277 Jobs in Murbad
Analytical Researcher I
Posted 1 day ago
Job Viewed
Job Description
Date: Aug 20, 2025
Location:
Ambernath, India,
Company: Teva Pharmaceuticals
Job Id: 63604
**Who we are**
Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with.
**The opportunity**
+ Finished product testing and analytical method development by HPLC, GC, IC, UV etc.
+ Analytical method validation and transfers, analysis of API, Finished product R&D samples
**How you'll spend your day**
+ Analysis of Solid oral dosage i.e. Dissolution, Assay, CU, BU and Related substances etc.
+ Analysis of samples received from Formulation department (samples include in-process, finished product, pre-formulation study samples and stability samples etc.).
+ To carry out analytical method development and method validation, in-process samples and finished products.
+ To carry out analytical method transfer activity to QC, Goa.
+ Handling and testing of hi-potent compounds/molecules
+ Trouble shooting of analytical instruments for difficulties faced during day-to-day operations.
+ Calibration and maintenance of analytical instruments. Maintenance includes activities such as Qualification, keeping track of AMC, History, Spares, Usage records etc.
+ Literature Search for development of analytical methods.
+ To ensure that all activities undertaken are executed in the framework of good laboratory and documentation practices and the existing quality systems are adhered.
+ To ensure safe practices are followed during the execution of activities and strict adherence to the EHS systems of the site.
**Your experience and qualifications**
+ M.Sc. / M. Pharm./ Ph. D
+ 3-8 Years relevant experience
+ Sound knowledge of Chemistry and analytical method development, method validation and transfer, Instrumental method of analysis and logical approach.
+ Hands on experience on Instruments viz., GC, HPLC, Ion Chromatography, UV and Dissolution apparatus etc.
+ Knowledge of regulatory requirements for different markets (US, EU, Canada etc.
+ Knowledge on ICH guidelines, forced degradation studies, impurity profile etc.
**Personal attributes**
+ Basic communication skills
+ Must be honest and trustworthy
+ Be respectful
+ Possess cultural awareness and sensitivity
+ Outgoing, personable, responsible, self-motivated and confident
**Teva's Equal Employment Opportunity Commitment**
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.
EOE including disability/veteran
Principal Scientific Publisher FRD
Posted 1 day ago
Job Viewed
Job Description
Date: Sep 12, 2025
Location:
Ambernath, India,
Company: Teva Pharmaceuticals
Job Id: 63885
**Who we are**
Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with.
**The opportunity**
+ The Principal Scientific Publisher will be responsible for the preparation of consistent and high-quality technical documents related to Pharmaceutical Research and Development for Formulation related documents in accordance with Teva's standards.
+ Execute all functions in accordance with current FDA regulations, ICH guide lines, USP methodologies, cGMPs and SOPs.
+ Maintain open communication with R&D members to ensure timely delivery of high-quality documents independently with minimal supervision.
**How you'll spend your day**
+ Preparation of documents and facilitation of documentation management in R&D while following established guidelines for correctness, completeness and clarity.
+ Preparation of documents such as Manufacturing Batch Records, Study Protocol and Reports, Stability Protocols, Product Development Report, Quality Overall Summary, response to regulatory queries, based on the scientific input from the Formulation team. Knowledge of QBD & DOE is essential. Knowledge of shelf-life extrapolation and statistical analysis would be preferred.
+ Preparation of high impact presentations including graphs and charts.
+ Submission of documents for signatures and coordinating their flow, archival and retrieval to ensure timely flow and publish monthly performance metrics.
+ Continuously improve documentation systems to increase efficiency and compliance with cGMP and/or other regulatory requirements.
+ Perform other duties as assigned or delegated.
+ Comply with FDA guidelines/Company Policies of Data Integrity.
**Your experience and qualifications**
Education: A minimum master's degree (M.Pharm) or a PhD in Pharmacy is required.
Industry Experience Required:
+ A minimum of 12 to 15 years of Formulation R&D experience with solid oral dosage forms for regulated markets is required. Knowledge of other dosage forms will be an added advantage.
+ Demonstrated knowledge and understanding of quality and regulatory guidance for SOD products for regulated market.
