• Job Description

  Req#: 4906298

  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

  As part of the North Creek Manufacturing Facility, you will develop and apply your knowledge of procedures, techniques, tools, materials and equipment. Your receptiveness to new ideas will enhance the team’s ability to achieve goals and targets. You will follow standard procedures to complete tasks and identify process issues or problems that involve direct application of your skills/knowledge.

  It is your hard work and focus that will help in making Pfizer ready to achieve new milestones and help patients across the globe. You desire the opportunity to significantly contribute to the development and commercialization of transformative cancer therapies. You will use your training and knowledge of biopharmaceutical manufacturing to execute operations in a cGMP Facility.

  How You Will Achieve It

  • Utilize standard operating procedures and documents cGMP activities within batch records and logbooks applying good cGMP documentation and data integrity practices.

  • Complete setup, use, and cleaning (as necessary) of cGMP production equipment.

  • Proactively works with senior associates, subject matter experts, and management to achieve training competency in production operations.

  • Maintains a clean and orderly production area. Positively engages and collaborates with other team members to ensure daily production tasks are completed promptly.

  • Ensure work executed in compliance with company and regulatory quality policy and systems.

  • Participates and supports a culture of continuous improvement. Effectively collaborates with cross functional partners such as Quality Assurance, Quality Control, Supply Chain, and Facilities.

  Job duties may include:

  • Media and buffer compounding, assembly and movement of materials and equipment into staving and production areas, wipe-down and sanitization of equipment/materials prior to and post-transfer, preparation and sterilization of parts and assemblies (including manual wash, equipment wash, and autoclave), stocking of materials, gowning, and supplies, and ensuring cleanliness and audit -readiness of the GMP Manufacturing areas.

  • Performs cell culture operations safely and compliantly in accordance with OSHA and cGMP guidelines. Cell Culture operations include but are not limited to; dispensing and sampling of raw materials, media preparation, small scale passaging, set-up and operation of single use bioreactor, product sampling, and depth filtration harvest set-up and operations.

  • Performs Downstream and Conjugation operations safely and compliantly with OSHA

  Qualifications

  Must-Have

  • Bachelor’s degree, preferably in Life Sciences or Engineering, or Associate degree, preferably in Life Sciences or a technical program, or High School Diploma with Biotech certificate from an approved program desirable.

  • Required 0-2 years related experience.

  • Must be able to work off-shifts, and overtime as required. Applicant must be willing and able to work reliably on a flexible schedule, some off shift work, to meet the project's demands.

  • Assigned shift will depend on the group to which the Manufacturing Associate is assigned.

  • Must be able to don gowning in the form of hospital scrub, gloves, safety glasses/goggles, head and beard covers, coveralls and safety toe footwear with shoe covers multiple times per shift.

  • Ability to handle and work with hazardous materials and chemicals per standard operating procedures and OSHA guidelines.

  • Good organizational and communication skills, both written and verbal, and the ability to prioritize competing tasks.

  • Excellent interpersonal skills with the ability to work well with others in a dynamic and highly collaborative environment. Ability to interact constructively with peers and support groups.

  Last day to apply 3/22/24

  The salary for this position ranges from $22.93 to $38.22 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 - Washington – Bothell 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

• About the company

  At Pfizer we know that great things happen anywhere people come together with one shared goal. And the greatest rewards are sometimes where you least expect them. The future of medicine is happening at Pfizer.

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