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Senior Engineer - MTS

LSNE Contract Manufacturing Manchester, NH
  • Expired: February 07, 2020. Applications are no longer accepted.

Senior Engineer - MTS

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Thrive in the dynamic and challenging environment of a contract development and manufacturing organization. Driven to excel through self-leadership and thriving team engagement. If this describes you, then look no further than LSNE. We have the experience, expertise and a successful track record in completing development of life-changing pharmaceuticals and medical devices. Together with our clients, we work to bring about treatment of many forms of cancers, Diabetes, communicable diseases, and many other illnesses. Come make a difference. Your work will matter and your contributions will be significant in these endeavors.
We offer a competitive compensation and benefits package and a very generous paid time off benefit. Join our team!
JOB SUMMARY
The Senior Engineer-MTS position will define relevant operational/technical standards and practices for LSNE sites that produce medical devices as well as the site and identify and drive implementation of improvements to maximize throughput and capacity utilization. The role will interface with other LSNE functions as well as external clients to implement new processes and technologies into LSNE GMP manufacturing as well as supporting validation efforts.
The individual will be a key contributor within a group responsible for performing process improvements, including timely completion of feasibility studies, scale-up, technology transfer and GMP floor support for programs that bring new biopharmaceutical products/devices to pre-clinical, clinical and commercial manufacturing phases.
The successful candidate will contribute during execution of process engineering activities for the department, including troubleshooting manufacturing issues, analyzing data and authoring technical reports. The scope includes enabling studies and contributions to the preparation of regulatory submissions. The feasibility studies include small and pilot scale to establish critical and key operating parameters including, but not limited to clinical and validation batches. The individual will effectively collaborate and communicate within the framework of cross-functional, multi-disciplinary teams. In addition, this person will interact with other internal departments such as research, internal manufacturing, facilities/engineering, project management, procurement, quality as well as with comparable functions at external clients. The individual will work autonomously to implement solutions for problems of moderate scope and complexity reporting to the Sr. Manager of MTS.
JOB DUTIES
+ Actively participate and provide input and feedback for the LSNE Safety Program to meet Health and Safety regulations and OSHA requirements in all duties
+ Provide technical mentorship to junior MTS Engineers and investigators
+ Experimentation and manufacturing support related work including development and pilot scale studies to support process development, optimization and characterization
+ Contributes to the evaluation of novel, generic platform technologies that can be applied across multiple programs
+ Participates during technology transfer of programs spanning all phases of biopharmaceutical/medical device lifecycle, including discussions of scale, equipment design and oversight of GMP and Engineering batches. Establish technical support initiatives for GMP operations in these multi-product sites
+ Interacts with manufacturing operations staff, troubleshoots problems and supports their operations
+ Compose technical documents (protocols, batch records) for conducting technical studies
+ Interpret and execute policies and procedures. Recommend modifications to operating policies
+ Function as a technical expert on equipment, systems, processes
+ Lead troubleshooting of operations, develop preventative maintenance procedures, and maintain engineering documentation (commissioning, protocols, test plans, functional/detailed design)
+ Establish equipment specifications in standard documentation User Requirements (URS), Functional Specification (FS) and Detail Design Specifications (DDS)
+ Lead efforts with manufacturing, process development, facilities, quality assurance and other departments in developing requirements and recommendations for system modifications
+ Execute tasks, under the minimal direction of project managers, to complete design, engineering, construction, commissioning, and qualification for projects within schedule and budget constraints
+ Coordinate the work of consultants and engineering firms on development of standard design documents
+ Provides technical support to external clients and internal operations, utilizing statistical data analysis. Develops solutions to complex problems using ingenuity and innovation, and ensures solutions are consistent with overall organization objectives
+ Drives key equipment, systems, and facility improvement projects, providing oversight of design, construction, testing, and turnover with responsibility for schedule and overall project performance
+ Provide technical input for product tech transfers, evaluation of process requirements versus facility capabilities
+ Provide technical support and analysis for the resolution of deviations, investigations, and process issues
+ Works independently to develop department procedures, standards, and specifications Writing and reviewing data summaries as per established company guidelines and procedures
+ Authors technical reports, technology transfer packages and presentations
+ Contributes to regulatory submissions. Develop project scopes, schedules and budgets
EDUCATION, PROFESSIONAL SKILLS, & EXPERIENCE
+ BS with 10+ years or Masters with 8+ years or PhD with 6 years of experience in Chemical/Biochemical Engineering or related discipline within a relevant GMP manufacturing environment
+ Process Engineering/development experience in the biotechnology/pharmaceutical/medical device industry with practical expertise around scale-up, tech transfer and manufacturing support to large scale GMP operations is required
+ Familiarity with the operation of large scale disposable technologies, devices and production equipment for unit operations is highly preferred
+ Proven track record of large scale process implementation
+ Excellent oral and written communication skills
+ Strong technical writing ability required
+ General understanding of fill finish, freeze drying (lyophilization), medical device, filtration, milling, mixing technologies, fluid metering, formulation, and purification
+ Knowledge of equipment in pharmaceutical manufacturing including autoclave, filling pump, vial washer, depyrogenation oven, lyophilizers, and process utilities (WFI, PW, Clean Steam, HVAC, etc)
+ Excellent interpersonal, teamwork, and leadership skills
+ Must be capable of multi-tasking and performing assignments that have loosely defined objectives which require investigation of numerous variables.
+ Ability to apply knowledge of multiple engineering disciplines to evaluate and develop solutions for operational issues.
+ Proficiency with Microsoft products and ability to learn additional applications as needed
+ Must be able to work on complex problems in which analysis of situations or data requires and in-depth evaluation of various factors
+ Applied knowledge of Quality by Design, six sigma, and operational excellence tools in creating efficient and high quality processes and end products
+ Understanding of new manufacturing technologies including single use disposables
PHYSICAL REQUIREMENTS -
+ Ability to wear personal protective equipment such as safety glasses/goggles, gloves and safety shoes.
+ Ability to gown and gain entry to controlled manufacturing areas.
+ Ability to lift, pull or push equipment weighing up to 25-50 lbs.
+ Occasional standing is required
COMMUNICATIONS & CONTACTS - Interacts with all departmental staff
MANAGERIAL & SUPERVISORY RESPONSIBILITIES - Not Applicable
The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified.

LSNE Contract Manufacturing

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Manchester, NH
03103 USA