Stability Coordinator/Associate QC Chemist

Eagle Labs, Inc•Seminole, FL

2d•$45,000 - $65,000•Onsite

About The Position

The Stability Coordinator/Associate Chemist is responsible for the administration of the stability program which includes, scheduling of the stability sample pull points, pulling samples, scheduling and sending out samples for testing, monitoring environmental stability storage chambers and setting the samples down on stability according to the relevant procedures, supporting the site's Stability Program coordinating sample management activities, and ensuring compliance with cGMP, SOPs, and ICH guidelines. Additional responsibilities are to perform testing, review, approve data, ensure cGMP/GLP practices are following regulatory requirements, equipment management/maintenance, lead investigations, deviations, out-of-specifications (OOS). Collaborate with Quality control manager, director and other departments.

Requirements

The successful candidate must be able to work independently on multiple projects and meet established timelines
Applicant must have a bachelor's degree with at least 3-5 years of experience
Stability program experience required
Relevant Quality experience, preferably in the bio/pharmaceutical/supplemental and/or nutraceutical industry
Knowledge of stability and cGMPs
An understanding of stability testing, FDA, ICH, and applicable stability regulations is required
Knowledge in statistical concepts for appropriate interpretation of stability data (e.g. trending analysis)
Strong technical writing skills
Proficiency with computer systems (Microsoft Office applications)
Experience with document management systems
Strong interpersonal and communication (written and oral) skills and the ability to work well in a team environment are essential)
Normal lifting, sitting, standing and walking requirements to facilitate support of staff in the office
Bachelor’s degree in related scientific discipline and 4-5 years of experience with documentation systems and cGMP-compliant environments required.
Strong organizational, technical writing, and communication skills.
Knowledge of stability program expectations, sample handling, data integrity, and QMS principles.
Proficiency with Microsoft Outlook, Excel, and Word.

Nice To Haves

Experience with sample tracking is preferred.

Responsibilities

Conducting and overseeing stability studies to ensure product quality and compliance with regulatory guidelines
Providing support for product testing and analysis, including sample preparation, data analysis, and report writing
Maintaining and updating quality control documentation and record
Identifying and resolving quality control issues and deviations in a timely manner
Collaborating with cross-functional teams to ensure timely completion of projects and adherence to quality standards
Communicating with external vendors and suppliers to ensure timely delivery and quality of materials and with outside contract laboratories on testing.
Schedule testing and sending out samples to contract laboratories and maintaining communication and follow ups on status and results
Participating in internal and external audits and inspections
Staying up to date with industry regulations and guidelines related to quality control
Participating in continuous improvement initiatives to enhance quality control processes and procedures
Prioritizing and managing multiple tasks and projects to meet deadlines
Ensuring compliance with company policies and procedures
Enter studies into the computerized stability management system in accordance with SOPs.
Compile, interpret, and evaluate data and identify impacts related to deviations, OOS/OOT results, or excursions.
Maintain inventory, coordinate final sample destruction, and reconcile stability materials.
Prepare samples for shipment, complete related documentation, and perform peer reviews.
Ensure compliance with cGMP, quality policies, and guidelines.
Review internally and externally produced laboratory data for finished products and raw materials.
All other duties as assigned.