Pharmaceutical Compounding & Tableting Technician

Zoetis Spain SL; Lincoln (NE); On-site; USD 42,000 - 52,000; Full time

Benefits offered by this job

Sign-on bonus

Paid vacation & holidays

401(k) with company match

Tuition reimbursement

Job summary

Zoetis in Lincoln, NE is seeking a Compounding/Tableting Technician to operate pharmaceutical bulk compounding equipment and tablet presses. You will maintain accurate batch records, follow cGMP SOPs, and work with DEA schedule III/IV materials in a team-based environment.

The role requires a high school diploma and 6–12 months manufacturing experience, with flexibility for overtime. Sign-on bonus and comprehensive benefits are offered.

Qualifications

• HS diploma or equivalent with 6–12 months of manufacturing experience.
• Ability to read and interpret procedures; basic math and manual dexterity.
• Familiarity with Windows-based PC tasks, hand tools and measuring devices.
• Understanding of cGMP/SOP requirements and safety practices.

Responsibilities

• Maintain and complete accurate records (timecards, batch records, logbooks).
• Operate PLC-controlled blenders, dryers, granulator, tablet presses and related equipment.
• Clean production equipment and facilities; set up/disassemble equipment.
• Use scales, moisture analyzers, calipers; manage material handling devices.
• Follow SOPs/cGMPs; practice housekeeping; adhere to dress and gowning policies.
• Apply proper safety practices, PPE, lock-out/tag-out when required.
• Communicate effectively with peers and supervisors; support team objectives.

Skills

Record keeping

Equipment operation

SOPs/cGMPs

Safety procedures

Teamwork

PC skills

Math skills

Mechanical basics

Education

HS Diploma or equivalent

Technical school certificate or 1-2 yrs college

Tools

Windows-based PC

PLC-controlled equipment

Job description

Zoetis in Lincoln, NE is seeking a Compounding/Tableting Technician to operate pharmaceutical bulk compounding equipment and tablet presses. You will maintain accurate batch records, follow cGMP SOPs, and work with DEA schedule III/IV materials in a team-based environment.

The role requires a high school diploma and 6–12 months manufacturing experience, with flexibility for overtime. Sign-on bonus and comprehensive benefits are offered.