Manufacturing Program Manager

We are seeking an experienced Program Manager – Manufacturing IT to lead and deliver complex IT programs that support pharmaceutical manufacturing operations. This role is responsible for overseeing multiple cross-functional initiatives, including Manufacturing Execution Systems (MES), automation, data integrity, and regulatory compliance programs, ensuring alignment with business objectives, GMP standards, and global IT strategies.

The ideal candidate will bring a strong background in program management, combined with extensive knowledge of pharmaceutical manufacturing systems, regulatory requirements (GxP, FDA, EMA), and digital transformation initiatives.

Position: Program Manager Manufacturing IT

· Location : Maccesfield / Luton / Cambridge - 3 days onsite & 2 days remote

· Start: ASAP

· Duration: 6 months+ Possible extension

· Rate : £ Outside IR 35

· Languages: English

Key Responsibilities

Program Leadership & Strategy

Lead the end-to-end delivery of Manufacturing IT programs across multiple sites and regions.

Define program scope, roadmap, governance structure, and success metrics aligned with business and IT objectives.

Partner closely with Operations, Quality, Engineering, and other business stakeholders to prioritize and execute strategic initiatives.

Drive digital transformation initiatives, including Industry 4.0, smart manufacturing, and advanced data analytics programs.

Project & Portfolio Management

Manage a portfolio of IT projects, including MES implementations, LIMS integrations, ERP interfaces, and manufacturing automation systems.

Ensure projects are delivered on schedule, within budget, and in accordance with defined quality standards.

Establish and maintain effective program governance, reporting frameworks, risk management processes, and escalation procedures.

Oversee relationships with external vendors, consultants, and system integration partners.

Regulatory Compliance & Quality

Ensure all Manufacturing IT programs comply with GxP regulations and applicable FDA, EMA, and global regulatory requirements.

Promote and enforce data integrity principles (ALCOA+) and validation standards (CSV/CSA) across all systems and processes.

Collaborate with Quality Assurance, Validation, and Compliance teams to support audits, inspections, and regulatory submissions.

If you are looking for a new contract opportunity kindly share your CV - npawar@redglobal.com

Thanks,

Nisha