Par Pharmaceuticals Work Values

Daily Duties at Par Pharmaceuticals:

Audited the manufacturing of customer and generic parenterals in an aseptic pharma environment. Conducted independent technical review of all batch-related documentation Performed tasks/deviations/investigations/ protocols of moderate and high complexity Performed Lyophilization/Sterilization reviews Performed audits of aseptic filling operations against cGMPs and SOPs Provided guidance and on-site training for new QA Auditors (I and II) Acted as liaison between Production and Quality Management teams Performed Standard Operating Procedure revisions

What they like about Par Pharmaceuticals:

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

21 CFR Parts 210 , FDA/EMEA Inspections, Deviation Investigation, CAPA Management, Project Management, Root Cause Analysis, Clinical Research, Lot Disposition/Batch Release, Aseptic Auditing

Skills

Data Management, Aseptic Auditing, Root Cause Analysis, Regulatory Audits, Customer Audits, Deviation/CAPA Management, Tech Transfer, Clinical Research, Lot Disposition / Batch Release, Deep Understanding of 21 CFR Parts 210 & 211, Project Management, Aseptic Manufacturing

These are some of the questions we asked our climbers about their experiences with Par Pharmaceuticals: