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Bioassay Development Scientist, Biosimilars Pharm Sci

Pfizer


Location:
Lake Forest, IL
Date:
04/17/2018
2018-04-172018-05-18
Pfizer
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Job Details

**ROLE SUMMARY**



Join one of the leading Biosimilars Pharmaceutical Sciences organizations in the industry. As a leader in the biosimilars sector with approved products in the U.S. and Europe and an industry-leading biosimilars pipeline, Pfizer offers an exciting opportunity for a strong scientist to join our global Biosimilars Analtyical R&D team. We currently have an opportunity for a bioassay scientist with a strong organizational and communication skills and experience in critical reagent management to join our global Biosimilars Pharmaceutical Sciences team in Lake Forest, IL.







The Scientist, Bioassay Development will manage global inventory in LIMS (including requesting shipment of biological materials) write study plans, protocols and reports to support maintenance and re-supply of critical reagents. He or she is a technical expert in one or more bioassay development areas (cell biology, molecular biology or immunology). He or she will participate in developing assay test methods and will generate and critically evaluate scientific data. He or she will be accountable for ensuring that experiments, analytical methods and data meet the requirements for the intended use of the data, which includes characterization, assessment of biosimilarity and comparability assessment as well as method development, optimization and qualification of methods.







**ROLE RESPONSIBILITIES**



The Scientist (Critical Reagent and Reference Standard Coordinator) will manage global inventory in LIMS (including international shipping of biological materials) write study plans, protocols and reports to support maintenance and re-supply of critical reagents. He or she will develop or evaluate tools for effective inventory management. He or she will follow good documentation and review practices, and effectively communicate scientific results and strategies in presentations and written reports. A high level of attention to detail is required.



He or she will participate in activities to support the biosimilar pipeline within established timelines and ensure the quality and integrity of data. He or she will participate in method development, optimization, qualification and validation as needed and ensure that methods are able to consistently meet the accuracy and precision required to support process development, similarity assessment and manufacturing. He or she will critically evaluate scientific literature and industry trends and will work with a continuous improvement framework.







**QUALIFICATIONS**







+ B.S. and 5 + years of relevant experience OR M.S. and 2+ years of relevant experience OR Ph.D with 0 years of relevant experience.



+ Must have a high level of attention to detail and be very organized.



+ Must have good oral and written communication and scientific documentation skills.



+ Experience with electronic laboratory notebook and LIMS systems is desired.



+ Demonstrated experience in working effectively in cross-functional and multi-geographic teams is highly desirable.







**PHYSICAL/MENTAL REQUIREMENTS**



Standing or sitting for several hours. Ability to lift 40 pounds. Data capture, organization, analysis and presentation using commercially available software such as GraphPad, JMP, PLA, SoftMax Pro, Excel, Microsoft Powerpoint, eLN and Sharepoint.







**NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS**







Flexibility in schedule to accommodate diverse time zones is required. This position requires understanding of and adherence to aseptic technique and biohazard safety guideline including wearing PPE. Job requires inventory of items which are stored in ultracold conditions.







**OTHER INFORMATION**







+ Eligible for relocation package



+ Eligible for employee referral bonus



+ Posting expiration date: Thursday, May 3, 2018







**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.







**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.



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