Job Description
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 Tech Transfer Engineer III will be joining the Pfizer Andover Clinical Manufacturing Facility (ACMF) team.
The ACMF is a facility located on the Pfizer Andover, MA campus and is responsible for cGMP production of phase I/II clinical drug substance supporting the Pfizer Biotherapeutics portfolio. The ACMF resides within the Research and Development organization.
The ACMF Tech Transfer Team is responsible for incoming product site assessment, preparatory activities, campaign readiness and overall product/project ownership to support ACMF manufacturing of clinical drug substance.
How You Will Achieve
Serve as tech transfer lead for incoming projects on a rotating basis (approximately 1-2 per year)
When not serving as TT lead, execute tech transfer activities in support of all ACMF campaigns (approximately 12-18 per year)
Work with BRD development lines to improve scale up processes and identify best TT practices
Partner with BRD development lines on complex technical initiatives
Lead/support the creation of manufacturing batch records and other GMP documentation
Execute and troubleshoot upstream and downstream processes in a cGMP environment
Authorship of SOP’s for upstream and downstream unit operations
Data analysis and communication/collaboration with tech transfer team, production operations, development labs, and quality
Support implementation of new technologies and equipment
Support and author investigations as needed
Support facility audits as needed
?Qualifications
Must-Have
BS/BA in Chemical Engineering, Biotechnology, Microbiology, Cell Biology, Biochemistry or equivalent +4 years of experience, or MS + 1 years of experience.
Previous experience in Biologics GMP manufacturing and/or Biologics Tech Transfer
Nice-to-Have
Experience with Tech Transfer, facility fit assessments, and engineering design
Advanced knowledge of bioprocessing techniques and equipment
Ability to identify and implement process improvements independently
Experience in a GMP manufacturing role
Experience with Production Control Systems (i.e. DeltaV), ERP Systems (i.e. Microsoft Dynamics and/or SAP) and other business systems (Document Management Systems, LIMS, Microsoft Word, Excel, etc.)
Ability to execute against SOP’s and document entries in a compliant manner
Demonstrated capability to assemble a matrix cross-functional team
Excellent oral and written communication skills
Ability to work under minimal supervision
PHYSICAL/MENTAL REQUIREMENTS
Other Job Details:
Last Date to Apply for Job: April 1st, 2024
Work Location Assignment: Flexible
Flexible colleagues are assigned a Pfizer site within a commutable distance where they work about 2-3 days weekly to connect and innovate with their team face-to-face. However, they also benefit from being able to work offsite regularly when it makes business sense to do so.
The annual base salary for this position ranges from $74,900.00 to $124,800.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% of the base salary. 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 does not apply to Tampa, FL or any location outside of the United States.
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
"An Equal Opportunity Employer M/F/D/V"
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