Formulations Technician

Lazarus Naturals•Portland, OR

5d•Onsite

About The Position

Etz Hayim Holdings operates Cycling Frog and Lazarus Naturals, encompassing a wide range of activities from farming and extraction to chemical processing, packaging, and warehousing. Lazarus Naturals focuses on making quality hemp-based CBD accessible, offering a 60% Assistance Program to specific groups. Cycling Frog aims to normalize casual use THC products, particularly through affordable, sessionable THC beverages. This role is based in Portland, Oregon.

Requirements

Basic computer skills and working knowledge of MS Office products (additional experience with systems such as ERP preferred).
Ability to receive instruction and follow directions.
Ability to interact positively with co-workers and management.
Ability to communicate effectively with written and oral communication skills.
Ability to follow company policies and procedures.
Ability to follow cGMP and other regulatory requirements.
Ability to operate and troubleshoot warehouse equipment.
Detail-oriented with the ability to identify errors and/or inconsistencies while performing tasks.
Excellent written and verbal communication and interpersonal skills with the ability to communicate effectively with multiple levels within the organization. Fluency in spoken and written English is essential.
Project management skills.
Comprehensive knowledge and practical experience with product/process development, processing laboratory techniques, and regulatory requirements
Strong critical thinking and problem-solving skills.

Nice To Haves

Previous experience in a manufacturing environment within pharmaceutical, nutraceutical or food processing industries is preferred.

Responsibilities

Inspects, prepares, measures and mixes raw materials and ensures product compliance and traceability at all times.
Ensures batch formulations are completed on schedule and to spec in a fast-paced environment.
Assists with Formulations scale-up and optimization of the manufacturing process; assist with the technology transfer from R&D to Production.
Plan and contribute to project-related scientific/technical activities (interpret results, provide a critical assessment of data, and draw relevant conclusions.)
Work collaboratively with other cross-functional groups to execute change controls associated with Manufacturing and Packaging master records, SOPs and protocols.
Create and review applicable SOPs, as well as review appropriate documentation and test results for accuracy, completeness, and compliance with SOPs/GMP requirements.
Reviews and revises batch records, process characterization reports, verification reports and investigation reports as needed.
In collaboration with QC, ensures raw material, WIP and finished product maintains cGMP standards at all times.
Conducts receipt and sampling of all raw materials required for production, and updates records as needed.
Completes all training requirements as needed.
Maintain work areas and performing job functions in a safe and efficient manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMPs), Standard Operating Procedures (SOPs) and Batch Production Record (BPR) instructions.
Responsible for performing additional related duties as assigned.