Product Designer, Chemistry Job at Benchling (San Francisco)

Product Manager, Chemistry

Biotechnology is rewriting life as we know it, from the medicines we take, to th...

Location

United States , Boston

Salary:

164000.00 - 247000.00 USD / Year

Benchling

Expiration Date

Until further notice

Requirements

5+ years of product management experience
Academic or professional experience in a scientific field, bonus points for chemistry
Deep knowledge of small molecule R&D or a strong desire to learn
Proven ability to drive 0→1 product development, especially in enterprise SaaS
Strong communicator who thrives in cross-functional, fast-moving environments
Empathetic collaborator who can bridge the gap between scientists, engineers, and business teams
Experience at the intersection of life sciences, data, and AI (e.g., cheminformatics, predictive modeling, or LLM-assisted workflows) is a strong plus

Job Responsibility

Define and execute the product vision and roadmap for Benchling’s small molecule R&D solution, from early discovery through development
Partner closely with customers and field teams to deeply understand our customer’s scientific workflows and pain points
Translate scientific and technical insights into intuitive, scalable software capabilities that integrate seamlessly across Benchling’s platform
Collaborate with engineering, design, and data teams to deliver high-quality products on time and with measurable impact
Leverage AI to enhance scientific productivity—partnering with AI and platform teams to build intelligent tools that accelerate decision-making for chemists
Drive alignment across stakeholders, communicating priorities, tradeoffs, and outcomes clearly and persuasively
Represent the small molecule domain internally and externally, influencing the future direction of Benchling’s multi-modal R&D platform

What we offer

Broad range of medical, dental, and vision plans for employees and their dependents
Fertility healthcare and family-forming benefits
Four months of fully paid parental leave
401(k) + Employer Match
Commuter benefits for in-office employees and a generous home office set up stipend for remote employees
Mental health benefits, including therapy and coaching, for employees and their dependents
Monthly Wellness stipend
Learning and development stipend
Generous and flexible vacation
Company-wide Winter holiday shutdown

Fulltime

Product Manager, Chemistry

Biotechnology is rewriting life as we know it, from the medicines we take, to th...

Location

United States

Salary:

164000.00 - 247000.00 USD / Year

Benchling

Expiration Date

Until further notice

Requirements

5+ years of product management experience
Academic or professional experience in a scientific field, bonus points for chemistry
Deep knowledge of small molecule R&D or a strong desire to learn
Proven ability to drive 0→1 product development, especially in enterprise SaaS
Strong communicator who thrives in cross-functional, fast-moving environments
Empathetic collaborator who can bridge the gap between scientists, engineers, and business teams
Experience at the intersection of life sciences, data, and AI (e.g., cheminformatics, predictive modeling, or LLM-assisted workflows) is a strong plus

Job Responsibility

Define and execute the product vision and roadmap for Benchling’s small molecule R&D solution, from early discovery through development
Partner closely with customers and field teams to deeply understand our customer’s scientific workflows and pain points
Translate scientific and technical insights into intuitive, scalable software capabilities that integrate seamlessly across Benchling’s platform
Collaborate with engineering, design, and data teams to deliver high-quality products on time and with measurable impact
Leverage AI to enhance scientific productivity—partnering with AI and platform teams to build intelligent tools that accelerate decision-making for chemists
Drive alignment across stakeholders, communicating priorities, tradeoffs, and outcomes clearly and persuasively
Represent the small molecule domain internally and externally, influencing the future direction of Benchling’s multi-modal R&D platform

What we offer

Competitive total rewards package
Broad range of medical, dental, and vision plans for employees and their dependents
Fertility healthcare and family-forming benefits
Four months of fully paid parental leave
401(k) + Employer Match
Commuter benefits for in-office employees and a generous home office set up stipend for remote employees
Mental health benefits, including therapy and coaching, for employees and their dependents
Monthly Wellness stipend
Learning and development stipend
Generous and flexible vacation

Fulltime

Product Manager, Chemistry

The demand for accelerating scientific research is greater than ever. Benchling ...

