Employer Active
Job Alert
You will be updated with latest job alerts via emailJob Alert
You will be updated with latest job alerts via emailWork Schedule
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 shift Will work with hazardous/toxic materialsJob Description
Summary:
Performs current Good Manufacturing Practices (cGMP) production of pharmaceutical Spray Dried Intermediates (SDI) and Solid Dosage Forms (tablets capsules granules). Manages process documentation in a fastpaced flexible manufacturing environment.
Crucial Functions:
1. Progresses towards Subject Matter Expertise on multiple process trains.
2. Reviews approves and updates quality documents.
3. Executes Production Batch Records to make pharmaceutical products.
4. Reviews completed Batch Records for compliance prior to QA review.
5. Assists with schedule adherence via prioritization of daily tasks.
6. Maintains Qualified Subject Matter Expert status to deliver employee training.
7. Drives continuous improvement activities and educates peers.
8. Maintains cleanliness required of equipment work areas and facility; performs visual equipment inspections.
9. Prepares manufacturing suites and components for Production Batch Record .
10. Operates in a safe manner wears appropriate PPE and identifies and raises any safety hazards.
11. Follows established waste disposal operations.
12. Mentors new team members.
13. Serves as backup for Team Lead as appropriate.
14. Supports new equipment commissioning and qualification activities.
15. Supports audits as needed.
16. Follows all appropriate SOPs Good Documentation Practices and Data Integrity procedures.
17. Exhibits the 4i Values (Integrity Intensity Innovation and Involvement).
18. Performs other responsibilities as vital.
Education:
HS Diploma or equivalent required.
Experience:
5 year of work experience in manufacturing/production environment; demonstrated pharma related formulation/production experience.
Equivalency:
Equivalent combination of education training and meaningful work experience may be considered.
Required Experience:
IC
Full-Time