1090 Formulation Jobs - Page 10

The role involves conducting quality inspections and testing for colour cosmetic products such as lipsticks, eyeliners, eyeshadows, and foundations. This includes performing physical, chemical, and sensory testing to ensure products meet defined quality parameters like color accuracy, texture, fragrance, and packaging integrity. You will also monitor raw materials and packaging components for compliance with quality specifications. You will be responsible for maintaining detailed records of inspections, test results, and deviations, as well as preparing quality reports and communicating findings to production and R&D teams. It is essential to ensure that all quality control activities are do...

You should have a comprehensive understanding of product development activities for all injectable dosage forms meant for the regulated market. This includes working with complex injectable products like suspension-based formulations, liposomal formulations, and Polymer based products. Your responsibilities will also involve preparing and reviewing product development reports, MFR, stability protocols, study protocols, and SOPs. Additionally, you should have a basic grasp of implementing QbD principles for formulation and development, including QTPP, CQA, CPP, CMA, risk assessment, and control strategy. Effective coordination with various departments such as regulatory affairs, manufacturing...

Basis knowledge of Telco Network operations. Primary responsibility is to Monitor the KPI & Alarms for the multivendor RAN nodes system. To oversee end to end Networks performance and maintain the acceptable level of network quality of service as per business objectives and a set of predefined network Key Performance Indicators Maintain a certain agreed level of Network performance, availability, reliability, integrity and usability by monitoring, analysing and reporting predefined Key Performance indicators (KPIs), measures and customer feedback. Good Performance management (RAN KPI) knowledge. Strong RCA & troubleshooting Skills. Creation of TT through tools within the agreed Response time...

Basis knowledge of Telco Network operations. Primary responsibility is to Monitor the KPI & Alarms for the multivendor RAN nodes system. To oversee end to end Networks performance and maintain the acceptable level of network quality of service as per business objectives and a set of predefined network Key Performance Indicators Maintain a certain agreed level of Network performance, availability, reliability, integrity and usability by monitoring, analysing and reporting predefined Key Performance indicators (KPIs), measures and customer feedback. Good Performance management (RAN KPI) knowledge. Strong RCA & troubleshooting Skills. Creation of TT through tools within the agreed Response time...

IP Strategy & Risk Management Conduct comprehensive patent landscape and whitespace analyses across global markets (India, US, EU, China, Brazil, Japan, etc.) to identify IP barriers and opportunities. Draft, file, and prosecute patent applications (including formulation, process, and use patents) to strengthen the company s IP portfolio. Perform Freedom to Operate (FTO) analysis to assess risk and enable informed product development and commercialization decisions. Predict potential blocking patents and assess the probability of patent grant or litigation risks. 2 . Portfolio & Lifecycle Intelligence Monitor competitor activities, brand pipelines, patent expiry timelines, and ongoing clinic...

Oversee and lead all activities of assigned teams /projects; meet customer needs. Work according to appropriate standards for quality, ethics, health, safety, environment, protection and information security; lead initiatives to ensure continuous improvement; all activities have to be aligned with organizational workflows and procedures. Evaluate and interpret results, draw relevant conclusions; supervise project related activities; perform complex tasks without having established procedures. Oversees and may also write protocols, scientific reports, lab procedures or process. related SOPs; write scientific documents intended for external partners or for generation of registration documents;...

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 t...

Clearly define the scope/solution of both Capital and RTB related projects and initiatives Capture, aalyze and organize business requirements into a logical order. Prioritize requirements based on business needs. Able to produce Tableau/Power BI dashboards Contribute toward technical discussion in arriving at new solutions Identify and document all non-functional requirements. Create business process maps and data flow diagrams. Communicate business requirements to business area experts and technical/development staff. Lead the identification and documentation of business metrics. Determine systems of record with the assistance of appropriate source system experts Help identify potential sou...

Manage ETO projects in an international environment from definition to final approval Coordinate all activities for the project and create the final design and pricing Define specifications in cooperation with other departments like product development, quality, procurement, MSAT,sales and marketing for more complex projects Making technical and feasibility analyzes of projects Design new custom products using in-house design tool according to customer needs and internal design rules (Use of computer software design tool) Ensure product is manufacturable and define any qualification/testing that might be needed Calculate product cost and define price of the product in collaboration with mark...

