IPQA Supervisor


Job ID 17-00158

Industry Pharma

Job Type Permanent

Location Dayton, NJ

Description

Want to work for a top Generic Pharma company with lots of growth potential? How about a company that you can be promoted quickly and be recognized for your work? We have a direct relationship with our Hiring Managers and can get you in for the interview! This client provides great benefits and bonus structure as well. Apply with us today!


JOB SUMMARY
Supervisor is to monitor all IPQA activities for all shifts if needed. Manage the scheduling for all IPQA.
Manage the syllabuses and training for all of IPQA. Help support the manager with all deviations, incidents, CAPA's, change controls for the IPQA and manufacturing floor. Be the backup and support batch record review and release activities when needed.
REPORTING RELATIONSHIPS
IPQA shall report to QA Manager. All of IPQA employees report to the supervisors.
DUTIES & ESSENTIAL JOB FUNCTIONS - PERCENT OF TIME - FREQUENCY - ESSENTIAL DUTIES
75% Daily
- Assist IPQA in all activities when needed
- Monitor IPQA and Manufacturing activities on the floor.
- Make decisions on quality and compliance issues.
- Follow up on action plans.
- Guide IPQA and Manufacturing on quality issues
- Train IPQA to improve their skills on specific activities.
- Investigate and close Deviations, CAPAs and Change Control as needed in a timely manner.
5% Daily
Review analytical data used for release of raw material and finished product. Approve certificates of analysis for raw material and finished product as needed.
5% Monthly
Revise applicable SOP. Train IPQA and others as applicable.
5% Monthly
Prepare syllabuses verify IPQA training and perform more training if required.
10% Weekly
Verify and transfer all APR data.
NOTE: These duties and job functions are inclusive of all above but not limited to IPQA activities. The responsibilities may change at the discretion of the QA Manager.
OTHER FUNCTIONS AND RESPONSIBILITIES
Perform any duties as assigned.
Monitor and trend the times it takes for IPQA room clearance and minimize this delay for all areas.
Manage the spot cleaning program for QA



Qualifications

QUALIFICATIONS
Preferably a 4 year degree in a scientific discipline.
Proficient in Microsoft Office.
REQUIRED
1-3 years of experience of manufacturing and packaging in a pharmaceutical manufacturing environment.
Minimum of 1 year of Supervisory experience in Quality Assurance/ quality Operations
Read, write and speak English