QUALITY SUPERVISOR IN-COMING

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, provide 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 in. 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: 

• Acts as a liaison between Quality and Production. Supervise and maintain quality inspection activities, including component inspections, raw material inspections, and other applicable inspections, and supervise 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 inspection activities.
• Performs daily verification of instrumentation (scales, gauges, etc.)
• Performs incoming inspection of packaging components.
• Accurately reviews and records data.
• Promote continuous improvement and customer satisfaction. 
• Participate in other activities as assigned by the Quality Manager.

QUALIFICATION:

REQUIRED:

• Minimum of 5 years’ experience, preferably in the pharmaceutical industry. 
• Experience 
• Capable of preparing cGMP and other laboratory documents. 
• Excellent knowledge of computer systems and software. 
• Good knowledge of cGMP and FDA regulations.
• Excellent interpersonal and organizational communication skills.

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 goals

Education and/or Training 

• Working knowledge of FDA regulations for drugs and/or medical devices.
• High School diploma or equivalent.

COMPUTER SKILLS:

• Basic computer skills

• Microsoft Office