Manager, QA R&D Job at Baxter (Marsa)

Manager, QA R&D

As a Quality System Leader: develop, maintain and manage the R&D Site(s) Quality...

Location

Malta , Marsa

Salary:

44800.00 EUR / Year

Baxter

Expiration Date

Until further notice

Requirements

Degree in Engineering (or equivalent) and 8-10 years of experience in the area of Medical Device Quality and/or Regulatory
5+ years team manager experience
Demonstrates leadership skills and ability to work independently
Working knowledge of ISO 13485:2016
Problem Solving – Apply DMAIC and statistical techniques to address issues and investigations
Resourceful and independent - Applies organizational and technical knowledge to move teams through issues
Recognized as a Quality System expert by peers and other design site personnel
Demonstrated success in delivering results

Job Responsibility

Ensure site compliance to applicable regulations and standards and maintain site certifications
Ensure Quality System processes are correctly implemented on site
Recommend, lead, and/or support projects for improvements to the quality system
Identify Key Quality Indicators to provide data for continuous improvement and potential escalation
Ensure site audit readiness for internal, external, and unannounced audits - Drive success in audits, compiling audit responses and tracking audit commitments
Support Supplier Quality responsibility for the R&D site, and participate in supplier audit, as needed
Implement and participate as auditor to the internal site audit program
Manage, identify, hire, develop and recognize the Quality System team
Ensure appropriate documentation is complete, correct, that the schedules of any reviews are met

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Competitive benefits
Discretionary bonuses
Long-term incentive

Manager, QA R&D

As a Quality System Leader: develop, maintain and manage the R&D Site(s) Quality...

Location

Malta , Marsa

Salary:

44800.00 EUR / Year

Baxter

Expiration Date

Until further notice

Requirements

Degree in Engineering (or equivalent) and 8-10 years of experience in the area of Medical Device Quality and/or Regulatory
5+ years team manager experience
Demonstrates leadership skills and ability to work independently
Working knowledge of ISO 13485:2016
Problem Solving – Apply DMAIC and statistical techniques to address issues and investigations
Resourceful and independent - Applies organizational and technical knowledge to move teams through issues
Recognized as a Quality System expert by peers and other design site personnel
Demonstrated success in delivering results

Job Responsibility

Ensure site compliance to applicable regulations and standards and maintain site certifications
Ensure Quality System processes are correctly implemented on site
Recommend, lead, and/or support projects for improvements to the quality system
Identify Key Quality Indicators to provide data for continuous improvement and potential escalation
Ensure site audit readiness for internal, external, and unannounced audits - Drive success in audits, compiling audit responses and tracking audit commitments
Support Supplier Quality responsibility for the R&D site, and participate in supplier audit, as needed
Implement and participate as auditor to the internal site audit program
Manage, identify, hire, develop and recognize the Quality System team
Ensure appropriate documentation is complete, correct, that the schedules of any reviews are met

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Competitive benefits, discretionary bonuses, and/or long-term incentive

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

R&D Group Manager

We are seeking a dynamic and visionary leader to join our team as R&D Group Mana...

Location

Romania , Bucharest

Salary:

Not provided

Global-e

Expiration Date

Until further notice

Requirements

Minimum of 3 years of experience in a similar leadership role within a high-scale SaaS development environment
Proven experience in a leadership role within R&D, managing cross-functional teams, with a focus on developing and supporting high-scale SaaS (Software as a Service) products
Proven experience in driving stack modernization projects
Extensive background in software development and a deep understanding of the full development life cycle, particularly in the context of large-scale, mission-critical SaaS applications
Strong technical background, experienced in cloud native, micro-services based SaaS products. Hands on is advantage
Passionate about leveraging AI within the development life cycle for boosting productivity and quality
Demonstrated expertise in implementing and optimizing QA processes, with a focus on automation, in the context of high-scale SaaS products
Hands-on experience in developing and maintaining production environments for SaaS products, ensuring reliability, scalability, and optimal performance
Excellent communication and interpersonal skills, with the ability to influence and inspire teams in the context of high-scale SaaS development
Strategic thinking and the ability to align R&D efforts with broader business objectives, especially in the dynamic landscape of SaaS

