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Job Details


Pfizer: One of the World's Premier Biopharmaceutical Companies

Technology Transfer Associate (4839510_Andover)

Pharmaceuticals

All

Yearly

Full Time

No

Andover, Massachusetts, United States

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

You will have knowledge of process equipment and systems and manufacturing operations with the primary responsibility to execute technology transfer, project improvements, and new technology and equipment introductions. Due to your expertise in the manufacturing technology transfer domain, you may participate in equipment qualifications, clinical and process validation campaigns and training of operational qualifications and assist the Technology Transfer team members as needed. You will conduct all activities in accordance with Company policies and standard operating procedures, Pfizer Values, and global regulatory guidelines, environmental guidelines etc.

As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative team environment for your colleagues.

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
  • Contribute to completion of project milestones and organize own work to meet project task deadlines.
  • Use operational and technical expertise to assist in troubleshooting activities, technology transfer and start-up activities.
  • Analyze data from multiple sources; investigations, daily/weekly KPIs, equipment/process performance, etc. and develop a strategy for shift to improve performance.
  • Ensure all production equipment and systems are in compliance with Current Good Manufacturing Practices.
  • Manage execution of relevant process activities by following established Standard Operating Procedures.
  • Perform process monitoring and data analysis, and data preparation for presentation in several forums including project team meetings.
  • Promote a safety, compliance and continuous improvement culture.
  • Drive changes that support Right First Time, Efficiency and/or reduced costs.
  • Provide coaching and mentoring to front-line staff to increase competency of the plant floor.
  • May initiate and lead investigations in support of manufacturing operations

QualificationsMust-Have
  • Bachelor's Degree with 2 years of experience
  • Previous experience in a GMP manufacturing environment

Nice-to-Have
  • Familiarity and experience with mammalian cell culture, centrifugation, and ultrafiltration
  • Previous experience with scale up of these unit operations is desirable.
  • Familiarity and experience with downstream purification process such as UF/DF, and Chromatography experience.
  • Experience with Six Sigma, Method 1, 5S and/or other operational excellence programs a plus.
  • Familiarity with aseptic technique and microbial control a plus


PHYSICAL/MENTAL REQUIREMENTS

  • Work will include walking throughout the manufacturing suite including up and down stairs.
  • Perform mathematical calculations and ability to perform complex data analysis
  • Ability to don cleanroom gowning

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

  • This position is M-F 830-500PM
  • May require off-shift support
  • This role may use a hybrid working remote model where you may be split between working from home and on-site
  • The role requires work / oversight in a GMP manufacturing suite which requires gowning

Pfizer requires all U.S. new hires to be fully vaccinated for COVID-19 prior to the first date of employment. As required by applicable law, Pfizer will consider requests for Reasonable Accommodations.

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