11,203 Research jobs in India

Research Scientist/Senior Research Scientist

Bhiwadi, Rajasthan ₹900000 - ₹1200000 Y Kusum

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Role & responsibilities

  • Responsible for formulation and process development (QbD approach) of following categories of Pharmaceutical products:
  • Oral Immediate-Release Dosage Forms.
  • Oral Modified-Release Dosage Forms Including Pelletization technology and Wurster technology.
  • Topical Semisolids (Creams, Ointment and Gels).
  • Oral Liquid Dosage Forms
  • Topical Liquid Dosage forms.
  • Solid (Suppositories), Semisolid & Liquid dosage forms for Rectal and Vaginal applications.
  • Design and execute formulation trials and evaluate stability data to finalize formulation composition.
  • Execution of technology transfer batches for manufacturing processes from laboratory scale to production scale.
  • Oral Immediate-Release Dosage Forms.
  • Oral Modified-Release Dosage Forms Including Pelletization technology and Wurster technology.
  • Topical Semisolids (Creams, Ointment and Gels).
  • Oral Liquid Dosage Forms
  • Topical Liquid Dosage forms.
  • Solid (Suppositories), Semisolid & Liquid dosage forms for Rectal and Vaginal applications.
  • Knowledge of patent non infringing strategy based product development
  • Knowledge of Bioequivalence study & clinical study protocol and criteria
  • Independent contributor for batch planning, batch execution & technology transfer
  • Develop manufacturing processes for R&D formulations so that the technical transfer is successful for large-scale batches.
  • Responsible for all formulation/ process related CMC documents which will be part of regulatory filings.
  • Write/review master formulas, manufacturing procedures, SOPs, stability protocols, process validation protocols, Product Development Reports etc.
  • Prepare/review specifications for pharmaceutical products and packaging components, etc.
  • Support the manufacturing of exhibit/submission batches per regulatory requirements.
  • Work with Cross-functional teams (Analytical, Regulatory Affairs, Pharmacovigilance, Bioequivalence, Quality Control, Quality Assurance, Inventory Control, etc.) to expedite the development and approval of new products by different Agencies for Regulated and ROW Markets.
  • Assure that all formulation and process development activities are documented in the notebook as per company procedures and cGLPs.
  • Provide recommendations for continuous improvements in practices and systems to improve performance and enhance efficiency and quality.
  • Communicate with outside vendors and laboratories.

Preferred Skill Set:

  • Thorough knowledge of the pharmaceutical industry, particularly drug delivery industry, and formulation and process development including guidelines.
  • Knowledge for development of formulations comes under category of medical devices, Dietary Supplements and Cosmetics.
  • Knowledge of ICH/GMP regulations.

Behavioral /Managerial Skill Sets

  • Skills building and maintaining productive relationships with organizational partners including teamwork.
  • Skills related to develop and deliver products well with in specified timelines.
  • Being a team player
  • Appropriate communication with all stakeholders
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Research Scientist/ Senior Research Scientist

Umbergaon, Gujarat ₹900000 - ₹1200000 Y Sulphur Mills

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Position: Research Scientist/ Senior Research Scientist

Position Summary: The successful candidate will primarily be accomplished through the implementation of fungicide screening trials in the laboratory, greenhouse.

Qualification: M Sc./Ph.D (Agri) in plant pathology/Microbiology,

Experience: More than 3 years experience in research and development crop protection.

Location: Umergaon, District: Valsad, South Gujrat

Skills:

  • Implementing and evaluation of fungicide screening trials in the laboratory and greenhouse.
  • Design and execute greenhouse studies to evaluate efficacy of novel crop protection products including disease control phytotoxic assessment.
  • Create/ standardize testing methodologies for screening new active ingredients via. Implementing new screening methods & platforms for existing or emerging diseases against NCEs & formulations under controlled condition.
  • Used to split between green house and laboratory work viz. preparation of microbiological media and culture of plant pathogens, isolation and multiplication of plant pathogens.
  • Thorough understanding of disease identification and other nutritional deficiencies and disorders.
  • Experienced in use of automated greenhouse systems, precision agriculture tools.
  • Excellent analytical, organizational and people skills. Proficiency of statistical analysis. Ability to use statistical software to interpret biological data, prepare technical report/presentation for internal team.
  • Work with chemistry, biology and field teams to transition promising candidates from green house to field trials.
  • Summarize trial data and provide development recommendations, identify development opportunities for product label expansion new uses and new solutions
  • Strong research, decision making, critical thinking and problem-solving skills
  • Resource planning and management-lab chemicals, lab supplies and lab instrument maintenance, calibration and validation.

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Research Scientist

Mumbai, Maharashtra Abbott

Posted 5 days ago

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**Key** **Accountabilities** **and** **Responsibilities:**
**·** **Analytical Method Development of various** **pharmaceutical dosage forms like oral solid, oral liquid, Injectables, Nasal Spray.**
**·** **Analytical Method Validation of various** **pharmaceutical dosage forms like oral solid, oral liquid, Injectables, Nasal Spray.**
**·** **Analytical Method Transfer of various** **pharmaceutical dosage forms like oral solid, oral liquid, Injectables, Nasal Spray.**
**JOB** **SPECIFICATION**
+ Analytical method development and validation for pharmaceutical dosage forms.
+ Literature search related to the drug substance, create analytical profiles.
+ Execution of analytical method transfer for pharmaceutical dosage forms.
+ Analysis of routine samples (product development batches, stability study samples, raw materials etc.).
+ Operation and Calibration of analytical instruments/equipment's.
+ Qualification of working standards.
+ Data Review and Release (as assigned).
+ Documentation of analytical activities as per Good documentation practices.
+ Work in laboratory as per Good laboratory practices.
+ To use PPEs and follow safe practices in lab.
+ Preparation of SOPs, STPs, Specifications, COAs and stability reports
+ Preparation of RM Specification and STPs
+ Trouble shooting of analytical issues/problems/queries.
+ Review of Analytical development & stability data.
+ Analytical Activities related to Quality Control Department.
+ Any other task assigned by management.
**Competencies** **Required:**
+ Good Knowledge about Analytical Method development, Validation and method transfer
+ Knowledge about the Regulatory requirement and Quality requirement
+ Must be able to perform the analysis as per the Good Laboratory Practices
**Functional** **Skills/** **Know-how:**
+ Hands on experience on HPLC, GC, UV spectrophotometer, IR spectroscopy, Dissolution Test Apparatus, Disintegration Test Apparatus, Viscometer, Differential Scanning Calorimetry (DSC), Malvern Particle sizer.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
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Research Scientist

Mumbai, Maharashtra Abbott

Posted 5 days ago

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_MAIN PURPOSE OF ROLE_
+ Under general supervision, responsible for designing new products and processes and improving and maintaining existing products.
+ May execute less complex projects.
_MAIN RESPONSIBILITIES_
-
May conduct design analysis on components and/or assemblies to assist in the development process by ensuring designs are cost efficient, manufacturable, and reliable.
-
Communicates with the other engineering personnel to coordinate the interrelated design and assure project completion.
_Education_
_Education Level:_ Associates Degree (± 13 years)
_Experience/Background_
_Experience Details:_ Minimum 1 year
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
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Research Scientist

