Job Description: Develops and validates manufacturing processes for drug products, including new or revised dosages or presentations, taking into consideration problems inherent in the transfer of technology from research, other sites, or other areas within the site to production. Conducts tests and measurements throughout the stages of production to determine control over applicable variables. Job Responsibilities: Ensures that projects are completed on schedule following established procedures and schedules. Work is performed independently, with only general direction. Recommends actions and independently determines and develops approach to solutions. Contributes to the completion of specific programs and projects. Decisions frequently impact the department/project team and delivery of objectives. Applies technical expertise to develop solutions to a wide range of problems of varying complexity, may refer to precedents and policies. Job Requirements: Demonstrated ability to interact effectively with all levels of the organization including diverse educational and cultural backgrounds. Ability to perform laboratory studies and analyze and interpret data from a variety of sources. Excellent written and oral communication skills Strong aptitude for learning process technology and equipment Bachelor’s degree in Engineering (Chemical, Mechanical, Industrial, Biomedical Engineering) or Life Sciences (Chemistry, Biochemistry, Microbiology) & a minimum of 5 years of relevant manufacturing experience OR a master’s degree in engineering or science and a minimum of 3 years of relevant manufacturing experience. Experience in formulation, process development, or manufacturing Job Details: Company: Pfizer Vacancy Type: Full Time Job Location: Grand Rapids, MI, US Application Deadline: N/A Apply Here careers-trivia.com
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