Cannabis Jobs in Research Triangle Park, NC

Company Description
Job Description

The incumbent is highly detailed oriented with excellent documentation skills. The incumbent will become trained and skilled at most or all unit operations in their area, often leading the execution of procedures, and performs most functions with minimal supervision.

• Executes manufacturing processing steps and/or manufacturing support activities, monitoring the process against the batch record and control system. May coordinate or lead process steps as requested.
• Documents/Records and Reviews cGMP data and information (including documentation of deviations) for processing steps and/or equipment activities, following standard operating procedures. Revises or creates documents as instructed. Key documentation includes batch records, SLRs, and equipment logbooks.
• Actively participates in training activities, managing their individual training plan. Trains other associates as required.
• Executes validation protocols with minimal supervision/direction of others.

Qualifications

• High School Diploma or equivalent
• Targeted biopharmaceutical training (Bioworks or equivalent) and/or related military training also preferred.
• Detailed oriented with excellent documentation skills.
• Operates in a safe manner in order to avoid injury to self and others.
• Strong peer and team leadership skills
• Adaptable to changing needs and demands, comfortable navigating in a changing environment.
• Comfortable with ambiguity; quickly understands the needs based on the situation at hand.
• Influencing and leading a positive attitude throughout team.
• Ability to communicate clearly and effectively to all levels of the organization.
• Ability to interact with others in a professional and courteous manner in accordance with Biogen’s Core Behaviors.
• Capable to work a 12-hour shift, both day shift or night shift.

Additional Information

The Manufacturing Associate performs and documents daily manufacturing operations in a cGMP environment that involves operation of process equipment, execution of validation protocols, creating/ revising cGMP documents and other assignments.

Apply for this job with Biogen

Apply now →

By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company. Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply. Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.

The Role

RISE Patient Care Specialists engage in one-on-one interaction with patients from the time they enter the retail area until they check out and exit the store. Our ideal Patient Care Specialist candidate should be friendly and upbeat, much like a barista in your favorite coffee shop. Our incredible Patient Care Specialists are GTI's secret to success—they connect each unique customer with just the right product and method of consumption for their needs. The Patient Care Specialist is a master of our menu and knows exactly how to help anyone who walks through the dispensary's doors. If you have a smile that can light up a room, as well as a bowl, we're looking for you!

Responsibilities

• Assist patients in a customer-facing, intimate retail environment
• Utilize product and consumption-method knowledge to successfully recommend a safe and effective regimen suited to each patient's specific needs
• Ensure sales floor is properly stocked and presence of the store is well maintained
• Own responsibility for remaining up-to-date with product knowledge
• Play an active part in patient education on products, methods of consumption, and safety as part of patient interaction
• Complete duties assigned during scheduled shift including:
  
  • Correct cash handling and discount application
  • Verification of proper paperwork, documentation and ID for patients
  • Accurate use and maintenance of the Point of Sale (POS) system; accurate and timely data entry of patient profiles in both the POS system and the state's electronic verification system
  • Maintenance of hard copy files (when required)
  • Assist in verifying order deliveries for accuracy
  • Security measures and safety compliance
  • Maintain visitor log
  
  
• Provide necessary support to management team to ensure retail store operations run smoothly, properly and in compliance with the applicable rules and regulations, including: daily activities, maintenance, and patient information for any reported issues and/or complaints
• Promote a work environment that is positive, communicative, patient-oriented, and compliant

Qualifications

• 1+ year of customer service experience; preference for candidates with specialty, customer-facing retail experience
• High school diploma, or equivalent
• Consistent demonstration of excellent customer service skills
• Previous experience with POS systems
• Desire to continuously learn (more) about cannabis, cannabinoids and the endocannabinoid system, GTI products, and cannabis therapies – previous knowledge a HUGE plus!
• Ability to listen well and effectively communicate, both verbally and in writing, with various audiences
• Ability to use standard office equipment, computer equipment and software including word processing, database management, spreadsheet applications and email
• Understanding of applicable federal, state and local laws and regulations as they pertain to the industry, personnel law, safety regulations, local municipal codes and organizational rules, regulations, directives and standard operating procedures

Additional Requirements

• Must be 21 years or older
• Must pass any and all required background checks.
• Possess valid driver's license or state ID.
• Must be and remain compliant with all legal or company regulations for working in the industry.

