Product Manager - Medical Devices Job at Kimal (Bromsgrove)

Senior Product Manager, Prenatal

Lead the UNITY Fetal Risk Screen product line. Collaborate with world-class team...

Location

United States , Menlo Park

Salary:

168961.00 - 190081.00 USD / Year

BillionToOne

Expiration Date

Until further notice

Requirements

5–7 years of experience in product management (clinical products such as medical devices or molecular diagnostics) or product marketing in molecular diagnostics
A proven track record of launching clinical products for provider audiences
Strong insight generation skills, with experience conducting market research and gathering user feedback
Demonstrated ability to lead large cross-functional teams through complex product launches
Hybrid role requirements: Onsite 3 days/week. Fully remote candidates will not be considered

Job Responsibility

End-to-end ownership of UNITY Fetal Risk Screen: Take full ownership of the product lifecycle—from early concept development to continuous improvement
Drive Product Roadmap Execution: Plan, manage, and execute the product roadmap with a focus on timely delivery and strategic alignment with company goals
Champion Continuous Improvement: Monitor user feedback, behaviors, and market trends to uncover opportunities for enhancements
Leverage Data for Strategic Decision Making: Analyze key metrics to make data-informed decisions and refine product offerings
Be the Voice of our Customers: Deeply understand the needs of patients and obstetric providers, becoming the company’s authority on their challenges, desires, and the market landscape
Lead Program Execution: Mobilize cross-functional teams, to achieve ambitious product milestones and deliver exceptional results

What we offer

Working alongside brilliant, kind, passionate and dedicated colleagues, in an empowering environment, toward a global vision, striving for a future in which transformative molecular diagnostics can help millions of patients
Open, transparent culture that includes weekly Town Hall meetings
The ability to indirectly or directly change the lives of hundreds of thousands patients
Multiple medical benefit options
employee premiums paid 100% of select plans, dependents covered up to 80%
Extremely generous Family Bonding Leave for new parents (16 weeks, paid at 100%)
Supplemental fertility benefits coverage
Retirement savings program including a 4% Company match
Increase paid time off with increased tenure
Latest and greatest hardware (laptop, lab equipment, facilities)

Fulltime

Senior Product Manager - CORTRAK Specialty Nutrition Systems, North America

Senior Product Manager role for CORTRAK Specialty Nutrition Systems, North Ameri...

Location

United States , Alpharetta

Salary:

Not provided

Avanos

Expiration Date

Until further notice

Requirements

Bachelor's degree required
At least 7 years of product management and sales experience in the health care industry (or other regulated industry)
Ability to travel at least 25%
Ability to manage cross-functional teams without direct reporting relationships
Ability to collaborate successfully and influence decisions
Exceptional written, verbal and communication skills
Experience in forecasting and demand planning
Development of strategic business plans
Development of key tactics and execution plans that drive strategic goals
Ability to assess the market and competitive landscape

Job Responsibility

Provides leadership to the Specialty Nutrition Systems product portfolio managing the CORTRAK and CORGRIP businesses with a focus on growing these categories through the development and execution of the strategic business/ marketing plans
To be successful in the role this will require developing a financial budget that drives growth and is achieved each calendar year
This individual will also drive the development and execution of the business/ marketing plans that will include market assessments, pricing strategy, key GPO/IDN strategies and competitive landscape
This role will also have responsibility for key customer management, new product launches, developing and running SABs (Sales Advisory Boards), improving GP and OP, tradeshow management and advising Global Strategic Marketing on future pipeline decisions
Assist in the development and execution of effective plans and programs, both strategic and tactical, to drive net sales, operating profit, and market share for categories
Maintain full P&L management responsibility for product portfolios
Develop long-term strategic business plans and marketing plans for product portfolio segments
Develop pricing strategies that support the growth and profitability of the business
Collaborate with Sales, Planning and Finance teams to develop timely and accurate forecasts to ensure required fill rates on existing and new products, supporting sector goals to improve return on working capital and working closely with sales team to develop a financial and demand forecast with a high degree of accuracy
Support in the development of GPO/ IDN strategies to grow and maintain the business

What we offer

benefits on day 1
free onsite gym
onsite cafeteria
HQ region voted 'best place to live' by USA Today
uncapped sales commissions
generous 401(k) employer match of 100% of each pretax dollar you contribute on the first 4% and 50% of the next 2% of pay contributed with immediate vesting

Fulltime

Senior Project Manager

As a Senior Project Manager at Delve, you’ll be the guiding force behind multi-d...

