2,328 Analytical Scientist jobs in India

Job Description

Job Summary
We are seeking a highly skilled Analytical Scientist in to join our Research and Development team for Injectable Division for developing and validating analytical methods for injectable products, ensuring compliance with the regulatory requirements, conducting literature reviews, scaling up for manufacturing of batches, coordinating manufacturing readiness, overseeing plant execution, and facilitating seamless technology transfer. This role demands a strong understanding of analytical principles, excellent documentation skills, and the ability to work effectively in a collaborative team environment. scaling up for manufacturing of batches, coordinating manufacturing readiness, overseeing plant execution, and facilitating seamless technology transfer.

Roles & Responsibilities

• You will be responsible Analytical method development and validation of injectable products. 
• You will be responsible to perform the Drug Master File/Literature review and procure the relevant columns and standards in order to initiate the analytical method development. Stay updated with the latest literature and industry developments in the field.
• You will be responsible to develop analytical methods, conduct validation studies to ensure the accuracy and reliability of the methods, and transfer validated methods to the Quality Control (QC) department.
• You will be responsible to execute analytical activities as per defined procedures, document the data and send the respective record of analysis to group leader/analytical expert for the review and release in order to provide the approved results to formulation team. 
• You will be responsible for analytical method development for drug products for various tests mentioned in the specification in order to analyse the product development batches for the prototype screening. 
• You will be responsible for analytical method validation activities at the manufacturing sites providing method development reports to verify the validation parameters and ensure the execution of method validation as per the regulatory requirement in order to provide the authentic analytical validation report for the regulatory filing. 
• You will be responsible for analytical method transfer to plant locations successfully in order to train the Quality Control (QC) team on the methods for the Exhibit and commercial batch analysis at plant.
• You will be responsible to ensure proper maintenance of laboratory equipment as per Good Laboratory Practices (GLP) standards to guarantee accurate and reliable results.
• You will be responsible to calibrate instruments as per the calibration schedule and strictly follow Standard Operating Procedures (SOPs) to maintain consistency and accuracy.
• You will be responsible to maintain a clean and organized work area, and ensure that the laboratory environment is controlled at the required temperature for optimal analytical conditions.
• You will be responsible to keep all relevant documents well-maintained and organized for easy access and compliance with internal and external auditing requirements. 

Qualifications

Educational qualification: Masters in Science/ Organic chemistry/ Pharmaceutical Sciences

Minimum work experience: 5 years of experience in analytical method development

Skills & attributes:

Technical Skills

• Extensive work experience in analytical method development and validation of injectable products.
• Proven experience with injectable, ophthalmic, peptide, and suspension products.
• Demonstrated expertise in sameness and characterization studies for complex molecules.
• Proficient understanding of various analytical techniques including HPLC, GC, UV, FTIR, KF, and mass spectrometry.
• Advanced skills in troubleshooting analytical methods and instruments.
• Comprehensive understanding of Abbreviated New Drug Application (ANDA) filing requirements.
• Strong knowledge of regulatory guidelines and industry standards related to pharmaceutical product development and analysis.
• Proven experience in method development, validation, transfer, and documentation in compliance with regulatory requirements.
• Familiarity with Quality by Design (QbD) principles and their application in analytical method development.
• Experience with stability testing and forced degradation studies for injectable products.
• Knowledge of current Good Manufacturing Practices (cGMP) and ICH guidelines.

Behavioral Skills

• Strong analytical and problem-solving abilities, with a keen attention to detail
• Excellent communication and interpersonal skills, with the ability to effectively present complex analytical data to diverse audiences.
• Ability to work collaboratively with own team and cross-functional teams in a fast-paced environment.
• Demonstrated project management skills and ability to handle multiple projects simultaneously.
• Adaptability and willingness to learn new techniques and methodologies.
• Strong commitment to safety protocols and environmental regulations in laboratory settings.

Additional Information

About the Department

Integrated Product Development Organisation   

We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) & Other dosages
Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years.

Benefits Offered
At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs.
The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.

