Senior Manufacturing Process Engineer
Senior Manufacturing Process Engineer Contract Duration 12 Months
Job Description:
As a Senior Manufacturing Process Engineer, you will be responsible for implementing and maintaining the effectiveness of the quality system.
Leads and participates in planning and conducting work requiring judgment in the independent evaluation, selection, and substantial adaptation and modification of standard techniques, procedures, and criteria within the engineering specialty.
Performs work that has a limited number of complex variables.
Devises new approaches to problems encountered.
Senior Manufacturing Process Engineer develops the most financially feasible alternative.
What You'll DoIndependently conceives and develops approaches to the solution of problems that require the application of advanced technical knowledge.
Applies working knowledge of related disciplines.
Plans, schedules, conducts, or coordinates detailed phases of the engineering work in a part of a major project or in a total project of moderate scope.
The Senior Manufacturing Process Engineer will solve problems with a variety of complex features such as conflicting design requirements, unsuitability of conventional materials, and difficult coordination requirements.
Directs the work of technical, clerical support, and less experienced engineering staff.
Participates in the technical evaluation of assigned staff and in the identification of development needs.
Interfaces with product team members, department managers, designers, R&D, marketing, and internal regulatory.
Frequent inter-divisional collaborations.
Represents department/ division on projects.
Acquires business skills Learn business fundamentals (finance, accounting, etc.
) and apply business skills to projects.
Education And Experience You'll BringB.
S.
Engineering degree with 5 years of experience or equivalent plus progressive technical experience and demonstrated competence.
B.
S.
Polymer or Science degree preferred.
Knowledge of regulations and standards affecting IVDs and BiologicsPreferred QualificationsExperience working in a medical device manufacturing environmentExperience in leading cross-functional teams to support large-scale projects including the implementation of New Products into manufacturing at supplier sitesPrior experience and familiarity with cGMP, FDA, and ISO-regulated environmentUnderstanding & knowledge of equipment software & GAMP guidelinesExperience in work with design & FAT qualification activitiesEquipment design and specification with Validation experience
Benefits:
Medical, Vision, and Dental Insurance Plans401k Retirement FundAbout The Company:
Our client is a globally diversified healthcare company with a central purpose of helping people live their healthiest possible lives.
They offer a broad portfolio of market-leading products that align with favorable long-term healthcare trends in both developed and developing markets.
Working with this company, you'll tackle a wide array of problems including some of the world's greatest healthcare challenges while experiencing myriad cultures, geographies, and technologies.
They are creating the future of healthcare through life-changing technologies and products that make you healthier and stronger, quickly identify when you have a medical need, and treat conditions to help you get back to doing what you love.
It serves people in more than 160 countries with leading medical devices, diagnostics, nutrition products, and branded generic medicines.
If you are looking for a great company to work for, look no further because our client has received an average of a four-star rating from its thousands of employees who have written positive reviews on Glassdoor and Indeed.
#gttnonit#LI-GTT%1974607% %%engid%% Recommended Skills Accounting Biopharmaceuticals Finance Leadership Problem Solving Research And Development Estimated Salary: $20 to $28 per hour based on qualifications.
Job Description:
As a Senior Manufacturing Process Engineer, you will be responsible for implementing and maintaining the effectiveness of the quality system.
Leads and participates in planning and conducting work requiring judgment in the independent evaluation, selection, and substantial adaptation and modification of standard techniques, procedures, and criteria within the engineering specialty.
Performs work that has a limited number of complex variables.
Devises new approaches to problems encountered.
Senior Manufacturing Process Engineer develops the most financially feasible alternative.
What You'll DoIndependently conceives and develops approaches to the solution of problems that require the application of advanced technical knowledge.
Applies working knowledge of related disciplines.
Plans, schedules, conducts, or coordinates detailed phases of the engineering work in a part of a major project or in a total project of moderate scope.
The Senior Manufacturing Process Engineer will solve problems with a variety of complex features such as conflicting design requirements, unsuitability of conventional materials, and difficult coordination requirements.
Directs the work of technical, clerical support, and less experienced engineering staff.
Participates in the technical evaluation of assigned staff and in the identification of development needs.
Interfaces with product team members, department managers, designers, R&D, marketing, and internal regulatory.
Frequent inter-divisional collaborations.
Represents department/ division on projects.
Acquires business skills Learn business fundamentals (finance, accounting, etc.
) and apply business skills to projects.
Education And Experience You'll BringB.
S.
Engineering degree with 5 years of experience or equivalent plus progressive technical experience and demonstrated competence.
B.
S.
Polymer or Science degree preferred.
Knowledge of regulations and standards affecting IVDs and BiologicsPreferred QualificationsExperience working in a medical device manufacturing environmentExperience in leading cross-functional teams to support large-scale projects including the implementation of New Products into manufacturing at supplier sitesPrior experience and familiarity with cGMP, FDA, and ISO-regulated environmentUnderstanding & knowledge of equipment software & GAMP guidelinesExperience in work with design & FAT qualification activitiesEquipment design and specification with Validation experience
Benefits:
Medical, Vision, and Dental Insurance Plans401k Retirement FundAbout The Company:
Our client is a globally diversified healthcare company with a central purpose of helping people live their healthiest possible lives.
They offer a broad portfolio of market-leading products that align with favorable long-term healthcare trends in both developed and developing markets.
Working with this company, you'll tackle a wide array of problems including some of the world's greatest healthcare challenges while experiencing myriad cultures, geographies, and technologies.
They are creating the future of healthcare through life-changing technologies and products that make you healthier and stronger, quickly identify when you have a medical need, and treat conditions to help you get back to doing what you love.
It serves people in more than 160 countries with leading medical devices, diagnostics, nutrition products, and branded generic medicines.
If you are looking for a great company to work for, look no further because our client has received an average of a four-star rating from its thousands of employees who have written positive reviews on Glassdoor and Indeed.
#gttnonit#LI-GTT%1974607% %%engid%% Recommended Skills Accounting Biopharmaceuticals Finance Leadership Problem Solving Research And Development Estimated Salary: $20 to $28 per hour based on qualifications.
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