Job description

This is a hybrid position requiring team members to be onsite 3 days a week.This position offers relocation assistance. At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future? There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families. We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts. Job Summary Reporting to the Director, Global Device Manufacturing & Technology, this role will support the engineering and commercial teams within the Device network in West. This role is responsible for the coordination of the technical RFQ (Request for Quotation) and Development Agreement process within the global engineering functions (Manufacturing Assembly Automation & Injection Moulding). This role will have functional responsibility for compiling the manufacturing strategy and costs associated with the RFQs and Internal DAs. Essential Duties and Responsibilities • Responsible for leading key activities within the Global Device Engineering Group specifically related to the quotation of commercial bids and development agreements. • Work with internal stakeholders across global sites to understand customer & business needs and translate to technical outputs and costs. • Identifying deliverables, time and cost, setting priorities and reporting to meet the needs of the business and the customer. • Responsible for the co-ordination and preparation of commercial bids within the engineering function for new business within existing and new accounts, including coordinating cross functional teams in support of this process. • Establish relationships with equipment suppliers in pursuit of new business, product development, manufacturing process development, continuous improvement, and on-going business development. • Manage equipment suppliers during the RFQ phase to ensure deliverables are met in a timely manner. • Represent Global Engineering where applicable at customer meetings to ensure that the needs of the business are met. • Ensure that the procedures and systems are in place to facilitate the introduction of new processes and equipment. Education • Bachelor's Degree In Engineering or Science field required • Master's Degree In Engineering or Science field preferred Basic Qualifications • Must have a minimum of a Bachelor of Engineering (preferably a concentration in Mechanical/Manufacturing Engineering or Tooling Engineering) and at least 3 - 5 years’ experience in technical role. • A background or knowledge of Injection mould tooling and design and general moulding systems would be an advantage. • Have a good understanding of operational processes. • Have a good understanding of business development and the ability to interpret customer requirements. • Have excellent knowledge of manufacturing automation, injection moulding, machine design, development, and validation processes. • Must have good working understanding of manufacturing processes, Inc. automation from Low Volume to High Volume. Preferred Knowledge, Skills and Abilities • Preferably worked in either the medical, packaging or technological industries with a good understanding of the regulatory requirements including working knowledge of ISO 13485; EU GMP, CFR Part 820. • Have the ability to work with customers. • Must have strong data analysis capabilities. • Have a good understanding of resource requirements to implement project. • Excellent written and verbal communication skills as well as the ability to accurately document work performed. • Must be able to work in a fast-paced environment. • Must be able to organize and prioritize tasks; must be detail orientated and self-motivated. • Must be able to work independently on own projects while working concurrently with all departments / sites and levels of employees. • Must maintain the ability to work well with others in a variety of situations. • Must be able to multi-task, work under time constraints, problem solve, and prioritize tasks. • Ability to make independent and sound judgments based on facts. • Analytically minded with strong problem-solving skills. • Observe interpret and evaluate situations in a solution focused manner. • Learn and apply new information or new skills. • Work to meet deadlines which may involve situations constrained by time. • Able to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description • An ability to collaborate across functional teams and work effectively in a matrixed team environment. • Must be able to work independently on own projects while working concurrently with all departments. • Good understanding on GAMP 5 guidelines will also be an advantage • Perform additional tasks at the discretion of the manager. Travel Requirements 30%: Up to 78 business days per year Physical Requirements Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. Additional Requirements • Must be able to perform job duties as required with limited physical demands. West embraces diversity and equality of opportunity. We foster an environment where all individuals are safe, treated fairly, valued and respected. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, disability status or other applicable legally protected characteristics. Where permitted by law, employment with West Pharmaceutical Services, Inc. or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of post-offer background screening and/or drug screening.   #LI-Hybrid #LI-BC1

Requirements

Must-haves

This is a hybrid position requiring team members to be onsite 3 days a week.This position offers relocation assistance.
We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.
Essential Duties and Responsibilities
Responsible for leading key activities within the Global Device Engineering Group specifically related to the quotation of commercial bids and development agreements.
Work with internal stakeholders across global sites to understand customer & business needs and translate to technical outputs and costs.
Identifying deliverables, time and cost, setting priorities and reporting to meet the needs of the business and the customer.
Establish relationships with equipment suppliers in pursuit of new business, product development, manufacturing process development, continuous improvement, and on-going business development.
Manage equipment suppliers during the RFQ phase to ensure deliverables are met in a timely manner.
Represent Global Engineering where applicable at customer meetings to ensure that the needs of the business are met.
Ensure that the procedures and systems are in place to facilitate the introduction of new processes and equipment.
Bachelor's Degree In Engineering or Science field required
Must have a minimum of a Bachelor of Engineering (preferably a concentration in Mechanical/Manufacturing Engineering or Tooling Engineering) and at least 3 - 5 years’ experience in technical role.
A background or knowledge of Injection mould tooling and design and general moulding systems would be an advantage.
Have a good understanding of operational processes.
Have a good understanding of business development and the ability to interpret customer requirements.
Have excellent knowledge of manufacturing automation, injection moulding, machine design, development, and validation processes.
Must have good working understanding of manufacturing processes, Inc. automation from Low Volume to High Volume.
Preferably worked in either the medical, packaging or technological industries with a good understanding of the regulatory requirements including working knowledge of ISO 13485; EU GMP, CFR Part 820.
Have the ability to work with customers.
Must have strong data analysis capabilities.
Have a good understanding of resource requirements to implement project.
Excellent written and verbal communication skills as well as the ability to accurately document work performed.

Nice-to-haves

Master's Degree In Engineering or Science field preferred
Preferred Knowledge, Skills and Abilities

Application prep

Use the role’s language and application details while tailoring your materials.

Platform: successfactors
Effort: medium