Why Patients Need You

Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.

What You Will Achieve

You will be recognized as a subject matter expert with specialized knowledge and skills in procedures, techniques, tools, materials and equipment. You will be entrusted with adapting standard methods and procedures by applying your knowledge, prior work experience and requirements. Your business awareness of cross-organizational impact on project delivery will elevate the quality of project deliverables. You will arrive at decisions on which methods and procedures are the best fit for different work situations.

You will train others and reinforce behaviors that will help us achieve our goal of providing the best healthcare to our patients.

How You Will Achieve It

• Manage own time, professional development and be accountable for own results.
• Prioritize own workflow, allocate work of others and assist in establishing their priorities, pushing self and others to exceed goals.
• Responsible for providing input to performance assessment on team members.
• Ensure compliant and timely documentation and resolution of events.
• Develop working process to enhance Good Manufacturing Practices {also cGMP} standards for the team.
• Maintain a high level of personal safety and housekeeping considerations.
• Identify Continuous Improvement opportunities and participates in Continuous Improvement projects.
• Author /review QC (Quality Control) documentation and document all results in accordance to Good Manufacturing Practices and Good Laboratory Practices requirements.
• Responsible for the endorsement of Good Laboratory Practices {part of GxP} Environment, Health & Safety requirements and Pfizer Quality Standards (PQS) requirements.
• Ensure compliance with all policies and procedures in accordance with the Company Handbook.
• Provide an efficient customer focused service by representing the area at designated meetings, and by ensuring laboratory processes, equipment and services are maintained in an operational state.
• Provide training for team members and perform peer reviews of data and logbooks.

Qualifications

Must-Have

• High School Diploma or GED
• 8+ years' experience
• Certification in assigned area, if applicable
• Ability to write clear technical document.
• Good organizational and time management skills
• Good oral and written communication skills
• Good Microsoft Office skills

Nice-to-Have

• Bachelor's Degree
• Pharmaceutical, quality control, and stability experience
• Effective problem-solving skills
  
  

PHYSICAL/MENTAL REQUIREMENTS

Be able to work for 8 hours at time while wearing personal protection gear.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

No travel or environmental requirements, ability to work off shift hours as needed to support business needs.

Work Location Assignment: On Premise

The salary for this position ranges from $27.64 to $46.07 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 - Rocky Mount location.

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 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.

Quality Assurance and Control