Job Responsibility

Develop and execute a forward-thinking R&D strategy aligned with the company’s overall business objectives
Provide visionary leadership to multiple teams, fostering a culture of innovation, collaboration, and continuous improvement
Drive architecture principles, technology selection, engineering practices and stack modernization
Lead and enforce engineering practices across groups
Lead and mentor 5-6 cross-functional teams, ensuring they are motivated, engaged, and working cohesively towards common goals
Promote a culture of accountability, ownership, and excellence within each team
Oversee the end-to-end product development life cycle for multiple cross non foundation domains
Collaborate with product managers, architects, and other stakeholders to ensure successful delivery of high-quality products
Drive a robust quality assurance process, while implement effective and modern testing strategies and ensure product reliability
Champion a culture of quality across the R&D organization, emphasizing the importance of innovation, quality and agility in every phase of development

Personal Care Indonesia R&D Oral Care Manager

Lead the growth agenda of Oral care category in PT Unilever Indonesia to ensure ...

Location

Indonesia , Banten

Salary:

Not provided

Unilever

Expiration Date

Until further notice

Requirements

Oral care background from R&D or Supply Chain
R&D formulation
R&D from non formulation i.e. packaging, CTIC
Oral care Formulation Technology & Process Knowledge
Innovation Project Management including Risk management process
Strategic, Analytical and Systematic thinking
Problem Solving
Communication & Influencing Skill
Complexity Management Skill
Presentation skill

Job Responsibility

Lead the growth agenda of Oral care category in PT Unilever Indonesia to ensure that we land innovation OTIF fully supported by strong claims and demos so we can assert our leadership
support all initiatives that is margin accretive to the business and drive our agenda for planet positive
Asserting our leadership through product innovation delivery supported by strong claims and demos
Making the business profitable through saving and simplification
Ensuring that we meet Planet positive agenda
To manage, coach and develop the Oral care R&D team ensuring good collaboration with the capability R&D team (pack, CTIC, Digital, Regulatory affairs) and with the cross functional team and with the Global team
Responsible for all technical contents in specification, artwork, communication, claims and demos maximizing the use of digital tools where possible
Ensure full product compliance with Unilever guidance and local regulatory guidance
Drive value improvement programmes to support margin improvement through smart product saving, iGP and complexity reduction
R&D Business partner to Indonesia Oral care team, Acting as the first point of contact for all issues related to Oral care

Fulltime

R&D Global Skin Cleansing Men's Packaging Manager

The Personal Care Category is seeking a dynamic, flexible, and innovative packag...

Location

United States , Trumbull

Salary:

103000.00 - 154400.00 USD / Year

Unilever

Expiration Date

Until further notice

Requirements

B.S Degree (Packaging Science or Engineering equivalent)
Minimum 7+ years in R&D packaging development within Personal Care, Beauty & Wellbeing or Prestige categories within both regional and global experience
Technical Project Lead experience on multiple complex innovation programs
Project Management experience with a proven track record of delivering multiple projects in tandem in a fast paced environment
Experience as the R&D lead responsible for a complex brand program
Highly Skilled and Experienced in managing and coaching people
Expertise in key packaging materials for category – rigid plastics, bottles, closures, dispensers, aerosols, flexibles and paperboard and basic awareness of all packaging materials
Technical Specification & Supply Chain Support
Fully Operational Project Management Skills
Fully operational knowledge of the package development process and engineering principles

Job Responsibility

Packaging workstream leader, working with Brand Development and the cross functional project team, ensuring packaging is fit for purpose to meet the packaging brief, and delivered on time, in full
Deliver packaging which not only meets the required quality and technical standards, but also delights the consumer and builds brand love, through using Unilever’s Packaging Excellence best practices
Development of complex custom delivery systems which deliver key consumer benefit and open up new market spaces and address business needs from premiumization to plant positive solutions
To help develop packaging capability within the team, and lead relevant group activities, at both a packaging, and at a category R&D, level
Where assigned, to be the Technical Project Leader of a project, accountable for delivery of all R&D deliverables, and managing the programme of the R&D workstream leaders assigned to the project
Manage, coach and develop WL1’s
Develop comprehensive development testing protocols for all critical aspects of pack performance and ensure pack is tested against these
Budget responsibilities where relevant
To develop and test packaging in accordance with the One Unilever Packaging Process (1UPP), and ensure that the packaging team is fully trained and adopting the 1UPP
To comply with the Unilever Code of Business Principles and all SHE and QA policies, including the support of product claims, risk management and environmental awareness