Location

United States , Boston

Salary:

Not provided

Delve

Expiration Date

Until further notice

Requirements

7+ years’ experience in Project Management, Product Management, Engineering Program Management, and/or other client-facing roles
5+ years’ work experience in medical device electromechanical product development
Experience planning and maintaining client projects from start to finish
Well-versed and knowledgeable about MS Excel, MS Project, Smartsheet, and internal project management systems
Familiarity with and/or interest in consulting environments and how they work

Job Responsibility

Be the connection point between the internal project team and client. Work in collaboration with a Technical Lead or other senior team members to run client projects
Work with Technical Lead to define product requirements, track adherence to requirements, and ensure deliverables are met per client expectations
Identify potential change of scope issues as they arise and communicate them to the team, account management, and the client
Create proposals and budgets and manage schedules of internal and external support, document all decisions, and track action items
Maintain responsibility for project data accuracy and organization for internal project management database and server
Regularly review project budget status with Account Manager and Technical Lead and request resources to complete project work as necessary
Oversee and support the planning/preparation of presentation materials, in cooperation with Technical Lead and other team members
Work with studio account directors and client partners to ensure project health across project financials, work quality and internal and client team’s happiness

Fulltime

Quality Production Operations

Join the Quality Production Operations team to drive excellence in manufacturing...

Location

Italy , Rome

Salary:

Not provided

Cosmo Intelligent Medical Devices

Expiration Date

Until further notice

Requirements

Knowledge of 2017/745(MDR) and 21 CFR 820
Knowledge of 13485: 2021
Strong technical troubleshooting and problem-solving skills
Excellent communication and collaboration abilities
Good English Level (writing and speaking)
Ability to work independently and collaboratively across multifunctional teams
Resilient and able to work effectively under stress and tight deadlines
Willingness to travel as needed
Minimum of 2 years of experience in the quality assurance role within the medical devices or healthcare industry, with a strong focus on production processes
Bachelor’s degree in engineering, or a related field

Job Responsibility

Oversee all processes related to the collection and review of the production records
Review the Device History Records related to medical device products and ensure the correctly storage of records
Support the Medical Device Production Manager in the planning of the production process
Ensure that all production activities comply with regulatory standards, quality control protocols, and company policies
Incoming Inspection: support the R&D ensure that the procedure for deciding when the lot under inspection is to be rejected or accepted
Equipment Management: manage the equipment calibration and archive the records
Non conformities management: open and manage the non conformities issued during the production process, correction and corrective action
Problem Solving: support the Medical Device Production Manager in the implementation of the corrective actions to minimize disruptions and maintain continuous production flow. Ensure that activities are correctly carried out and registered
Supplier Management: perform the supplier qualification and supplier monitoring process and support the Quality Assurance Manager during the audit at the supplier
Training: ensure that the training and guidance to production staff are correctly registered

RA Manager

Eitan Medical is a fast-growing global medical device company, developing and ma...

Location

Israel , Netanya

Salary:

Not provided

Eitan Medical

Expiration Date

Until further notice

Requirements

BSc in a scientific area, (Bio-medical or Quality Engineering - an advantage) or acknowledged regulatory course graduate
2-4 years medical device/pharmaceutical post market experience
Knowledge and experience with the following regulatory systems: EU / Canada /US - advantage to other regulation
Minimum 2 years management experience
Strong verbal and written communication skills
Good technology expertise is essential
Experience in front of the authorized authorities
Understanding of risk management disciplines
English – very high level, verbal and written
Ability to work under pressure and in tight schedules

Job Responsibility

Managing the post market RA team
Support design and post market compliance of products from a regulatory perspective
Handling Vigilance, MDR and authorities’ inquiries of complaints
Support the investigation process from a regulatory perspective
Responsible for managing product field action
Responsible on regulatory assessment related QMS process
Responsible of company’s PSUR

Fulltime

Program Manager

The Program Manager establishes with expertise leaders the budget to execute the...

