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 Pfizers 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.
This incumbent is a member of the Formulations operational support team within the Plant Supply & Logistics focus factory. Under the supervision of the Formulations team lead the incumbent may be responsible for material inventory management maintenance of equipment including tanks and pump systems conducting quality control assays and formulating medically active solutions according to validated recipes. Incumbent responsibilities will also include safe handling of controlled substances and List I chemicals in-process and investigational sampling as well as isolator and respirator usage. All activities shall be performed according to applicable Standard Operating Procedures (SOPs) and/or Batch Records and shall maintain compliance with all relevant regulatory body and license requirements (i.e. FDA USP etc.). Accurate records of activities performed will be maintained per data integrity regulations prescribed by current Good Manufacturing Practices (cGMP) and incumbent is responsible for providing communication of all process and specification deviations as they occur. Incumbent actively participates in teamwork adheres to safety practices and strong working knowledge to perform role functions independently. Additional responsibility may include assisting with metrics reporting as well as initiating and developing project plans for continuous improvements within the department.
Material Handling Participates in management of inventory transportation and disposal of all applicable raw materials used in the Formulations department. Shall receive and maintain fork truck license through safety trainings and certification processes.
Equipment Cleaning Assists with cleaning of product contact equipment necessary for batch manufacture per applicable regulation standards and operating procedures. Verifies appropriate cleaning prior to use of equipment and effectively communicates all atypical or unclean appearances to management in a timely manner.
Conducting Assays Accurately performs quality control assays as required to complete in-process batches and identify variations according to provided standard operating procedures. Communicates effectively all basic technical issues atypical or out-of-specifications test results instrument malfunctions and methodology problems as they occur. May participate in active investigational analyses as well.
Solution Formulating Precisely weighs measures and charges APIs controlled substance and List 1 chemicals according to validated recipe instructions to generate homogenous medically active solutions used in batch manufacturing. Safely handles API controlled substance and List 1 chemical material as per site specific safe handling programs. Inspects solution for characteristics such as pH dissolution and abnormalities.
Teamwork Participates as a contributing member of the operational support team in sharing the performance of all listed responsibilities including general area maintenance tasks such as daily/weekly cleanings and equipment preventative maintenance (PM). Performs data review of peers. Supports mentorship and training of new staff as needed.
Safety Practices Contributes to the housekeeping and cleaning of designated production areas. Safely handles / disposes of chemical and hazardous waste. Complies with all Safety Environmental and Security policies as required. Communicates all safety concerns incidents and events as they occur.
Operational Support Has opportunity to participate in non-routine activities/projects to support the team goals. May initiate and develop project plans for the purpose of continuous improvement within the department.
Basic Qualifications Minimum High School Diploma or GED with 4 years of relevant experience or Specialized Certifications: 1 to 18 months of relevant experience depending on the certifications depth and relevance Knowledge of basic chemistry mathematical calculations and metric system usage. Skills training in basic chemical assays and both physical and computerized record keeping. Preferred Qualifications 3-6 years of relevant experience in an industrial pharmaceutical production setting preferred.
PHYSICAL/MENTAL REQUIREMENTS
Ability to stand for 10 to 12 hours at a time sit for 5 to 6 hours at a time and regularly walk long distances climb stairs/ladders walk on catwalks. Ability to regularly lift up to 50 lbs without mechanical assistance at least once a shift and lift >50 lbs with assistance. Intellectual capability to perform complex mathematical problems and complex data analysis.
NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS
Ability to work in a controlled temperature environment wearing clean room attire. On occasion steam noise chemical odours and fumes may be present; personal protective equipment must be worn for safety reasons. Ability to maintain shift work on a 12 hour 2-2-3 rotating schedule. Day or night shift schedule will be required.
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 providers 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 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. 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.
Required Experience:
IC
Erfahren Sie mehr über uns als forschendes und produzierendes Pharmaunternehmen: Von unserem Beitrag zum medizinischen Fortschritt bis zur nachhaltigen Produktion.