Location

United States , San Francisco

Salary:

164000.00 - 247000.00 USD / Year

Benchling

Expiration Date

Until further notice

Requirements

5+ years of product management experience
Academic or professional experience in a scientific field, bonus points for chemistry
Deep knowledge of small molecule R&D or a strong desire to learn
Proven ability to drive 0→1 product development, especially in enterprise SaaS
Strong communicator who thrives in cross-functional, fast-moving environments
Empathetic collaborator who can bridge the gap between scientists, engineers, and business teams
Experience at the intersection of life sciences, data, and AI (e.g., cheminformatics, predictive modeling, or LLM-assisted workflows) is a strong plus

Job Responsibility

Define and execute the product vision and roadmap for Benchling’s small molecule R&D solution, from early discovery through development
Partner closely with customers and field teams to deeply understand our customer’s scientific workflows and pain points
Translate scientific and technical insights into intuitive, scalable software capabilities that integrate seamlessly across Benchling’s platform
Collaborate with engineering, design, and data teams to deliver high-quality products on time and with measurable impact
Leverage AI to enhance scientific productivity—partnering with AI and platform teams to build intelligent tools that accelerate decision-making for chemists
Drive alignment across stakeholders, communicating priorities, tradeoffs, and outcomes clearly and persuasively
Represent the small molecule domain internally and externally, influencing the future direction of Benchling’s multi-modal R&D platform

What we offer

Broad range of medical, dental, and vision plans for employees and their dependents
Fertility healthcare and family-forming benefits
Four months of fully paid parental leave
401(k) + Employer Match
Commuter benefits for in-office employees and a generous home office set up stipend for remote employees
Mental health benefits, including therapy and coaching, for employees and their dependents
Monthly Wellness stipend
Learning and development stipend
Generous and flexible vacation
Company-wide Winter holiday shutdown

Fulltime

Medical Device Regulatory and Quality Consultant

We are seeking a highly skilled consultant with experience in medical device and...

Location

United Kingdom , Melbourn

Salary:

Not provided

PA Consulting

Expiration Date

Until further notice

Requirements

A technical background in Engineering (systems, biomedical, mechanical, electrical, software, or related field) or Applied Science (physics, chemistry, biology, materials science, etc.)
Demonstrated prior direct experience in the design, development, or testing of medical devices and/or combination products
At least five years' experience in MedTech, pharmaceuticals, or life sciences, with a strong track record in regulated product development
Deep expertise in regulatory frameworks (FDA, EMA, MDR/IVDR, ISO 13485, IEC 62304, ISO 14971, GAMP, 21 CFR 4/ 820)
Proven ability to work cross-functionally with engineering, quality, and regulatory teams, contributing practical insights from previous technical roles
Strong problem-solving skills, troubleshooting expertise and the ability to drive technical decision-making in a highly regulated environment ensuring alignment with business and regulatory needs
Ability to manage multiple concurrent projects

Job Responsibility

Provide expertise on global regulatory requirements for medical devices and combination products ensuring compliance with FDA, EMA, MHRA, MDR/IVDR, and ISO standards
Guide processes for hardware, software, and AI-driven medical device development to ensure compliance with applicable regulatory standards and guidance, including ISO 13485, ISO 14971, IEC 62304, and related standards and guidance for AI-driven medical technologies
Advise cross-functional teams of designers, mechanical, electrical, software and usability engineers on requirements and best practices for regulatory and quality compliance
Ensure requirements traceability from user needs through design, development, verification, and validation
Lead risk management activities in accordance with ISO 14971, ensuring safety and efficacy through robust design and process controls
Develop and optimise clients’ Quality Management Systems (QMS) to streamline compliance and lifecycle management
Work closely with clients’ R&D teams, business stakeholders, and notified bodies to align project goals with industry requirements
Facilitate cross-functional collaboration, ensuring smooth integration between engineering, quality, and regulatory disciplines
Translate complex technical and regulatory requirements into actionable development strategies for medical technologies