+ Demonstrated knowledge and working understanding of basic concepts of Good Manufacturing Practices (GMP), regulatory documentation required.
**Knowledge, Skills and Abilities**
Communication Skills
+ Communication skills with the ability to speak and write with clarity and structure.
+ Fluency in English and Advanced technical writing abilities a must.
+ Well versed with business, scientific communication platforms.
Computer Skills
+ Proficient skills level with using Microsoft applications, including Word, Excel, & PowerPoint.
+ Other software knowledge related to statistical tools for data mapping / trending experience preferred but not required.
+ Awareness, Adaptation and Facilitation of communication technology channels is preferred.
+ Demonstrated computer literacy, including spreadsheets, structural drawings, databases, and communication packages preferably in a Windows environment.
Other Skills
+ Proficiency in English spelling, grammar and punctuation.
+ Strong organization skills, attention to detail, and the ability to work in a team fast pace environment.
+ Good documentation skills and working knowledge of technical writing principles and practices.
+ Good subject knowledge and problem solving skills required.
+ Attention to detail, and the ability to work within a team in a fast pace environment is desired
+ Ability to work in a highly independent and self-directed work environment is desired.
**Teva's Equal Employment Opportunity Commitment**
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.
EOE including disability/veteran
Analytical Researcher I
Posted 4 days ago
Job Viewed
Job Description
Date: Aug 25, 2025
Location:
Ambernath, India,
Company: Teva Pharmaceuticals
Job Id: 63605
**Who we are**
Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with.
**How you'll spend your day**
+ Shall have FDA approval in Microbiology
+ To carry out Microbiological testing of various products like in-process, finished products, pre-formulation study samples and stability samples etc.
+ Check analytical results and suggest further course of action.
+ To carry out Microbial method development, method validation and transfer activity.
+ Preparation and updating of STP and analytical related SOPs.
+ Regulated market experience (US/EU/Canada etc)
+ Laboratory resources management.
+ To execute Microbial method validation as per the protocol and to complete the required documentation.
+ Calibration and maintenance of analytical instruments. Maintenance includes activities such as Qualification, keeping track of AMC, History, Spares, Usage records etc.
+ To ensure that all activities undertaken are executed in the framework of good laboratory and documentation practices and the existing quality systems are adhered to.
+ To ensure safe practices are followed during the execution of activities and strict adherence to the EHS systems of the site.
+ Any other activity assigned by the line manager.
**Your experience and qualifications**
+ M.Sc. / M. Pharm in Microbiology
+ Overall Pharma industry experience: 4 plus years
+ Sound knowledge of Microbiology and Microbial analysis, Microbial method development and method validation. Microbiological testing of various products like in-process, finished products, pre-formulation study samples and stability samples etc.
+ Regulated market experience (US/EU/Canada)
+ FDA approval in Microbiology.
**Teva's Equal Employment Opportunity Commitment**
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.
EOE including disability/veteran
Quality Engineer / Senior Quality Engineer
Posted 1 day ago
Job Viewed
Job Description
RUD India is a leading manufacturer of high-quality equipment for bulk and unit material handling. Established in 2007 and part of the German Group, we develop innovative, patented solutions for a wide range of industries. Our products, compliant with ASME, DIN/EN, and VDI standards, are trusted in over 125 countries. We pride ourselves on indigenization, quality, and delivering cost-effective, reliable
solutions that give our clients a sustainable competitive edge.
As part of our strong growth path, RUD India is expanding its operations with the construction of a state-of-the-art, world-class manufacturing facility in Murbad, near Mumbai. This strategic expansion not only strengthens our production capabilities and technological excellence but also opens up exciting opportunities for professionals to build rewarding careers in a dynamic, innovation-driven environment.
Job Summary:
We are seeking a proactive Quality Engineer to uphold and enhance our world-class quality standards. The ideal candidate will be the guardian of our product quality, responsible for ensuring that all processes and outputs meet stringent internal and international specifications.
Key Responsibilities:
• Conduct Incoming, In-Process, and Final Inspection.
• Manage and resolve customer complaints by leading root cause analysis (RCA) and implementing effective corrective and preventive actions (CAPA).
• Maintain and control all quality documentation, including inspection reports, test certificates, and quality records.
• Play a key role in the implementation, maintenance, and auditing of ISO 9001 and other relevant management systems.
