Senior Quality Assurance Specialist - GxP & Investigations

tendersglobal.net 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 a member of Pfizer’s dedicated and highly effective quality assurance team. You will evaluate and review Pfizer’s clinical and commercial batches of drugs. You will make sure that product and process documents match the specifications based on established sampling and statistical process control procedures. Your expertise will help in identifying deviations from established standards, in the manufacturing and packaging of products. In the relevant cases you will approve investigations and change control activities to ensure compliance with configuration management policies. As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate in explaining difficult issues and establishing consensus between teams. It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe. How You Will Achieve It Ensure overall compliance of Clinical and Commercial products for all regions Ensure post-release surveillance commitments are met, including participation in product complaint investigations, Biological Product Deviation Reporting, Field Alerts, and Recalls Support product launch activities for introduction of product into new countries Assure compliance of products released to distribution and market, including Regulatory compliance check to Product Specification File, Filings, etc. Assure compliance of products released for use in Investigator Sponsored Trials and Patient Access Programs Participate in Regulatory inspections Ensure label requirements for each country are defined Participate in Material Review Board meetings as needed Provide administrative support for Material Review Board meetings, such as schedule and facilitate meetings, scribe, and distribute meeting minutes, and draft executive summaries Participate in investigations to support timely regulatory actions and communication when warranted Support Product Recall team, participating in investigations to determine product impact and distribution, and lead for quality operations communication to impacted parties Support Quality Agreement negotiations with vendors or partners to Seattle Genetics Develop knowledge on regulatory requirements in United States and Canada, where product is actively distributed for both Clinical and Commercial use, as well as potential future markets Assess current business processes for the team, and identify opportunities for continuous improvement to drive efficiency, scalability, and risk reduction Influence cross-functional teams to meet compliance and business needs Qualifications Must-Have Bachelors Degree with at least 3 years of experience OR Masters with more than 1 year of experience OR High School Diploma (or Equivalent) and 8 years of relevant experience OR an Associates Degree with 6 years of experience Experience in Quality administered systems Knowledge of current Good Manufacturing Practices and the applicable GxP regulations and standards Proactive approach and strong critical thinking skills Must be able to work in a team environment within own team and interdepartmental teams Excellent communication and interpersonal skills Good working knowledge of Microsoft Excel and Word Nice-to-Have Relevant pharmaceutical experience Willing to lead by example and jump right in, desire to get to root cause, collaborative and active listener Effectively manages stressful situations, able to focus on task at regardless of circumstances and stress induced pressure Physical/Mental Requirements Ability to work effectively and efficiently Ability to multitask without loss of efficiency or accuracy Ability to complete assigned tasks without direct supervision Ability to exercise independent judgment and make decisions Other Job Details Last day to apply: March 20th, 2024 Relocation support available Work Location Assignment:Flexible (Required to be On Premise an average of 2.5 days per week) The annual base salary for this position ranges from $78,000.00 to $130,000.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 10.0% of the base salary. 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 tendersglobal.net (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States. 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 SunshineAct. 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 #J-18808-Ljbffr Pfizer