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This is where you make a difference in our patients’ safety. As a member of the Baxter Quality team, you will play an essential part in our mission of saving and sustaining lives. Quality is important throughout the entire product lifecycle and works collaboratively with all areas of the organization. Because Quality touches everything Baxter does, a role in Quality provides many opportunities for growth, learning and a successful career that has a daily impact on people’s lives. You will be responsible for supporting various assignments supporting Baxter quality systems and ensuring label copy control, sample management, documentation review, Oversight floor shop activities, and other quality department functions. This is a 2/2/3 day shift position, will work 12-hour shift from 6:00 am - 6:30 pm.
Job Responsibility:
Makes detailed observations, analyzes data, and interprets results
Maintains department equipment and inventory levels for controlled materials
Owns monthly inventory cycle count initiation and variance follow-up
Perform routine inspections as the provider of floor shop oversight, quality checks, and in-process product inspections of finishing product areas
Interacts with manufacturing and supervision to address quality process or batch-related concerns
Performs process compliance audits of all manufacturing areas to ensure quality of product/process (TIQs) is achieved
Performs troubleshooting, works independently, and makes decisions based on general guidance and existing procedural requirements
Performs product functional testing in support of equipment validations
Identifies process improvements and escalates to Line Operations Supervision and/or Management
Ability to work independently and as part of a team in a fast-paced environment
Requirements:
The candidate must not be allergic to penicillin or cephalosporin drugs
6 months of experience in manufacturing/quality preferred
HS Diploma or equivalent is required
Basic science, math, and computer skills (including Microsoft Word and Excel) are required
Good writing, verbal communication, and problem-solving skills are required
Ability to work in a team environment and make independent decisions based on procedural and regulatory requirements
It is desirable for the candidate to have experience with the requirements of current Good Manufacturing & Documentation Practices in pharma manufacturing facilities
The candidate must be able to work flexible hours in a dynamic environment with minimal direct supervision
Will work in both Drug Delivery and Penicillin facilities as needed
Overtime may be required to meet the production schedule
Must be able to work every other weekend
Visual Acuity 20/20 Near Vision with or without corrective vision required
Nice to have:
6 months of experience in manufacturing/quality
Experience with the requirements of current Good Manufacturing & Documentation Practices in pharma manufacturing facilities
What we offer:
Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts
Educational assistance programs
Paid holidays
Paid time off ranging from 20 to 35 days based on length of service