21 jobs in Reckitt

The position is accountable to the GCMA Manager and finally to the GCMA Director, working closely with others as part of the matrix. The role interacts as appropriate with other internal functions including Regulatory and Safety (RAS), Quality, Evidence Generation and Clinical Research (EG&CR), R&D, Marketing, Professional Relations etc. The role also supports interactions with external partners, including key opinion leaders.

Specific tasks and responsibilities include, but are not limited to:

• Represent the GCMA Germ Protection team and contribute expertise in cross-functional project meetings

• Conduct a fair-balanced assessment of efficacy and safety data and provide advice on the best approach to drive brand growth with support from GCMA Manager

• Support and educate teams with understanding of the literature, new clinical data and current medical opinion on category topics including healthy skin and germ protection

• Partner with the other Medical Science team members under supervision to:

o Provide strategic medical input in category development leading brand science for product innovation and claims, mainly related to cosmetics and germ protection products like biocides

o Proactively partner with the project teams, providing medical input and strategic advice to ensure the feasibility and success of product development initiatives

o Provide ideas/concepts for constructing the product pipelines (e.g. new products, new combinations, new technologies, novel evidence generation techniques)

o Provide medical support and oversight for promotional activities

o Assist in registration and development of Reckitt products globally

• These include but are not limited to:- clinical overviews and summaries, integrated summaries of safety and efficacy, clinical documents such as Study Protocols and other Medical documents

• Collaborate with subject matter experts across multiple departments to ensure quality and technical accuracy of documentation

• Prepare responses to Medical Information requests where appropriate

• Conduct systematic literature searches/reviews as necessary

• Ensure that working documents and other appropriate documentation are updated and current

• Understand clinical and medical data for the product and competitors

• Bachelor's Degree preferably associated to healthcare or the life sciences (eg basic science, pharmacy, nursing or medical) is required

• Postgraduate qualifications preferred

• Experience in the medical and pharmaceutical / consumer health industry and knowledge of the role of Medical Affairs is a distinct advantage

• Experience in systematic searches, reviewing scientific data, and preparing medical or scientific documents (e.g. post graduate experience in relevant science, publications and experience in medical writing, systematic review and clinical data appraisal) to a high standard is highly desirable.

• Knowledge of research methodology, information management and regulatory requirements and an understanding of healthcare compliance and guidelines related to cosmetics or consumer products is desirable. Proven ability to generate, analyse and interpret scientific and clinical data is required.

• Previous experience of work in Product Research and Development, or experience of Clinical studies, with examples of successful product launches is an advantage

• Proven ability as a team player, able to work within a matrix, with excellent oral and written communication skills.

The Candidate will demonstrate the following capabilities:

• Leadership capability – demonstrated ability to lead specific tasks within projects as well as working strategically according to the portfolio priorities

• Strategic Thinking – maintains competitive advantage by carefully considering the issues and competing priorities within a situation, program or portfolio and then developing a strategy that includes the strategic application of available principles, tools and systems.

• Business Acumen – Understands the implications of decisions related to human, financial, material and information resources, from a business perspective and uses this knowledge to plan, implement and manage clinical research within R&D.

• Project Management – Demonstrates the discipline of risk-based planning, organising and managing resources to bring about the successful completion of specific project goals and objectives in accordance with defined quality and time-based metrics.

Key Attributes:

• Proactive mindset.

• Passion for strategy development and delivery.

• Team player

• Strong skills in managing multiple projects simultaneously with an ability to prioritise appropriately.

• Track record of building strong internal and external networks.

• Strong interpersonal, verbal and written communication skills.

• Fluency in English (oral and written).

• Thrives working in fast paced, innovative environment while remaining flexible, resourceful and reliable.

• Proven ability to develop appropriate research strategy and conduct a systematic review of available published data including retrieval, critical appraisal and appropriate citing of literature

Responsibilities:

To monitor the site quality system compliance requirement of Schedule M, MHRA, SAHPRA, ISO 9001 and other regulatory authorities.

To Monitor planning and conduct of Self Inspection. Initiate and approve the corrective action plans. Compliance follow-ups for external audits.

Investigate, review Deviations, Quality incidents and ensure adequate CAPA plans, its implementation and close-out in Quality One software.

Ensure change controls are initiated, reviewed, & documented in Quality One software.

Investigate, review consumer complaints & ensure appropriate CAPA implementation.

Monitor the annual supplier audit schedule, Assessments and conduct audits for raw material and packing material suppliers as per schedule.

