Qa Production Tech - Weekend Shift

Come Grow with Us!

Vitality Works mission is to create efficacious and therapeutic herbal, vitamin and nutraceutical supplements to help people get and stay well. While the FDA defines minimum quality, we strive for the highest level of quality. Vitality Works also operates in an environmentally sustainable way, recycling, composting, reducing energy and water consumption in a conscientious way. Our dedicated and passionate employees strive to produce amazing products in an uncompromising yet affordable way so that these products are affordable and effective.  

** 7am to 7:30pm, Friday, Saturday, Sunday, and every other Monday **

10 % Shift Differential

Job Summary

Vitality Works is looking for a dedicated and motivated individual that is responsible for checking and verifying that the product is made in accordance with the production records, regulatory requirements and applicable SOPs and evaluate the quality of each product.

Duties and Responsibilities include but are not limited to:

• Monitor processing/packaging conditions to assure cGMP compliance to specifications (SOP’s)
• Perform Quality Assurance activities as defined in SOP’s (i.e. line startup and line clearance)
• Perform AQL checks to confirm product meets quality attributes
• Monitor and document results of quality tests and inspections as required (i.e. torque testing, liquid levels, pill/capsule counts, vacuum testing, pH testing)
• Perform allergen testing for production areas
• Perform batch record reviews
• Provide transfer approvals for production
• Verify quantities of finished product for encapsulation
• Verify labels prior to use in packaging
• Communicate significant issues or developments identified during work activities and provide recommended process improvements to QA Supervisor/Manager
• Coach production operators on quality requirements
• Provide on the floor support to manufacturing operations
• Assist in performing investigations
• Assist in preparing for internal audits
• Maintain all SOP’s relevant to current position
• Complete projects and other duties assigned by QA Supervisor/Manager

Knowledge, Skills, and Abilities:

• The ability to work in a fast-paced environment.
• Working knowledge and understanding of current Good Manufacturing practices for the Dietary Supplement industry
• Knowledge of 21 CFR 11 a plus
• Proficient in MS Office (Excel, Word, Outlook, PowerPoint)
• Ability to communicate at all levels of the company pertaining to manufacturing and laboratory activities
• Strong math and analytical skills
• Must display strong interpersonal skills, along with strong organizational abilities
• Must be detail oriented
• Strong technical writing and documentation skills
• Must be a self-starter who is able to work independently
• Ability to multitask and work under pressure to produce positive outcomes

Requirements

• High School Diploma, GED, or sufficient experience pertaining to this position.
• Bachelors of Science in Biology, Chemistry. Biochemistry or related field or 5 years of relevant experience
• Ability to lift up to 50 lbs. on a regular basis. This position requires strenuous physical activity throughout the day.
• Previous experience in manufacturing/warehouse in a GMP setting
• At least 2 years of experience in Quality Control or Quality Assurance in an herbal, dietary supplement or pharmaceutical industry

Employee Perks:

• Great benefits!
• 2 free Product Samples Per Month
• On-site Gym and Basketball Court!

Benefits:

• 401(k) & Matching
• Medical Insurance
• Dental Insurance
• Vision Insurance
• Employee Assistance Program
• Employee Discounts
• Free Life Insurance, STD, LTD
• Vacation & Sick Time Off
• Referral Program

Apply Today on our Career Portal!