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Bioprocess Technician IV - Night Shift , mAbs

Job in Greensboro, Guilford County, North Carolina, 27497, USA
Listing for: Pfizer
Full Time position
Listed on 2026-02-19
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Quality Engineering
Salary/Wage Range or Industry Benchmark: 25.88 - 43.14 USD Hourly USD 25.88 43.14 HOUR
Job Description & How to Apply Below
Position: Bioprocess Technician IV - Night Shift 6pm-6am, mAbs

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:

  • 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 issue resolution associated with process equipment commissioning, qualification and validation.
  • Drive troubleshooting, technical support/analysis and resolution of equipment, automation, and process issues on the manufacturing floor.
  • Drive right‑first‑time and continuous improvement execution, timely review of daily documentation, and complete data entry; identify and/or communicate process and compliance concerns in real time.
  • Support audits and observation improvements.
  • Collaborate with the Subject Matter Expert for manufacturing operations in support of QTS investigations and CAPA implementations.
  • Remain current on assigned training.
  • Implement Lean Manufacturing, Sustainability, Operational Excellence initiatives; facilitate the drive towards continuous improvement in all manufacturing areas.
  • Collaborate in the escalation process through various levels of management when operations, personnel safety, equipment functionality, product supply and/or quality compliance are at risk.
  • Ensure work requests are generated when issues arise with facility or manufacturing equipment.
  • Be proficient in enterprise systems to support manufacturing operations including but not limited to SAP, LIMS, AMPS, PDOCS and/or QTS.
  • Participate in performance of cleaning, inventory, and maintenance of the 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 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 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 must take the necessary safety precautions when working with pressurized systems, steam, and corrosive chemicals.
  • The incumbent must attain knowledge of the operational equipment.
  • The incumbent will be required to assist in solving problems regarding site assessment and specific units used in biopharmaceutical manufacturing.
  • The incumbent must follow SOPs, MBRs and 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. Night shift 6pm‑6am.
Other Job Details

Last Date to Apply for Job:
Feb 19, 2026.

Referral Bonus Eligibility: YES

Eligible for Relocation Package: NO

Work Location Assignment:
On Premise

The salary for this position ranges from $25.88 to $43.14 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…

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