Technical Writer

vor 18 Stunden


Zurich, Schweiz Pharma Resource Group, Inc. Vollzeit

**Notes from Manager**:
Some Scientific knowledge will be important. 3-6 yrs exp. is fine. we also consider resume with less exp. then required.

**Main responsibilities include the following**:

- Develop/edit a broad range of technical documents related to biopharmaceutical raw materials, including memos, assessments, specifications, and reports based upon compilation and analysis of supplier-provided and internal data.
- Compile raw material information from various sources (e.g. suppliers, CMOs, internal sites., regulatory/industry, compendia); organize data for broader use within the LM Material Science team.
- Support life cycle management of raw materials used in the clinical and commercial supply chain as part of tech transfer to both internal and external manufacturing sites.
- Maintain documentation, adhering to standards, templates, and best practices, in the document management system.
- Track tasks to support project completion and reporting.

**Additional Responsibilities may include the following**:

- Participate in meetings to gather and/or share information to support deliverables.
- Support raw material investigations and life cycle activities related to raw materials.

**Requirements**:

- Bachelors in Chemistry, Biology, Materials Science and Engineering, Biochemical Engineering, Chemical Engineering, or Pharmacy/Pharmaceutics required
- 3+ years of Technical Writing Experience in a Pharmaceutical environment
- Superior written and verbal communications skills
- Proficient with MS Word, including TOC, creating/using styles, footnotes, and cross references
- Competent with MS Excel, PowerPoint, and Outlook
- Familiar with SharePoint and electronic document management systems
- Able to multi-task and quickly adjust to changing priorities without sacrificing quality or timely completion of tasks

**Preferred Experience**
- 3-5 years of industry experience
- Demonstrated competency and experience with raw material specifications development and management, including compendia testing
- Demonstrated competency and experience in product development within the pharmaceutical industry.

**Job Types**: Full-time, Permanent

Edit job

Open

Schedule:

- 8 Hour Shift
- Day shift
**Experience**:

- Writing of Pharmaceutical industry: 2 years (required)


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