What we offer

Health and lifestyle perks accompanying private healthcare for you and your family
25 days annual leave (plus a bonus half day on Christmas Eve) with the opportunity to buy 5 additional days
Generous company pension scheme
Opportunity to get involved with community and charity-based initiatives
Annual performance-based bonus
PA share ownership
Tax efficient benefits (cycle to work, give as you earn)

Fulltime

Medical Laboratory Scientist Group Lead

Medical Laboratory Scientist Group Lead - Mount Kisco, NY, Monday to Friday, 8:0...

Location

United States , Mount Kisco

Salary:

35.59 - 58.75 USD / Hour

Quest Diagnostics

Expiration Date

Until further notice

Requirements

Three (3) to five (5) years of clinical experience as a Medical Technologist within the designated discipline
Foreign educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation)
United States educated candidates must provide a detailed original transcript
Bachelor's Degree Medical Technology, Chemistry or Biology or Previously qualified as a Technologist under 42 CFR 493. 1433 published in March 14, 1990
Comprehensive theoretical and operational job knowledge in designated specialty required
Knowledge of organizational/departmental policies and procedures
Proven leadership and problem-solving skills
Must be detail-oriented, have the ability to work independently, establish work priorities for self and others and to handle several tasks simultaneously for maximum department efficiency
Ability to schedule and manage resources to meet department goals
Interpersonal skills necessary to deal courteously and effectively with supervisors, co-workers and clients

Job Responsibility

Demonstrate proficiency in all duties of a Medical Technologist I and II
Perform and report on assigned analytical tests in accordance with applicable Standard Operating Procedures (SOP) ensuring that applicable quality control requirements are met
Actively support and comply with laboratory policies and procedures for specimen handling and processing, test analysis, reporting and maintaining records of patient test results
Adhere to analytical schedules to maintain turnaround time of results including STATS or critical results to clients
Perform, review and document QC analysis to ensure accuracy of clinical data and proper instrument function
Make quality control decisions regarding the disposition of an assay or test
Review requests for validity checks and recommend an appropriate course of action taking into account the limitations of specimen requirements and the effects of time and the quality of additional and/or repeat testing
Serve as a technical resource for the department by investigating and resolving analytical testing problems, recommending a course of action in instances identified as beyond acceptable limits, and responding to non-routine/complex inquiries and/or requests from clients and sales representatives
Assist Lab Supervisor by monitoring workflow to meet testing schedules
distributing and reviewing work assignments

What we offer

Day 1 Medical, supplemental health, dental & vision for FT employees who work 30+ hours
Best-in-class well-being programs
Annual, no-cost health assessment program Blueprint for Wellness
healthyMINDS mental health program
Vacation and Health/Flex Time
6 Holidays plus 1 'MyDay' off
FinFit financial coaching and services
401(k) pre-tax and/or Roth IRA with company match up to 5% after 12 months of service
Employee stock purchase plan
Life and disability insurance, plus buy-up option

Fulltime

Technical R+D Manager, Food/Bev

The Food Research and Development Manager provides technical leadership across t...

Location

United States , Irving

Salary:

Not provided

7-Eleven, Inc

Expiration Date

Until further notice

Requirements

Bachelor's degree in food science, Food Engineering, Chemistry, or related field
6-12 years of relevant work experience
5+ years of project management experience
Strong technical knowledge of food chemistry, microbiology, and processing technologies
Expertise in formulation development, ingredient functionality, and food product optimization
Proficiency in experimental design, product testing methodologies, and data analysis
Understanding food safety principles, HACCP, and regulatory requirements for food products
Experience with sensory evaluation techniques and consumer testing methodologies
Strong project management skills with ability to manage multiple projects simultaneously
Excellent problem-solving abilities with a solutions-oriented approach

