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:

A hiring company that offers alternative approaches to pay, performance bonuses, and/or equity in the firm is very attractive to you. You're generally less interested in working for an organization offering only traditional, salary-based compensation, one with limited opportunity to acquire equity in the firm, or one that does not actively promote skill development. In addition, you are more likely to choose a company that offers a variety of internal career options, with defined career paths. You view the learning of new skills and development of your expertise as key to your career advancement. These aspects of an organization may become even more important to you as you progress in your field, and are especially critical if you change career or occupation.

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: