Packaging Line Coordinator - 3rd shift

## Packaging Line Coordinator - 3rd shift

Apply:
United States
- Michigan
- Kalamazoo:
Full time:
Posted Today:
4963085
** Use Your Power for Purpose
** Our breakthroughs would not reach the hands of patients without our dedicated pharmaceutical manufacturing team. We rely on agile members who understand the critical impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and continuously strive to improve outcomes. Your efforts ensure that patients and physicians have timely access to the medicines they need.
** What You Will Achieve
** In this role, you will:
• Perform manual and/or automated packaging and/or inspection duties as required by the operating unit
• Changeover, set up, and assist with troubleshooting of all production lines
• Perform line cleaning and clearances; verifies line is cleaned and cleared prior to starting a production order
• Perform necessary process checks including but not limited to package checks, hourly audits, etc.
• Monitors production output, checks product quality and makes adjustment to ensure equipment is operating efficiently
• Maintain entries into GMP documents with daily review for completeness & accuracy
• Utilize computer skills to interact with multiple systems, performing entries is systems such as but not limited to SAP, AMPs (E ), Serialization, and WPM
• Display robust communication between shifts
• Train and mentor new colleagues and TCWs
• Working safely and compliantly following all applicable SOPs and standards including recording of GMP documentation
• Completing and maintaining all required training on time
• Consistently displays Pfizer Core Value behaviors of Courage, Excellence, Equity, and Joy
• Utilize downtime effectively and learn production principles
• Maintains training requirements per Site and unit goals

Other duties as assigned by the supervisor
• Safety Orientation
• LOTO• Unit safety audits and inspections
• GMP record entries
• Access to area specific gowning
• Meets daily GMP requirements - with assistance
• Maintains training requirements per Site and Unit Goals
• Monitors production output
• Checks product quality
• Makes needed adjustments to ensure equipment is operating efficiently
• Performs accurate and efficient Tier 0 handoffs with incoming and outgoing
• Is the primary SME for critical program interfaces such as SAP / AMPs (E ) /
• Conducts area audits - GMP/5S/Safety
• Conduct equipment changeovers on manual production lines
• Weekend Rotation (participation) as a line leader/coordinator
• Verifies that line is clean and cleared prior to starting production order
• Perform material and finished goods reconciliation
• Responsible for accuracy of batch record related documentation and batch record review
• Complete LOTO, line logs, maintenance logs as needed
• Complete visual inspection training and be able to perform visual inspections of parts.
• Conduct equipment changeovers on automated lines
• Conduct minor set up activities
• Performs work in professional, self-directed, responsible, and timely manner
• Responsible for the direction of colleagues and TCWs while leading the work center / production line
** Here Is What You Need** (Minimum Requirements)
* High School Diploma or GED with 2+ years of relevant experience
* Proficiency in math and reading skills for understanding Standard Operating Procedures, Good Manufacturing Practices (also cGMP), and Batch Record comprehension
* Ability to follow instructions provided in written, oral, or diagram form
* Capability to perform tasks under demanding conditions
* Basic computer skills for data entry and equipment operation
** Bonus Points If You Have** (Preferred Requirements)
* Experience in a pharmaceutical or manufacturing environment
* Knowledge of Good…