Our Work Culture
Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic.
For more details, please visit our career website at

• Analytical method development
• Routine Analysis by HPLC, GC, LCMS, KF and FTIR
• Analytical documentation as like Protocols, specifications etc.
• Calibration of HPLC, GC instruments
• Aware about data integrity and ALCOA
• Chiral method development

Skills Required
Ftir, data integrity, Kf, Gc, Lcms

A world-leading research institution is seeking a highly experienced Principal Scientist in Analytical Chemistry to lead critical research initiatives in Lucknow, Uttar Pradesh . This position offers an unparalleled opportunity to work on cutting-edge scientific projects and contribute to significant advancements in the field. You will be responsible for developing, validating, and implementing advanced analytical methodologies for the characterization of complex chemical substances and biological samples. Key duties include overseeing laboratory operations, managing analytical instrumentation (e.g., HPLC, GC-MS, NMR, ICP-MS), troubleshooting instrument performance issues, and ensuring data integrity and compliance with regulatory standards (e.g., GLP, GMP). You will mentor and guide junior scientists and technicians, lead research projects from conception to completion, and contribute to grant writing and scientific publications. We are looking for a candidate with a Ph.D. in Analytical Chemistry, Physical Chemistry, or a related field, with a minimum of 8-10 years of post-doctoral or industry experience in analytical method development and validation. A proven track record of publications in high-impact journals and experience in managing research projects and teams are essential. Expertise in spectroscopic, chromatographic, and mass spectrometric techniques is required. Excellent leadership, communication, and problem-solving skills are critical. This role is based in a state-of-the-art facility and offers a competitive salary and benefits package, along with excellent opportunities for professional growth and scientific discovery.

Our client, a leading pharmaceutical research and development company, is seeking an accomplished Senior Research Scientist with expertise in Analytical Chemistry to join our esteemed, fully remote research team. This position is instrumental in advancing drug discovery and development through the application of sophisticated analytical methodologies. You will lead the development, validation, and implementation of cutting-edge analytical techniques for the characterization of active pharmaceutical ingredients (APIs) and finished drug products. Responsibilities include designing and executing analytical studies, troubleshooting complex analytical challenges, and ensuring the quality and reliability of data generated. You will collaborate closely with formulation scientists, chemists, and regulatory affairs specialists to support project milestones and regulatory submissions. Expertise in various analytical techniques, such as HPLC, GC, Mass Spectrometry, NMR, and dissolution testing, is essential. The ideal candidate will hold a Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, or a related field, with a minimum of 8 years of progressive experience in pharmaceutical R&D. A proven track record in developing and validating analytical methods according to regulatory guidelines (e.g., ICH) is mandatory. Strong understanding of pharmacopeial standards and regulatory requirements for drug development is crucial. Excellent analytical, problem-solving, and communication skills are paramount. You should be adept at managing multiple projects, mentoring junior scientists, and contributing to a culture of scientific excellence and innovation within a completely remote working environment. This is an outstanding opportunity to shape the analytical strategy for critical pharmaceutical projects and contribute to bringing life-changing medicines to patients worldwide.

