Mindlance
Job Title
Scientist, Data Analytics
Location
Seattle (Dexter), WA OR Devens, MA OR Summit, NJ (50% Onsite | Hybrid)
Project Duration
12 months (Possible to extend) (W2 Contract)
Work Schedule: M-F 8-5
Position Overview:
Client is seeking a Scientist in Data Analytics within the Analytical Science & Technology (AS&T), Cell Therapy Quality (CTQ) organization. The ideal candidate will have prior experience working in data analytics and will help drive efficiencies, improvements, and alignment on common practices and strategies in support of routine GMP release and stability testing activities. The candidate will develop high quality descriptive, analytical, statistical models, insights, patterns and visualizations that can be used to improve decision making in Quality Control operations. The candidate will be responsible for ensuring compliance with current and prospective global regulatory requirements and should be aware of and adopt effective and efficient industry standard practices. Work scope will include commercial and clinical manufacturing for all manufactured cell therapy products. This role will work with IT, Quality Control, Manufacturing, AS&T and other technical functions to collect and analyze data. Global travel up to 10% of time may be required.
Duties/Responsibilities:
Provide multivariate analysis (MVA) modeling for improved analytical method understanding and robustness. Assist with script development and analytical modeling to automate data transformation and analysis. Perform data verification, transformations, preprocessing, exploratory data analysis and model development by interacting with a variety of databases and programs. Continuously monitor critical method parameters and evaluate trending events. Collaborate and support investigations by providing data and analysis Establish and support predictive process monitoring analytics Supporting proactive initiatives or investigations related to product or assay performance Responsible for documentation of all technical work both within and outside of formal document management systems. This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.
Specific Knowledge, Skills, Abilities:
Excellent knowledge of evaluating data using statistics and statistical tools, to make data driven decisions. Proficiency in major statistical software packages and programming languages (e.g., R, JMP, MINITAB, or SAS). JMP software preferred. Proficiency in Microsoft Office, specifically, Excel and Powerpoint. Experience with data mining and analysis techniques across disparate data sources. Some experience with one or more computer science languages (SQL, python, C++, Java, html/css). Dashboard development experience (Tableau, Spotfire, Domino) Self-motivated to identify and propose novel methodologies that will drive increased efficiency. Must be detail oriented with a proven track record of meeting timelines. Possess strong verbal/written communication skills to enable working with internal/external parties and/or collaborating with cross-functional teams. Knowledge of cGMPs and multi-national biopharmaceutical/cell therapy regulations.
Education, Experience/Licenses/Certificates:
Bachelors and/or Masters Degree required in scientific discipline with a technical understanding of data analytics. Minimum of 3+ years (BS) or 1+ year (MS) of industry experience in a technical data analytics role(s) supporting biopharma programs Excellent verbal and written communication skills Ability to prioritize and balance work from multiple projects in parallel
EEO:
Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.
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Scientist, Data Analytics
Location
Seattle (Dexter), WA OR Devens, MA OR Summit, NJ (50% Onsite | Hybrid)
Project Duration
12 months (Possible to extend) (W2 Contract)
Work Schedule: M-F 8-5
Position Overview:
Client is seeking a Scientist in Data Analytics within the Analytical Science & Technology (AS&T), Cell Therapy Quality (CTQ) organization. The ideal candidate will have prior experience working in data analytics and will help drive efficiencies, improvements, and alignment on common practices and strategies in support of routine GMP release and stability testing activities. The candidate will develop high quality descriptive, analytical, statistical models, insights, patterns and visualizations that can be used to improve decision making in Quality Control operations. The candidate will be responsible for ensuring compliance with current and prospective global regulatory requirements and should be aware of and adopt effective and efficient industry standard practices. Work scope will include commercial and clinical manufacturing for all manufactured cell therapy products. This role will work with IT, Quality Control, Manufacturing, AS&T and other technical functions to collect and analyze data. Global travel up to 10% of time may be required.
Duties/Responsibilities:
Provide multivariate analysis (MVA) modeling for improved analytical method understanding and robustness. Assist with script development and analytical modeling to automate data transformation and analysis. Perform data verification, transformations, preprocessing, exploratory data analysis and model development by interacting with a variety of databases and programs. Continuously monitor critical method parameters and evaluate trending events. Collaborate and support investigations by providing data and analysis Establish and support predictive process monitoring analytics Supporting proactive initiatives or investigations related to product or assay performance Responsible for documentation of all technical work both within and outside of formal document management systems. This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.
Specific Knowledge, Skills, Abilities:
Excellent knowledge of evaluating data using statistics and statistical tools, to make data driven decisions. Proficiency in major statistical software packages and programming languages (e.g., R, JMP, MINITAB, or SAS). JMP software preferred. Proficiency in Microsoft Office, specifically, Excel and Powerpoint. Experience with data mining and analysis techniques across disparate data sources. Some experience with one or more computer science languages (SQL, python, C++, Java, html/css). Dashboard development experience (Tableau, Spotfire, Domino) Self-motivated to identify and propose novel methodologies that will drive increased efficiency. Must be detail oriented with a proven track record of meeting timelines. Possess strong verbal/written communication skills to enable working with internal/external parties and/or collaborating with cross-functional teams. Knowledge of cGMPs and multi-national biopharmaceutical/cell therapy regulations.
Education, Experience/Licenses/Certificates:
Bachelors and/or Masters Degree required in scientific discipline with a technical understanding of data analytics. Minimum of 3+ years (BS) or 1+ year (MS) of industry experience in a technical data analytics role(s) supporting biopharma programs Excellent verbal and written communication skills Ability to prioritize and balance work from multiple projects in parallel
EEO:
Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.
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