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Associate, Oncology Operations

Pfizer


Location:
Pearl River, NY
Date:
03/24/2017
Job Code:
1049025-1852
Pfizer
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Job Details

Job Title Associate, Oncology Operations

JobID 1049025-1852

Location: Pearl River, NY

Description *About Pfizer*

A career at Pfizer offers opportunity, ownership and impact.All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to impact the health and lives of millions of people. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives.



*Role 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 incumbent's projects. Actively develop technical and operational leadership on all aspects of the manufacturing operations and contribute to the success of the department.



*Responsibilities*

*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, etc. Heavy "hands-on" operations and irregular work schedules occasionally required. Function as a member of self-directed high performance team.*Perform manufacturing of commercial and clinical batches in compliance with cGMP, Safety, and Environmental regulations. Meet the production demand. Ensure all Investigations and commitments are performed in a timely manner. Ensure 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 changes. Evaluate 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 solutions. Work 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 procedures. Incorporate cGMP and regulatory compliance into all assigned projects scope and design.*Provide project team support as required by team leads.



*Qualifications*

*BS in Chemical Engineering or related scientific discipline*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 requiredPHYSICAL/MENTAL REQUIREMENTS *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.NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS *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.



*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.





*Associate, Oncology Operations*
*Pearl River, New York*
*1049025-1852*


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