**Description**
At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health.
USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds-regardless of background-to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment.
**Brief Job Overview**
This is a non-supervisory position to support process development and scale-up of Active Pharmaceutical Ingredient (API) and related materials. The successful applicant in this role will work on projects including Analytical Method Development and evaluation for in-process samples for synthetic chemistry. The successful candidate will also perform a variety of non-routine and routine analytical tests, maintains safety & GLP environment in the lab including development/validation of methods, stability studies and research projects in analytical chemistry. The successful applicant will direct, troubleshoot, and share insights on complex projects while drawing independent conclusions about the results and determining how to proceed with the project. They closely collaborate with other scientists and/or other USP personnel.
**How will YOU create impact here at USP?**
As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.
Additionally, USP's People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.
The Scientist IV has the following responsibilities:
+ Support reaction monitoring, scale-up and final analysis of samples as per monograph /in-house procedures including method development/validation if required. Prepare development reports for Synthetic Support projects. Execute projects per the approved test protocols if assigned.
+ In collaboration with the synthetics team evaluate, implement and grow Process Analytical Technologies (PAT) capabilities and expertise. This includes evaluation of process monitoring, understanding, and control via in line, online and at line techniques. Serve as technical expert and champion for PAT and/or process model building.
+ Plan, execute, and complete the projects as per specifications, timelines, and budget.
+ Responsible for preparation and review of SOPs, protocols, reports, etc.
+ Ensure project requirements by coordinating with external vendors and all internal relevant departments.
+ Responsible for ensuring the required maintenance and calibrations of the equipment
+ Responsible for preparing, executing and completing IQ/OQ/PQ of new instruments as assigned
+ Preparation and planning for ISO-9001 certification/recertification by participating actively, verification of protocols and related documents and take an active role in the internal as well as external QA audits and address the audit issues in a timely manner.
+ Maintain GLP & implement safety procedures while working in Lab.
+ Work on any other assigned tasks/ lab management activities.
+ Conversant with lab safety norms and strictly follow them.
+ Collaborate within the team and cross functional teams
+ Learn and practice Diversity, Equity, Inclusion & Belonging culture
**Who is USP Looking For?**
The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience:
The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience:
+ MSc. in Analytical Chemistry / Organic Chemistry/M. Pharm, having 8-10 years of experience in Analytical Research and Development or Ph.D. with 4-7 years of experience in Analytical Research and Development.
+ Must have hands on experience in working with chemical methods and handling instruments like HPLC, GC, LC-MS, GC-MS, FTIR, UV-Visible, wet chemistry, etc.
+ Understanding of process analytical technology, chemometrics, and knowledge of in-line, online, at line process analytical tools (e.g., IR, Raman, HPLC)
+ Experience in analytical testing and development with focus on process analytical chemistry and to understand, monitor and control chemical processes/reactions.
+ A comprehensive understanding of the science involved in the development of synthetic organic molecules and analytical chemistry.
+ Ability to perform analytical method developments and method validations as and when required.
+ Excellent technical writing and verbal communication skills
+ Good interpersonal skills and proven ability to function in a team-oriented environment are necessary.
We especially welcome applications from those who hold historically marginalized and/or underrepresented identities. This job description provides a portrait of an ideal candidate. Candidates who possess many, though perhaps not all, qualifications are encouraged to apply.
**Additional Desired Preferences**
+ Hands on experience with PAT instruments, techniques, and models such as in line, at line, or online IR, Raman, HPLC, NMR, etc.
+ Experience with a wide variety of software and laboratory information systems, including chemometric modeling software
+ Working knowledge of API manufacturing and product testing (e.g. ICH guidelines, USP general chapters and monographs)
+ Expertise with USP compendial methods and requirements (e.g. monographs and general chapter) and ICH quality guidelines
+ Pharmaceutical laboratory experience, method development and method implementation in manufacturing environments, and/or continuous manufacturing experience.
+ Strong project management skills with ability to be effective both independently and in collaborative teams
+ Skilled in evaluation and interpretation of data; Ability to multi-task.
+ Skilled in anticipating, troubleshooting, and solving technical problems.
+ Takes personal responsibility to ensure work is delivered on time and is of the highest quality.
**Supervisory Responsibilities**
NA
**Benefits**
USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.
Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP.
**Job Category** Chemistry & Scientific Standards
**Job Type** Full-Time

SPI Pharma , a part of Associated British Foods plc, is a trusted global leader in providing innovative solutions to the pharmaceutical and nutraceutical industries. With decades of expertise, SPI Pharma specializes in the development and supply of high-quality excipients, antacid actives, drug delivery systems, and taste-masked technologies.

Our products help pharmaceutical companies create better-tasting, patient-friendly, and more effective oral dosage forms , including tablets, capsules, soft gels, and liquid suspensions. We support our customers from concept to commercialization through our advanced technical services, dedicated R&D teams, and a strong commitment to quality and compliance.

At SPI Pharma, we value scientific excellence, collaboration, and innovation to deliver meaningful healthcare solutions worldwide.

