Sr. Specialist, Engineering (m/f/d)

MSD; Italia; Hybrid; GBP 70,000 - 95,000; Full time

Job summary

MSD is seeking a highly motivated engineer to support sterile drug product manufacture within our External Manufacturing Network in Europe. You will work with strategic partners and senior management to drive technical excellence across multiple facilities, ensuring robust sterilization, validation, and process transfer.

You will lead technical issues, support regulatory inspections, and champion continuous improvement in a global, fast-paced environment with approximately 25% travel.

Qualifications

• Bachelor's degree in engineering or related discipline.
• 7+ years of relevant work experience in manufacturing, startup, and/or tech transfer.
• 3+ years in sterile/aseptic Drug Product processing including formulation and filling.
• Experience in Relationship Management

Responsibilities

• Manage technical issues related to global external manufacturing of commercial Drug Product.
• Provide technical leadership within Technical Operations for sterile Drug Product management.
• Support technical transfers of new sterile Drug Product to contract manufacturing sites.
• Drive change with state-of-the-art technology and processes.
• Lead resolution of technical issues within product lines or major projects.
• Provide leadership for day-to-day technical activities in commercial manufacturing.
• Interface between Technical Operations and third-party drug product manufacturers.
• Support Change Controls, investigations, and CAPAs; assist inspections.
• Lead and coordinate critical technical projects in sterile manufacturing.
• Coordinate cross-functional investigations and CAPA/change control implementations.

Skills

Change Control

GMP Knowledge

Process Validation

Tech Transfer

Project Management

Regulatory Compliance

Risk Management

Root Cause Analysis

Cross-functional Collaboration

Strategic Thinking

Documentation

Education

Bachelor's degree in Engineering

Job description

Job Description

Our Large Molecule Technical Operations Unit is seeking a highly motivated individual to fill an open position to support sterile drug product manufacture within our External Manufacturing Network in Europe. This is an exciting opportunity to work with key strategic external partners, grow technical experience in sterile manufacturing, and work on high visibility network initiatives with direct access to senior management. Our team strives to provide technical excellence in our work and be strong partners, collaborators, and leaders within the large molecule lines of business at our company.

Our Engineers support internal and external manufacturing operations remain operational, continuously improve and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation.

Primary responsibilities

• Manages technical issues relating to the global external manufacturing of commercial Drug Product.
• Provide technical leadership within Technical Operations group for the management of sterile drug product.
• Support technical transfers of new sterile drug product to our contract manufacturing sites.
• Driving change both internal and external ensuring state of the art technology and processes are implemented and maintained.
• Lead to resolve technical issues relating to a product line or major technical projects within Technical Operation.
• Provide direct leadership for day-to-day technical activities for commercial drug product manufacturing –i.e., trouble shooting, process changes and improvements, new manufacturing technology implementation etc.
• Lead and act as the primary interface on technical issues between Technical Operations and third-party drug product manufacturers.
• Provide technical leadership on Change Controls, investigations, and CAPAs and support of Health Authority Inspections.
• Support / Lead critical technical projects relating to the manufacturing of commercial sterile drug product.
• Organize and lead ad hoc cross functional teams to manage investigations and implementation of CAPA and change controls.
• Coordinates and manages risk assessments and develops solutions to complex issues that require a high degree of ingenuity, creativity and innovation. Requires understanding and application of principles, concepts, practices and standards that govern the manufacturing of sterile products.
• This role includes approximately 25% travel.

Qualifications

Education and Minimum Requirements

• Bachelor’s degree in engineering, biological/chemistry sciences or related discipline
• A minimum of 7 years of relevant work experience in manufacturing, in the areas of process start up, routine manufacturing and/or technical transfer.
• A minimum of 3 or more years of experience in sterile/ aseptic Drug Product processing including formulation and filling.
• Experience in Relationship Management

Required Skills and Experience

• Ability to work effectively across boundaries to build strong collaborative relation with other internal teams, such as; Global Technical Operations, Sterile, External Services partner groups, Small and Large Molecule Sites and external partners.
• Strong professional and interpersonal communication skills are also required.
• Must be able to multi-task and work within tight deadlines.
• Flexibility and the ability to work independently as well as excellent organizational skills.
• Strong knowledge of Quality systems, Change Control Drug Product Manufacturing and Validation
• Strong analytical problem-solving skills, root cause analysis and risk assessment/mitigation
• Proven team building skills
• Excellent command of English (both written and oral).

Preferred Experience and Skills

• Experience managing direct reports (none assigned to the role at the moment)
• Lean Manufacturing / Six Sigma Experience
• Project management experience
• Knowledge of worldwide regulatory requirements, experience supporting regulatory inspections.

Additional location(s) Compensation Information

The base salary range for the additional location (Italy) of this position is: (EUR 45`300 - 77`000)

This range reflects the Company's reasonable expectation of the base salary applicable to this role at the time of posting. This will be based on an individual’s experience, skills, effort, responsibilities, organization needs and compensation levels within their peer group. If applicable, employees may also be eligible for annual bonus and long-term incentives or other benefits. This role is part of a collective bargaining agreement / national collective labor agreement. Our Talent Acquisition team will provide further information to you, if applicable. The applicable NCBA is CCNL Chimico-Farmaceutico, Classification ‘Quadro’, Level A3.

Required Skills

Business Agility, Change Control Processes, Controls Management, Cross-Functional Project Management, Customer-Oriented, Deviation Management, Good Manufacturing Practices (GMP), Manufacturing Process Validation, Manufacturing Production, Multitasking, Process Innovation, Process Optimization, Regulatory Compliance, Relationship Management, Risk Avoidance, Root Cause Identification, Schedule Adherence, Strategic Thinking, Task Management, Technical Support, Technical Transfer

Employee Status: Regular

Relocation: No relocation

VISA Sponsorship: No

Travel Requirements: 25%

Flexible Work Arrangements: Hybrid

Shift: Not Indicated

Valid Driving License: No

Hazardous Material(s): N/A

Job Posting End Date: 10/31/2026*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.