MES Integration Lead

We are seeking an experienced

MES Integration Lead

to support the integration of manufacturing equipment with our

Manufacturing Execution System (MES)

in a highly regulated pharmaceutical environment. This role will work closely with

site engineering, automation, and manufacturing teams

to deliver robust, GMP-compliant MES solutions that support digital manufacturing and electronic batch record initiatives.

Key Responsibilities Provide

technical leadership and guidance

for the integration of manufacturing equipment with the MES platform. Own and manage the

MES integration roadmap, integration pack, and key deliverables

. Collaborate with

site engineering leads, automation engineers, and manufacturing teams

to ensure successful MES deployment. Facilitate and drive

Agile planning and delivery

for MES integration projects. Analyse and resolve

technical issues related to MES integration and system performance

. Lead the creation and management of

URS, FRS, and MES software documentation

. Oversee

software configuration, coding activities, and MES documentation practices

. Ensure compliance with

cGMP regulations and validated computer system lifecycle requirements

. Coordinate with

MES platform providers, engineering contractors, and equipment vendors

across the project lifecycle.

Required Skills & Experience 10+ years’ experience in MES integration

, ideally within pharmaceutical or life sciences manufacturing. Strong experience with

MES platforms, particularly Rockwell FactoryTalk PharmaSuite (FTPS)

. Proven ability to

configure, customise, and extend MES platforms

for GMP-compliant manufacturing processes. Experience integrating MES with

ERP, LIMS, SCADA, and shop-floor equipment

. Strong knowledge of

industrial communication technologies such as APIs, OPC UA, and middleware solutions

. Advanced

SQL expertise

, including stored procedures and database management. Experience with

scripting languages such as Python or JavaScript

for automation and reporting. Deep understanding of

pharmaceutical manufacturing workflows

, including: Electronic Batch Records (EBR) Weigh & Dispense Batch execution processes Strong knowledge of

cGMP requirements and validated computer system lifecycle practices

.

What We’re Looking For A proactive

technical leader with strong collaboration skills Experience working in

cross-functional engineering and IT teams Passion for

digital manufacturing and Industry 4.0 transformation If you're an experienced

MES professional looking to lead complex integration projects in a regulated manufacturing environment

, we’d love to hear from you.