1090 Formulation Jobs - Page 31

Alembic Pharmaceuticals Ltd. is looking for Research Scientist/ Senior Research Scientist- Analytical Development Advanced characterization Laboratory (Peptides and Complex Generics) based at our Injectable R&D Vadodara Role & responsibilities : 1) Develop and validate analytical methods for various aspects of peptide and complex injectable formulations, including purity, identity, degradation products and stability. 2) Expertise in relevant techniques like HPLC, LC-MS, UV/Vis Spectrophotometry, GC, Particle size, In vitro release etc. 3) Data analysis and interpretation, prepare analytical protocols, reports and contribute to regulatory submissions. 4) Identify and resolve analytical issues...

We are hiring for Production Assistant Manager & Executive to work with our manufacturing operations, ensuring consistent production of high-quality branded generics across our diverse portfolio of oral liquids, solids, and topical dosage forms. This is a critical role for our organization, and the ideal candidate will be a strategic leader with a proven track record of driving productivity improvements, operational excellence, optimizing efficiency, and ensuring strict adherence to cGMP compliance. Responsibilities: • Oversee the day-to-day operations of all production departments, including: Oral Liquids Manufacturing Solid Dosage Manufacturing Collaboration with Quality Control, Quality A...

Role & responsibilities This is a full-time on-site role for a Regulatory Affairs Manager located in Chennai. The Regulatory Affairs Manager will be responsible for ensuring regulatory compliance, managing regulatory submissions, and overseeing the implementation and maintenance of quality systems. Day-to-day tasks include tracking regulatory requirements, preparing and submitting regulatory documents, and collaborating with cross-functional teams to ensure adherence to regulatory standards. Experience in Technology Transfers will be an added advantage. Preferred candidate profile Regulatory Compliance, Regulatory Requirements, and Regulatory Affairs skills Experience with Regulatory Submiss...

Position Title : Polymer Scientist / Engineer Department: Research and Development (R&D) Qualification : MSc in Polymer Science OR Organic Chemistry / B.Tech in Polymer Science Job Description / Responsibilities / KRA : Develop and optimize formulations for paints, coatings, textile binder, textile printing and construction chemicals to meet industry and client requirements. Conduct research on polymer-based materials for improved performance and cost-effectiveness. Perform product testing and quality evaluations in alignment with standard protocols. Collaborate with cross-functional teams, including production and quality assurance, to implement innovations. Stay updated on advancements in ...

Network Design Architecture design discussion with Customer together with Nokia team Document and identify and perform analysis of all networking technologies Prepare research plans and documented projects for all LAN and WAN based methods Identify and resolve all technical issues in matter of formulation and creation of strategies Develop multi functional technology and multi vendor network based action plans Prepare and implement three tier upgrade program and resolve all network issues Coordinate Dedicated design document delivery (HLD/LLD/Migration Strategy) to project(internal repository) Handover Customer approved HLD/LLD and golden configs to IntegrationEngineer(s)/MoP Creators Suppor...

Understanding of product development related activities of all injectable dosage forms for regulated market. Exposure to injectable dosage form which includes exposure in development of complex injectable products like suspension-based formulation, liposomal formulations, Polymer based products etc. Experienced in preparation and review of product development report, MFR, stability protocol and other study protocols and SOP etc. Basic understanding of implementation of QbD principles for formulation and development (QTPP/CQA/CPP/CMA, risk assessment and control strategy etc.) Effective co-ordination with different departments like regulatory affairs, manufacturing warehouse, quality assuranc...

Executive, Process Plant safety POSITION PURPOSE: Responsible for Process and Plant safety ensuring minimum risk to people, property and community Responsible for leading Process and Plant safety risk assessments MAJOR TASKS AND RESPONSIBILITIES: Interpret Process and Plant safety policy as laid down by Bayer Group and implement using Best Practices (PPS guidelines) Perform risk assessments for management of change with site management team and provide recommendations for the safe implementation of management of change in line with accepted Bayer guidelines Carry out periodic revalidation to ensure that safety concepts as agreed and documented during previous risk assessments are in place an...

