Why Patients Need You 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 The clinical manufacturing technical specialist is part of a multi-disciplinary team responsible for cGMP production of phase I/II clinical drug products supporting the Pfizer Biotherapeutics portfolio. Technical Operations 3 of Biotherapeutics Drug Product Manufacturing is a GMP Drug Product manufacturing position responsible for the execution of batch records following site approved standard operating procedures (SOP) inside the Andover Liquid Dose Manufacturing Facility (AN-LDM). This position will maintain and prepare equipment, revise SOPs, Train personnel, formulate drug products, aseptically fill drug products. As part of the Technical Operations team, your prior work experience and ability to apply your breadth of knowledge will help you adapt the standard methods and procedures. You will help us identify required delivery and process improvements that drive increased efficiency, throughput and quality. You will arrive at decisions on which methods and procedures are the best fit for different work situations. It is your hard work and focus that will help in making Pfizer ready to achieve new milestones and help patients across the globe. How You Will Achieve It Manage own time, professional development, and be accountable for own results. Prioritize own workflow and assist in prioritizing the workflow of less-experienced colleagues. Adhere to Good Manufacturing Practices and standard operating procedures, and material sampling instructions. Responsible for the equipment preparation, formulation and aseptic filling of biologic drug products. Complete recurring assignments independently and select the most appropriate method or approach to do so within prescribed limits of authority. Identify opportunities for continuous improvements and enable implementation. Perform troubleshooting of production support equipment and operations. Understand scientific principles in order to problem solve and troubleshoot test results. Report any deviation or observation that might lead to adverse impact to product quality. Complete work instructions and maintains clean room environment to comply with regulatory requirements. Qualifications Must-Have High School Diploma or GED 5 years of experience Certification in assigned area, if applicable Drug product filling/ Final fill experience Demonstrated experience in a biotechnology manufacturing or laboratory environment Experience in cGMP (Current Good Manufacturing Practices) compliance as related to manufacture of biologics Ability to think critically and demonstrate troubleshooting and problem-solving skills Strong workload planning skills, organization, and attention to detail, and follow through Excellent written and verbal communication skills Strong computer skills in Microsoft Office required e.g. MS Word, MS Excel Nice-to-Have Bachelor's Degree Liposome manufacturing experience PHYSICAL/MENTAL REQUIREMENTS Role tasks will include frequent bending, lifting (up to 40 pounds) and twisting motions. Ability to stand for several consecutive hours Absence of any medical restrictions which could restrict completion of all required duties Must be able to meet gowning requirements NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS Shift is 7am to 5:30pm (4 by 10 hour work day rotating week to week, Monday through Friday schedule) Overtime may be required Aseptic Gowning required Work Location Assignment: On Premise The salary for this position ranges from $28.68 to $47.79 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 - Massachusetts - Andover 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. Manufacturing Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives. We’re looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place.