Job Description
Job Summary:
- Performs current Good Manufacturing Practices (cGMP) production of pharmaceutical Spray Dried Intermediates (SDI) and Solid Dosage Forms (tablets, capsules, granules).
- Completes process documentation in a fast-paced, flexible manufacturing environment.
Crucial Functions:
- Maintains cleanliness required of equipment, work areas, and facility.
- Prepares manufacturing suites and components for Production Batch Record execution.
- Completes Production Batch Records to make pharmaceutical products.
- Verifies baseline GMP activities.
- Operates safely, wears appropriate PPE, and promptly identifies and reports safety hazards.
- Follows established waste disposal operations.
- Evaluates processes for continuous improvement.
- Performs tasks of growing complexity with a higher degree of independence.
- Performs all duties in a cGMP manner.
- Follows all appropriate SOPs, Good Documentation Practices, and Data Integrity procedures.
- Exhibits the 4i Values (Integrity, Intensity, Innovation, and Involvement).
- Performs other technician responsibilities as vital.
Education:
- HS Diploma or equivalent required.
Experience:
- 1+ year of work experience in manufacturing/production environment; pharma preferred.
Equivalency:
- Equivalent combination of education, training, and meaningful work experience may be considered.