• Ensure all products and processes comply with relevant ASME, DIN/EN, and VDI standards.
• Utilize quality control tools (e.g., Calipers, Micrometers, Hardness Testers, etc.) for precise measurement and validation.
• Collaborate with production and engineering teams to drive continuous quality improvement initiatives.
Required Qualifications & Skills:
• Diploma or Degree in Mechanical / Production Engineering.
• 5 to 10 years of hands-on experience in a quality assurance role within a manufacturing/fabrication environment.
• In-depth knowledge of ISO 9001 standards and experience in internal audits.
• Experience in handling customer complaints.
• Proficiency in using various measuring and inspection instruments.
• Excellent documentation and communication skills.
• Familiarity with international standards like ASME, DIN, or VDI is a significant advantage.
Admissions Counsellor
Posted 1 day ago
Job Viewed
Job Description
About the BITS Law School, Mumbai:
A premier institute focused on generating the next cadre of legal leaders in India and across the globe, situated in Mumbai. Founded in March 2023, the School offers high-quality multidisciplinary legal education in times of increasing demand for well-rounded, tech-savvy and industry-ready law graduates across disciplines.
The website of BITS Law School is
About the job Job Title: Admissions Counsellor
Department: Admissions & Outreach
Reports To: HOD, Admissions & Outreach
Location: Work from Home
Employment Type: Contractual
Job Purpose:
To engage with prospective students via telephone or digital channels to provide information about the BITSLAW's - 5year Law programme, support the admissions process, and contribute to enrollment targets by effectively guiding applicants through their decision-making journey.
Job Responsibilities
- Explain the admission procedure and program distinguishing features to prospective students and their parents through incoming/outgoing phone calls, emails and face to face meetings (external situation permitting)
- Support applicants throughout the admission process by helping them register on the admission portal and addressing their queries in order to help them complete the online application
- Follow-up with students to verify any application issues, including discrepancies or missing information
- Maintain regular communication with students, parents, colleagues and external agencies for coordinating admission activities, explaining USPs of the BITSLAW's programme and addressing any related queries
- Collaborate with the program coordinators to organize presentations, information sessions, and recruitment related activities
- Build broad knowledge on admission activities and guidelines
- Any other admission related activities as intimated by manager
Experience / Education:
- Undergraduate/Postgraduate from a reputed university in India or abroad
- Outstanding communication and interpersonal abilities and good command over the language
- Understanding of Indian higher education landscape and related policies would be a plus
- Quick learner and a strong team player
- Passion for building world class institutions of higher education
- Proficiency in MS Office Desirable Experience
- 2–3 years of relevant experience e.g. academic advising, or admissions in a higher education institution
- Experience working in a target-driven sales or student recruitment environment
- Exposure to education technology platforms and student information systems
*Job responsibilities stated are not to be taken as an exhaustive statement of duties. Employees may be required to perform other job-related duties as necessary
Sr. Associate/ Associate, Programmes
Posted 1 day ago
Job Viewed
Job Description
About the BITS Law School, Mumbai:
A premier institute focused on generating the next cadre of legal leaders in India and across the globe, situated in Mumbai. Founded in March 2023, the School offers high-quality multidisciplinary legal education in times of increasing demand for well-rounded, tech-savvy and industry-ready law graduates across disciplines.
The website of BITS Law School is
Job Responsibilities*
- Providing administrative and technical support to programme management and delivery, including (but not limited to) developing and managing academic calendars, timetables, and assessment schedules; monitoring attendance, class conduct, and mentor–mentee/tutorial groups; visiting faculty or short course arrangements, administering teaching feedback, READ program, and other academic support initiatives; coordinating daily operations including class swaps or re-scheduling, field visits, venue booking, and coordinating on hospitality related information, etc.
- Liaising with academic team (Dean, faculty, TRFs, tutors, Exam office, Registrar’s office) on academic planning components such as course planning, policy development and execution, etc.
- Working with the student representatives to assess and resolve student grievances and queries, channel student feedback to relevant stakeholders as and when necessary.
- Overseeing and execution of academic events and awards such as the freshers’ orientation, student elections, awards ceremonies, Dean’s list, convocation, alumni meet, guest lectures, workshops, LBC/SLC, conferences & symposia etc.