What we offer

Bonus eligible
Long-Term Incentive (LTI) eligible
Eligible to participate in benefits plan (e.g., health insurance including prescription drug, dental, and vision coverage
retirement savings benefits
life insurance and disability benefits
parental leave
sick leave
paid vacation and holidays
access to numerous voluntary benefits)

Fulltime

R&D Quality Laboratory Oversight (Associate Director)

Be a key quality leader ensuring high-quality, compliant analytical testing acro...

Location

Japan , Kanagawa

Salary:

Not provided

BioLife Plasma Services

Expiration Date

Until further notice

Requirements

Bachelor's degree in Life Sciences, Chemistry, Biochemistry, or related field
MS/PhD preferred
7+ years' experience in GxP laboratory quality oversight (GMP/GLP, analytical testing, inspections)
Strong knowledge of analytical methods and lab operations for small molecules and biologics
Proven skills in data integrity, deviation/CAPA management, and quality risk management
Clear communicator and collaborator, effective in a global matrix environment with competing priorities

Job Responsibility

Provide quality oversight for GxP and non-GxP labs across the R&D pipeline
Review and approve critical GMP/GLP documentation (methods, validations, deviations, CAPAs)
Ensure robust ALCOA+ data integrity controls in lab systems, processes, and records
Lead or support lab-related investigations, audits, and inspections with clear, timely CAPA
Collaborate with Pharmaceutical Sciences, Regulatory, Manufacturing, and QA to align on quality expectations

What we offer

Allowances: Commutation, Housing, Overtime Work
Salary Increase: Annually, Bonus Payment: Twice a year
Holidays: Saturdays, Sundays, National Holidays, May Day, Year-End Holidays etc. (approx. 123 days in a year)
Paid Leaves: Annual Paid Leave, Special Paid Leave, Sick Leave, Family Support Leave, Maternity Leave, Childcare Leave, Family Nursing Leave
Flexible Work Styles: Flextime, Telework
Benefits: Social Insurance, Retirement and Corporate Pension, Employee Stock Ownership Program, etc.

Fulltime

R&D Systems & Lab Operations Specialist

Join our team as a R&D Systems & Lab Operations Specialist and play a pivotal ro...

Location

India , Noida

Salary:

Not provided

AquSag Technologies

Expiration Date

Until further notice

Requirements

Proven expertise with ELNs and LIMS, including workflow design and system configuration
Exceptional written and verbal communication skills to convey complex information clearly across diverse audiences
Strong analytical mindset and attention to detail in the review and optimization of digital lab processes
Experience translating laboratory protocols into structured, digital formats with robust traceability
Solid understanding of quality assurance principles in R&D settings
Ability to work independently and as part of a remote, expert-driven team
Demonstrated experience developing or reviewing rubrics for laboratory or scientific operations.

Job Responsibility

Review and refine rubrics to validate the accuracy and usability of laboratory processes within electronic lab environments
Translate experimental protocols into structured workflows using Electronic Lab Notebooks (ELNs) and Laboratory Information Management Systems (LIMS)
Assess and enhance the clarity of documentation to ensure written protocols are actionable, logical, and ready for digital adoption
Collaborate with cross-functional teams to identify workflow improvements and ensure realistic QA pairs that mirror everyday lab operations
Monitor and track protocol execution, providing feedback to ensure compliance with best practices in digital lab management
Champion quality assurance by identifying gaps, inconsistencies, and opportunities for automation in lab processes
Serve as a key contributor to the development of scalable and reproducible lab data management strategies.

Fulltime

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Manager, QA R&D

Job Description

Job Responsibility

Requirements

What we offer

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