Sonipat, Haryana Crystal Crop Protection Limited

Posted 1 day ago

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Roles & Responsibility-

  • Analytical Method Development: Highly skilled in designing, optimizing, and implementing analytical methods (both for technical actives / APIs and formulations), using HPLC / UPLC, GC (including headspace), LC‑MS / LC‑MS‑MS or equivalent.
  • Method Validation: Deep experience with validation protocols in compliance with regulatory standards (ICH, SANCO / SANTE, OECD GLP or equivalent), including parameters like specificity, accuracy, precision, LOD/LOQ, linearity, range, robustness, stability.
  • Wet Lab & Physical‑Chemical Testing: Strong competence in sample preparation, moisture content determination, physical property evaluation, chemical assays of formulations and technical materials, IPQC support.
  • Troubleshooting & Non‑Routine Testing: Able to identify, diagnose and correct issues in analytical measurements, instrument performance, method interference, reproducibility, sensitivity issues etc.
  • Regulatory & Quality Compliance: Familiar with regulatory guidelines; experience in maintaining compliance with GLP (if applicable), safety standards, documentation, calibration and maintenance of instruments, controlled environment of lab operations.
  • Documentation & Reporting: Able to generate, review and approve validation protocols, SOPs, technical and validation reports; ensure data integrity, method transfer documentation; maintain good laboratory practices in record keeping.
  • Cross‑Functional Collaboration: Capability to work with R&D formulation, regulatory, QA/QC, project management, ensure analytical support is aligned to product development and registration timelines.


Experience & Background

  • Requires 7–10 years of demonstrated expertise in analytical R&D or development of analytical methods in the agrochemical industry.
  • Prior work should be in one or more of these domains: agrochemical technical substances, agrochemical formulations.
  • Must have been leading or managing a team of 4‑8 analysts or scientists continuously for the past 2‑3 years , including supervision, mentoring, allocation of tasks, and performance evaluation.
  • Experience in regulatory / quality driven environments where analytical methods are developed, validated and used for regulatory filings.

Educational Qualification

  • Essential: Master of Science (M.Sc) in Organic Chemistry or Analytical Chemistry .
  • Preferred: Doctor of Philosophy (Ph.D) in Organic Chemistry or Analytical Chemistry.
  • The educational background should demonstrate strong foundation in chemical theory, separation science, and instrumental analysis.
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Research Scientist

Noida, Uttar Pradesh ₹500000 - ₹1500000 Y Mabbit Communications

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Patent Writing for United States Patent and Trademark Office

Kindly provide minimum two references with resume

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Research Scientist

Bengaluru, Karnataka ₹1200000 - ₹3600000 Y GE Vernova

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Job Description Summary
GE Vernova's Advanced Research business is the central innovation engine for GE's portfolio of energy businesses, which is unified under one banner called GE Vernova. The research organization is made up of 300+ researchers representing virtually every major scientific and engineering discipline. Collectively, they are driving major research programs and initiatives to decarbonize power, accelerate renewables, and promote electrification and the creation of a 21st century grid fit to power a zero-carbon energy future.

We are seeking a highly motivated and skilled researcher to join our team in the field of Artificial Intelligence, Machine Learning (AIML). As a Research Engineer, you will have the opportunity to work closely with our experienced engineers and researchers on cutting-edge projects that leverage AIML techniques for the development of state-of-the-art prognostics, diagnostic and modelling solutions.

Job Description
Roles and responsibilities

  • Develop innovative algorithms and methodologies in artificial intelligence and machine learning (AIML) tailored for process and product development.
  • Analyse extensive datasets to identify patterns, trends, and insights, focusing on diagnostics and prognostics for large-scale energy equipment.
  • Implement and enhance AIML algorithms and models for optimal performance.
  • Design and execute experiments to evaluate the efficacy and reliability of AIML-based solutions.
  • Document research findings, methodologies, and implementation details for effective knowledge sharing and future reference.
  • Collaborate with cross-functional teams, including engineers, researchers, and product managers, to integrate AIML solutions into existing system platforms.
  • Stay informed on advancements in AIML, control systems, and signal processing engineering through literature reviews and participation in relevant conferences and seminars.
  • Research, conceptualize, and develop AI solutions for complex industrial challenges.
  • Work collaboratively with fellow researchers on ongoing and new projects.
  • Demonstrate the value of AI through early prototypes and solutions addressing real-world problems.
  • Utilize software libraries, tools, and practices to implement efficient, scalable, and reusable solutions.
  • Contribute to intellectual property development by writing invention disclosures and filing patents.
  • Publish research in scientific journals and present findings at conferences.