Working Conditions

• While performing the duties of this job, the employee is regularly required to perform grasping, talking, hearing, seeing and repetitive motions
• PHYSICAL DEMANDS: Must be able to lift, carry and balance up to 30 pounds (100 pounds with assistance), may include sitting or standing for extended periods of time, as well as stooping, bending over and/or crouching

Apply for this job with Green Thumb Industries

Apply now →

By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company. Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply. Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.

Company Description
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Job Description

The incumbent is highly detailed oriented with excellent documentation skills. The incumbent will become trained and skilled at most or all unit operations in their area, often leading the execution of procedures, and performs most functions with minimal supervision.

• Executes manufacturing processing steps and/or manufacturing support activities, monitoring the process against the batch record and control system. May coordinate or lead process steps as requested.
• Documents/Records and Reviews cGMP data and information (including documentation of deviations) for processing steps and/or equipment activities, following standard operating procedures. Revises or creates documents as instructed. Key documentation includes batch records, SLRs, and equipment logbooks.
• Actively participates in training activities, managing their individual training plan. Trains other associates as required.
• Executes validation protocols with minimal supervision/direction of others.

Qualifications

• High School Diploma or equivalent
• Targeted biopharmaceutical training (Bioworks or equivalent) and/or related military training also preferred.
• Detailed oriented with excellent documentation skills.
• Operates in a safe manner in order to avoid injury to self and others.
• Strong peer and team leadership skills
• Adaptable to changing needs and demands, comfortable navigating in a changing environment.
• Comfortable with ambiguity; quickly understands the needs based on the situation at hand.
• Influencing and leading a positive attitude throughout team.
• Ability to communicate clearly and effectively to all levels of the organization.
• Ability to interact with others in a professional and courteous manner in accordance with Biogen’s Core Behaviors.
• Capable to work a 12-hour shift, both day shift or night shift.

Additional Information

The Manufacturing Associate performs and documents daily manufacturing operations in a cGMP environment that involves operation of process equipment, execution of validation protocols, creating/ revising cGMP documents and other assignments.

Apply for this job with Biogen

Apply now →

By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company. Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply. Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.

Job Description

The incumbent is highly detailed oriented with excellent documentation skills. The incumbent will become trained and skilled at most or all unit operations in their area, often leading the execution of procedures, and performs most functions with minimal supervision.

• Executes manufacturing processing steps and/or manufacturing support activities, monitoring the process against the batch record and control system. May coordinate or lead process steps as requested
• Documents/Records and Reviews cGMP data and information (including documentation of deviations) for processing steps and/or equipment activities, following standard operating procedures. Revises or creates documents as instructed. Key documentation includes batch records, SLRs, and equipment logbooks.
• Actively participates in training activities, managing their individual training plan. Trains other associates as required.
• Executes validation protocols with minimal supervision/direction of others.

Qualifications

• High School Diploma or equivalent
• Targeted biopharmaceutical training (Bioworks or equivalent) and/or related military training also preferred.
• Detailed oriented with excellent documentation skills
• Operates in a safe manner in order to avoid injury to self and others
• Strong peer and team leadership skills.
• Adaptable to changing needs and demands, comfortable navigating in a changing environment
• Comfortable with ambiguity; quickly understands the needs based on the situation at hand
• Influencing and leading a positive attitude throughout team
• Ability to communicate clearly and effectively to all levels of the organization
• Ability to interact with others in a professional and courteous manner in accordance with Biogen’s Core Behaviors
• Capable to work a 12-hour shift, both day shift or night shift

Additional Information

The Manufacturing Associate performs and documents daily manufacturing operations in a cGMP environment that involves operation of process equipment, execution of validation protocols, creating/ revising cGMP documents and other assignments.

Apply for this job with Biogen

Apply now →

By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company. Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply. Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.