What are the responsibilities and job description for the QUALITY SUPERVISOR position at FORMULATED Solutions LLC?
Formulated Solutions Innovates, Formulates and Creates consumer brands. We put together a broadly talented team of experts in manufacturing, production, laboratory, regulatory, distribution and marketing, that possesses an unparalleled drive to deliver market-ready products of the highest quality. Our in-house technologies in Aerosol, Biochemistry, Cosmetic, Pharmaceutical and Polymer Chemistry, coupled with innovative package design and strategic marketing services, provides clients with one of the fastest design-to-market solutions in the world. We serve companies in pharmaceutical, cosmetic, personal care and specialty chemical applications. We also support small and large companies in generating and producing unique products for the retail market.
Formulated Solutions offers a wide range of benefit options for our full-time employees, allowing them to find the right plan to enroll into. We also offer 401k with a company match and much more! If you are hard-working, self-motivated and looking for a new and exciting career opportunity, apply today!
PRIMARY PURPOSE:
· Performs in-process inspections and finished product inspections.
- Verifies pre and post clearance activities during production runs.
- Performs daily verification of instrumentation (scales, gauges, etc.)
- Performs monitoring (temperature,etc) of retain area.
- Performs incoming inspection of packaging components.
- Accurately reviews and records data.
- Acts as a liaison between Quality and Production.
- Participates in other activities as required by Quality management.
- Supervise and maintain quality inspection activities, including in process inspections,
and supervising the inspectors. Performs quality inspector activities when
necessary. Reviews all quality inspection activities for in process, incoming
materials, components and determines disposition. Ensuring inspection
activities meet FDA and ISO requirements, as well as implementing continuous
improvements as necessary.
- Quality monitoring of quality production activities and quality inspection activities.
- Accurately reviews and records data.
- Promote continuous improvement and customer satisfaction.
- Participate in other activities as assigned by the Quality Manager.
QUALIFICATION:
A. Required
- Position requires approximately 10% sitting and 90% standing/walking.
- Must be able to occasionally lift up to 25 pounds.
CRITICAL SKILLS AND ABILITIES:
· Working knowledge of FDA regulations for drugs and/or medical devices.
- Ability to use a personal computer and peripheral equipment to accurately enter and analyze data and produce reports.
- Ability to make quality decisions and act accordingly.
- Ability to establish priorities, work independently, productively, and proceed with objectives without supervision.
- Ability to perform effectively under conditions of fluctuating workload.
- Ability to handle and resolve recurring problems.
- Communicate with others clearly and concisely.
- Ability to work in a fast paced environment – sometimes rapidly shifting priorities. Ability to concentrate in such an environment and perform quality work.
- Strong initiative, technical commitment and contribution to company and departmental
COMPUTER SKILLS:
Technical Skills and Experience (if applicable) (i.e., computing,negotiating)
EDUCATION AND/OR TRAINING
· Working knowledge of FDA regulations for drugs and/or medical devices.
- High School diploma or equivalent.