Responsibilities Key Deliverables Independent Shift handling coordination with Production for seamless execution of maintenance activities. Coordination with vendors for outsourced activities. Spare parts management i.e.. procurement, Storage, and consumption monitoring. Analysis of chronic and repeated breakdowns and formulation of Countermeasures to tackle the same with preventive, proactive predictive approach. Maintaining different performance parameter related to department viz. RFI, MTBF, MTTR and analyzing of the same for adopting suitable maintenance program. Chalking out of annual, monthly, weekly preventive maintenance Plan of plant in consultation with respective shops. Execution ...

Treasury TTG INTERNAL USAGE No. of Vacancies 1 Reports to Is a Team leader No Team Size 1 Grade Deputy Manager, Manager Business Department Treasury Sub - Department Treasury TTG Location About Treasury The primary function of the treasury department of any banks is to ensure that its assets match its liabilities in every possible way. Treasury department profoundly influences both deposit taking and loan sanctioning functions of the bank. Apart from ALM function, Treasury Department also undertakes Foreign exchange dealing, Forex and Rupee Derivatives transactions and Investment in SLR (Govt Securities) and Non SLR Securities (Corporate Bonds/CP-CD/Equity). About the Role Treasury & Markets...

We are looking for a highly enthusiastic & passionate candidate for the post of R&D Associate to develop next-generation dental materials, including cements, 3D printing resins, sealers, and composites. You will be part of a high-energy team driving innovation from concept to commercial launch. 3-5 years of hands-on R&D experience for mid-level roles in polymer or biomaterial development, including formulation, characterization, and scaling from lab to production Relevant sector : Dental Materials & Products, Medical Device & Biomaterials, Polymer & Chemical manufacturing, Additive Manufacturing/ 3D printing, Advanced Materials Science & nanotechnology Role & responsibilities : Formulate and...

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 & Packing Aseptic operations/ QMS / SKID / Multi-vessel / SVP / Visual Inspection / Packing / VI (Senior Officer / Officer / Associate) Experience - 02 to 07 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI Engineering (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experienc...

We are looking for a dedicated and detail-oriented Manufacturing Chemist to join our production team. The ideal candidate will have a strong background in chemistry and practical experience in a manufacturing setup, preferably in the cosmetics, pharmaceutical, or chemical industry. Your key responsibilities will include assisting in the manufacturing and formulation of chemical products according to company standards, handling and operating lab and production equipment safely and efficiently, monitoring and ensuring the quality of raw materials and finished products, maintaining proper documentation of batch records, test results, and manufacturing data, ensuring compliance with GMP (Good Ma...

Job Title: Production Machine Operators (6 Positions) Nourish Pharmaceutical Pvt Ltd is a leading manufacturer of finish dosage formulations, including tablets, capsules, and oral liquids. We are seeking skilled Production Machine Operators to join our team. Positions: 1. Granulation Operator 2. Compression Machine Operator 3. Primary Packing Operator 4. Coating Operator 5. Capsule Operator 6. Oral Liquid Packing Operator Job Descriptions: 1. Granulation Operator - Key Responsibilities: - Operate and maintain RMG (Rapid Mixer Granulator), FBD (Fluid Bed Dryer), and Paste Cattle Blender equipment - Ensure smooth granulation process and maintain product quality - Monitor and control process pa...

Job Title: Quality Assurance Officers (4 Positions) Company: Nourish Pharmaceutical Pvt Ltd Location: Kheda, Gujarat Job Type: Full-time Nourish Pharmaceutical Pvt Ltd is a leading pharmaceutical company committed to delivering high-quality products. We're expanding our Quality Assurance team and looking for talented professionals to join us. Positions: 1. Quality Assurance Officer - Production 2. Quality Assurance Officer - QMS 3. Quality Assurance Officer - Validation & Qualification 4. Quality Assurance Document Control Officer Job Descriptions: 1. Quality Assurance Officer - Production - Key Responsibilities: - Ensure cGMP compliance in production areas - Manage and review Batch Manufact...

At Cognyte we create mind-blowing security analytics software to speed up investigations and allow customers to detect and respond to real security threats like terror, crime, fraud, cyber threats, crypto crime, and more We did a spinoff in early 2021 and are independently traded on Nasdaq Were young, develop cutting-edge technology, and were going far, fast, So, if you rock at DevOps and being a technical expert, and want in on the action, lets talk! Your impact Designing and implementing cloud native best practices over our advanced and innovative security product Develop new tools to support our CI\CD infrastructure Design and implement Cloud native security best practices Working with cu...