#Gracure Pharmaceuticals Ltd Hiring For Production (Primary Packing) Designation - Operator (Primary Packing) Qualification - ITI /Diploma Experience: 4 to 8 Years Location : Bhiwadi Note: Experience Required from Pharmaceutical Industry Only. Interested candidates can share their resume at Shivani.singh@gracure.com

Job Title : Design Engineering Manager Location : Gandhinagar, Gujarat, India Company: Hitachi Industrial Equipment Systems India Salary Range: As per the industry Company Overview: Backed by the latest technologies, extensive research and development and innovation, Hitachi offers advanced industrial components, equipment and solutions that are helping manufacturing businesses across verticals attain increased operational efficiencies, cost reduction, agility, high uptime, and throughput. Job Purpose: Drive talent development within the Sustaining Engineering organization to develop a high-functioning design engineering team. The Sustaining Engineering Manager is responsible for technically...

Select how often (in days) to receive an alert: Select how often (in days) to receive an alert: Formulation Researcher II Jun 11, 2025 Ambernath, India, 421506 Who we are The opportunity This section is where we attract the attention of potential candidates and sell the role. How has the role come aboutWhat makes it appealingWhat are the key responsibilitiesHow is the role better with Teva than with another companyWherever possible, we should bring through the essence of our EVP pillars, i. e. , we care, we re in it together, and we make work fulfilling. How you ll spend your day Your experience and qualifications Enjoy a more rewarding choice Make a difference with Teva Pharmaceuticals In p...

#Gracure Pharmaceuticals Ltd Hiring For Production (Primary & Secondary Packing) Designation - Sr. Officer/Executive (Primary & Secondary Packing) Qualification - B. Pharma/M.sc Experience: 5 to 8 Years Location : Bhiwadi Note: Experience Required from Pharmaceutical Industry Only. Interested candidates can share their resume at Shivani.singh@gracure.com

Stedman Pharmaceuticals is looking for a dynamic and experienced candidate for the Quality Control (QC) department with hands-on experience in Analytical Method Validation for various dosage forms. Resume to hrd@stedmanpharma.com / 9786920463

Role & responsibilities Develop and execute a robust out-licensing strategy for pharmaceutical products (formulations/APIs/biologics) targeted at the U.S. market. Identify, evaluate, and engage with potential U.S. partners for licensing, co-development, or distribution deals. Manage the end-to-end out-licensing process from opportunity identification, due diligence, deal structuring, negotiation, and closure. Collaborate with R&D, regulatory, IP, legal, and finance teams to support business development initiatives. Stay abreast of market trends, competitive landscape, and regulatory changes in the U.S. pharmaceutical market. Represent the company at key global business development and partne...

PRINCIPLE ACCOUNTABILITIES: Conduct formulations experiments, coordinate for analysis of samples and carry out the required stability studies. Troubleshoot technical problems related to the manufacturing processes and formulations independently, in order to meet the project goals. Guide fellow scientists and trainees on technical matters. Manage a Quick run innovation project independently. Communicate with the project manager(s) and other stakeholders. Presentations with due connect to the overall technical and business goals. Coordinate with analytical department for analysis of formulation samples. In-time documentation of experiments, trial reports, stability studies and other technical ...

As Executive Procurement, you will be responsible for RM/PM planning. You will also be responsible for Productivity of certain P2P units and related operations work. In addition to this you will be responsible for ensuring 100% order execution of Exports Orders. Key Responsibilities: Material resource planning & scheduling Co-ordinating 100% execution of Export Orders. Optimize the raw material and packaging material inventory by better scheduling and other initiatives. Vendor management and coordination for the timely supply of the RM/PM Coordinate with operations / Quality Control for smooth functioning To control inventory levels at factories by ensuring minimal obsolescence. Optimization...

Job description Department : New Product Development Experience Required : 0-2 years Salary Range : 2. 5 LPA 3.0 LPA Roles & Responsibilities: Develop and formulate cosmetic products across various categories such as skincare, hair care, and grooming products, ensuring high-quality formulations. Facilitate the successful transfer of formulations from R&D to production, ensuring seamless scaling up of manufacturing processes. Collaborate with production and manufacturing teams to ensure efficient and accurate technology transfer. Prepare and manage all necessary documentation related to technology transfer. Conduct stability testing to ensure the shelf life and quality of products under vario...

Grade G - Office/ CoreResponsible for providing technical leadership and advice on the development of our portfolio of products, using advanced technical capabilities to design and develop new products and test methods that differentiate against competitors and meet the changing demands of global markets, whilst keeping internal stakeholders appraised of trends that may influence our technical or business strategy and providing strategic advice on future development direction. Entity: Technology Research & Technology Group Job Description: The role is embedded in the Product Development team and has numerous touch points with both internal and external customers and is part of the Data Cente...

