**Use Your Power for Purpose**

The qualified candidate will provide support for new and existing analytical method development and validation in a cGMP quality control analytical (QCA) laboratory. Supported activities include initial analytical method development, validations, qualifications and compendial verifications in support of clinical and commercial drug substance production. Analytical method validations for PAT methods within production suites will also be supported. A host of analytical techniques will be utilized, spanning a wide range of materials, including small molecules, gases, nucleotides, custom media, resins, polymers, salts, sugars, enzymes and others. This is a fast-paced group managing activities that are tied directly to the Andover production record. This role will also have a direct impact on Network Lab Strategy efforts aimed at harmonizing global analytical method strategy across 40 Pfizer sites.

**What You Will Achieve**

+ Develop...