MSD

About MSD

The Associate Director, Process Engineering within Global Engineering Solutions (GES) will lead capital project Process Engineering deliverables ranging from early pre-charter activities, to process design & specification, and through commissioning & qualification, process implementation & realization of the solution. The Associate Director will participate in a high performing team as Process Lead and be responsible for implementation of capital project scope, application of Lean methods, and execution of technical studies that support our business objectives. The Associate Director also provides consulting to peer projects and network initiatives. 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. Due to continued growth and investment, we are hiring an Associate Director, Process Engineering within GES supporting the Capital Project Portfolio. The Associate Director will support a portfolio of capital projects and initiatives for the Large Molecule (Biologics/Vaccines/Sterile) Line of Business, with initial assignments supporting Sterile Drug Product Projects. A preferred candidate will have appropriate subject matter expertise in Isolated Filling and/or Lyophilization applications and is expected to maintain advanced technical knowledge in their respective area(s) of expertise. In addition to initial assignment(s), the Associate Director will have opportunities to support the wider portfolio of Biologics, Vaccines, and Sterile needs, as well as to be exposed to multiple business areas. The Associate Director will exhibit advanced leadership, interpersonal & communication skills, and provides guidance to assigned engineers. Successful performance requires advance technical knowledge in own field, knowledge in a variety of other areas including new products, processes, systems and facilities, and imaginative and innovative approaches to new and diverse problems. POSITION RESPONSIBILITIES Responsible for development of project scope, front-end planning, and providing innovative designs & solutions that meet business objectives Provides technical guidance during project, assesses viability of technology in proposed configuration, verifies adherence to our company standards and practices, and ensures deliverables are technically sound Leads preliminary designs, including P&ID development and HAZOP facilitation Provides leadership during project implementation, including Commissioning & Qualification Collaborates with other Integrated Project Team members and directs the work of vendors/suppliers in preparation of project related deliverables. Participate in the development and review of engineering guidelines, standards, safety/environmental policies, and change requests. Skills Creative, innovative, thinks outside of the box, self-motivated, applies problem-solving skills, and solid base in engineering fundamentals and equipment troubleshooting Demonstrated leadership and teamwork skills. Ability to get results in a cross functional environment and has ability to effectively collaborate with and influence partners. Effective written and verbal communication skills Project/Time Management skills which deliver on-time and quality work Travel Requirement Percent of travel: >30% for projects assignments outside of primary location. Travel and flexibility in project assignment location is required; assignments may require short term travel assignments Reporting Structure This role will report to the Director, Process Engineering, GES. Qualifications, Knowledge & Experience Bachelor of Science degree (or higher) in Engineering or applicable Science Minimum 8 years Pharmaceutical/Biotech industry in engineering, technology and/or manufacturing in biologics or vaccines. Advanced understanding of isolated filling and/or lyophilization unit design & operations, including hygienic, CIP, SIP design and unit operations familiarity. Experience in Large Molecule unit operation design, startup, and/or operation is preferred. Experience with equipment life cycle approach and Capital Management stage gate process Our Manufacturing & Supply Division is committed to be the most trusted supplier of bio-pharmaceuticals worldwide. Our facilities, along with our external contractors, suppliers, and partners, create an interdependent global manufacturing network that’s committed to delivering a high quality, reliable supply to customers and patients on time, every time. We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace. Who we are … We are a global biopharmaceutical leader with a diverse portfolio of prescription medicines, oncology, vaccines and animal health products. We are driven by our purpose to develop and deliver innovative products that save and improve lives. With 69,000 employees operating in more than 140 countries, we offer state of the art laboratories, plants and offices that are designed to Inspire our employees as we learn, develop and grow in our careers. We are proud of our 125 years of service to humanity and continue to be one of the world’s biggest investors in Research & Development. What we look for … In a world of rapid innovation, we seek brave Inventors who want to make an Impact in all aspects of our business, enabling breakthroughs that will affect generations to come. We encourage you to bring your disruptive thinking, collaborative spirit and diverse perspective to our organization. Together we will continue Inventing For Life, Impacting Lives while Inspiring Your Career Growth. INVENT. IMPACT. INSPIRE. THE COMPANY As a company we are committed to ‘Inventing for Life’ in all that we do. We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world’s most challenging healthcare needs. OUR COMMITMENT TO IRELAND In Ireland we are one of the country’s leading healthcare companies, having first established here over 50 years ago. We currently employ over 2,200 people, across four sites in Ballydine, Co Tipperary, Brinny, Co Cork, Carlow and Dublin and, in addition, operate substantial Human Health (Commercial) and Animal Health businesses. To date, we have invested $2.5 billion in our Irish operations and our annual turnover ranks us as one of Ireland’s top 20 companies. Currently, our Irish sites manufacture approximately half of our companies top twenty products, saving and enhancing lives around the world. Our Brinny site in Cork is a leading facility for the development, testing and manufacturing of new biologics and vaccines, exporting to over 90 countries across the world. With a team of approximately 500 people, the Brinny site specialises in the late-stage development and commercial supply of biotech products, including some of the company's most successful and life-changing treatments for oncology, hepatitis C and rheumatoid arthritis. The Brinny site has been a vibrant part of the local Innishannon community for nearly 35 years and is now one of the region’s largest employers. The Company has invested €130m in the site since 2016 as a result of increased global demand for medicines and vaccines which will see the Brinny site further expand its production facilities and capacity to meet this demand. We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace. Search Firm Representatives Please Read Carefully Merck & Co., Inc., Kenilworth, NJ, USA, also known as Merck Sharp & Dohme Corp., Kenilworth, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: No relocation VISA Sponsorship: Travel Requirements: 25% Flexible Work Arrangements: Shift: Valid Driving License: Hazardous Material(s): Number of Openings: 1 Requisition ID:R42306

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Company Info

Legal Form: S A DeCV

Company Type: Public

Company Size: 5001 - 10000

Revenue: ~ 10 million (USD)

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