Job Responsibility

Lead end-to-end technical research and development and commercialization for innovation, renovation, and maintenance initiatives across the Private Brands portfolio
Apply and continuously improve technical development and commercialization systems that embed food safety, regulatory compliance, QA standards, and shelf-life considerations
Translate product concepts into scalable, manufacturable formulations and processes, ensuring technical readiness for launch
Own product performance over shelf life, including defining test strategies, validating assumptions, and managing technical risk for formulation, process, and supplier changes
Ensure all products comply with applicable food regulations and brand QA standards
Partner closely with QA, Regulatory, Legal, and Sensory to support approvals, audits, testing, and ongoing compliance
Serve as a primary technical partner to co-manufacturers, establishing expectations for quality, performance, and compliance
Identify opportunities for continuous improvement and lead implementation with suppliers and internal teams
Support supplier performance management, including technical input to scorecards, corrective actions, and continuous improvement
Partner with Strategic Sourcing to identify, qualify, and onboard new suppliers through technical evaluations and capability assessments

Fulltime

Research Associate I, R&D Complex Product Development

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

India , Ahmedabad

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Masters (Pharmacy, or equivalent discipline) with 6 to 10 years of experience, or, PhD (biophysics, biochemistry or equivalent discipline) with 0 to 5 years of experience in SEC-UV-MALS and related methods encompassing liquid chromatography, light scattering, diffraction and light obscuration
Competency in the acquisition, processing and data analysis by SEC-UV-MALS and light scattering/diffraction/obscuration techniques for analysis of peptides and iron colloidal products for regulatory submissions is mandatory
Expertise in computational chemistry, molecular modeling and statistical methods are beneficial attributes
Basic understanding of working principles of biophysical & spectroscopic methods, like CD, FTIR, UV, EPR, Mossbauer, and fluorescence spectroscopy, particle XRD, microscopy methods (AFM & EM) & related orthogonal methods to assess structural properties of proteins and iron colloids
Proficiency in literature search through publication and patent databases, repositories (e.g. Pubmed), scientific webinars by regulatory agencies, etc, to remain updated on advanced characterization methods and recent scientific developments
Knowledge of pharmacopoeia, ICH Guidelines and means to implement them for product development
Experience in the operation, calibration and preventive maintenance of NMR and other instruments to ensure continued usage
Trouble shooting of various problems obtain during the product development
Knowledge of good laboratory practices and good documentation practices
Communication skills

Job Responsibility

To perform advanced characterization of complex injectable drugs, including iron formulations, proteins & peptides, oligonucleotides, carbohydrates & other biomolecular APIs and various impurities in lyophilized, liquid, emulsions & other formulations for regulatory submission following GLP norms
To manage outsourced studies at CROs, academic institutes & other external facilities, from study design, execution, analysis and report preparation. Traveling to external facilities, as and when required, is a mandatory requirement for this position
To demonstrate subject matter expertise and help overcome technical challenges in product development, by liaising with formulation and other cross-functional teams as a Subject Matter Expertise (SME)
To understand the project with guidance of Sub-department Manager and follow their instructions
To provide necessary assistance for various procurement activities, review quotations, engage suppliers to procure required goods & services in a timebound manner
To complete the planned work in the stipulated time frame, inform the Sub-department Manager if any deviation or issues are observed
To keep track of each activity related to product analysis and development activities
To carry out all the testing and data recording according to the approved SOPs/ ALCOA++ principle and current pharmacopoeia. Data recording in ELN and sign off must be completed on time
To verify the shelf life of the chemical or reagent before performing analysis of the material or product
To follow Good Documentation Practices & Good Laboratory Practices, maintain lab notebooks & other records appropriately

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Manufacturing Design Engineer, Optical

The RL (Reality Labs) Team at Meta is helping more people around the world come ...

Location

China , Shanghai

Salary:

Not provided

Select Country

Product Designer, Chemistry

Job Description

Job Responsibility

Requirements

Nice to have

What we offer

Looking for more opportunities?