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Bioprocess Technician IV

Job in Sanford, Lee County, North Carolina, 27330, USA
Listing for: Pfizer, S.A. de C.V
Full Time position
Listed on 2026-01-28
Job specializations:
  • Manufacturing / Production
    Quality Engineering, Pharmaceutical Manufacturing, Manufacturing Engineer, Operations Engineer
Salary/Wage Range or Industry Benchmark: 60000 USD Yearly USD 60000.00 YEAR
Job Description & How to Apply Below

Location

United States - North Carolina - Sanford

Overview

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.

Use Your Power for Purpose

Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team. We rely on a team of dedicated and agile members who understand the importance and impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and always look to improve outcomes. You will help to ensure that patients and physicians have the medicines they need when they need them.

Responsibilities
  • Serve as a key resource and potentially lead lower levels within your area of expertise.
  • Manage personal time and professional development, taking accountability for results and prioritizing workflow.
  • Contribute to project and department tasks, providing direction and training to team members, and may act as a lead worker.
  • Be recognized as a "LEAD" or "Subject Matter Expert" within your field.
  • Proactively identify and resolve potential problems, considering wider implications beyond immediate issues.
  • Complete assignments independently, selecting appropriate methods and ensuring team assignments are completed.
  • Review non-standard work for technical soundness and may review the work of others.
  • Adhere to Pfizer standards, guidelines, and values, influencing teams and contributing to the development of departmental standards and guidelines.
  • Leverage knowledge of process equipment, systems, manufacturing operations, and automation control to plan and execute activities.
  • Ensure compliance with Company policies, standard operating procedures, and global regulatory and environmental guidelines, adapting methods and procedures as necessary.
Minimum Requirements
  • High School Diploma or GED
  • 6+ years of experience
  • Experience with in the biopharmaceutical industry, including knowledge and experience with relevant biopharmaceutical unit operations and/or laboratory operations
  • Understanding of continuous improvement processes
  • Proficiency in process equipment, systems, manufacturing operations, and automation control
  • Ability to manage personal time and professional development
  • Strong problem-solving skills with the ability to identify and resolve potential issues
Preferred Requirements
  • Bachelor's Degree
  • Advanced knowledge of biopharmaceutical manufacturing processes
  • Strong communication and interpersonal skills
  • Proficiency in project management
  • Familiarity with global regulatory and environmental guidelines
  • Ability to adapt to changing priorities and work effectively under pressure
  • Familiarity and basic understanding of common AI tools and a curiosity for learning how they can be used to enhance productivity
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 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
Work Location Assignment

On Premise

Compensation

The salary for this position ranges from…

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