Use Your Power for Purpose At Pfizer, our purpose is to deliver breakthroughs that change patients’ lives. Your work will directly support the discovery sciences, ensuring drug safety and efficacy, and aiding clinical trials. By leveraging cutting-edge design and process development capabilities, you will help accelerate the delivery of top-tier medicines to patients globally, making a significant impact on improving patients' lives. The In Vivo Technician within the Drug Safety R&D organization is responsible for performing accurate, high quality in‑life study work for rodent and non-rodent safety studies in compliance with the study protocol, Standard Operating Procedures (SOPs), Good Laboratory Practice (GLP) regulations, Environmental Health and Safety (EHS) standards, animal welfare regulations, and departmental policies/procedures. The data collected on these studies by the In Vivo Technician enable candidate selection, clinical programs, early research and target safety, and investigative work. What You Will Achieve In this role, you will: Perform assigned in vivo study activities in compliance with applicable regulatory requirements, study protocols, SOPs, and company procedures. Support the in-life phase of rodent and non-rodent safety/toxicology studies, including study set-up, test article administration, animal observations, sample collection, data collection, and documentation. Read, understand, and follow study protocols and associated Pristima protocols to ensure study activities are performed as required. Accurately enter, review, and document study data and correct errors in accordance with established procedures. Perform self-review and, as appropriate, peer review of in-life data for accuracy, completeness, and protocol compliance. Prepare study materials, forms, labels, supplies, and equipment needed for study activities. Use, maintain, and perform required checks or calibrations of laboratory equipment, such as balances and IV pumps. Identify and communicate equipment or technical issues and assist with troubleshooting as appropriate. Communicate with Study Directors, Management, Comparative Medicine, and support personnel regarding study activities, animal observations, and unexpected findings. Follow established animal welfare practices and promptly communicate observations or issues to appropriate personnel. Support preparation of study data and documentation for quality assurance review and archiving. Manage assigned activities to meet study timelines while maintaining data quality. Maintain clean, organized, and safe work areas. Participate in departmental training, SOP updates, and continuous improvement activities. As training and experience progress, may serve as a Primary Technician for assigned studies. Here Is What You Need (Minimum Requirements) High School Diploma with 5+ years of relevant experience Demonstrated ability to handle multiple projects simultaneously Strong organizational and time management skills Detail-oriented with strong interpersonal and communication skills Proficiency in using laboratory equipment and software Basic understanding of laboratory protocols and procedures Bonus Points If You Have (Preferred Requirements) A Bachelor's Degree Experience in a biological laboratory, specifically in vivo work Ability to work independently and as part of a team Meticulous attention to detail Excellent problem-solving abilities Strong analytical and critical thinking skills Familiarity and basic understanding of common AI tools and a curiosity for learning how they can be used to enhance productivity PHYSICAL/MENTAL REQUIREMENTS Must be able to lift 40 lbs and to stand for at least 3 hours. Must also have the ability to perform mathematical calculations. NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS Overtime, weekend and holiday work is required. Work Location Assignment: On Premise The salary for this position ranges from $26.86 to $44.77 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 - Connecticut - Groton 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. Research and Development A career at Pfizer offers opportunity, ownership and impact. All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to impact the health and lives of millions of people. Pfizer, a global leader in the bio pharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives.

In Vivo Technician.

more at Pfizer.

Senior Oncology Account Specialist Hematology Detroit South, MI

Validation and Compliance Specialist- GMP/Pharma Industry

Global Clinical Supply (GCS) Product Area Business Lead (Senior Manager)

similar roles.

Assistant Professor, Education

Assistant Professor, Family Nurse Practitioner

Praktikums-/Werkstudentenstelle Sportmanagement (10-20h / 6-12 Monate)

Initiativbewerbung (m/w/d)

Customer Service & Operations Agent

Air Import Operations Agent