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Pharmaceutical Material Specialist II - Dispensing

Job in Vacaville, Solano County, California, 95688, USA
Listing for: Lonza
Full Time position
Listed on 2026-02-21
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Manufacturing Production, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 65000 - 105000 USD Yearly USD 65000.00 105000.00 YEAR
Job Description & How to Apply Below

Pharmaceutical Material Specialist II - Dispensing

The Pharmaceutical Material Specialist II - Dispensing is responsible for the dispensing of raw materials liquids and powders (hazardous and non-hazardous), acids/bases, under cGMP conditions to support the manufacture of therapeutic proteins (API).

What you will get:

The full-time base annual salary for this position is expected to range between $65,000-$105,000. In addition, below you will find a comprehensive summary of the benefits package we offer:

  • Performance‑related bonus
  • Medical, dental and vision insurance
  • 401(k) matching plan
  • Life insurance, as well as short‑term and long‑term disability insurance
  • Employee assistance programs
  • Paid Time Off

Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.

What you will do:

Recognized as Subject Matter Expert (SME) of shift and primary point of contact for communication.

Required to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique and cross contamination awareness in handling of products and materials.

Expected to follow and adhere to all written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, and sampling as required. All tasks will be completed while gowned and wearing required PPE while working in a Class C environment.

Expected to execute process recipes.

Ability to report to production via written and electronic documents in accordance with current good manufacturing practice (cGMP) and good documentation practice (GDPs). Complete documentation reviews as appropriate.

Ability to qualify and perform required functions and scheduled cleans on all Dispensing equipment through routine cleaning and sanitization.

Become involved in Track Wise and DMS tasks to support area for updates to documentation and required CAPA tasks ; document owner of suite SOPs, allowing for involvement of change and ownership of process; complete training on Work Notifications in order to generate work orders as applicable for Manufacturing Suites.

What we are looking for:
  • Associates Degree or Bachelor’s degree in related field or equivalent experience.
  • Microsoft suite (Word, Excel and PowerPoint).
  • Use of SAP, Syncaid and Orchestrate.
  • Leadership experience is plus.
  • Comprehend and follow instructions and works as an active member of team.
  • Able to interpret data.
  • Demonstrates critical thinking skills and decision making abilities.
About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.

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