Role & responsibilities Job Responsibilities: 1.Market samples receiving, entry and stock maintenance. 2.List updations, equipment and SOPs, Product code list updation 3.RM BOM preparation and checking of new product solid, liquid and semi-solid dosage form. 4.Preparation of MFR/MPR/PDR of solid, liquid and semi-solid, injectable dosage form. 5.Sample upkeep Withdrawal and Storage of Sample. 6.RA related mail communication, document follow ups, preparation and send as per urgency and priority of documents. 7.List updations (RM/PM/Stability samples)/ Innovator samples/ Equipments. 8.BOP preparation and corresponding mail correspondence. Responsible for QMS activity ,MFR preparation and corres...

Role & responsibilities 1. To ensure that all required information is included in the regulatory filing. 2. To collect the documents require for dossier preparation. 3.To evaluate the country wise requirements for dossier preparation as per checklist. And compile a draft dossier as per requirements and in the format provided by the authority of the country. 4.To co-ordinate with Artwork, Purchase, QC, QA, R&D, Packaging, Licensing Department for necessary documents/data. Prepare documents for courier purpose and send the courier. 5. Keep a track of the courier to check delivery on time. Providing comments on the product, preparing and submitting a regulatory application, and working with oth...

Job Overview We are looking for a qualified and experienced Manufacturing Chemist having worked in cosmetics and OTC production background to oversee the manufacturing processes of cosmetics and OTC products in accordance with industry standards, regulatory requirements, and company protocols. The ideal candidate will ensure accurate batch preparation, maintain compliance with GMP standards, and support production efficiency. Key Responsibilities Take batches of cosmetic & OTC Supervise and manage the manufacturing of cosmetic and OTC topical formulations (creams, ointments, gels, etc.). Oversee end-to-end production management, including planning, scheduling, and resource optimization. Ensu...

You would have complete knowledge of relevant categories. Total understanding of the various agency functions You would have been able to understand the client working style and deliver on their day-to-day requirements and start building relationships with the key decision makers within the current pipeline Demonstrate good understanding of clientsbusiness and challenges and ability to apply the knowledge in the formulation of campaign strategy and recommendation. Build a good relationship with clients, internal and external stakeholders, and partners Proactively drive the business initiatives and response to the client requirements & briefs. Have full understanding of what is happening on c...

Assist in R&D tasks and activities. Develop and implement R&D policies and procedures. Monitor and report on R&D performance metrics. Collaborate with R&D teams and stakeholders. Ensure compliance with R&D standards and regulations.

Walk In Drive For Production OSD In Formulation Division @ Kothur Department:- Production OSD Qualification :-ITI | Diploma | BSC | B Pharmacy | M Sc | M Pharmacy Experience :- 2 To 8 Years Skills :- Packing Operators :- Primary Packing:- Cam MNX | ACG|B Max|BQS|IMAPG||EL Mach|Pharma Pack|CVC Secondary Packing:- HI-Cart|IC-150|CAMHV1|CVC| IMA A 300 Cartonator & Pharma Pack| Labelling Packing Supervisors| Inchargers|Bottle Line Supervisors QMS Supervisors : Handling deviation|Change Controls|Market Complaint&Investigations|Audit Complaince&Intiations of Quality Intiatives Manufacturing:- Compression | Coating | Granulation | Capsule Filling| Executives | Operators| Supervisors Division :- For...

Responsibilities As a regulatory affairs officer: ensure that a company's products comply with the regulations of the regions where they want to distribute them keep up to date with national and international legislation, guidelines and customer practices respond to queries from medical bodies like the Medicines and Pertaining to that Guidelines. collect, collate and evaluate scientific data from a range of sources develop and write clear arguments and explanations for new product licences and licence renewals prepare submissions of licence variations and renewals to strict deadlines monitor and set timelines for licence variations and renewal approvals work with specialist computer software...

Review and manage SOPs, BMRs, BPRs, other GMP documents Ensure proper documentation practices (GDP) are followed across departments Support in preparation for regulatory inspections and audits WALK IN INTERVIEW LOCATION PUNE (31/08/2025 Sunday) Required Candidate profile Coordinate with production, QC, warehouse, and engineering departments to resolve quality issues. Support tech transfer and validation activities as required. Good analytical and communication skills.