Job Description

Ability to perform detailed tasks and document activities accurately.

Able to work in a aseptic controlled environment which includes wearing PPE, aseptic gowning qualifications, and subsequent gowning re-qualification's.

Specific vision requirements include 20/20 near vision (can be corrected with eyeglasses or contacts).

Ability to work and communicate with others in a professional and effective manner, within a team-oriented environment.

Ability to read, comprehend, write, and communicate effectively in English.

Basic user knowledge and understanding of Windows based computer systems such as Microsoft Office, with an ability to learn other computer-based systems.

Required Knowledge, Skills, and Abilities

• One (1) year experience in pharmaceutical manufacturing, chemistry lab or similar laboratory experience.

  Intermediate Microsoft Office skills. Experience with LIMS, QMS and Trackwise preferred.

  Experience working in a GMP regulated environment preferred.

• Organizes and performs testing of raw materials (including USP water), bulk samples, and finished product to assure the chemical quality of the product.

  Evaluates stability of raw materials, bulk samples, and finished product per established protocols.

  Maintains accurate notebook of all sample identifications, raw data, and calculations associated with assigned analysis duties.

  Reports anomalies in analyses and malfunctions of equipment to laboratory supervisor.

  Works effectively with chemists to complete special sample analyses as required.