R&D Technical Writer

Curaleaf

Newton, MA, USA

Full time

Aug 5

This job is no longer accepting applications.

Curaleaf Holdings, Inc. (CSE: CURA) (OTCQX: CURLF) (Curaleaf) is a leading U.S. provider of consumer products in cannabis, with a mission to improve lives by providing clarity around cannabis and confidence around consumption. As a vertically integrated, high-growth cannabis operator known for quality, expertise, and reliability, the company and its brands, including Curaleaf and Select provide industry-leading service, product selection, and accessibility across the medical and adult-use markets. Curaleaf currently operates in 23 states with 106 dispensaries, 22 cultivation sites, and over 30 processing sites, and employs over 4,600 team members across the United States. Home | Curaleaf | Cannabis with Confidence

Our corporate social responsibility is Rooted In Good  Diversity, Equity, Inclusion + Social Equity + Sustainability Social Responsibility | Curaleaf | Cannabis with Confidence We believe in taking corporate and social responsibility very seriously, from our educational outreach to national partnerships, state-wide initiatives and local causes. Giving back to the communities where we operate is important to us, and helps to change old attitudes by showing the positive impact of cannabis in creating jobs, changing lives, and helping local communities.

We educate. We advocate. We give.

Job Description:

As a Research and Development Technical Writer, you will ensure all scientific documents are prepared, maintained and controlled at the highest standard of quality and compliance before they are submitted to both external and internal clients. You will be working with multiple electronic databases to extract data and generate quality scientific documents to follow existing style guides and templates. This role will work with various departments moving the physical files from one location to another as the document works through the life cycle.

We are looking for a quality-oriented individual who enjoys detail, accuracy, and working on multiple projects. You must be able to work in a fast-paced environment with demonstrated ability to juggle multiple competing tasks and demands. We are looking for a candidate who is detail-oriented with outstanding work ethic and has a strong knowledge of scientific writing and grammatical rules. This person also needs the ability to manage multiple priorities successfully and meet deadlines in a fast-paced environment.

Responsibilities:


Conduct interviews with various users and technical staff to gather data for documentation

Research and translate technical information into documents for nontechnical and technical users

Recommend formats responsive to technical and customer requirements

Perform quality control (QC) checks of draft documents to ensure the accuracy of the data and resulting subsequent conclusions

Review documents for style, clarity, grammar, and punctuation

Produce products that conform to the company documentation and quality assurance standards


 

Experience/Education:


Bachelor’s Degree required

At least 4 years of relevant experience in a Medical Device, Pharmaceutical organization or regulated laboratory setting.

Authorship of SOP’s, Manufacturing batch records, Product Specifications

Demonstrates strong working knowledge of systems/applicationsin use within Research and Development, (Sharepoint, Power BI, Power Automate, Power Apps,Microsoft Office applications, Microsoft Teams, Visio etc.)

Proficient and is comfortable using DAX/PowerQuery formulas and scripts in Power BI and Power Apps.


 

 

Curaleaf is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

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Cannabis with confidence

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