Manager, R&D Process Quality Job at Amgen (Hyderabad)

Project Manager - R&D

The EU Product Change Management (PCM) department is part of the International C...

Location

Netherlands , Mijdrecht

Salary:

Not provided

SC Johnson

Expiration Date

Until further notice

Requirements

Degree in Science, Engineering or Supply Chain preferred, or a related science supported by experience that demonstrates fit with the role
At least 2 years of progressive RD&E/GSC experience in the FMCG industry
Influence of teams either within a project or through special assignments
Has shown a solution-driven and strategic approach to deliver on commitments, showing adaptability and ability to deal with ambiguity
Able to effectively communicate new ideas, technical stories and approaches to different audiences in a clear and structured way
Demonstrate strong cross-functional skills including effective communication, financial acumen, integrated risk management, project management, quality & robustness, regulation & safety, scientific rigor and technical curiosity

Job Responsibility

Develop and manage a detailed project schedule to meet launch commitments in each country defined in the project scope
Manage the project scope and coordinate cross-functional conversation if any changes occur during the project execution
Lead project kick-off and regular meetings with subject matter experts, identifying project risks and developing the relevant mitigation plans to achieve project objectives
Guarantee the SCJ processes are followed and lead communication with relevant Stakeholders or Sponsors in case of escalations, process deviations or scope changes
Participate in, Identify and occasionally Lead improvement initiatives within project management tools and processes
Track project progress against deliverables & milestones, issue project status reports, and provide synthesized summaries to support communication to Stakeholders & Sponsors
Maintain Project Documentation (Data in Project Tracking tool, MS Project Timeline, Stage Gate documents & templates, Risk register, Close Out Report, etc.)
Ensure the processes within the region are followed (E2E process, Regional Project Approval, Stage Gate, Technical Reviews, etc.)
Be an RD&E representative for a specific category of products working with regional business partners while being a consulting expert with ICB RD&E category counterparts on the regional spécificatives to influence portfolio decisions, as well as timing and execution of regional projects and global rollo-uts
Within the category, develop expertise on specific product forms

What we offer

We offer an attractive annual salary (including 13th month installment and holiday allowance)
Participation in the SC Johnson bonus plan
Participation in our pension plan
Participation in our cafeteria system
Opportunity to benefit from our health insurance package with VGZ
Excellent opportunity for career development and progression, a highly collaborative work environment and an autonomous and flexible working culture where you will be able to add value and be recognized and rewarded

Fulltime

Manager, R&D Claim Enquiry & Resolution

This is a critical, high-impact role responsible for safeguarding the claims of ...

Location

United Kingdom , London

Salary:

Not provided

EmpowerRD

Expiration Date

Until further notice

Requirements

Proven experience (3+ years) in UK R&D Tax Relief, with significant exposure to managing and successfully resolving HMRC enquiries or compliance checks
Strong technical understanding of R&D tax legislation (including SME and RDEC schemes) and the Department for Science, Innovation and Technology (DSIT) guidelines on R&D for tax purposes
Demonstrable experience in managing complex projects or a high-volume case portfolio simultaneously
Excellent written and verbal communication skills, specifically the ability to articulate complex technical and financial concepts to both HMRC and non-tax professionals
Strong commercial acumen and a pragmatic approach to dispute resolution

Job Responsibility

Manage the end-to-end portfolio of all active HMRC R&D tax credit enquiries, ensuring all statutory deadlines and internal SLAs are met
Develop, implement, and execute robust enquiry defence strategies for complex claims, focusing on technical and financial justifications in line with UK R&D legislation (CTA 2009/HMRC Guidelines)
Own and lead direct written and verbal correspondence and negotiations with HMRC caseworkers (ISBC/WMBC/Large Business Compliance Teams) to achieve timely and favourable closure notices
Review and quality-assure all documentation and supporting evidence (technical narratives, project costing, payroll, contracts) provided to HMRC to ensure it is clear, comprehensive, and addresses specific compliance risks
Manage and cultivate a flexible bank of external expert contractors (e.g., specialist engineers, sector-specific consultants, legal counsel) who can provide specialised technical evidence and support during enquiries
Define scopes of work, manage budgets, and oversee the output of all third-party experts to ensure their contribution aligns with the overall resolution strategy
Lead the internal feedback loop by analysing trends, common errors, HMRC concerns, and legislative risks identified during enquiries
Develop and deliver training sessions to the Claim Delivery and Sales teams, embedding new learnings and best practices back into our claims process and technology product
Proactively refine and update internal methodology and technical guidance to mitigate future enquiry risk and ensure all new claims are resilient and compliant
Support in reviewing technical narratives of ongoing claims to align with enquiry learnings

What we offer

Competitive salary
generous holiday allowance
pension contribution
private healthcare
a commitment to continuous professional development

Fulltime

R&D Process Engineer - Software Development

We are seeking a dedicated and experienced (Senior) Process Engineer for softwar...

Location

Germany , Munich

Salary:

Not provided

Brainlab

Expiration Date

Until further notice

Requirements

University degree Computer Science or equivalent
Knowledge of IEC 62304 and its successful implementation in organizations
Knowledge of other medical device software related standards and regulations such as FDA 21 CFR Part 820 and ISO 13485 desired
Solution orientation and a structured nature
Strong communication and documentation skills and ability to work cross-functionally
Experience in software development in a regulated industry (medical devices preferred)
Basic to intermediate proficiency in programming languages (e.g. Python, Java) and/or experience with scripting and automation tools to enhance process efficiency
Fluent in written and spoken English, German is a plus

Job Responsibility

Design, implement, and optimize software development processes within R&D in accordance with relevant medical device standards (e.g., IEC 62304, ISO 13485, ISO 14971, MDR/FDA)
Work cross-functionally with R&D, Quality Management, Quality Assurance to maintain a compliant yet efficient development environment
Ensure audit readiness and support internal and external audits related to R&D processes
Align software development processes within the Brainlab agile methodology
Provide process training and coaching to R&D colleagues and facilitate knowledge sharing across the organization
Align and integrate tools that support process automation and collaboration within R&D

What we offer

30 vacation days, plus December 24th and December 31st
Flexible working hours
Hybrid work model within Germany
Bike leasing via cooperation partner "BikeLeasing"
Parking garage and safe underground bike storage
Award-winning subsidized company restaurant and in-house cafes
Variety-rich fitness program in our ultra-modern 360m2 company gym
Regular after work, team, and company events
Comprehensive training and continuing education opportunities

Fulltime

R&D Manager, Product Development

The Manager, Product Development is responsible for executing and managing new p...

Location

United States , Ontario, California

Salary:

110000.00 - 120000.00 USD / Year

Ajinomoto Foods North America, Inc.

Expiration Date

Until further notice

Requirements

Strong foundation in food chemistry, microbiology, and/or process engineering
Advanced expertise in research methodologies, statistical analysis, and experimental design
Extensive experience in the full cycle of food product development, from recipe formulation and ingredient selection to factory-scale commercialization
Culinary experience is an asset, with proven success in formulating and developing recipes, and managing products from benchtop to commercial launch
Skilled in assessing team members' capabilities and fostering opportunities for growth and development
Proven project management experience, with the ability to set priorities and drive multiple projects to successful outcomes
Willingness to travel, with flexibility to accommodate up to 25% travel annually, based on business and project needs

Job Responsibility

Execute and manage new product development, continuous quality improvement, production transfers, profit enhancement, and technology development within the assigned product category, from benchtop to manufacturing scale-up
Execute the development of new products while continuously enhancing quality to meet company and customer specifications
Collaborate with and advise sales, marketing, and customer service representatives on new product requirements and specifications, target product quality, and resolution of customer complaints
Manage various aspects of product development, including cost analysis, packaging design, photo shoots, and other R&D initiatives
Create new and improved product samples for internal testing and provide prototypes to potential clients
Conduct product testing in the test kitchen, develop specific processing methods in the laboratory, and finalize them through Commercial Production (CP) tests in the production facility
Develop and implement monitoring methods and procedures for projects, including preparing records for expenditures, research findings, progress reports, and staff meetings to keep management informed of project status
Follow the New Product Introduction (NPI) process, developing recipes, production control sheets, and procedures for approval during product assessments
Support the presentation of new products and technologies to customers by providing technical assistance as requested by the marketing department
Cultivate and maintain relationships with vendors and customers, understanding their needs and identifying opportunities for growth, innovation, and improvement

What we offer

annual bonus

Fulltime

R&D Manager

The R&D Manager will lead local end-to-end Product Development activities across...

