Bioprocess Technician III - 3rd Shift - 12hrs 6pm to 6am

Posted Yesterday
Be an Early Applicant
Sanford, NC, USA
In-Office
23-39 Hourly
Junior
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
Perform hands-on bioprocess manufacturing tasks on third shift, follow GMP and SOPs, support production of active biological ingredients, maintain equipment and housekeeping, complete data entry and reporting, and contribute to continuous improvement under moderate supervision.
Summary Generated by Built In
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:
  • Take responsibility for individual contributions to achieve team deliverables, working effectively as a team member and coordinating with others.
  • Manage personal time and professional development, being accountable for results.
  • Follow standard procedures to complete tasks of varying scope, sequence, and complexity within the agreed timeframe.
  • Identify and solve moderately routine problems.
  • Complete assignments with moderate supervision using established procedures, referring deviations from standard procedures to the supervisor.
  • Ensure work is reviewed for accuracy, quality, and adherence to standards.
  • Be responsible for the production of drug substances or active biological ingredients (ABI), assisting in various activities and functions within a manufacturing facility, and ensuring equipment functionality.
  • Support technical operations, maintain housekeeping standards, keep training status current, and assist in the implementation of new technology for process execution and analysis.

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

Other Job Details:
  • Work Location Assignment: On Premise
  • Last day to apply: August 4
  • Shift: 12hrs 6pm to 6am
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.
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 provider's 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 www.pfizer.com/careers accessible 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 [email protected] . 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.
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

Skills Required

  • 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
  • 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

What the Team is Saying

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Pfizer
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The Company
HQ: New York, NY
121,990 Employees
Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.

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Employees engage in a combination of remote and on-site work.

Typical time on-site: 2.5 days a week
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