DEPARTMENTS: QA, TECH TRANSFER, SAFETY (EHS), PRODUCTION & PACKING WORK LOCATION: Vemgal, Bengalore JOB DESCRIPTION: PRODUCTION Experience: (01 07 Years) •Granulation, Compression, Coating, Capsule filling PACKING Experience: (01 07 Years) •Bottle Packing (Primary & Secondary), Blister Packing (Primary & Secondary) QA Experience: (03 08 Years) •IPQA, Validation & QMS Safety Experience: (01- 05 Years) •EHS, Risk Assessment, ETP, STP Tech Transfer Experience: (01- 05 Years) •Technology Transfer, QUALIFICATIONS : ITI/ B.Sc/ Diploma/ B. Pharm/ M.Sc with relevant experience DESIGNATIONS: Jr Operator/ Operator/ Jr. Officer/ Officer/ Jr Executive/ Executive• INTERVIEW VENUE: Hotel: RK Gardenia, No....

Excellent written and verbal communication skills in Marathi and English. Excellent report writing and drafting skills in Marathi and English. Computer typing in Marathi and English. In-depth knowledge of air quality monitoring techniques, air pollution control technologies, and regulatory frameworks. Expertise in air quality data analysis, reporting, and interpretation using industry-standard software and tools. Knowledge of best practices in urban air quality management and emission reduction strategies. Strong project management skills, including the ability to streamline and execute activities within a given timeframe. Prepare EOI for Vendor identification and checking their competency a...

Role Responsibilities: Conduct thorough market research and data analysis to support company objectives. Collect and evaluate data from primary and secondary sources. Develop and manage research projects, ensuring timelines and budget compliance. Provide actionable insights that inform strategic decision-making. Prepare detailed reports and presentations to communicate findings. Collaborate with cross-functional teams to identify research needs. Assist in the formulation of research methodologies and strategies. Monitor industry trends and competitive landscape. Present research outcomes to stakeholders clearly and concisely. Support the analysis of data sets using statistical software. Iden...

Urgent Requirement For Regulatory Affairs - FML Department in FML Division - MSN Laboratories, R&D Center Regulatory Affairs FML Department in FML Division , Job Description: ( Regulatory Affairs - FML Division ) Should have minimum of 13 to 23 years of experience in FML Regulatory Affairs Job Title: Deputy Manager / Manager / Senior Manager / AGM Experience: 13 to 23 years in FML RA field Candidates Only. Education: B Pharm \ MSc \ M Pharm Department : Regulatory Affairs - FML Markets : China, Europe, Australia, US, ROW Key Skills Regulatory Guidelines Knowledge, Documentation, Problem-solving, Strong Communication, Collaboration, Organization Skills Role & responsibilities International Pr...

Role & responsibilities Bsc / MSc Chemistry / Diploma in printing with 2 to 5 years experience in water based inks, and roto gravure printing experience, familiar with ink mixing / formulation, Delta E, Density, Customer experience in shade card preparation and approval, knowledge in SAP etc. Preferred candidate profile From same / Similar industry working on Ink Management Profile leading a team on subject matter.

To involve from start and investigate level 2 & 3 incidents, by working closely with site CFT and operating people to arrive at proper Root cause, CA and PA and in report writing. To Involve in valid OOS and other cases as relevant, by working closely with site CFT and operating people to arrive at proper Root cause, CA and PA and in report writing. To review level 1B incidents and give feedback for improvement. To periodically trend level 1A incidents and highlight/escalate key observations. To review any other referred reports associated with incidents/events in association with sites. To possess high level of integrity to have unbiased, independent and objective closure of incidents and m...

This note describes the role and requirements for Procurement professional based in Mysore, Karnataka India. Expected 8-10 years Purchase operations experience in OSD Plants , R&D and QC site's Raw Material, Excipients, Chemicals and Packaging. Roles and Responsibilities Strongly prefer candidate from OSD (Pharma) Plant purchase experience . Raw Materials, Excipients, Chemical & Packing material purchase across OSD manufacturing sites, R&D sites and QC sites including CAPEX investments. Should have minimum 1Cr (monthly) purchasing experience connected to approval and transactions of PO. Lead the negotiations process with vendors with the aim to get the best competitive price and supply secur...

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities Injectable Manufacturing & Visual Inspection Aseptic operations/ QMS / SKID / Multi-vessel / SVP / Visual Inspector (Senior Officer / Officer / Associate) Experience - 01 to 05 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI OSD – Manufacturing / QMS (Senior Officer / Officer / Executive) Experience - 02 to 07 Years Qualification – B. Pharmacy/ M Pharmacy Engineering ...