Lead and manage the local Quality Assurance team.

Ensure that finished products released as per the release procedure

Review and approval of Supplier based on document assessment and audit outcome

Prepare audit compliance reports and ensure CAPA in co-ordination with suppliers

Monitor the Out of Specification & Out of trend results investigations

Review audit trails for laboratory instruments.

Review and approval of batch records and release of FG.

Review, approve the Quality assurance SOP's and SOP's related to Mysore site.

To review the site policy and procedure's like VMP, SMF, PVMP, Protocols, specifications, test methods, batch documents & other site documents.

Trend analysis of quality management system key performance indicators.

To ensure that appropriate qualification, requalification and validations are done for site equipment's, area, and systems.

Ensure control, maintenance, and issue of documentation for manufacture, compliant with the marketing and manufacturing authorizations requirements (regulatory bodies) and effective/efficient delivery of operational activities.

To ensure the management review and annual product review program are maintained according to concerned GMP and QMS requirement.

Ensure store checks are performed as per procedure

Ensure the maintenance of department and premises.

To manage Quality Critical Event and ensure that event is escalated to the concerned party according to concerned global policy. To contribute as a member of quality critical event for reviewing of decision for the event such as continuing production and sales and level of recall etc.

To ensure and monitor key quality process during NPD/EPD roll out from site.

Ensure appropriate qualification and validations for site equipment's, area and systems

Ensure required initial and continuing training of department personnel & adapted according to need. Provide GMP trainings.

To support all key initiative at the site as key member of the Site leadership team.

Site Management review meetings & ensure completion of follow up actions.

Other responsibilities assigned by the management time to time.

Motivate and drive the Quality team to continually improve the Quality Culture at site.

To perform, review of the site risk register and evaluation.

Ensure the monitoring and control of the manufacturing environment, plant hygiene, process validation, training.

This role of Category R&D Associate is to support the development of NPD, EPD & BDI initiatives based on relevant consumer insights for the bar soap format.

The R&D Associate will be responsible for formulation development, analytical testing and project planning to ensure all project milestones are met as per timelines.

• Lead regional technical developments on key bar soap initiatives for Reckitt's Dettol brand by leveraging prior experience/expertise to help drive pipeline growth.
• Oversee a small technical team on all aspects of development including bar soap formulation, processing, manufacture/scale-up and R&D capability in region.
• Develop technical plans to meet project brief objectives and conduct all technical testing to ensure high quality output & impact.
• Initiate and leverage partnerships with local and global raw material suppliers to deliver existing and new bar soap innovation needs.
• Work with R&D colleagues, regulatory and marketing to support and validate new bar soap claims.
• Partner with supply and quality to conduct all required industrial trials to ensure successful delivery; issue trial reports with findings/recommendations.
• Build a cohesive, motivated and professional team with a result-oriented culture, where personal responsibility/initiative, teamwork, and mutual respect are key.
• Be responsible for the development of his/her colleagues to enable them to achieve their full potential including formulation development experience on GP PC segments.
• Responsible for ensuring that all development activity within the team conforms to health & safety and quality requirements.

QUALIFICATIONS

• Master's Degree (Chemistry, pharmacy, chemical engineering or other relevant field of science).

EXPERIENCE

• Minimum 5-10 years R&D experience with a proven track record of delivery.
• Experience of working in cosmetic formulation environment is desirable.
• Strong technical background in bar soap formulation and processing.
• Strong interpersonal skills and willingness to work in a cross functional environment including marketing, supply, procurement, regulatory, clinical and legal team
• Oral & written communication skills to effectively provide feedback to reporting manager and cross functional team members.
• Global mindset, commercial understanding of corporate & operational business issues.
• Strong analytical skills with the ability to think strategically, develop tactics and measurable implementation plans and able to transform solid thinking into action.

The position is accountable to the GCMA Manager and finally to the GCMA Director, working closely with others as part of the matrix. The role interacts as appropriate with other internal functions including Regulatory and Safety (RAS), Quality, Evidence Generation and Clinical Research (EG&CR), R&D, Marketing, Professional Relations etc. The role also supports interactions with external partners, including key opinion leaders.

