Quality Engineer at WEST PHARMACEUTICAL SERVICES SINGAPORE PTE LTD

, Puerto Rico, United States -

Full Time

Start Date

Immediate

Expiry Date

18 Jul, 26

Salary

0.0

Posted On

19 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality engineering, ISO 9001, cGMP, Root cause failure analysis, CAPA, PFMEA, SPC, Coordinate measuring machine, Lean manufacturing, Six Sigma, Data analysis, Trend analysis, Quality system maintenance, Technical documentation, Process improvement, Calibration

Industry

Pharmaceutical Manufacturing

Description

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 In this fully onsite role, you will be responsible to control all Quality functions including the expansion and maintenance of the Quality System, provide support for product and process improvements by collecting, compiling, and analyzing inspection and process date, and ensure the effective use of resources to meet site quality requirements.Essential Duties and Responsibilities Drive site and departmental goals/KPI’s in the improvement of Cost of Poor Quality and Yield Opportunity to 100%Meet Company and Department goals in the continuous improvement of tooling products, services, and processesProvide accurate quality reports and perform trend analysis on assigned areas of responsibilityWork independently and with project teams to develop design control deliverables including quality plans, manufacturing and inspection documentation, test methods, and any necessary records for filing tooling product history files.Support quality assurance improvement activities by evaluating products, processes, and data to develop control or improvement strategies intended to improve the Customer Experience.Participate in the development and maintenance of product risk and hazard analysis (PFMEA)Assumes responsibility for various assigned projects designed to improve product quality, reduce costs and/or validate facility products or processes, including development and implementation of any new or required inspection methods and in-process SPC programs.Work with management and technical staff in performing root cause failure analysis and implementing corrective and preventative actions to preclude recurrence (CAPA).Identify and remedy equipment and/or process documentation gaps and provide appropriate training where needed.Support both Corporate and facility driven initiatives intended to meet defined objectives, including Quality System planning and audit support.Analyze data, process capabilities, customer concerns and expectations and any other leading or lagging indicators which may be used to improve product and process knowledge.Interact with customers to understand and integrate those requirements into West manufacturing and quality system requirements.Perform supplier non-conformance investigation and response.Conduct activities in accordance with the company Quality Policies/Procedures at all times - Comply with company cGMP regulations and be responsible for defect recognition.Schedule and maintain department machine calibration requirements and results.Monitor and document daily output performance and unmanned hours in your department.Perform other duties as assigned based on business needs.Conform with and abide by all regulations, policies, work procedures, instructions, and all safety rules - exhibit regular, reliable, punctual, and predictable attendance.Education Bachelor's Degree in Engineering, Business required Work Experience Minimum 3 years of experience in a Quality engineering role at an engineering, pharmaceutical, or medical device manufacturer required andMinimum 3 years of experience in the use of computer-based measuring equipment (e.g., Coordinate Measuring Machine). required and Experience in conventional toolroom machinery (mills, lathes, surfaces grinders). preferred Preferred Knowledge, Skills and Abilities Knowledge of ISO 9001, cGMPProficiency in all Microsoft Office applications.Flexibility in providing support beyond normal working hours when necessary.Awareness of all relevant SOPs/SOIs as per Company policy as they are related to the position covered by this job description.Always comply with the Company’s Safety and Quality PoliciesTrained Quality Auditor.Demonstrate innovativeness in tactical matters relating to proposing alternate solutions for process improvement.Support and contribute to Lean Sigma programs and activities towards delivery of the set target.Formal apprenticeship or training in an engineering background.Knowledge of SPCKnowledge of “Lean Manufacturing” techniques.Knowledge and experience in all processes involved in the manufacture of rubber compression molds.Qualified Lead Auditor.Formal qualification in Quality ManagementLicense and Certifications Manufacturing\Six Sigma Green Belt Certification Upon Hire preferred andManufacturing\Lean Six Sigma Black Belt with DOE experience. Upon Hire preferred Travel Requirements 10%: Up to 26 business days per yearPhysical Requirements Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently, and/or up to 10lbs/4kgs of force constantly to move objects.Additional Requirements 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.Self-motivated with the ability to make independent and sound judgments.Read and interpret data, information, and documentsLearn and apply new information or skills 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.  #LI-KR1#LI-Onsite

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Responsibilities

The Quality Engineer will manage quality functions, including maintaining the Quality System and performing root cause failure analysis to drive process improvements. They will also develop design control deliverables and ensure compliance with cGMP regulations and site quality requirements.