Location

United States , Jeffersonville, Indiana

Salary:

Not provided

1440 Foods Manufacturing

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Food Science, Food/Chemical Engineering, or equivalent required
Advanced degree preferred
8+ years of experience in Food/Beverage Consumer Packaged Goods industry
At least 4 years of experience managing teams through the entire product development cycle
Experience in Dairy and/or Nutritional products preferred
Active knowledge and experience in planning and conducting sensory evaluations
Experience working with nutritional software, technical and quality systems
Experience with Excel, ESHA Genesis, project management software, and/or Trace Gains preferred
Strategic technical mindset
Operates effectively in a matrixed environment

Job Responsibility

Lead local end-to-end Product Development activities across nutritional bars and powdered beverage portfolio
Plan and execute product development activities (innovation, cost-reduction, business continuity, efficiencies)
Lead R&D team through entire product development cycle from benchtop to commercial production
Ensure initiatives meet product development brief (technical requirements, cost, operational feasibility)
Drive data- and scientific-driven product development process
Lead team in addressing technical challenges (ingredient scouting, formulation, process scale-up)
Oversee planning and execution of benchtop, pilot, and full-scale plant production
Establish and execute best R&D practices (lab management, agile development, rapid prototyping)
Manage multiple concurrent projects, prioritize tasks, allocate resources
Act as role model for effective teamwork, build relationships with internal and external partners

Fulltime

Employee in quality management and/or regulatory affairs

As a professional QM/RA associate, you will be responsible for tasks in Quality ...

Location

Austria , Salzburg

Salary:

Not provided

Brainlab

Expiration Date

Until further notice

Requirements

Experience or training in Quality Management, preferably in the medical device sector (ISO 13485) or any industry with high regulatory standards
Knowledge of EU MDR (Medical Device Regulation) and experience with Class II or higher medical devices is an advantage
Familiarity with clinical evaluations and post-market surveillance processes under MDR guidelines is highly desirable
Knowledge of international regulations and certifications for medical devices is a plus
Fluent in German and English (written and spoken)
Flexible, team-oriented, and eager to work in an international environment

Job Responsibility

Support and collaborate across all areas of Quality Management (QM)
Ongoing control, improvement, and optimization of quality management processes and standards
Assist in creating and reviewing deviation reports, risk management plans, and CAPA (Corrective and Preventive Actions), ensuring thorough monitoring of corrective actions
Ensure the implementation and monitoring of regulatory requirements for medical devices
Assist with international product certifications and approvals
Liaise with regulatory bodies and authorities, including correspondence with notified bodies (globally)
Support clinical evaluations, ensuring that medical devices meet clinical safety and performance requirements in accordance with regulatory standards
Participate in post-market surveillance activities, including monitoring product performance in the market and managing feedback loops to continuously improve device safety and effectiveness
Support internal and external audits as well as supplier audits
Assist R&D with documentation and support the development process

What we offer

A motivating work atmosphere in a young, dynamic team
An exciting and varied scope of assignments customized for your skills and interests
The opportunity to grow with us, be directly involved and participate in our company’s success
A secure, permanent full-time contract
Generous social benefits within our culturally diverse enterprise
Freshly-cooked meals and healthy snacks provided daily
Good public transport connections and parking facilities available
Flexible working hours
Support for daily obligations (childcare, etc.)

Fulltime

Quality Compliance Manager

The Quality Compliance Manager will lead the implementation of a customized, ris...