We are looking for a skilled and motivated Research Scientist – Analytical Development to join our R&D team. The ideal candidate will have a solid background in pharmaceutical sciences or chemistry, with strong hands-on experience in analytical method development, validation, and routine testing of pharmaceutical dosage forms — especially soft gelatin capsules and solid orals.

The role requires excellent technical knowledge of key analytical instruments, good documentation skills, regulatory awareness, and the ability to work independently and in cross-functional teams.

Key Responsibilities:

• Execute all laboratory activities safely and reliably, strictly adhering to Pharmaceutical GLP/GMP guidelines and internal SOPs.

• Develop, validate, and implement robust analytical methods for drug substances, reference standards (RS), impurities, and finished dosage forms.

• Perform routine analytical testing such as Assay, Dissolution, Related Substances, Content Uniformity, and other quality tests with a special focus on soft gelatin capsules and other solid orals.

• Conduct analytical testing for formulations under stability studies as per ICH guidelines.

• Independently troubleshoot analytical or instrumental issues and recommend effective solutions in a timely manner.

• Ensure proper calibration and maintenance of analytical instruments such as HPLC, UPLC, UV-Vis Spectrophotometer, FTIR, DSC/TGA, Dissolution Apparatus, KF Titrator, Rheometer , etc.

• Maintain accurate and up-to-date lab notebooks, raw data, and reports in line with Good Documentation Practices (GDP) .

• Prepare comprehensive method development and validation reports, technical presentations, and, where appropriate, support the publication of technical data in reputable journals.

• Support regulatory submissions by providing necessary analytical data and documentation.

• Collaborate closely with cross-functional teams including formulation R&D, quality control, manufacturing, regulatory affairs, and external partners.

• Travel to other company locations, customer sites, or contract manufacturing organizations (CMOs) for method transfer, troubleshooting, or technical support as required.

• Meet project priorities, timelines, and deliverables while maintaining high standards of quality and compliance.

Required Knowledge & Skill Set:

Education:

• Master's degree in Pharmaceutical Sciences (M.Pharm) or M.Sc. in Chemistry .

• B.Pharm acceptable for junior roles (optional).

Technical Expertise:

• Strong knowledge and practical experience in analytical method development and validation.

• Proficiency in operating and troubleshooting instruments like HPLC, UPLC, GC-MS, LC-MS/MS, ICP-MS, UV-Vis, FTIR, XRPD/XRD, DSC, TGA, Dissolution Apparatus, KF Titrator , and other relevant tools.

• Sound understanding of pre-formulation and stability study protocols .

• Experience in handling soft gelatin capsules and various dosage forms like tablets, capsules, ODTs, ER, DR, etc., is an added advantage.

• Familiarity with ICH guidelines , FDA/EMA requirements , and GLP/GMP compliance .

Soft Skills:

• Proactive and solution-oriented mindset for addressing analytical challenges.

• Strong documentation and report-writing skills.

• Effective verbal and written communication.

• Ability to work both independently and within a cross-functional team.

• Organized, detail-oriented, and committed to timelines and quality standards.

2. Propose and identify efficient and robust synthetic routes for the preparation of API’s/Intermediates/RSMs/Impurities.

3. Laboratory experimentation, participation on API project team and work in collaboration with scientists from Analytical R&D and other disciplines such as engineering to further develop synthetic routes into synthetic processes.

4. Interpretation of analytical data to drive synthetic experimental plans and ability to utilize electronic tools (such as electronic notebook) to document information.

6. Participate in the preparation of technical transfer documents for manufacture internally or at third parties. Compliance on safety and regulatory requirements is expected and documented through our internal training program.

7. Participate in key initiatives for CRD and contribute to continuous improvement work in the department and advancement of the Process Chemistry discipline through technology, workflow or business impact

8. Independent, science-based and innovative thinking and the ability to collect advance scientific literature and databases wherever needed.

9. Understands the principles of operation of specialized scientific equipment and teaches subordinates how to operate the

equipment.

10. Effective contribution to the raw material/supply chain quality related investigation and extending the work till fixing the

problem.

