Bioprocessing Technician III

Use Your Power for Purpose

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:

• Supports manufacturing operations on the production floor for Buffer/Media/Process Support 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

• 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 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 

This is a 1st shift position on a 6 AM to 6 PM rotating schedule.

Other Job Details:

• Last day to Apply: June 25, 2026

• Work Location Assignment: On Premise


The salary for this position ranges from $23.40 to $39.01 per hour. In addition, this position offers eligibility for overtime, weekend, holiday and other pay premiums depending on the work schedule and the Company’s policies. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided applies only to the United States - North Carolina - Sanford location.





Relocation assistance may be available based on business needs and/or eligibility.




Candidates must be authorized to be employed in the U.S. by any employer.

U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.






To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.


Manufacturing