Bioprocess Technician III Day shift 6 am-6 pm, Vaccines
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Job Location:
Sanford, FL - USA
Hourly Salary:
$ 22 - 38
Posted on:
5 hours ago
Vacancies:
1 Vacancy
Job Summary
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 Pfizers 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 Vaccines 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 DeltaV 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 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 ro environment requirements
hour shift (straight days)
Other job details
Last day to apply: December 22nd 2025
Work Location Assignment:On Premise
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care providers name address and the type of payments or other value received generally for public disclosure. Subject to further legal review and statutory or regulatory clarification which Pfizer intends to pursue reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse your name address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race color religion sex sexual orientation age gender identity or gender expression national origin disability or veteran status. Pfizer also complies with all applicable national state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
Pfizer endeavors to make to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing please email. This is to be used solely for accommodation requests with respect to the accessibility of our website online application process and/or interviewing. Requests for any other reason will not be returned.
Required Experience:
IC
Key Skills
- Quality Analysis
- Facility
- ISO
- Inventory Levels
- Root cause Analysis
- Shift operations
- General Maintenance
- Daily Operations
- Supervision
- Analysis
- PLC
- Safety Standards
- Quality Standards
- Time management skills
- Troubleshooting
About Company
Erfahren Sie mehr über uns als forschendes und produzierendes Pharmaunternehmen: Von unserem Beitrag zum medizinischen Fortschritt bis zur nachhaltigen Produktion.
