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Bioprocess Technician III - Day Shift , mAbs

Job in Sanford, Lee County, North Carolina, 27330, USA
Listing for: Pfizer, S.A. de C.V
Full Time position
Listed on 2025-12-28
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Quality Engineering, Validation Engineer, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 22.94 - 38.24 USD Hourly USD 22.94 38.24 HOUR
Job Description & How to Apply Below
Position: Bioprocess Technician III - Day Shift 6am-6pm, mAbs

Bioprocess Technician III - Day Shift 6am-6pm, mAbs

  • 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.

Transforming Delivery of high quality products

Pfizer, We are one

PGS - Manufacture the Future

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:

  • Executes manufacturing operations on the production floor for buffer/media make-up tanks, glass washers, autoclaves, bioreactors / fer mentors, filtration equipment, inoculum preparation, chromatography skids and/or UF/DF skids with varying levels of automation.
  • Follow SOPs and batch records for unit operations.
  • Supports operation of manufacturing equipment associated with process equipment commissioning, qualification and validation.
  • Assists troubleshooting, technical support/analysis and resolution of equipment, automation, and process issues on the manufacturing floor.
  • Strives for Right first time execution and continuous improvement, the timely review of daily documentation and completes data entry;
    Identify and/or Communicate process and compliance concerns in real time.
  • Participate in audits, as required.
  • Assists the Subject Matter Expert for manufacturing operations in support of QTS investigations and CAPA implementations.
  • Responsible for remaining current on assigned training.
  • Supports Lean Manufacturing, Sustainability, Operational Excellence initiatives; facilitate the drive towards continuous improvement in all manufacturing areas.
  • Assists in the escalation process through various levels of management when operations, personnel safety, equipment functionality, product supply and/or quality compliance are at risk.
  • Escalates the need for work requests when issues arise with facility/manufacturing equipment.
  • Utilizes enterprise systems to support manufacturing operations including but not limited to, SAP, LIMS, AMPS, PDOCS and/or QTS.
  • Assists 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 with 2+ years of relevant experience, Associate 0 years of experience
  • Strong verbal and written communication skills
  • Proficiency in using standard manufacturing equipment and tools
  • Basic understanding of Good Manufacturing Practices (GMP)
  • Ability to follow detailed instructions and standard operating procedures
  • Strong problem-solving skills in a structured environment
  • Capability to work effectively in a team setting
  • Basic computer skills, including familiarity with data entry and reporting systems
Bonus Points If You Have (Preferred Requirements)
  • Experience in a pharmaceutical or biotechnology manufacturing environment
  • Knowledge of regulatory requirements and quality systems
  • Strong organizational skills and attention to detail
  • Ability to adapt to changing priorities and manage multiple tasks
  • Demonstrated ability to take initiative and drive continuous improvement
  • Strong analytical skills and the ability to interpret technical data
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…
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