Formulation Operator - 2nd Shift

The Formulation Operator will:

Align with cGMP’s, SOPs and site safety procedures, as well to follow good housekeeping rules.

 • Communicate and work collaboratively within a team to achieve operational delivery within a complex or multidisciplinary production environment to meet monthly/weekly demand requirements

 • Demonstrate ability to properly operate equipment, perform equipment set-up/change-over/clean-ups, assist in preventative maintenance and perform minor equipment troubleshooting in a safe and efficient manner.

• Verify raw materials, components and products meet the product specification and are available to meet the agreed production schedule

• Responsible for visual inspection, cleaning (including quarterly cleanings) and tightening of equipment.

• Apply Standard Work Instructions and advance issues and opportunities to improve. Responsible for execution and improvement of changeover of formulation assets including, assembly / disassembly, and center line adjustment to optimize equipment performance, where appropriate.

• Provide ownership of the process & equipment performance (OEE).

• Use a continuous improvement approach, alerts supervision of any irregularities in procedures or equipment operations. Partner with other Operators/Mechanics/Technicians/Facilitators/Engineers to correct.

• Accountable for accurately and contemporaneously documenting formulation and cleaning activities in batch records/electronic batch records, paper or electronic Logbooks, and within applicable performance tracking systems (Traksys, Discoverant, etc.)

 • Can lift up to 50 lbs, push/pull large vessels and carts, and transfer full drums off of and onto a pallet.

• Use a pallet jack to transport pallets.

 • Must be comfortable wearing a Powered Air Purifying Respirator (PAPR) while working in the process area.

•  Attend regular SHE, GMP, PET (FIT) and Site meetings.

• Able to work other shifts, weekends, alternative schedules when production demands require.

• Able to perform duties with minimum supervision.

 • Able to demonstrate good interpersonal skills and work in a robust team environment, with other operators, mechanics, technicians, supervision and project management with the goal of completing planned production and furthering Newark Site and AstraZeneca initiatives.

Conduct activities and interactions consistent with things we value and in compliance with the Code of Conduct and supporting Policies and Standards relevant to your role. Complete all required training on the AZ Code of Conduct and supporting Policies and Standards on time. Report potential issues of non-compliance.

Essential Requirements:

Minimum of a High School Diploma

Minimum of 2 years of experience in a GMP setting

Demonstrated problem solving and troubleshooting skills

Basic mechanical competence

Basic computer skills

Good interpersonal, communication and writing skills

Ability to perform duties with minimal supervision

Desirable Experience:

Experience in a production environment

Knowledge of pharmaceutical cGMP's

Date Posted

Closing Date

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.