Recipe Author

Pfizer • Kalamazoo, MI

3d • Onsite

About The Position

The recipe author will become proficient with the standard functionality of MES (Manufacturing Execution System) PharmaSuite and work with production units to convert paper records to EBR (Electronic Batch Record). The EBR recipe author will focus on authoring and configuring master batch records, templates, revisions, validation and change controls of EBR Recipes at the Kalamazoo Manufacturing Site.

Requirements

• Applicant must have a bachelor's degree with 0+ years of experience; OR an associate's degree with 4 years of experience; OR a high school diploma (or equivalent) and 6 years of relevant experience.
• Pharmaceutical experience
• HTML, Java, or object-oriented programming.
• Focused in Systems Analyst/Data Management.
• EBR/MES build experience.
• Experience working in Quality Tracking Systems.
• Ability to perform mathematical calculations and ability to perform complex data analysis
• Candidates must be authorized to be employed in the U.S. by any employer.
• This position requires permanent work authorization in the United States.

Nice To Haves

• Certifications: M1, Yellow Belt and/or Pfizer Human Performance methodology.

Responsibilities

• Design, preparation and revision of Electronic Batch Records (EBR).
• Supporting end users on EBR execution and usage.
• Manage EBR design and configuration changes, process reviews and alignment with associated documentation used to the continuity plan.
• Initiating and own change controls related to documents and equipment.
• Ensuring their closure and implementation of changes within specific time.
• Participate in process mapping of business processes.
• Engagement of SME’s, Leads and Operators to ensure critical parameters are being captured.
• Point of contact for electronic batch record manufacturing issues as part of sustainment team.
• Escalation of electronic manufacturing execution issues to subject matter expert or supporting team.
• Having thorough knowledge of manufacturing execution system (MES), recipe design, baseline configuration, create and execute functional verification protocols.
• Act as part of sustainment team to support continuous improvement and batch record changes as applicable.
• BT ticket follow ups and ensuring its resolution with EBR Issues.
• Ensure all the performed activities comply with respective procedures.
• Identify deviations/exceptions and escalate to leadership by appropriate procedures.
• Adherence to safety procedure/GMP & GDP practices.
• Reassess and participate in an agile change environment to enhance the process at intervals to eliminate non-value-added activities and drive continuous improvement including supporting projects and deployments.
• Participate in cross functional teams to support, enhance, and upgrade AMPS.
• Ensure compliance of operations to cGMP, safety and Pfizer integrity principles at all stages of activity
• Assist Manager in controlling tracking and periodic EBR procedure updates and manages emergency changes appropriately.
• To attend the training of all applicable procedures as per schedule.
• Colleague will be responsible for cross training to be able to support all AMPS areas being deployed or sustained.

Benefits

• 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
• paid vacation, holiday and personal days
• paid caregiver/parental and medical leave
• health benefits to include medical, prescription drug, dental and vision coverage.
• Relocation assistance may be available based on business needs and/or eligibility.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Associate degree