Specific tasks and responsibilities include, but are not limited to:

• Represent the GCMA Germ Protection team and contribute expertise in cross-functional project meetings

• Conduct a fair-balanced assessment of efficacy and safety data and provide advice on the best approach to drive brand growth with support from GCMA Manager

• Support and educate teams with understanding of the literature, new clinical data and current medical opinion on category topics including healthy skin and germ protection

• Partner with the other Medical Science team members under supervision to:

o Provide strategic medical input in category development leading brand science for product innovation and claims, mainly related to cosmetics and germ protection products like biocides

o Proactively partner with the project teams, providing medical input and strategic advice to ensure the feasibility and success of product development initiatives

o Provide ideas/concepts for constructing the product pipelines (e.g. new products, new combinations, new technologies, novel evidence generation techniques)

o Provide medical support and oversight for promotional activities

o Assist in registration and development of Reckitt products globally

• These include but are not limited to:- clinical overviews and summaries, integrated summaries of safety and efficacy, clinical documents such as Study Protocols and other Medical documents

• Collaborate with subject matter experts across multiple departments to ensure quality and technical accuracy of documentation

• Prepare responses to Medical Information requests where appropriate

• Conduct systematic literature searches/reviews as necessary

• Ensure that working documents and other appropriate documentation are updated and current

• Understand clinical and medical data for the product and competitors

• Bachelor’s Degree preferably associated to healthcare or the life sciences (eg basic science, pharmacy, nursing or medical) is required

• Postgraduate qualifications preferred

• Experience in the medical and pharmaceutical / consumer health industry and knowledge of the role of Medical Affairs is a distinct advantage

• Experience in systematic searches, reviewing scientific data, and preparing medical or scientific documents (e.g. post graduate experience in relevant science, publications and experience in medical writing, systematic review and clinical data appraisal) to a high standard is highly desirable.

• Knowledge of research methodology, information management and regulatory requirements and an understanding of healthcare compliance and guidelines related to cosmetics or consumer products is desirable. Proven ability to generate, analyse and interpret scientific and clinical data is required.

• Previous experience of work in Product Research and Development, or experience of Clinical studies, with examples of successful product launches is an advantage

• Proven ability as a team player, able to work within a matrix, with excellent oral and written communication skills.

The Candidate will demonstrate the following capabilities:

• Leadership capability – demonstrated ability to lead specific tasks within projects as well as working strategically according to the portfolio priorities

• Strategic Thinking – maintains competitive advantage by carefully considering the issues and competing priorities within a situation, program or portfolio and then developing a strategy that includes the strategic application of available principles, tools and systems.

• Business Acumen – Understands the implications of decisions related to human, financial, material and information resources, from a business perspective and uses this knowledge to plan, implement and manage clinical research within R&D.

• Project Management – Demonstrates the discipline of risk-based planning, organising and managing resources to bring about the successful completion of specific project goals and objectives in accordance with defined quality and time-based metrics.

Key Attributes:

• Proactive mindset.

• Passion for strategy development and delivery.

• Team player

• Strong skills in managing multiple projects simultaneously with an ability to prioritise appropriately.

• Track record of building strong internal and external networks.

• Strong interpersonal, verbal and written communication skills.

• Fluency in English (oral and written).

• Thrives working in fast paced, innovative environment while remaining flexible, resourceful and reliable.

• Proven ability to develop appropriate research strategy and conduct a systematic review of available published data including retrieval, critical appraisal and appropriate citing of literature

The position is accountable to the GCMA Manager and finally to the GCMA Director, working closely with others as part of the matrix. The role interacts as appropriate with other internal functions including Regulatory and Safety (RAS), Quality, Evidence Generation and Clinical Research (EG&CR), R&D, Marketing, Professional Relations etc. The role also supports interactions with external partners, including key opinion leaders.

Specific tasks and responsibilities include, but are not limited to:

• Represent the GCMA Germ Protection team and contribute expertise in cross-functional project meetings

• Conduct a fair-balanced assessment of efficacy and safety data and provide advice on the best approach to drive brand growth with support from GCMA Manager

• Support and educate teams with understanding of the literature, new clinical data and current medical opinion on category topics including healthy skin and germ protection

• Partner with the other Medical Science team members under supervision to:

o Provide strategic medical input in category development leading brand science for product innovation and claims, mainly related to cosmetics and germ protection products like biocides

o Proactively partner with the project teams, providing medical input and strategic advice to ensure the feasibility and success of product development initiatives

o Provide ideas/concepts for constructing the product pipelines (e.g. new products, new combinations, new technologies, novel evidence generation techniques)

o Provide medical support and oversight for promotional activities

o Assist in registration and development of Reckitt products globally

• These include but are not limited to:- clinical overviews and summaries, integrated summaries of safety and efficacy, clinical documents such as Study Protocols and other Medical documents