11. Remains competent and current through self-directed professional reading, developing professional contacts with colleagues, attending professional development training, and attending training and/or courses required by the supervisor.

12. Contributes to a work environment that encourages knowledge of, respect for, and development of skills to engage with those of other cultures or backgrounds.

Qualification:
Doctorate in chemistry

1+ years relevant experience (Especially in pharmaceutical industry with synthesis experience)

Strong knowledge of synthetic organic chemistry principles

Strong knowledge in analytical, good communication and adequate computer skills are preferable.

Work Location Assignment: On Premise

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Research and Development

LI-PFE

Reference Number: 51830:  Medical Laboratory Scientist Anatomical Pathology - Maternity Leave Cover  
Employment Type: Fixed Term Full Time (FT)  
Location: Northern Health (All Campuses)  
 

About Northern Health:

As an organisation we have a clear focus on how we service and partner with our community, including our strategy of helping the community stay well when at home. Our reputation of community minded, inclusive and progressive is matched to none. 

Northern Health is located in the rapidly growing northern suburbs with projected growth the biggest in the state. With a booming, culturally rich and diverse community, and less than an hour’s drive from the CBD (still within the bounds of Myki and ride-sharing), Melbourne’s North is fast

Northern Health are seeking applications from motivated and suitably experienced Medical Laboratory Scientist to join the Anatomical Pathology team on a fixed term contract. 

Northern Health is the major provider of acute, maternity, sub-acute, mental health, specialist, community and home-based services in Melbourne’s rapidly growing outer north.

Services are provided through our five main campuses:

Northern Hospital Epping, Broadmeadows Hospital, Bundoora Centre, Craigieburn Centre, and Kilmore District Hospital.  In addition, Mental Health Services are provided at Epping, Broadmeadows, Jacana, Preston, Mill Park and Coburg.

About the Role:

This role would suit an experienced Medical Laboratory Scientist who enjoys working as aprt of a team to contribute to the production of high-quality work and on-going patient care and enjoys working in a fast paced envrionment. Based within the Anatomical Pathology team the key responsibilities would be (but not limited to); routine histopathology duties including specimen reception, tissue cut-up, tissue discard, processing and processor maintenance, embedding, microtomy, frozen sections, H&E and special stains evaluation, troubleshooting and IHC duties. Assisting in mortuary duties and participating in a rotating roster with a variety of shifts including mornings and afternoons based on the department’s requirements may form part of this position. 

To be successful in this role you will have:.

• Experience and good working knowledge of diagnsotic Anatomical Pathology.
• Proven ability to work both independetly and as part of a team with a determination to see tasks through to completion. 
• Demonstrated knowledge of laboratory services, ability to adhere to established procedures, and high attention to detail. 
• Well-developed communication, organisation, problem solving and time management skills.
• Professional appraoch to pateint care

Next Steps . . .

If this opportunity sounds like the next step in your career, then we would love to hear from you. Please click on the 'Apply' button and follow the prompts.

For further details, please refer to the Position Description. Alternatively, you can contact Imogen Campbell, Senior Scientists of Anatomical Pathology on 03 94859401

Applications close on 31 August 2025

Why work at the Northern Health?

NH offer a range of benefits which support and reward staff both personally and professionally.

Our staff benefits include award winning facilities and campus partnerships, Professional development and events, an award winning Health and wellbeing program and financial benefits.

• Health and Wellbeing programs, including our new ‘Thrive’ program
• Flexibility in the workplace and extra leave options and support
• An inclusive and culturally safe space
• Access to salary packaging, EAP, our online library and onsite car parking

Work with us! Northern Health is an equal opportunity employer and is committed to attracting and retaining a diverse workforce which reflects the community we serve. Applications from Aboriginal and Torres Strait Islander people, as well as applicants who are LGBTIQ+, who have different abilities, or are from culturally and Linguistically Diverse Backgrounds are encouraged.

Kenvue Is Currently Recruiting For A:

Principal Scientist R&D Materials Analytical

What We Do

At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we're the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON'S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.

