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Bioprocess Technician IV - Day shift Vaccines

Job in Sanford, Lee County, North Carolina, 27330, USA
Listing for: Pfizer, S.A. de C.V
Full Time position
Listed on 2026-01-19
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Manufacturing Engineer, Quality Engineering, Validation Engineer
Job Description & How to Apply Below
Position: Bioprocess Technician IV - Day shift 6 am - 6 pm, Vaccines

United States - North Carolina - Sanford.

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.

To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.

Pfizer Global Supply proudly shoulders the responsibility of manufacturing and distributing our wide-ranging pharmaceutical products.

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

What You Will Achieve
  • Executes manufacturing operations on the production floor for Downstream/Purification with varying levels of automation.
  • Follow SOPs and batch records for unit operations.
  • Supports operation of manufacturing equipment and issue resolution associated with process equipment commissioning, qualification and validation.
  • Drives troubleshooting, technical support/analysis and resolution of equipment, automation, and process issues on the manufacturing floor.
  • Drives right‑first‑time and continuous improvement execution, the timely review of daily documentation and completes data entry; identifies and/or communicates process and compliance concerns in real time.
  • Supports audits and observation improvements.
  • Collaborates with the subject matter expert for manufacturing operations in support of QTS investigations and CAPA implementations.
  • Responsible for remaining current on assigned training.
  • Implements Lean Manufacturing, Sustainability, Operational Excellence initiatives; facilitates the drive towards continuous improvement in all manufacturing areas.
  • Collaborates in the escalation process through various levels of management when operations, personnel safety, equipment functionality, product supply and/or quality compliance are at risk.
  • Ensures work requests are generated when issues arise with facility or manufacturing equipment.
  • Proficient in enterprise systems to support manufacturing operations including but not limited to SAP, LIMS, AMPS, PDOCS and/or QTS.
  • Ensures and participates in performance of cleaning, inventory, and maintaining facility in a safe and GMP compliant manner.
Here Is What You Need (Minimum Requirements)
  • High School Diploma or GED and 4+ years of experience, particularly in a pharmaceutical or other cGMP (Current Good Manufacturing Practices) environment OR Associate plus 2 years of work experience OR Bachelors plus 0 years of work experience preferred.
  • Effective verbal and written communication.
  • Proficiency in operating and troubleshooting production equipment.
  • Strong understanding of cGMP and safety regulations.
  • Ability to maintain accurate documentation and records.
  • Experience in a clean room environment.
  • Competence in using automated and enterprise systems.
  • Effective cross‑functional communication skills.
Bonus Points If You Have (Preferred Requirements)
  • Experience in a pharmaceutical manufacturing environment.
  • Knowledge of process improvement methodologies.
  • Ability to train and mentor less‑experienced colleagues.
  • Ability to work independently and as part of a team.
  • Attention to detail and commitment to quality.
  • Adaptability and flexibility in a dynamic work environment.
Physical / Mental requirements
  • Requires the moving of heavy equipment and the ability to lift ~40 pounds.
  • Moderate repetitive standing, sitting, bending, and ladder climbing on a daily basis.
  • The incumbent needs to take the necessary safety precautions when working with pressurized systems, steam, and corrosive chemicals.
  • The incumbent is required to attain knowledge of the operational equipment.
  • The incumbent will be required to assist in solving problems regarding site assessment, specific units used in Biopharmaceutical manufacturing.
  • The incumbent must be able to follow SOPs, MBRs and be able to use a multitude of enterprise systems including SAP, Delta‑V, etc.
Non Standard work schedule, travel or environment requirements
  • Supports a 24/7 facility.
  • 2‑2‑3 schedule. Day shift 6am‑6pm.
Other job details
  • Last day to apply:
    December 24th, 2025.
  • Work Location Assignment:
    On Premise.

The…

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