• Collaborate with subject matter experts across multiple departments to ensure quality and technical accuracy of documentation

• Prepare responses to Medical Information requests where appropriate

• Conduct systematic literature searches/reviews as necessary

• Ensure that working documents and other appropriate documentation are updated and current

• Understand clinical and medical data for the product and competitors

• Bachelor’s Degree preferably associated to healthcare or the life sciences (eg basic science, pharmacy, nursing or medical) is required

• Postgraduate qualifications preferred

• Experience in the medical and pharmaceutical / consumer health industry and knowledge of the role of Medical Affairs is a distinct advantage

• Experience in systematic searches, reviewing scientific data, and preparing medical or scientific documents (e.g. post graduate experience in relevant science, publications and experience in medical writing, systematic review and clinical data appraisal) to a high standard is highly desirable.

• Knowledge of research methodology, information management and regulatory requirements and an understanding of healthcare compliance and guidelines related to cosmetics or consumer products is desirable. Proven ability to generate, analyse and interpret scientific and clinical data is required.

• Previous experience of work in Product Research and Development, or experience of Clinical studies, with examples of successful product launches is an advantage

• Proven ability as a team player, able to work within a matrix, with excellent oral and written communication skills.

The Candidate will demonstrate the following capabilities:

• Leadership capability – demonstrated ability to lead specific tasks within projects as well as working strategically according to the portfolio priorities

• Strategic Thinking – maintains competitive advantage by carefully considering the issues and competing priorities within a situation, program or portfolio and then developing a strategy that includes the strategic application of available principles, tools and systems.

• Business Acumen – Understands the implications of decisions related to human, financial, material and information resources, from a business perspective and uses this knowledge to plan, implement and manage clinical research within R&D.

• Project Management – Demonstrates the discipline of risk-based planning, organising and managing resources to bring about the successful completion of specific project goals and objectives in accordance with defined quality and time-based metrics.

Key Attributes:

• Proactive mindset.

• Passion for strategy development and delivery.

• Team player

• Strong skills in managing multiple projects simultaneously with an ability to prioritise appropriately.

• Track record of building strong internal and external networks.

• Strong interpersonal, verbal and written communication skills.

• Fluency in English (oral and written).

• Thrives working in fast paced, innovative environment while remaining flexible, resourceful and reliable.

• Proven ability to develop appropriate research strategy and conduct a systematic review of available published data including retrieval, critical appraisal and appropriate citing of literature

Responsibilities:

To monitor the site quality system compliance requirement of Schedule M, MHRA, SAHPRA, ISO 9001 and other regulatory authorities.

To Monitor planning and conduct of Self Inspection. Initiate and approve the corrective action plans. Compliance follow-ups for external audits.

Investigate, review Deviations, Quality incidents and ensure adequate CAPA plans, its implementation and close-out in Quality One software.

Ensure change controls are initiated, reviewed, & documented in Quality One software.

Investigate, review consumer complaints & ensure appropriate CAPA implementation.

Monitor the annual supplier audit schedule, Assessments and conduct audits for raw material and packing material suppliers as per schedule.

Lead and manage the local Quality Assurance team.

Ensure that finished products released as per the release procedure

Review and approval of Supplier based on document assessment and audit outcome

Prepare audit compliance reports and ensure CAPA in co-ordination with suppliers

Monitor the Out of Specification & Out of trend results investigations

Review audit trails for laboratory instruments.

Review and approval of batch records and release of FG.

Review, approve the Quality assurance SOP’s and SOP’s related to Mysore site.

To review the site policy and procedure’s like VMP, SMF, PVMP, Protocols, specifications, test methods, batch documents & other site documents.

Trend analysis of quality management system key performance indicators.

To ensure that appropriate qualification, requalification and validations are done for site equipment’s, area, and systems.

Ensure control, maintenance, and issue of documentation for manufacture, compliant with the marketing and manufacturing authorizations requirements (regulatory bodies) and effective/efficient delivery of operational activities.

To ensure the management review and annual product review program are maintained according to concerned GMP and QMS requirement.

Ensure store checks are performed as per procedure

Ensure the maintenance of department and premises.

To manage Quality Critical Event and ensure that event is escalated to the concerned party according to concerned global policy. To contribute as a member of quality critical event for reviewing of decision for the event such as continuing production and sales and level of recall etc.

