Vesta Pharmaceuticls Work Values

Daily Duties at Vesta Pharmaceuticls:

Managed all quality functions of the company as outlined in facility SOPs. Researched and developed new product documentation for manufacturing and Quality functions for this start up pharmaceutical company. Reviewed and approved all GMP documentation. Managed contractors on site at Eli Lilly Company Interpreted cGMPs for facility and responsible for training programs. Prepared, reviewed, and implemented SOPs and enforced compliance. Developed and administered operational Quality budgets.

What they like about Vesta Pharmaceuticls:

Working in an organization that is technologically advanced, creative, and innovative is critical in your assessment of hiring companies. Less important to you are stability of the organization, the length of time an organization has been in business, and the business' plans for the future. You prefer a fast-moving company that will take risks to achieve its goals and objectives. The length of time the company has been in business is irrelevant. Maintaining status quo is unnecessary. You thrive on change, uncertainty and the upside of potential business risks, especially those associated with innovation. Stability for the long haul is not nearly as important as is working in an atmosphere that is charged with a sense of urgency and constant change.

Tags

CQE, CQA, CQM, CQM/OE, ISO, ICH, CFR211, FDA, Quality Assurance, Quality Control, Document Control, Quality Auditing, Pharmaceuticals, Regulatory Compliance, ISO Auditor, CAPA, Corrective Action, Preventive Action, CFR820, CFR Part11, 21CFR211, 21CFR820, 21CFR Part 11, Quality Management, Validation, IQ, OQ, PQ, Regulatory Inspections, EMEA, Standard Operating Procedures, SOPs, QC, QA, Excipient, Quality Engineer, Project Manager, CGMP, GMP documentation, Solid Dose Products, Biopharmaceutical, Aseptic Manufacture

Skills

Ecommerce Strategy and digital marketing channels optimization - SEO, SEM, email, affiliates - for high-profile accounts., Sales Support, Software Implementation, Requirements Analysis & Specification, Leadership , Quality Auditing, Proces and equipment validation, Regulatory agency interface, Documentation Control systems, CAPA and complaint resolution, Review and approval of manufacturing records, Employee training, Technical writing, Pharmaceutical product recall process, Microsoft Office suite, JMP, Quality Engineering, Stattisical Process Control

These are some of the questions we asked our climbers about their experiences with Vesta Pharmaceuticls: