Sr Tech Sup Metrology, Lab, LN
- Salary
- €30.4K–€38.7K
- Moves you to
- France
- Support
- Relocation support
- Posted
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Work Location Logistics:
This is an onsite position requiring the team member to be onsite for all scheduled workdays.
Relocation:
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
Essential Duties and Responsibilities
- Procurement, validation, set-up and maintaining metrology and measurement systems/equipment.
- Metrology fixture design and validation (GRandR)
- Perform and review QFD (Quality Function Deployment) in support of product design, development and operations.
- Conduct data trend analysis to identify short and long-range patterns so that recommendations can be made to effect continuous improvement necessary to satisfy customer requirements.
- Document metrology system validation via protocols and reports using West procedures
- Ensures that all metrology equipment is correctly calibrated through auditing, managing and scheduling the calibration of inspection equipment through external vendors.
- Training of metrology operators, ongoing re-fresher training and assessment to determine level of competency on a frequent basis.
- Establish and maintain documentation in line with West Contract Manufacturing and West Pharmaceutical Services.
- Liaise with customers and suppliers on new and existing projects.
- Maintain good communications both internally and externally.
- Makes periodic audits as requested and completes necessary documentation.
- Support to operations, development and quality departments.
- Chairing customer meetings reviewing measurement systems, data analysis and first article inspection reports.
- Perform additional duties at the request of the direct supervisor.
- Drives a culture of continuous improvement and lean operations.
- Act in accordance with the company’s Guiding Principles and adherence to the corporate Code of Conduct.
- Other duties as assigned
Education
- Bachelor's Degree in Mechanical/Manufacturing Engineering or Bachelor's of Science dedgree in related field, or equivalent experience required
Work Experience
- Minimum 3 years of experience in a similar role, ideally in the Medical Device Industry; or
- Minimum 2 years of technical data review experience in cGMP laboratory; or
- Minimum 3 years’ experience in cGMP pharmaceutical industry
Preferred Knowledge, Skills and Abilities
- Training/certification in dimensional measurement preferred. (i.e. NPL, AUKOM)
- Knowledge of programming coordinate measuring machines is essential using software like: PC-DMIS, Calypso, Volume Graphics.
- Proficient knowledge of ISO/ASME GDigital and Transformation requirements, interpreting 2D engineering drawings and 3D models for various levels of medical device components, assemblies, and subassemblies using CAD system (e.g. SolidWorks).
- Knowledge and experience with in-house calibration procedures and calibration management software including day to day inspections of equipment.
- Proven experience of Measurement System Analysis (MSA) development, Minitab and statistical packages is essential.
- (i.e. Measurlink)
- CT scanning knowledge would be a distinct advantage.
- Strong problem solving and critical thinking skills to troubleshoot issues and identify root causes.
- Computer literacy required including all Microsoft Office utilities.
- Must possess good communication/interpersonal skills; must be detail orientated, organized, flexible and be able to handle multiple tasks and time critical projects/deadlines.
- Working knowledge of ISO 9001:2000 / ISO 13485.
- Knowledge of generating validation documentation and subsequent reporting
- Knowledge of generating Standard Operating Procedures and Work Instructions
- Knowledge of Internal Quality and Systems Auditing.
- Ability to motivate a team toward a common goal.
- Ability to work, lead and empower team members
Travel Requirements
Physical Requirements
Shift
Pay Transparency:
The annual base salary range for this position is €30,400.00 - €38,700.00. Total target compensation is determined using objective and gender-neutral criteria, including relevant experience, qualifications, skills, market benchmarks, geographic location, and the scope and responsibilities of the role.
This position may be eligible for variable compensation and other incentive programs in accordance with the terms of the applicable plans within the country of employment. In addition, team members are eligible to participate in the company’s benefits and total rewards programs applicable to their location and employment status.
West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to Apply.Accommodation@westpharma.com. Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening.