- Documenting and monitoring academic & extra-curricular performance, attendance, discipline, and other student relevant data, drawing reports and analysing trends and projections that may be relevant to academic planning.
- Liasoning with other departments, Dean’s Office, Registrar’s Office, Exam Office and other stakeholders as needed. Providing administrative support and PT feedback to relevant committees.
- Maintaining or creating SoPs and ensuring policy compliance
Essential Qualifications:
- Good academic record with a Bachelor or equivalent degree
- Fluent in English language, written and conversational
- High level of professionalism, and ability to keep confidentiality regarding departmental activities.
- Compliance with data protection and confidentiality regulations
- Ms Office skills (Excel particularly) necessary
Preferred Qualifications
- Prior experience of 2-3 years in program management (or relevant profile in academic management roles) at a reputable higher education institution
- Technical skills in academic management systems and learning management software (DigiCampus/Collpoll preferred)
- Professional communication and student centred approach
- experience in large data handling and analysis
- Able to work in a fast-paced environment in a new school/campus, where new challenges and demands sometimes arise on short notice
- Counselling experience or certification desirable
- Understanding of Indian Higher Education landscape and BCI related policies with a keen interest in legal education
*Job responsibilities stated are not to be taken as an exhaustive statement of duties. Employees may be required to perform other job-related duties as and when necessary.
Graphic Designer & Video Editor
Posted 1 day ago
Job Viewed
Job Description
About the Opportunity: BITSDES is a world-class centre of learning for design under the aegis of BITS Pilani, an Institution of Eminence. We are looking to hire a Graphic Designer + Video Editor with basic photography and videography skills to join the marketing team.
Job Summary:
The role will be responsible for designing visual concepts, creating digital and print graphics, and basic video editing and packaging for our social platforms, website, and marketing campaigns. It will report to the Head of Marketing, BITSDES and work in close coordination with members of the marketing team.
Job Responsibilities*
- Develop creative concepts and designs for digital and print media, including social media, websites, brochures, etc. as per the brief.
- Edit video content for social media, YouTube, website, and marketing campaigns.
- Conduct on-campus video and photo shoots on mobile phone and/or institution equipment.
- Communicate with printers and other vendors to ensure quality of the final product.
- Manage multiple projects simultaneously, meet deadlines, and work collaboratively with stakeholders.
Qualifications, Skills & Experience:
- Should have received formal education for a minimum of 5 years in visual/graphic design.
- At least three years of experience in graphic design and video editing.
- Proficient in using Adobe Creative Suite, especially - Photoshop, Illustrator, Premiere Pro.
- Should have basic photography and videography skills, understand DSLR/mirrorless camera functions and be able to shoot in manual mode.
- You must have an online portfolio – on Behance, Dribbble, or other website. Please share that along with your resume.
- You must be willing to travel to our campus at Kalyan, District Thane. This is an on-site position and we do not offer work from home.
Nature of engagement:
On contract for one year, extendable thereafter.
*Job responsibilities stated are not to be taken as an exhaustive statement of duties. You may be required to perform other job-related duties as necessary.
Be The First To Know
About the latest All Jobs in Murbad !
Assistant General Manager
Posted 2 days ago
Job Viewed
Job Description
Purpose
The prerequisite is the ability to handle large teams (30+ members) in QC, including an AMV team. The primary responsibility for leading the LC-MS, Nasal analytical, FT-NIR analytical teams for regular testing/method validation activities. The secondary is responsible for back-up support to the QC-HOD with daily updates, monthly sample status, Lab management, training, monthly review meetings and co-ordination with all stakeholders to align the work as per requirements.
Location: Ambernath, Maharashtra
Job Responsibilities:
- Primarily responsible for leading the QC-AMV team size of 30+members (LC-MS, Nasal and FT-NIR team) for regular testing/method validation activities and with sound analytical knowledge and good leadership qualities to achieve company goals.
- Secondary responsible for back-up support to the QC HOD with daily update, commercial output, monthly sample status, Training, monthly review meeting and co-ordination with all stakeholders to align the work as per requirements.