To ensure and monitor key quality process during NPD/EPD roll out from site.

Ensure appropriate qualification and validations for site equipment’s, area and systems

Ensure required initial and continuing training of department personnel & adapted according to need. Provide GMP trainings.

To support all key initiative at the site as key member of the Site leadership team.

Site Management review meetings & ensure completion of follow up actions.

Other responsibilities assigned by the management time to time.

Motivate and drive the Quality team to continually improve the Quality Culture at site.

To perform, review of the site risk register and evaluation.

Ensure the monitoring and control of the manufacturing environment, plant hygiene, process validation, training.

Responsibilities:

To monitor the site quality system compliance requirement of Schedule M, MHRA, SAHPRA, ISO 9001 and other regulatory authorities.

To Monitor planning and conduct of Self Inspection. Initiate and approve the corrective action plans. Compliance follow-ups for external audits.

Investigate, review Deviations, Quality incidents and ensure adequate CAPA plans, its implementation and close-out in Quality One software.

Ensure change controls are initiated, reviewed, & documented in Quality One software.

Investigate, review consumer complaints & ensure appropriate CAPA implementation.

Monitor the annual supplier audit schedule, Assessments and conduct audits for raw material and packing material suppliers as per schedule.

Lead and manage the local Quality Assurance team.

Ensure that finished products released as per the release procedure

Review and approval of Supplier based on document assessment and audit outcome

Prepare audit compliance reports and ensure CAPA in co-ordination with suppliers

Monitor the Out of Specification & Out of trend results investigations

Review audit trails for laboratory instruments.

Review and approval of batch records and release of FG.

Review, approve the Quality assurance SOP’s and SOP’s related to Mysore site.

To review the site policy and procedure’s like VMP, SMF, PVMP, Protocols, specifications, test methods, batch documents & other site documents.

Trend analysis of quality management system key performance indicators.

To ensure that appropriate qualification, requalification and validations are done for site equipment’s, area, and systems.

Ensure control, maintenance, and issue of documentation for manufacture, compliant with the marketing and manufacturing authorizations requirements (regulatory bodies) and effective/efficient delivery of operational activities.

To ensure the management review and annual product review program are maintained according to concerned GMP and QMS requirement.

Ensure store checks are performed as per procedure

Ensure the maintenance of department and premises.

To manage Quality Critical Event and ensure that event is escalated to the concerned party according to concerned global policy. To contribute as a member of quality critical event for reviewing of decision for the event such as continuing production and sales and level of recall etc.

To ensure and monitor key quality process during NPD/EPD roll out from site.

Ensure appropriate qualification and validations for site equipment’s, area and systems

Ensure required initial and continuing training of department personnel & adapted according to need. Provide GMP trainings.

To support all key initiative at the site as key member of the Site leadership team.

Site Management review meetings & ensure completion of follow up actions.

Other responsibilities assigned by the management time to time.

Motivate and drive the Quality team to continually improve the Quality Culture at site.

To perform, review of the site risk register and evaluation.

Ensure the monitoring and control of the manufacturing environment, plant hygiene, process validation, training.

The position is accountable to the GCMA Manager and finally to the GCMA Director, working closely with others as part of the matrix. The role interacts as appropriate with other internal functions including Regulatory and Safety (RAS), Quality, Evidence Generation and Clinical Research (EG&CR), R&D, Marketing, Professional Relations etc. The role also supports interactions with external partners, including key opinion leaders.

Specific tasks and responsibilities include, but are not limited to:

• Represent the GCMA Germ Protection team and contribute expertise in cross-functional project meetings

• Conduct a fair-balanced assessment of efficacy and safety data and provide advice on the best approach to drive brand growth with support from GCMA Manager

• Support and educate teams with understanding of the literature, new clinical data and current medical opinion on category topics including healthy skin and germ protection

• Partner with the other Medical Science team members under supervision to:

o Provide strategic medical input in category development leading brand science for product innovation and claims, mainly related to cosmetics and germ protection products like biocides

o Proactively partner with the project teams, providing medical input and strategic advice to ensure the feasibility and success of product development initiatives

o Provide ideas/concepts for constructing the product pipelines (e.g. new products, new combinations, new technologies, novel evidence generation techniques)

o Provide medical support and oversight for promotional activities

o Assist in registration and development of Reckitt products globally

• These include but are not limited to:- clinical overviews and summaries, integrated summaries of safety and efficacy, clinical documents such as Study Protocols and other Medical documents

