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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. It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.

Sanford North is recently a new Pfizer facility that serves as a Clinical, Commercial, and Contract Development and Manufacturing Organization (CDMO) site. It is designed to cater to the diverse needs of the pharmaceutical, biotechnology, and life sciences industries, offering comprehensive services across various staged of drug development and manufacturing.

ROLE SUMMARY

The Technical Operator IV will be responsible for performing all aspects of biologics upstream and downstream production in a single use facility, including cell vial thaw and flask expansion inside a Bio-Safety Cabinet (BSC), operation of wave/STR bioreactors up to 2000L, chromatography systems, and TFF systems.

ROLE RESPONSIBILITIES

• Performs manufacturing activities per current Good Manufacturing Practices (cGMPs).

• Perform all aspects of biologics upstream and downstream production.

• Operate production equipment safely in accordance with established standard operating procedures.

• Conduct activities in support of production schedules as directed by leadership.

• Manage multiple projects simultaneously.

• Review SOPs, master batch records, specifications, and other applicable cGMP documentation for Manufacturing.

• Maintain GMP records to comply with regulatory requirements and assist with in-process testing.

• Ensure compliance to training on an activity prior to GMP execution.

• Review completed batch records daily for GMP compliance and completeness.

• Inventory manufacturing supplies and ensure items are properly stocked.

• Operate to the highest ethical and moral standards.

• Adhere to quality standards set by regulations and policies, procedures, and mission.

• Work effectively in a team environment

BASIC QUALIFICATIONS

• High School Diploma/GED.

• 6 - 8 years of experience in a GMP pharmaceutical or biotech environment of which 2+ years of experience in Upstream or Downstream processing or combined education and experience.

• Good written and communication skills.

• Ability to follow detailed instructions and to maintain accurate records.

• Working knowledge and understanding of Microsoft Office Applications.

PREFERRED QUALIFICATIONS

• Ability to successfully multitask, when required.

• Bioworks Certification.

PHYSICAL/MENTAL REQUIREMENTS

• Frequently lift and or move objects at least 30 pounds.

• Stand/walk for extended periods of time.

• Ability to climb, balance, stoop, kneel, crouch, or crawl.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

• Ability to work a 12-hour schedule with nights and weekends.

• Ability to travel up to 10%.

Work Location Assignment: On Premise

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.

Manufacturing

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