Location

Taiwan , Taipei

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Bachelor’s degree in appropriate discipline or equivalent (e.g.: Biomedical Science / Nursing etc.)
Minimum 5 years in pharmaceutical industry and good in-depth knowledge of ICH GCP standards
2 years or more experience in Quality Management, Quality Assurance, or other relevant areas of the pharmaceutical/biotech industry where risk-based quality and quality by design are a core responsibility
Oversight and implementation of Quality Management Systems and experience managing quality in electronic QMS such as Veeva or TrackWise
Thorough understanding of Clinical R&D activities and Global/local Regulations
Knowledge of Regulatory Submission and local/Foreign Inspection Management procedures
Quality Oversight of Clinical Trials, including clinical trial protocol development, execution, and submissions
Excellent verbal and written communication skills, including strong business writing abilities and active listening
Ability to transform business and stakeholder feedback into clear, efficient processes using a straightforward language and format
Strong analytical, critical-thinking, and decision-making abilities

Job Responsibility

Review clinical trial protocols to ensure simplification, integration of lessons learned, and identification of critical data and processes
Provide quality oversight by assessing trial risks using the Risk Assessment Categorization Tool (RACT), ensuring accurate prioritization and mitigation of risks to patient safety, data integrity, and regulatory compliance—including country-specific risks relevant to Taiwan
Lead the development and implementation of Taiwan-specific Quality Plans, establishing local expertise to ensure adherence to applicable regulations
Collaborate with Clinical Quality Therapeutic Leads to support TA-specific data integrity, including technologies for data collection and measurement (e.g., biomarkers, imaging)
Contribute to the design and execution of TA and affiliate-specific Quality Assurance plans, including audit strategies (e.g., investigator site, affiliate, and study-level audits)
Support local clinical trial and cross-functional teams in managing quality activities such as issue resolution (e.g., deviations, CAPAs, serious breaches, privacy concerns), inspection readiness, and audit/inspection management
Monitor, analyze, and report compliance metrics and trends to key stakeholders and senior leadership, providing actionable recommendations
Drive innovation by exploring and applying sophisticated quality oversight methodologies, including AI, Natural Language Processing (NLP), and data analytics

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Fulltime

Director of R&D

The Director of R&D will lead a large engineering team in developing systems, so...

Location

Israel , Tel Aviv

Salary:

Not provided

Hewlett Packard Enterprise

Expiration Date

Until further notice

Requirements

First level university degree or equivalent experience required
15 or more years of related work experience, including 10 years of people management experience
Strong leadership skills, including coaching, team-building, and conflict resolution
Organizational and strategic management skills, including budget and business planning and forecasting
Strong analytical and problem solving skills
Ability to manage human capital across multiple geographies and organizations to drive workforce development and achieve desired results
Advanced communication skills catered to a wide variety of audiences (e.g., written, verbal, presentation)
mastery in English and local language
Extensive business acumen, technical knowledge, and industry experience encompassing one or more engineering, technology, and product domains
Advanced multi-tasking and prioritization skills

Job Responsibility

Provides direct and ongoing strategic leadership for a department or functional organization of multiple subordinate managers and high-level individual contributors designing and developing engineering solutions utilizing multiple engineering disciplines
Creates strategic and tactical operations and resource plans, goals, and priorities for assigned organization based on business and technology roadmap and functional objectives
Manages headcount, deliverables, schedules, and costs for the organization, ensuring that resources are appropriately allocated and that goals, objectives, timelines, and budgets are met in accordance with organizational metrics and business plans
Engages with program managers, marketing, supply chain, technical leaders, and executives to communicate program status, escalate issues, and guide and influence strategic decision-making
Manages senior relationships and escalated issues with outsourced partners and suppliers, including setting expectations regarding deliverables, product quality, schedules, and costs
ensures that organization is effectively leveraging outsourced resources
Identifies opportunities for and drives organizational initiatives and programs to support business process improvements and cost reductions
Provides overall people-care management for direct reports, including hiring, setting and monitoring of annual performance plans, coaching, and career development
drives and fosters organization-wide performance standards, expectations, and practices to support ongoing team member and process development.

What we offer

Comprehensive suite of benefits that supports physical, financial, and emotional wellbeing
Programs catered to career goals, including advancing skills or transitioning to other divisions
Unconditional inclusion, celebrating individual uniqueness
Flexibility to manage work and personal needs.

Fulltime

Manager, R&D Process Quality

Amgen

Location:
India , Hyderabad

Category:
-

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
January 06, 2026

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