What are the responsibilities and job description for the JT398 - MANUFACTURING ASSOCIATE position at Quality Consulting Group, LLC?
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.
Responsibilities:
- Manufacturing support role responsible for manual visual inspection and packaging of post-inspected units
- Manual visual inspection
- Interface with GMP systems
- Under minimal supervision, performs manufacturing according to Standard Operating Procedure
- Operate critical processing equipment
- Assist in ensuring operations are completed per manufacturing schedule
- Responsible for identifying and communicating problems during operations
- Review, revise, and audit documents
- Perform computer operations (MES, EBR, MAXIMO, LIMS and SAP Knowledge)
Qualifications:
- Associate degree preferred
- 1-year minimum GMP background manufacturing, computer savvy, SAP Knowledge is helpful as candidate will need to use Manufacturing Execution System
- Experience with manual visual inspection of drug product or in a GMP regulated environment
- Experience with PAS X Werum software for electronic batch records with some understanding of editing and validation
- Knowledgeable of manual visual inspection or strong understanding of related disciplinary areas in bioprocessing (Drug Product operations)
- Require a passing eye exam, which includes color
- The current shift structure is 6am-3pm
- Some training does require an earlier start time of 4am/5am
- Some processes may require earlier shift start times and/or weekend work to meet production demand
- Possibility to move to graves/swing shift but job seekers should be flexible.