West Point, PA

Senior Specialist Quality Assurance - Level II

Experis, a ManpowerGroup company, has an exciting contract opportunity with one of our key clients, a global biopharmaceutical company that is engaged in the discovery, development and manufacturer of healthcare products. On this team, you will perform a critical role in the team and In this role, you will be teaming up with client staff analysts to receive, store, label, and ship samples to support stability studies. You will also author stability testing protocols, as well as review and approve test results and escalate any atypical results.

Title: Senior Specialist Quality Assurance - Level II (Associate)

Location: West Point, PA 19486

Hybrid role (Onsite + Remote), need to be flexible for onsite work at least 3 days/week at west point, PA. Shift flexibility (7a-4p/8a-5p/9a-6p).

Contract: 5 Months

Qualifications:

Education: * BS /MS - Biology, Microbiology, Pharmacy, Chemistry, Chemical Engineering (or equivalent) * 2-5 years' experience in the Pharmaceutical Industry/Laboratory/quality control * Should have experience with GMP's * Previous experience as a Quality Assurance professional * Working knowledge of Microsoft Excel & Macros * Experience with Midas and LIMS & GLIMS. Preferred - statistical knowledge is helpful * Experience with statistical platforms such as JMP and Spotfire, SAS, SDMS. Nice to have: Veeva Vault Quality Docs. Personality: - You have impeccable attention to detail and a quality mindset! You are a fast-learner; a team-player! Accountable and adaptable, you are willing and able to jump in and help when and wherever needed! You are collaborative and open to new ideas! *Note*: Position: 2 available. The main goal is to help us complete implementation and migration of all our studies in the new LIMS system. Hybrid role (Onsite + Remote), need to be flexible for onsite work at least 3 days/week at west point, PA. Shift flexibility (7a-4p/8a-5p/9a-6p). This is not a lab based role for sample testing but will require sample handling, GMP documentation, and sample storage management. This role requires the understanding of stability study, techniques used for sample testing. Exposure and interactions globally and cross functionally

APPLY TODAY!

Recommended Skills

  • Adaptability
  • Attention To Detail
  • Biology
  • Chemical Engineering
  • Chemistry
  • Curiosity
Browse other jobs