Bioprocess Technician BPT IV (Night Shift: 6 PM - 6 AM)
Pfizer
July 02, 2026
On-site
North Carolina, United States
Operations
What You Will Achieve
In this role, you will:
- Execute manufacturing operations on the production floor for Downstream/Purification with varying levels of automation.
- Follow SOPs and batch records for unit operations.
- Support operation of manufacturing equipment and resolve issues related to commissioning, qualification, and validation.
- Troubleshoot and provide technical support/analysis to resolve equipment, automation, and process issues.
- Drive right-first-time and continuous improvement; review daily documentation, complete data entry, and identify/communicate process and compliance concerns in real time.
- Support audits and observation improvements.
- Collaborate with the Subject Matter Expert for manufacturing operations to support QTS investigations and CAPA implementations.
- Maintain current on assigned training.
- Implement Lean Manufacturing, Sustainability, and Operational Excellence initiatives to enable continuous improvement.
- Escalate when operations, personnel safety, equipment functionality, product supply, and/or quality compliance are at risk.
- Generate work requests when issues arise with facility/manufacturing equipment.
- Use enterprise systems supporting manufacturing operations (e.g., SAP, LIMS, AMPS, PDOCS, QTS).
- Perform cleaning, inventory, and maintain the facility in a safe and GMP-compliant manner.
Here Is What You Need (Minimum Requirements)
- High School Diploma or GED with 4+ years of experience in a pharmaceutical or other cGMP environment; or Associate + 2 years; or Bachelor’s + 0 years (preferred).
- Effective verbal and written communication.
- Ability to operate and troubleshoot production equipment.
- Strong understanding of cGMP and safety regulations.
- Ability to maintain accurate documentation/records.
- Clean room experience.
- Competence using automated and enterprise systems.
- Effective cross-functional communication.
Bonus Points If You Have (Preferred Requirements)
- Experience in pharmaceutical manufacturing; process improvement methodologies.
- Train/mentor others; work independently and as part of a team.
- Attention to detail, quality focus; adaptability.
Application instruction (from posting)
- Last day to apply: July 9th, 2026.
In this role, you will:
- Execute manufacturing operations on the production floor for Downstream/Purification with varying levels of automation.
- Follow SOPs and batch records for unit operations.
- Support operation of manufacturing equipment and resolve issues related to commissioning, qualification, and validation.
- Troubleshoot and provide technical support/analysis to resolve equipment, automation, and process issues.
- Drive right-first-time and continuous improvement; review daily documentation, complete data entry, and identify/communicate process and compliance concerns in real time.
- Support audits and observation improvements.
- Collaborate with the Subject Matter Expert for manufacturing operations to support QTS investigations and CAPA implementations.
- Maintain current on assigned training.
- Implement Lean Manufacturing, Sustainability, and Operational Excellence initiatives to enable continuous improvement.
- Escalate when operations, personnel safety, equipment functionality, product supply, and/or quality compliance are at risk.
- Generate work requests when issues arise with facility/manufacturing equipment.
- Use enterprise systems supporting manufacturing operations (e.g., SAP, LIMS, AMPS, PDOCS, QTS).
- Perform cleaning, inventory, and maintain the facility in a safe and GMP-compliant manner.
Here Is What You Need (Minimum Requirements)
- High School Diploma or GED with 4+ years of experience in a pharmaceutical or other cGMP environment; or Associate + 2 years; or Bachelor’s + 0 years (preferred).
- Effective verbal and written communication.
- Ability to operate and troubleshoot production equipment.
- Strong understanding of cGMP and safety regulations.
- Ability to maintain accurate documentation/records.
- Clean room experience.
- Competence using automated and enterprise systems.
- Effective cross-functional communication.
Bonus Points If You Have (Preferred Requirements)
- Experience in pharmaceutical manufacturing; process improvement methodologies.
- Train/mentor others; work independently and as part of a team.
- Attention to detail, quality focus; adaptability.
Application instruction (from posting)
- Last day to apply: July 9th, 2026.