Location

United States , Chicago

Salary:

100000.00 - 140000.00 USD / Year

Nemera

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Engineering, science or related field
Experience with leading multi-disciplinary project teams
Experience directly interacting with customers
Strong leadership with exceptional communication skills
Excellent interpersonal and organization skills

Job Responsibility

Lead and manage the customer (internal or external) in collaboration with the key account manager by being the main communication interface
Manage and coordinate the whole program and allocated program team from the request for quotation to the validation of small-scale processes and product design freeze in respect to quality, costs and timing targets
Manage program risks and proactively drive any associated action plans
Actively participate and coordinate the effective presentation of program status at periodic governance meetings
Manage multiple programs at the same time
Be capable of providing appropriate effort depending on the program complexity
Create program and project plans to track development progress and expenses
Coordinate with the finance controller to ensure accurate tracking of finances
Participate in the technical decisions and supplier selection with the team

Fulltime

Key Account Manager

Key Account Manager for the South Belgium & the Grand-Duchy of Luxembourg to rei...

Location

Belgium

Salary:

Not provided

Flen Health GmbH

Expiration Date

Until further notice

Requirements

Degree in biology, pharmacy, biomedical, economics or equivalent based on relevant experience
5-10 years of experience in developing relationships with clients and KOL within the pharma/medical sector
In-depth knowledge of territory, purchasing dynamics and tender procedures
Excellent negotiation and both oral and written communication skills
Strong customer focus and entrepreneurial spirit
Data savvy and comfortable with numbers, ability to effectively use Microsoft Office, CRM system & Showpad
Native French speaker and fluent in English
Valid Driving License
Problem solver, work with line manager to find innovative approaches to resolve situations and develop turnover

Job Responsibility

Key Account & KOL Management: develop and manage key opinion leaders (KOLs) and strategic accounts to generate new business opportunities in South Belgium and Luxembourg
Build and maintain strong relationships: establish and maintain strong relationships with regional healthcare organizations and key stakeholders within region
Market Insights & Strategic Decision-Making: stay up to date with changes in the healthcare landscape and leverage this knowledge to engage with key and strategic decision-makers
Impactful Partnerships: initiate and manage collaborations and joint projects with international, national, and regional stakeholders to support business growth
Commercial Expertise & Analysis: provide commercial expertise by gaining strategic insights through the analysis of sales, marketing, and health economic data
Sales Strategy & ROI Analysis: develop sales strategies and action plans for new products and conduct ROI calculations to assess their impact
Sales Management Support: support the sales manager/director in enhancing the sales team’s effectiveness, creating sales plans for existing products, and identifying new business opportunities
Training & Knowledge Sharing: contribute to the development and implementation of training programs to strengthen the sales team’s skills

What we offer

Excellent working conditions
Innovative and inspiring work environment
Independent project work & responsibilities within a professional team
Career prospect
Learning and development opportunities
Competitive remuneration according to experience

Fulltime

Principal Product Development Engineer

The individual in this role is highly skilled and experienced and can lead and d...

Location

United States , Lake Forest

Salary:

130000.00 - 150000.00 USD / Year

Manufacturing For Design

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in mechanical or biomedical engineering or equivalent experience
7 – 10 years industry experience with a medical device company
Demonstration of excellent communication (written and oral) skills
Demonstration of excellent organizational skills with the ability to adapt to a rapidly changing environments
Prior experience with non-invasive medical devices (catheters)
Ability to present/teach detailed technical information, to all levels of company personnel and customers
Extended periods of sitting
Extended usage of a microscope
Moderate lifting

Job Responsibility

Lead and manage the product development process, from concept through to commercialization, ensuring that projects are delivered on time and within budget
Define product specifications and requirements in collaboration with cross-functional teams
Conduct thorough risk assessments and implement strategies to mitigate potential issues
Collaborate with regulatory affairs and quality assurance team to ensure compliance with all relevant regulations and standards
Collaborate with R&D on the creation of prototypes and conduct experiments to determine validity of designs
Perform and/or manage design verification, equipment qualification and product and process validation
Use CAD software (Solidworks) for part and assembly design and detail drawings
Work closely with manufacturing team to facilitate the transition from development to production
Manage the budget for product development, optimizing costs while maintaining high product quality and compliance
Engage in completing necessary documentations as well as maintaining comprehensive documentation of all product development activities, including design specifications, test results, and regulatory submissions

What we offer

Medical Insurance, Dental Insurance, and Vision Insurance, 100% paid for employee
401K Plan

Fulltime

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Product Manager - Medical Devices

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