These roles sit at theintersection of operations, engineering, and digital/automation systems, and weare keen to review relevant profiles from your end.
.Please note that all roles needto be filled within one month. Kindly share only serious and suitablecandidates.
Kindly find the open positionsbelow.
Role 1: Operations Engineer
Key Responsibilities:
- Support and manage production equipment (e.g., pH meters, weighing scales)
- Handle single-use systems (SUS) in manufacturing
- Coordinate incoming material readiness
- Drive process qualification (PQ) execution
- Support DeltaV system operations (basic troubleshooting, run logic understanding)
- Work with SAP for production coordination
Requirements:
- 5+ years in biopharma manufacturing
- Strong GMP operations & qualification exposure
- Hands-on shopfloor and equipment experience
- Familiarity with DeltaV / automation environments
Role 2: MSAT Engineer - CleaningValidation
Key Responsibilities:
- Lead cleaning validation strategy
- Design and optimize CIP (Clean-in-Place) processes
- Develop GMP-compliant cleaning approaches
- Collaborate with Operations & QA on validation execution
Requirements:
- 5-8 years of experience
- Strong expertise in cleaning validation & process science
- Ability to translate scientific approach into site execution
Role 3: MSAT Engineer - EquipmentSupport
Key Responsibilities:
- Provide technical support for process equipment
- Drive optimization and troubleshooting of UF & centrifugation systems
- Support process performance and equipment readiness
- Work closely with automation (DeltaV) and operations teams
Requirements:
- 5-8 years in biopharma manufacturing
- Strong knowledge of:
- Ultrafiltration (UF)
- Centrifugation systems
- Hands-on DeltaV exposure
- Strong ability to bridge process + equipment + automation
Role 4: Process Engineer - PharmaSuite /Catalyst
Key Responsibilities:
- Configure and support MES workflows within PharmaSuite / Catalyst
- Support electronic batch record (EBR) design and execution
- Work closely with operations, QA, and IT teams for system integration
- Perform testing, validation, and troubleshooting of MES workflows
- Support change control, system upgrades, and hypercare activities
Requirements:
- 4-8 years of experience in MES within pharma manufacturing
- Hands-on experience with PharmaSuite / Catalyst systems
- Strong understanding of GMP, ISA-95, and batch processes
- Exposure to system interfaces (ERP / DeltaV / PLC) and validation lifecycle
Role 5 : DeltaV Engineer - DeltaVprotocols, basic control modules to recipe design.
Key Responsibilities:
- Develop and configure DeltaV control modules (CM), equipment modules (EM), and basic phase logic
- Support recipe design and configuration aligned to ISA-88 batch standards
- Assist in DeltaV protocol development, testing, and documentation
- Support commissioning, IO checks, and troubleshooting during manufacturing operations
- Work closely with process, QA, and validation teams to ensure compliant system delivery
- Support change control, system upgrades, and hypercare activities
Requirements:
- 3-5 years of hands-on experience in Emerson DeltaV within pharma/biotech manufacturing
- Strong fundamentals in control modules, equipment modules, and batch/recipe configuration
- Exposure to DeltaV protocols, testing (FAT/SAT), and commissioning activities
- Understanding of GMP, GAMP5, and ISA-88 batch processes
- Basic knowledge of system integration (MES / PLC / ERP interfaces) preferred
- Good troubleshooting mindset and ability to support live operations
