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First Shift (Days)Environmental Conditions
Able to lift 40 lbs. without assistance Adherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.) Standing for full shiftJob Description
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:
1. Maintains cleanliness required of equipment work areas and facility.
2. Prepares manufacturing suites and components for Production Batch Record execution.
3. Completes Production Batch Records to make pharmaceutical products.
4. Verifies baseline GMP activities.
5. Operates safely wears appropriate PPE and promptly identifies and reports safety hazards.
6. Follows established waste disposal operations.
7. Evaluates processes for continuous improvement.
8. Performs tasks of growing complexity with a higher degree of independence.
9. Performs all duties in a cGMP manner.
10. Follows all appropriate SOPs Good Documentation Practices and Data Integrity procedures.
11. Exhibits the 4i Values (Integrity Intensity Innovation and Involvement).
12. 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.
Required Experience:
IC
Full-Time