• Associate, Oncology Operations Jobs in New York City

  • Pfizer Inc.
  • New York City

Job Description:


The position performs manufacturing of commercial and clinical conjugate related products Primary duties include performing all required complex manufacturing activities including production, investigation, equipment validation, writing SOPs, in compliance with company policy and regulations Assist developing detailed plans and prioritize the routine tasks within the plan to achieve goals of incumbents projects Actively develop technical and operational leadership on all aspects of the manufacturing operations and contribute to the success of the department


Muti-task all activities associated with manufacturing of commercial and clinical antibody drug conjugates including but not limited to operation, cleaning, investigation, change control, conducting training, etcHeavy hands-on operations and irregular work schedules occasionally requiredFunction as a member of self-directed high performance team
Perform manufacturing of commercial and clinical batches in compliance with cGMP, Safety, and Environmental regulationsMeet the production demandEnsure all Investigations and commitments are performed in a timely mannerEnsure all production equipment and systems are in compliance with cGMP
Create or modify Standard Operating procedures (SOPs) for commitment implementation or as related to new projects, facility and equipment changesEvaluate and approve Preventive Maintenance Orders (PMOs)Initiate change controls related to new projects, facility and equipment changes, BR and PMO revision, etc
Assist in problem solving efforts for manufacturing processes Troubleshoot process issues, diagnose technical problems and identify short- and long-term solutionsWork closely with cross-functional groups to resolve system problems to minimize contamination and cost
Conduct manufacturing deviation investigations and write investigation reports (MIRs)Identify root causes and corrective/preventive actions (CAPAs) Implement CAPAs commitments
Compliance - Perform other technical tasks as required to ensure GMP and safety compliance Promote cGMP compliance within the work place by following site cGMP proceduresIncorporate cGMP and regulatory compliance into all assigned projects scope and design
Provide project team support as required by team leads


BS in Chemical Engineering or related scientific discipline with 0-2 years of experience
On the job and hands-on training will be provided drug substance intermediate, drug substance and drug product operation
Lean Six Sigma education or certification preferred but not required


Lifting, sitting, standing, walking, bending, ability to perform mathematical calculations and ability to perform complex data analysis
Ability to apply general engineering techniques/principals
Ability to operate automated process control systems
Ability to analyze operational process problems and implement appropriate corrective and preventative actions
Effectively interact with team members within and across functions Can articulate the issues and solutions to both team and to management Ability to organize and present data to related team meetings or sr management and poster presentations at external meetings, communicating effectively in both written and oral forms
Ability to make timely and sound decisions
Assimilates new knowledge skills, and job-related information that may vary in complexity, and applies them to work assignments in a timely manner

Generate different creative or novel solutions to business processes Evaluate the latest technology advances and apply to appropriate business problems


Potential for non-standard work hours (2nd or 3rd shift) during manufacturing activities
Operator gowning requirements, including full facemask or respirator

Adherence to departmental procedures and safety policies

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

Last Date to Apply for Job 27 June, 2019

N (Other) (United States of America)

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates

Profile Summary:

Employment Type : Full Time
Eligibility : Any Graduate
Industry : Biotechnology/Pharmaceutical/Medicine, Manufacturing/Industrial
Functional Area : Production/Manufacturing/Maintenance/Packaging
Role : Production/Manufacturi ng/Maintenance
Salary : As per Industry Standards
Deadline : 18th Mar 2020

Key Skills:

Company Profile:

Pfizer Incarfix

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