Non-Sterile Operator – Cleaning & Equipment Preparation

The non-sterile operator- cleaning and equipment preparation, is responsible for supporting the effective manufacturing of sterile pharmaceutical products as per the production schedule, in line with specifications and with accurate batch documentation.

POSITION RESPONSIBILITIES

Percent of Time (sum of responsibilities should equal to 100%)

Primary responsibility for providing cleaning and sterilization services as per production schedule while ensuring they meet all relevant targets including line OEE, Quality, right first time, adherence to schedule, health & safety.20

Responsible for Booking in, storage and distribution of the cleanroom garb and maintenance of consumables stocks in all areas, e.g. cleanroom supplies20

Providing cover for manufacture, sampling and dispensing of batches. Supporting the formulation, filling and packing process.25

Effectively resolve or escalate problems in the manufacturing area to ensure problem solving can occur when and where issues happen5

Completion of all relevant documentation, batch EBR (electronic batch record) and training records5

Attend and contribute to line meetings / daily huddles and visual workplace meetings for their lines / rooms. Identify improvement opportunities and contribute to continuous improvement projects.5

Attend and contribute to line meetings / daily huddles and visual workplace meetings for their lines / rooms. Identify improvement opportunities and lead / contribute to continuous improvement projects.5

Work effectively with their colleagues through timely and relevant communication to ensure the shift meets its production goals and that a smooth handover exists between shifts.5

Assist in 5S activities and help sustain the required 5s standards within their area.5

Organize, prepare for, and participate in Line Changeovers in order to maximize the OEE potential5

ORGANIZATIONAL RELATIONSHIPS

• Production Lead
• Production Operator
• Warehouse Personnel
• Quality Personnel

EDUCATION AND EXPERIENCE

• Experience in a pharmaceutical environment desirable.
• Knowledge and understanding of cGMP principles and manufacturing desirable.
• Lean manufacturing experience desirable.

PHYSICAL POSITION REQUIREMENTS

Note the physical conditions in which work will be performed, if applicable to the position.  Examples: Lifting, sitting, standing, walking, ability to travel, drive, unusual attendance requirements, weekend work or travel requirements, etc.

Lifting, sitting, standing, shift-hours.

 

 

Full time

 

 

Regular

 

 

Colleague

 

 

Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.

Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search.

 

 

Notice: Zoetis Recruiters will contact candidates via email from an address ending in @zoetis.com and may also initially connect with candidates through LinkedIn, including LinkedIn InMail. Zoetis does not use Gmail, Outlook, Yahoo, or other web-based/generic email domains to communicate about job opportunities, interviews, or offers of employment. If you receive a recruitment-related email message claiming to be from Zoetis that does not come from @zoetis.com, please treat it as suspicious. For your security, do not reply, click links, open attachments, share personal or financial information, or send money in response to unexpected or questionable recruitment communications.