Required Qualifications

  • PhD with 2 - 5 Years Experience or Master's degree with 5 - 7 Years Experience from a reputed institution in Computer Science or other engineering field.
  • Strong understanding of fundamental concepts in statistics, machine learning, and artificial intelligence.
  • Proficiency in programming languages commonly used in AIML applications such as Python, PySpark, PyTorch, Pandas, or similar.
  • Experience with data analysis and manipulation using tools like Pandas and NumPy.
  • Familiarity with software development best practices, including version control (e.g., Git) and agile methodologies.
  • Basic knowledge of cloud-based architectures
  • Excellent problem-solving skills and ability to think critically and creatively.
  • Strong communication skills and ability to work effectively in a collaborative team environment.
  • Demonstrated ability to build prototypes and quickly develop proof of concepts to show solution feasibility.

* *Additional Information*
*Relocation Assistance Provided:
Yes

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Research Scientist

Ernakulam, Kerala ₹500000 - ₹1000000 Y Agappe Diagnostics

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Role & responsibilities:

Outline the day-to-day responsibilities for this role.

Preferred candidate profile:

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Research Scientist

₹60000 - ₹80000 Y Pharmanza

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Job Description

  • Position: Junior research scientist (JRS)/Research scientist (RS)
  • Job Location: - Plot No. 214, Borsad - Tarapur Road, Ta: Petlad, Dist: Anand, Gujarat, India.
  • Department: R&D / Formulation
  • Experience: 3-6 years in Nutraceuticals Formulations.
  • Industry: Nutraceutical / Food / Pharma Manufacturing
  • Reports To: Manager FRD.
  • Job Type: Full-Time

Company Profile: -

Pharmanza Herbal Pvt. Ltd. is one of the few companies which is focusing on standardizing and proving the efficacy of Herbal products. Our strong supplier base, fully equipped R&D facility, FDA approved manufacturing facility, infrastructure for conducting human trials as well as our formulations unit provides a one stop solution to our valued customers. Pharmanza Herbal Pvt Ltd. is one of the leading research-oriented companies, manufacturing herbal extracts used in the Ayurvedic and nutraceutical segment. Our journey began in 1997 with Pharmanza India, our group company located in Khambhat, India, where we started producing herbal extracts. While Pharmanza India primarily focuses on veterinary allopathic formulations, we leveraged its facilities to manufacture herbal products such as Garcinia cambogia, Commiphora Mukul, and Withania somnifera from 1997 to 2004. As the business expanded, and we began exporting our products to countries like the US, Japan, and Germany. Pharmanza Herbal was established in Dharmaj, India, to continue our commitment to quality and innovation in herbal solutions. The facility is certified by Food safety authority of India (FSSAI), Food and drug Administration, India (Gujarat office) with NSF-GMP International. Current certifications include ISO9001:2015, ISO22000:2018, NSF-GMP, NSF-SPORT,USP-GMP,USP Ashwagandha,Bosewelia with Kosher and Halal and USDA/APEDA organic certifications for products. Additionally, we are also certified SEDEX 4 Pillers and ECOVADIS.

Job Overview: -

We are seeking a highly motivated and detail-oriented Formulation Scientist with 2-4 years of experience to join our team. The ideal candidate will have expertise in formulation development and optimization, along with a strong understanding of dosage forms, excipients, and manufacturing processes. As a key member of our R&D department, you will be responsible for designing and developing solid, semi-solid, or liquid dosage forms, performing stability studies, and ensuring regulatory compliance throughout the formulation process.

Responsibilities and Duties: -

  1. Research & development along with optimization of formulations for Nutraceutical and Health Supplement as per the organization requirements.

  2. Development of solid, semisolid, and liquid dosage forms for herbal and nutraceutical ingredients for domestic, and regulated markets like US, EU, Brazil, and Canada.

  3. Ensure adherence to regulatory requirements and customer expectations during product development.

  4. Collaborate with cross-functional teams, including Analytical Development, Quality Control, and Manufacturing, to ensure smooth transition from development to production.

  5. Contribute to total product development activity from material procurement to stability studies and technology transfer to the manufacturing units. Troubleshooting as required during these operations.