• Collaborate with subject matter experts across multiple departments to ensure quality and technical accuracy of documentation

• Prepare responses to Medical Information requests where appropriate

• Conduct systematic literature searches/reviews as necessary

• Ensure that working documents and other appropriate documentation are updated and current

• Understand clinical and medical data for the product and competitors

• Bachelor’s Degree preferably associated to healthcare or the life sciences (eg basic science, pharmacy, nursing or medical) is required

• Postgraduate qualifications preferred

• Experience in the medical and pharmaceutical / consumer health industry and knowledge of the role of Medical Affairs is a distinct advantage

• Experience in systematic searches, reviewing scientific data, and preparing medical or scientific documents (e.g. post graduate experience in relevant science, publications and experience in medical writing, systematic review and clinical data appraisal) to a high standard is highly desirable.

• Knowledge of research methodology, information management and regulatory requirements and an understanding of healthcare compliance and guidelines related to cosmetics or consumer products is desirable. Proven ability to generate, analyse and interpret scientific and clinical data is required.

• Previous experience of work in Product Research and Development, or experience of Clinical studies, with examples of successful product launches is an advantage

• Proven ability as a team player, able to work within a matrix, with excellent oral and written communication skills.

The Candidate will demonstrate the following capabilities:

• Leadership capability – demonstrated ability to lead specific tasks within projects as well as working strategically according to the portfolio priorities

• Strategic Thinking – maintains competitive advantage by carefully considering the issues and competing priorities within a situation, program or portfolio and then developing a strategy that includes the strategic application of available principles, tools and systems.

• Business Acumen – Understands the implications of decisions related to human, financial, material and information resources, from a business perspective and uses this knowledge to plan, implement and manage clinical research within R&D.

• Project Management – Demonstrates the discipline of risk-based planning, organising and managing resources to bring about the successful completion of specific project goals and objectives in accordance with defined quality and time-based metrics.

Key Attributes:

• Proactive mindset.

• Passion for strategy development and delivery.

• Team player

• Strong skills in managing multiple projects simultaneously with an ability to prioritise appropriately.

• Track record of building strong internal and external networks.

• Strong interpersonal, verbal and written communication skills.

• Fluency in English (oral and written).

• Thrives working in fast paced, innovative environment while remaining flexible, resourceful and reliable.

• Proven ability to develop appropriate research strategy and conduct a systematic review of available published data including retrieval, critical appraisal and appropriate citing of literature

This role of Category R&D Associate is to support the development of NPD, EPD & BDI initiatives based on relevant consumer insights for the bar soap format.

The R&D Associate will be responsible for formulation development, analytical testing and project planning to ensure all project milestones are met as per timelines.

• Lead regional technical developments on key bar soap initiatives for Reckitt’s Dettol brand by leveraging prior experience/expertise to help drive pipeline growth.
• Oversee a small technical team on all aspects of development including bar soap formulation, processing, manufacture/scale-up and R&D capability in region.
• Develop technical plans to meet project brief objectives and conduct all technical testing to ensure high quality output & impact.
• Initiate and leverage partnerships with local and global raw material suppliers to deliver existing and new bar soap innovation needs.
• Work with R&D colleagues, regulatory and marketing to support and validate new bar soap claims.
• Partner with supply and quality to conduct all required industrial trials to ensure successful delivery; issue trial reports with findings/recommendations.
• Build a cohesive, motivated and professional team with a result-oriented culture, where personal responsibility/initiative, teamwork, and mutual respect are key.
• Be responsible for the development of his/her colleagues to enable them to achieve their full potential including formulation development experience on GP PC segments.
• Responsible for ensuring that all development activity within the team conforms to health & safety and quality requirements.

QUALIFICATIONS

• Master’s Degree (Chemistry, pharmacy, chemical engineering or other relevant field of science).

EXPERIENCE

• Minimum 5-10 years R&D experience with a proven track record of delivery.
• Experience of working in cosmetic formulation environment is desirable.
• Strong technical background in bar soap formulation and processing.
• Strong interpersonal skills and willingness to work in a cross functional environment including marketing, supply, procurement, regulatory, clinical and legal team
• Oral & written communication skills to effectively provide feedback to reporting manager and cross functional team members.
• Global mindset, commercial understanding of corporate & operational business issues.
• Strong analytical skills with the ability to think strategically, develop tactics and measurable implementation plans and able to transform solid thinking into action.