Quality Compliance Specialist- Softgel

ABOUT THE COMPANY:

ANS provides industry-leading nutritional solutions to promote health and wellbeing, enabled by a world class team dedicated to service, excellence, quality, and innovation. As an organization we take pride in achieving our objective of “More than Supplements... Solutions”...Safely. We want to be a “solution” through an engaged, accountable and CARING culture.

If you are looking for an exciting career opportunity with a company that offers exceptional benefits packages, then you have come to the right place!

Most Competitive Pay in the Industry

·         401K Program

·         Paid holidays

·         Paid Time Off

·         Medical/Dental benefits

·         Employee and Family Events

·         Annual Awards Program

·         Best Employee Referral Program

The Opportunity…

• Strong track record of internal promotions
• Comprehensive Training program to encourage promotions
• Detailed Progression model to outline promotional opportunities
• Cross-functional opportunities to multiple different areas in the company

POSITION SUMMARY:

Ensure that finished products meet quality standards. Build relationships with Sales and customers to be sure that customers’ needs are met. Review, approve, and release finished goods for shipment. Maintain control of company retentions: logging them into boxes, and storing according to regulatory and company guidelines, fulfilling retention requests for various business needs. Generate Certificates of Analysis. Maintain accurate and complete records.

Status: Exempt.

RESPONSIBILITIES:

Must be Bilingual (English/Spanish)

·         Essential Duties – Order does not necessarily indicate duty importance.

·         Follow all company policies and procedures.

·         Follow and ensure compliance to quality system and cGMP programs.

·         Review batch records for completeness and accuracy and ensure that Current Good Manufacturing Practices/Good Procurement Practices were followed, consulting with a supervisor if needed.

·         Release or reject product based on testing results against specifications and completeness of batch record documentation

·         Generate Certificates of Analysis for finished goods and send them to the appropriate salesperson, Customer Service Representative, and/or customer.

·         Catalog, box up and store sample retentions. If needed, pull retention from storage and ensure completeness of necessary documentation. Pull retention for investigations and control of database for Retained samples.

·         Request and control of logbooks Issued/received at the facility.

·         Print, control and archival of Batch records needed for the production and packaging process at the facility.

Additional ¬

·         Perform other duties as assigned or needed.

·         Reports to Quality Control Manager, Miami Facility

QUALIFICATIONS

·         Non-supervisory role.

·         Must have a high school diploma or equivalent. College degree preferred.

·         Two years of work experience.

·         No certifications or licenses required.

·         Must have basic math skills.

·         Complex reading skills required for SOPs and FDA guidelines.

·         Must have moderate computer skills in MS Office.

·         Must have moderate language skills.

·         Must have moderate writing skills

·         Must be willing to learn new tasks and procedures.

·         Ability to perform all essential position duties and responsibilities efficiently and effectively with or without reasonable accommodation without posing a direct safety threat to self or others.

·         Maintain a regular and dependable work attendance record with few instances of unplanned and/or unexpected absences.