Pharma Manufacturing Operator II | Process & Packaging

Tevapharm; Cincinnati (OH); On-site; USD 25,000 - 36,000; Full time

Benefits offered by this job

Health Insurance

401(k) Retirement Savings with company

Paid Time Off

Life and Disability Insurance

Employee Stock Purchase Plan

Job summary

Teva in Cincinnati, OH is seeking an entry to mid-level manufacturing operator to support the manufacturing and packaging of pharmaceutical products. The role requires following batch records, SOPs and WI’s, with responsibilities ranging from setup and operation to cleanup and documentation.

Ideal candidates will have a High School Diploma, a background in pharma/healthcare manufacturing, and a proven ability to follow cGMP, SOPs, and regulatory requirements while maintaining 100% training

Qualifications

• Requires High School Diploma or equivalent.
• Prefer previous experience in a manufacturing environment within pharmaceutical, nutraceutical or food processing industries.

Responsibilities

• Learn manufacturing and/or packaging processes by following BRs, WIs, SOPs, etc.
• Set up, changeover, programming and operation of manufacturing/packaging equipment.
• Clean facilities, equipment and utensils per SOPs and WI's.
• Complete documentation for manufacturing/packaging activities.
• Maintain 100% training compliance and safety.
• Operate, set up and troubleshoot manufacturing/packaging equipment.

Skills

Follow directions

Team interaction

Written & verbal communication

Policy adherence

cGMP compliance

Training compliance

Set up & troubleshoot

Education

High School Diploma or equivalent

Job description

Teva in Cincinnati, OH is seeking an entry to mid-level manufacturing operator to support the manufacturing and packaging of pharmaceutical products. The role requires following batch records, SOPs and WI’s, with responsibilities ranging from setup and operation to cleanup and documentation.

Ideal candidates will have a High School Diploma, a background in pharma/healthcare manufacturing, and a proven ability to follow cGMP, SOPs, and regulatory requirements while maintaining 100% training