Pfizer Associate Technology Scientist/Associate Process Engineer I in Andover, Massachusetts
The Associate Technology Scientist/Associate Process Engineer I will provide oversight and support for manufacturing process monitoring for a suite/product, which requires basic project and meeting management skills. This position is responsible for performing and facilitating root cause analyses for process monitoring flags following the basic Six Sigma methodology. This individual will work closely with Manufacturing and Quality Control Analytical colleagues to observe and understand operations and methods to determine the potential sources of variability. The information gained while observing the processes will be the fundamental knowledge to assist with root cause analyses of the process monitoring flags.
This position offers an excellent opportunity to learn the Biotechnology drug substance manufacturing process and Quality Control Analytical methods, as well as an opportunity to be trained in the Six Sigma methodology, with the potential to work towards Six Sigma Certifications.
Regular review of applicable data and control charts to understand how process is performing and looking for incomplete data
Facilitate weekly cross functional process monitoring meetings, tracking flag progression and resolution
Perform initial assessment of flags prior to process monitoring weekly meetings by facilitating communications with manufacturing operators and quality control analysts
Perform root cause analysis of process monitoring flags using the Six Sigma methodology. This activity may be performed independently or as part a small cross functional team of subject matter experts. Some flag evaluations may be complex and advanced Six Sigma projects which provide an opportunity for learning more advance Six Sigma techniques and receiving formal Six Sigma Green or Black belt training
Identify and communicate changes and improvements for the univariate and multivariate process monitoring charts to STS system owner, including establishing and maintaining statistical limits
Work closely with STS Continued Process Verification SMEs to ensure process monitoring process meets requirements and works to optimize overall process to ensure it is efficient and effective
Assist with maintenance of univariate and multivariate monitoring models as needed
Observe and understand manufacturing unit operations and quality control analytical methods as needed
Communicate outcomes for process monitoring program to the appropriate stakeholders
BS in Engineering, Science or related discipline with no experience or equivalent combination of education and experience
MS in unrelated discipline with no experience or equivalent combination of education and experience
Solid understanding of Biotech Drug Substance Manufacturing processes
Basic knowledge of GMPs
Basic statistical data analysis skills
Basic project and meeting management skills
Excellent problem solving skills
Excellent attention to detail and communication skills, including both verbal and written.
Solid computer skills, including data extracting, querying, cleaning, manipulating (e.g., stack, split, join) and analyzing data
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.
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Other Job Details:
- Last Date to Apply for Job: 1/21/2019 Eligible for Employee Referral Bonus
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.