Senior Bioprocess Technician ( Rotating Nights / 6pm

MedDeviceJobs; Sanford (NC); On-site; USD 60,000 - 100,000; Full time

Benefits offered by this job

401(k) match

Retirement savings plan

Paid vacation

Job summary

Pfizer in North Carolina, Sanford location, seeks an experienced biopharma professional to support manufacturing operations and lead process improvements. You will oversee process equipment, automation control, and regulatory compliance, enabling reliable production of medicines for patients.

The role emphasizes leadership, continuous improvement, and collaboration across teams, with opportunities to train others and influence departmental standards at Pfizer.

Qualifications

• High School Diploma or GED.
• 6+ years of biopharmaceutical experience.
• Experience with biopharmaceutical unit operations or laboratory operations.
• Understanding of continuous improvement processes.
• Proficiency with 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.

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.

Skills

Lead worker

Problem solving

Time management

Communication skills

Education

High School Diploma or GED

Bachelor's Degree

Tools

SAP

Delta-V

Job description

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.

What You Will Achieve

• 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.

Here Is What You Need (Minimum Requirements)

• High School Diploma or GED
• 6+ years of experience
• Experience within 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

Bonus Points If You Have (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 the necessary safety precautions when working with pressurized systems, steam, and corrosive chemicals.
• The incumbent is required to be skilled and knowledgeable of the operational equipment.
• The incumbent will be required to solve problems regarding site assessment, specific units used in Biopharmaceutical manufacturing.
• The incumbent must be able to follow SOPs, MBRs and be skilled in a multitude of enterprise systems including SAP, Delta-V, etc.

Non-Standard work schedule, travel or environment requirements

• 12 Hour night shift 6pm-6am (2-2-3 schedule)

Other job details

• Last day to apply: October 16th, 2026
• Work Location Assignment: On Premise

The salary for this position ranges from $28.76 to $47.93 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 [e-mail]. 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