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Pfizer · 4 days ago

Sr. Associate Manufacturing Engineer (M - F)

United States - North Carolina - Sanford

Full-time

Onsite

Entry, Mid Level

$83K/yr - $134K/yr

2+ years exp

Pfizer is a leading pharmaceutical company dedicated to delivering medicines to patients globally. The Sr. Associate Manufacturing Engineer will play a crucial role in the design and development of manufacturing processes, ensuring operational efficiency and quality in production.

BiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine

No H1B

Responsibilities

Serve as the manufacturing area's technical SME, providing expertise in fields such as the process, equipment, automation, documentation

Act as a Manufacturing Point of Contact for operator-support and issue resolution

Acts as a departmental liaison with primary support groups such as engineering, technical services, quality control, quality assurance, development, and utilities and collaborate with the aforementioned groups to ensure a robust manufacturing operation

Capable of identifying technical problems and solving them with minimal guidance. Ability to analyze operational process issues and automation challenges to recommend / initiate appropriate corrective and preventative actions

Expertise in the Standard Work Plan and ability to coordinate batch activities with other Process Centric Teams (e.g., other manufacturing groups, Tech Services, QC, QA) to meet plan of record

Coordinate activities with maintenance to schedule routine work and to resolve corrective mechanical issues without impacting production operations

Act as AMPS (Agile Manufacturing Production System) subject matter expert for process. Author- change requests and participate in design reviews

Spend time on the production floor to proactively identify areas for improved efficiencies and ensure that product quality is maintained through all phases of production including operational parameters of manufacturing equipment, automation control, processing dynamics, and integrated utilities to identify and resolve quality, and technical, risk to manufacturing

Support batch record and SOP revisions, commitment ownership, project management and investigations as needed. Review and contribute to applicable documentation (i.e. MBRs, SOPs, etc)

Participates in process operational improvements

Know the processes and procedures, including the principles and practices of good data management (ALCOA), and be able to guide, advise, and coach their teams

Qualification

Manufacturing Process DesignTechnical Problem SolvingFDA Regulations KnowledgeAutomation Control SystemsLean Manufacturing PrinciplesSix Sigma MethodologiesMicrosoft ApplicationsTeam CollaborationLeadership Abilities

Required

Applicant must have a Bachelor's degree with at least 2 years of experience; OR a Master's degree with 0+ years of experience; OR an associate's degree with 6 years of experience; OR a High school diploma (or equivalent) and 8 years of relevant experience

Demonstrated ability to provide technical solutions for complex problems through equipment and process understanding

Working knowledge of Food and Drug Administration Regulations and Good Manufacturing Practices

Requires general knowledge of scientific principles, technical knowledge of production equipment, automation control systems, processing requirements and any related procedural requirements with emphasis on assigned production area

Proficiency in Microsoft Applications

Ability to work effectively in a team environment and collaborate with cross-functional teams