Who We Are

Our global team is 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.

Role Reports To:

Associate Director R&D APAC RMC

Location:

Asia Pacific, India, Maharashtra, Greater Mumbai

Work Location:

Fully Onsite

What You Will Do

Kenvue is currently recruiting for:

Principal Scientist – R&D Analytical Materials Team

This position reports to Manager, R&D Materials and is based at Mumbai, India.

Who We Are

At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we're the house of iconic brands - including Neutrogena, Aveeno, Tylenol, Listerine, Johnson's and BAND-AID® Brand Adhesive Bandages that you already know and love. Science is our passion; care is our talent. Our global team is made up of 22,000 diverse and brilliant people, passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact the life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.

Role reports to: Manager, R&D Materials team

Location: Mulund, Mumbai, India

Travel %: 10 %

What You Will Do

• The Principal Scientist, R&D Materials Analytical team is responsible for leading Raw Materials Analytical qualification team based in Mumbai to support various analytical qualification projects globally and serve as a Analytical SME for various raw materials related activities like defining critical to quality attributes, release testing strategy based on various GxP requirements, support for Regulatory submissions and/or queries.
  
  

Key Responsibilities

• Lead Analytical (Raw Material testing & Characterization) projects globally and ensure on time support to various projects for the raw materials used in personal care and Selfcare products.
• This person will manage internal and outsourced employees that performs assessments of Raw Materials specifications used at Internal and External Manufacturing sites to ensure alignment to current compendia, industry standards, product registrations, and internal procedures.
• This individual will collaborate with Global sites and the Specification team business partners and stakeholders (Internal/External Manufacturing Sites, Regulatory, Quality etc) to drive best practices for RM specifications aligned with company goals and objectives.
• This person will be responsible for understanding the impact of global Pharmacopoeia monographs on our products and owning changes to the impacted sites to ensure compliance, before effective dates.
• Support internal/external manufacturing sites for Analytical test method related trouble shootings & investigations linked to raw materials
• Drive or provide input to new policies, procedures, or significant changes to existing procedures, aligning with global partners to incorporate best practices
• Demonstrate a balanced and pragmatic approach to projects and challenges, emphasizing creativity alongside practicality. Maintain a results-oriented focus, consistently delivering on business objectives.
• Oversee the external partners for outsourcing activities, monitor the KPIs regularly and ensure the compliance to applicable Kenvue standards
• Make fact-based decisions regarding analyzing and interpreting data, drawing conclusions, and arriving at timely technical decisions
• Develop technical expertise in the team and ensure implementation & adherence to GxP practices.
• Lead and manage a team of direct and indirect reports including their development and career growth
  
  

Required Qualifications

What we are looking for

• Minimum of a bachelor's/ Masters degree in Chemistry /Pharmacy/Life Sciences with 10-12 years of experience; OR a PhD with 7-8 years of experience
• Minimum 2 years of experience in people management
  
  

Desired Qualifications /Skills

• Experience in a GxP environment is required
• Experience with use of Microsoft&aposs suite of products (Excel, Word, PowerPoint) is required
• Experience with quality compliance systems is preferred
• Experience with Consumer products (OTC and Cosmetic) is preferred.
• Effective communication skills, as this role requires consistent, frequent collaborations with global sites, project teams, and outsourced technical writers, via virtual meetings and email correspondences
• Strategic and operational skills to prioritize and execute projects based on business and compliance needs
• High level of learning agility and problem-solving skills
• Experience in talent development
  
  

What's In It For You

• Annual base salary for new hires in this position ranges from $XXX to $YYY. This takes into account a number of factors including work location, the candidate's skills, experience, education level & other job-related factors.
• Competitive Total Rewards Package*
• Paid Company Holidays, Paid Vacation, Volunteer Time & More!
• Learning & Development Opportunities
• Employee Resource Groups
• This list could vary based on location/region
• Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process.
  
  

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, or any other legally protected characteristic, and will not be discriminated against on the basis of disability.

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.

Skills Required
Consumer Products, Otc