Principal SAP Technical Architect, GMP Systems at Cellares

South San Francisco, California, United States

Apply Now

Not SpecifiedCompensation

Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level

Full TimeJob Type

UnknownVisa

Biotechnology, ManufacturingIndustries

Requirements

Bachelor’s degree in Computer Science or a related technical field
Minimum of 10+ years of experience within IT in a cGMP environment in the biotech/biopharma industry, including at least 5 years of leadership or lead developer experience
Strong, hands-on experience in SAP development, including ABAP programming, Fiori/UI5 app development, and related SAP technology stacks
Experience in interface development and management using platforms such as MuleSoft, Workato, or similar integration tools
Experience implementing and supporting Manufacturing, Quality, and Supply Chain applications, including ERP, MES, LIMS, QMS, etc
Ability to manage shifting priorities to meet critical deadlines in a fast-paced and dynamic environment while maintaining clarity of focus
Proven ability to deliver results independently with a proactive, hands-on approach to technical problem solving
Demonstrated success in building scalable, compliant, and supportable GMP systems with minimal supervision
Strong analytical and critical thinking skills with a detail-oriented mindset
Excellent teamwork and interpersonal skills; ability to communicate technical concepts to non-technical stakeholders
Strong written and verbal communication skills
Self-motivated with a passion for the role (inferred from description)

Responsibilities

Serve as a hands-on technical expert across SAP systems, actively engaging in ABAP programming, Fiori app development, SAP Basis administration, and SAP Security roles and authorizations
Participate in design, development, debugging, performance tuning, and deployment activities to ensure stable, secure, and scalable solutions
Develop and maintain a comprehensive technical blueprint for GMP systems, aligning technology services with business objectives and regulatory requirements
Provide architectural leadership in resolving inter-program and inter-project issues related to GMP systems
Partner with the IDMO Business to develop and execute against an IT roadmap and deliver on the IT infrastructure needed to manufacture autologous and allogeneic cell therapy products
Work closely with Validation and Quality in deploying and supporting IT GMP Systems
Manage and coordinate employees, contractors, and agencies involved in development projects to ensure alignment with project goals, timelines, budgets, and quality standards
Establish KPIs, monitor progress, and keep critical stakeholders informed of progress for IT projects and strategic initiatives
Establish key stakeholder relationships with internal and external stakeholders
Work closely with other functional areas to develop and execute against the strategic plan for all Cellares sites
Serve as a subject matter expert (SME) during audits or inspections by regulatory authorities

Skills

ABAP

Fiori

SAP Basis

SAP Security

MuleSoft

Workato

SAP Architecture

Cellares

Develops and manufactures cell therapies efficiently

About Cellares

Cellares develops and manufactures cell therapies in the biotechnology sector, operating as an Integrated Development and Manufacturing Organization (IDMO). Its proprietary "Smart Factory" technology features an automated single-use cartridge system, which increases productivity and reduces costs and process failures compared to traditional methods. The company serves a range of clients, including pharmaceutical companies, and aims to provide efficient and cost-effective manufacturing services for cell therapies. Cellares stands out by combining development and manufacturing processes under one roof, making it a competitive option in the industry.

South San Francisco, CaliforniaHeadquarters

2019Year Founded

$345.3MTotal Funding

SERIES_CCompany Stage

Industrial & Manufacturing, BiotechnologyIndustries

201-500Employees

Benefits

Health Insurance

Dental Insurance

Vision Insurance

401(k) Company Match

Stock Options

Risks

Emerging biotech startups threaten Cellares' market share with similar solutions.

Potential regulatory delays could impact scaling of new automated systems like Cell Q.

Supply chain vulnerabilities may disrupt production timelines for Cell Shuttle and Cell Q.

Differentiation

Cellares' Cell Shuttle offers 10x scalability over manual cell therapy manufacturing.

The Smart Factory technology integrates development and manufacturing, unlike traditional CDMOs.

Cell Q automates QC processes, addressing bottlenecks in cell therapy quality control.

Upsides

Partnership with Sony enhances precision in cell therapy manufacturing processes.

Strategic partnership with Bristol Myers Squibb provides financial boost and validation.

Ossama Eissa's appointment as COO accelerates global expansion and operational capabilities.

Land your dream remote job 3x faster with AI

Try Jobo Free