  6. Handling different equipment, performing experiments, and documenting the results in a prescribed format.

  7. Pre-formulation and excipient compatibility studies, assist in research activities as instructed. 8. Preparation of literature search, patent search, prepare product development reports, stability protocol, process validation protocol, reports and SOPs.

  8. Responsible for inventory management and lab management ensuring GDP during documentation and fulfilment of GLP requirements during routine lab work.

  9. Troubleshoot formulation-related issues during clinical trials and commercial production.

  10. Data compilations and record maintenance.

  11. Any other responsibility, as assigned by management.

Qualifications: -

  • Education level: Bachelor's or Masters degree in Pharmaceutical Sciences, Chemistry, or a related field
  • Experience: 3-5 years
  • Personal characteristics: Hands-on experience with various formulation techniques, Strong knowledge of drug delivery systems, excipient selection, and stability studies, Familiarity with regulatory guidelines (USFDA, EMA, ICH) and industry standards. Ability to work collaboratively in a fast-paced, team-oriented environment.
  • Salary Range: - Competitive
  • Computer Competency: -Efficient
  • Skills: -
  • Excellent problem-solving and analytical skills with keen attention to detail, Strong written and verbal communication skills

  • Benefits:

  • Competitive salary package.
  • Subsidized food facility.
  • Free Transportation facility from Vadodara location.
  • Medi-claim facility.
  • Opportunities for professional development and growth.
  • A dynamic and collaborative work environment committed to sustainability.

Join our dynamic team and contribute to the success of our mission to provide high-quality nutraceuticals and dietary supplements that positively impact people's health and well-being. If you possess the required qualifications and share our passion for quality, we encourage you to apply for this exciting opportunity as an JRS/RS in our manufacturing unit.

Company Website: - Company Email id: -

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Research Scientist

Mumbai, Maharashtra ₹900000 - ₹1200000 Y Abbott

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Pupose:Deliver formulations in defined timeframe to meet product delivery goals for I&D

Development of different formulations either as generic or differentiated generics. To demonstrate successful stability and scale up at manufacturing site.

Core Job Responsibilities

  • Development of formulation using scientific rationale in use of excipients to create a reproducible prototype formulation.
  • Ensure Proper documentation of every trial in the log note books and then using the information for creation of the Product Development Report for use in dossier for filing.
  • Use of QbD wherever required for Product and process optimization.
  • Ensure proper upkeep, maintenance and calibration of the equipment.
  • Ensure scale up of the developed formulation works at engineering batch level.

Key Deliverables:

  • Literature/Patent search to create drug profile
  • Prototype development with rationale use of excipients
  • Preformulation study as may be required for formulation development
  • Conduct 6 months accelerated stability studies to ensure stable formulation
  • Proof of concept studies to demonstrate BE or comparative PK as the case may be
  • Scale up studies at 1/10th scale or engineering batch
  • Technology transfer and manufacturing of Bio/Clinical batch

Job Title: Jr Research Scientist Formulation

Job Function: Innovation & Development

Location: Mumbai (Andheri MIDC)

Reporting to:Sr Group Leader Formulation

Critical Success Factors: Functional/ Technical: Functional / Technical:

1. Formulation and Product Development

a. Schedule and follow all the steps to deliver the drug as per QTPP

b. Select the suitable polymers / excipients based on either properties or scientific rationale

c. Evaluation of CQA of drug / excipients and estimate its implications for product development

d. Designs the process which is reproducible and scalable with higher yield, cost effective, and environment friendly

2. Design of Experiments

a. Executes the experiments as per DOE to optimize product and process

3. Pharmaceutical Development Report (PDR)

a. Prepares PDR as per Common Technical Document (CTD) module 3 requirements

b. Complies with regulatory requirements as defined in QTPP

4. Project Management

a. Is able to plan and prioritize multiple project deadlines to meet product delivery goals

Education & experience:

  • M. Pharm/Ph. D.
  • 5 to 7 yrs
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