- Responsible for Execution & approval of different types of QMS (OOS, OOT, Investigation etc) and identify scientific root causes with effective CAPA and maintain Lab compliance.
- Responsible to design and executing planning of analysis (Routine work, Method validation and Method transfer), data interpretation and presenting to HOD.
- Should be self-driven, have the capability to make self-decision and be a good learner. Providing guidance to team members for improving the work quality and monitoring and reporting on key performance indicators (KPIs).
- Shall be responsible for leading all types of QC-AMV work in the absence of QC-HOD and actively participate in departmental improvement programs to enhance the Output and Quality.
- Collaborating and coordinating with cross-functional teams like QA, RA, R&D and PMI to proceed the allocated task with ownership and accountability.
- Stay updated on industry developments and emerging trends to ensure they remain competitive for LC-MS and FT-NIR techniques.
- Responsible for adherence to GLP and Health, Safety Environment system in Laboratory and responsible for facing the FDA Audit (US, MHRA, EU) individually.
Qualifications & Pre-Requisites
Preferably have the following skill but not limit as mentioned below.
- Master Degree of Science / Bachelors or Master Pharma.
- Should have strong analytical knowledge and expertise in modern analytical instruments (Like: HPLC, GC, LC-MS or NIR or Nasal performance testing etc) with the ability to interpret complex data and generate insights.
- Preferably mix work experience in QC, AMV and AD departments.
- Strong leadership skills with a proven ability to motivate and develop team members.
- Exceptional problem-solving skills and a strategic mindset. Solid organisational and time management skills, with the ability to manage multiple projects and deadlines.
- Knowledge of Chromeleon 7.2 and Sciex software will be an added advantage.
- Should have good working experience in GMP and USFDA/EU Audit faced.
- Should have skill to achieve deliverable tasks with minimum support for analysis.
- Should have excellent written and verbal communication skills, with the ability to present findings clearly and effectively
Additional notes
- The role is expected to manage the work in all shifts.
- If required he might need to travel to Satara, Thane site, Indore site on work priority as per company policy.
- Responsible for ensuring compliance with GLP, Health, Safety and Environment. requirement.
Science Teacher - Physics/Chemistry
Posted 2 days ago
Job Viewed
Job Description
Company Description
Name: Rosary High School
Location: Yadav Nagar, Ulhas Nadi Bridge, Badlapur Gaon Road, Badlapur West, Thane, Maharashtra
Managing Trust: Saint Anthony Educational and Welfare Trust
Board Affiliation: CBSE (Central Board of Secondary Education)
Role Description
This is a full-time on-site role for a Science Teacher specializing in Physics and Chemistry at Rosary High School located in Ulhasnagar. The Science Teacher will be responsible for developing and implementing engaging lesson plans, instructing students in the subjects of Physics and Chemistry, evaluating student progress, and providing feedback to students and parents. The teacher will be expected to maintain up-to-date knowledge of curriculum and educational best practices, and participate in school activities, meetings, and professional development opportunities.
Salary - 40 K Per month
Qualifications
- Proficiency in Science Education and a strong understanding of Physics
- Qualified Teacher certification and experience in Lesson Planning
- Strong Mathematical skills
- Excellent communication and organizational skills
- Ability to engage and inspire students
- Experience with educational technology and tools is a plus
- Bachelor’s or Master’s degree in Education, Physics, Chemistry, or a related field
Interior Designer
Posted 7 days ago
Job Viewed
Job Description
The ideal candidate will have excellent creative thinking skills and be able to create designs based on conversations with a client. The candidate should be confident communicating regularly with the client in order to assess their needs and be able to adjust a given approach based on feedback. The candidate should maintain familiarity with the interior design landscape and trends in order to provide the best ideas for clients.
Responsibilities
- Create attractive designs and layouts for various projects
- Meet with client in order to understand the client's objectives and desires
- Communicate effectively with client, vendors and team in order to address client's needs
- Prepare presentations (3D, 2D,mock-ups and renderings) for clients
- Create quotes for clients and ensure full workflow is followed
- Maintain industry knowledge in order to stay relevant
Qualifications
- Bachelor's degree 1 - 3 years of experience in related field, Proficient in AutoCAD and Microsoft Office suite
- Strong creative and communication skills
- Demonstrated ability to execute
Apply here