DOCUMENT CONTROL SPECIALIST III Position Available In Pinellas, Florida

DOCUMENT CONTROL SPECIALIST III FORMULATED

Solutions

LLC – 2.3

Largo, FL Job Details Full-time Estimated:

$46.7K – $64.2K a year 1 day ago Benefits 401(k) matching Qualifications GMP Mid-level High school diploma or GED Analysis skills Math Quality assurance Computer skills Manufacturing Document management Associate’s degree 2 years Full Job Description 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

Knowledge of quality assurance/control methods, principles, and practice. Knowledge of the relationship of quality assurance to other activities such as production, engineering, and purchasing. Skill in interpreting and applying product specifications, technical data, regulations, policy statements, and other guideline materials. Accurately organize and maintain files for documents, records, specifications, certificates, labels, and other documents/data. Skill in written and oral communications and in establishing effective interpersonal relationships. Follow all safety and GMP procedures. Aid in ensuring that all departments are trained in new procedures or new revisions of existing procedures and help manage training files for all employees. Receive Document Change Order Request/Assessment from other departments or customers and send Document Change Order Request/Assessment for assessment and signatures. Review, implement, approve customer/ vendor specifications Create new item numbers and keep data base up to date Mange new items, description, specifications, BOMs Make changes to documents/procedures. Keep all documents organized and accessible. Promote continuous improvement and customer satisfaction. Perform other duties as assigned by Quality Control Manager

QUALIFICATION

Required:

High School diploma or GED is required. Two or more years experience working in quality assurance, quality compliance’s and/or document control. Experience following detailed procedures and maintaining accurate records is required.

Preferred:

Associate’s degree preferred or; equivalent combination of education, experience and training, Experience in a pharmaceutical industry and experience in a manufacturing environment preferred.

CRITICAL SKILLS AND ABILITIES

Ability to maintain detailed and accurate records. Ability to use a personal computer and peripheral equipment to accurately enter and analyze data and produce reports. Strong math and strong analytical skills. Must be able to recognize own limits and level of competence and ask for directions or help when needed. Communicate with others clearly and concisely, Ability to work in a fast-paced environment — sometimes with rapidly shifting priorities. Ability to concentrate is such an environment and perform error-free work.