Recipe Author Developer

Reposted 25 Days Ago
Be an Early Applicant
Pittsburgh, PA, USA
In-Office
Mid level
Information Technology • Mobile • Software • App development
The Role
The Recipe Author Developer will gather requirements, design and validate Master Batch Records, and provide project updates while ensuring compliance with pharma processes.
Summary Generated by Built In
Company Description

We provide creative and technology services and solutions in the areas of web design, customized web applications and e-commerce solutions, Mobile App development and much more services to organizations in the All over the world.

With well defined and documented processes and practices, we ensure successful implementation of all our projects. Our teams are highly trained in best practices of web and application developments and are managed by certified project managers who ensure highest levels of process control and management.

Job Description

Recipe Author Developer
Work location: Pittsburgh, PA
Duration: 6 months+ extendable.
Work experience: 4-10 years
Mandatory Skills
Manufacturing Execution systems
Functional knowledge of Pharma processes (Weigh & Dispense, SBM etc)
Rockwell FTPS (v8.2)
Preferred Skills
MES development & deployment on other products
Worked in Agile / complete SDLC project lifecyle
Integration with other L2/L3
Job Roles/Responsibilities

1. Gathering requirements for a MBR for a Unit Procedure/Product
2. Liaising with various product (operations, validation) experts and subject matter experts to determine the requirements for the new MBR
3. Creating a standard set of instructions to support site implementations Designing and developing State Diagrams in MES
4. Determining updates for Master Data, State Diagrams, Equipment management
5. Design and creation of complex MBR for Weighing & Dispensing
6. Site specific requirement analysis for processes
7. Validation of the created MBRs for site deployment
8. Providing status updates to the Project Manager on a day to day basis on progress, issues and risks.
9. Support execution of OQ w.r.t various interfaces (SAP, scales)
10. Provide guidance on MBR related issues during validation
11. Troubleshoot and defects resolution during validation of Master Batch Records

Additional Information

All your information will be kept confidential according to EEO guidelines.

Skills Required

  • 4-10 years of experience in related roles
  • Functional knowledge of Pharma processes such as Weigh & Dispense
  • Experience with Manufacturing Execution Systems (MES)
  • Proficient in Rockwell FTPS (v8.2)
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The Company
HQ: St. Louis, MO
68 Employees
Year Founded: 2012

What We Do

We provide creative technology services and solutions in the areas of web design, customized web applications and e-commerce solutions, Mobile App development and much more services to organizations all over the world. With well defined and documented processes and practices, we ensure successful implementation of all our projects. Our teams are highly trained in best practices of web and application developments and are managed by certified project managers who ensure highest levels of process control and management.

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