Bioprocess Technician BPT IV (Day Shift: 6 AM - 6 PM)
Pfizer
July 02, 2026
On-site
North Carolina, United States
Operations
What You Will Achieve (Responsibilities)
- Execute manufacturing operations (Downstream/Purification) for varying automation levels.
- Follow SOPs and batch records; support equipment commissioning, qualification, and validation.
- Troubleshoot and resolve equipment, automation, and process issues.
- Drive right-first-time and continuous improvement; review daily documentation and complete data entry; identify/communicate process and compliance concerns.
- Support audits/observation improvements; collaborate with SME on QTS investigations and CAPA.
- Remain current on assigned training; implement Lean/Sustainability/Operational Excellence initiatives.
- Escalate issues impacting safety, equipment, product supply, or quality compliance; generate work requests as needed.
- Use enterprise systems (e.g., SAP, LIMS, AMPS, PDOCS, QTS).
- Perform cleaning/inventory and maintain safe, GMP-compliant facilities.
Here Is What You Need (Minimum Requirements)
- HS Diploma/GED + 4+ years (pharma/cGMP) OR Associate + 2 years OR Bachelor + 0 years preferred.
- Effective verbal/written communication.
- Proficiency troubleshooting production equipment; strong cGMP & safety knowledge.
- Accurate documentation/recordkeeping.
- Clean room experience; ability to use automated/enterprise systems.
Bonus Points (Preferred)
- Pharma manufacturing experience; process improvement knowledge.
- Train/mentor; independent + team work; attention to detail/quality; adaptable.
Non-Standard Schedule
- 12-hour shift 2/2/3, 6AM–6PM; on-premise.
Compensation/Benefits & Application
- $25.88–$43.14/hour; eligibility for overtime/weekend/holiday premiums.
- Benefits include 401(k) with matching and retirement contribution, paid vacation/holidays/personal days, caregiver/parental and medical leave, and medical/dental/vision.
- Last day to apply: July 9, 2026.
- Execute manufacturing operations (Downstream/Purification) for varying automation levels.
- Follow SOPs and batch records; support equipment commissioning, qualification, and validation.
- Troubleshoot and resolve equipment, automation, and process issues.
- Drive right-first-time and continuous improvement; review daily documentation and complete data entry; identify/communicate process and compliance concerns.
- Support audits/observation improvements; collaborate with SME on QTS investigations and CAPA.
- Remain current on assigned training; implement Lean/Sustainability/Operational Excellence initiatives.
- Escalate issues impacting safety, equipment, product supply, or quality compliance; generate work requests as needed.
- Use enterprise systems (e.g., SAP, LIMS, AMPS, PDOCS, QTS).
- Perform cleaning/inventory and maintain safe, GMP-compliant facilities.
Here Is What You Need (Minimum Requirements)
- HS Diploma/GED + 4+ years (pharma/cGMP) OR Associate + 2 years OR Bachelor + 0 years preferred.
- Effective verbal/written communication.
- Proficiency troubleshooting production equipment; strong cGMP & safety knowledge.
- Accurate documentation/recordkeeping.
- Clean room experience; ability to use automated/enterprise systems.
Bonus Points (Preferred)
- Pharma manufacturing experience; process improvement knowledge.
- Train/mentor; independent + team work; attention to detail/quality; adaptable.
Non-Standard Schedule
- 12-hour shift 2/2/3, 6AM–6PM; on-premise.
Compensation/Benefits & Application
- $25.88–$43.14/hour; eligibility for overtime/weekend/holiday premiums.
- Benefits include 401(k) with matching and retirement contribution, paid vacation/holidays/personal days, caregiver/parental and medical leave, and medical/dental/vision.
- Last day to apply: July 9, 2026.