  • Wavre, Wallonie, Belgique GSK Temps plein

    Site Name: Belgium-WavrePosted Date: Aug 2 2023The purpose of the job is to partner with Business counterparts to guide them towards documentation and training excellence through continuous improvement and transformation projects.The role has a key strategic relevance for the partnership with the Business and to raise the culture of documentation & training...


  • Wavre, Wallonie, Belgique Parexel Temps plein

    The Initiation Clinical Research Associate II (iCRA II) specialises in performing all study start up activities for a clinical trial. You will participate in Pre SIV activities and be assigned & accountable for managing and driving the strategy for the Pre SIV / start up tasks of the study. The iCRA II can also support protocol amendments if applicable. This...

  • Specialist Qc Transfer

    il y a 4 semaines


    Wavre, Belgique Jefferson Wells Temps plein

    Location: **Wavre** - Type: **Contracting** **#20405** **Specialist QC Transfer**: Brabant Wallon - contracting **#QC #Transfer #Pharma** Our partner is looking for a **Specialist QC Transfer** to join its team. This international company is well-known for its pharmaceuticals and vaccines. **What are your responsibilities?**: You will Coordinate the...


  • Wavre, Belgique Parexel Temps plein

    Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep...


  • Wavre, Belgique GSK Temps plein

    **Site Name**: Italy - Siena, Belgium-Wavre **Posted Date**: Aug 29 2023 **Specialist R&D Third Party Quality GMP/GDP (maternity leave)** **Job Purpose**: Ensure QA Oversight of third parties involved in the Clinical Manufacturing and Supplies environment (including batch review activities). Be the quality contact of the RDC for all GMP topics. **Key...


  • Wavre, Belgique GSK Temps plein

    **Site Name**: Belgium-Wavre **Posted Date**: Apr 11 2023 Build, deploy and maintain one or more Vx R&D Foundation Quality System(s) in close partnership with R&D business and Operational Quality Partners, by promoting a culture of continuous quality improvement to ensure best practice in the delivery of Vx Quality for R&D and R&D objectives while meeting...


  • Wavre, Belgique Ansys Temps plein

    When visionary companies need to know how their world-changing ideas will perform, they close the gap between design and reality with Ansys simulation. For more than 50 years, Ansys software has enabled innovators across industries to push boundaries by using the predictive power of simulation. From sustainable transportation to advanced semiconductors, from...

  • Qualification Specialist

    il y a 3 semaines


    Wavre, Belgique Pauwels Consulting Temps plein

    In het kortwavre bediende, freelancer 40 uur per week - Jahlye GeeraertsTalent Acquisition Specialist Life Sciences 0032498179909 - **Qualification Specialist**: Pharma & Sciences - Validation - Plan, organize and manage Qualification activities (URS, FAT/SAT, IQ/OQ/PQ) - Perform Risk Analysis - Write and review Equipment or Qualification documents and...

  • Validation Specialist

    Il y a 2 mois


    Wavre, Belgique Pauwels Consulting Temps plein

    In het kortwavre bediende, freelancer 40 uur per week - Jahlye GeeraertsTalent Acquisition Specialist Life Sciences 0032498179909 - **Validation Specialist**: - Pharma & Sciences - Validation - Review and write Validation documentations, plans and reports - Plan, organize and manage Validation activities - Review and monitor change control - Identify and...

  • Validation Specialist

    il y a 3 semaines


    Wavre, Belgique Pauwels Consulting Temps plein

    In het kortwavre bediende, freelancer 40 uur per week - Jahlye GeeraertsTalent Acquisition Specialist Life Sciences 0032498179909 - **Validation Specialist**: Pharma & Sciences - Validation - Review and write Validation documentations, plans and reports - Plan, organize and manage Validation activities - Review and monitor change control - Identify and solve...


  • Wavre, Belgique GSK Temps plein

    Ready to help shape the future of healthcare? Your talent can bring our science to life! As a, we empower you to be yourself, share ideas and work collaboratively **_ Specialist QA Investigational Medicinal Product (IMPQ)_**: **Job purpose**: - You act with colleagues of CM&S Quality and our partners to ensure the continuous supply of clinical vaccines in...


  • Wavre, Belgique GSK Temps plein

    Ready to help shape the future of healthcare? Your talent can bring our science to life! As a, we empower you to be yourself, share ideas and work collaboratively **_ Specialist QA Investigational Medicinal Product (IMPQ)_**: **Job purpose**: - You act with colleagues of CM&S Quality and our partners to ensure the continuous supply of clinical vaccines in...

  • Automation Specialist

    il y a 1 semaine


    Wavre, Wallonie, Belgique GSK Temps plein

    Site Name: Belgium-WavrePosted Date: Mar 1 2023The role of Automation Specialist is a new role that has been announced as part of the R&D capital investment.The automation specialist is the expert on automation for equipment and systems in the dedicated MPUs, by delivering automation solutions for different technologies (process primary and secondary...


  • Wavre, Wallonie, Belgique GSK Temps plein

    Site Name: Italy - Siena, Belgium-WavrePosted Date: Aug Specialist R&D Third Party Quality GMP/GDP (maternity leave)Job Purpose:Ensure QA Oversight of third parties involved in the Clinical Manufacturing and Supplies environment (including batch review activities). Be the quality contact of the RDC for all GMP topics.Key Responsibilities: Be the quality...


  • Wavre, Belgique GSK Temps plein

    **Site Name**: Belgium-Wavre, GSK House, Stevenage, USA - Pennsylvania - Upper Providence, Warsaw **Posted Date**: Jul 21 2023 GSK is a place where outstanding people do amazing things. As a science-led global healthcare company, we exist to help people do more, feel better, live longer. Our goal is to be one of the most innovative, best performing, and...

  • Qualification Specialist

    il y a 1 semaine


    Wavre, Wallonie, Belgique Pauwels Consulting Temps plein

    In het kortwavrebediende, freelancer40 uur per week Jahlye GeeraertsTalent Acquisition Specialist Life Sciences- Qualification Specialist: Pharma & Sciences Validation Plan, organize and manage Qualification activities (URS, FAT/SAT, IQ/OQ/PQ) Perform Risk Analysis Write and review Equipment or Qualification documents and reports Identify and solve problems...


  • Wavre, Belgique Parexel Temps plein

    The **Initiation Clinical Research Associate II **(**iCRA II**) specialises in performing all study start up activities for a clinical trial. You will participate in Pre SIV activities and be assigned & accountable for managing and driving the strategy for the Pre SIV / start up tasks of the study. The iCRA II can also support protocol amendments if...