2048 Formulation Jobs - Page 28

Job Title: DGM – Corporate Quality (Audit) Business Unit: Global Quality & Compliance Job Grade G8 Location : Mumbai At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Job Summary : To manage quality audit of vendors ...

As an Assistant Manager/Manager (Technical Services and R&D Support) at our company, you will play a crucial role in supporting the research and development of personal care products, focusing on skincare, haircare, and body care categories. Your responsibilities will include assisting in the formulation, testing, and analysis of products, ensuring regulatory compliance, and supporting the day-to-day activities of the R&D team. Key Responsibilities: - Come up with new product ideas and implement ideas received from customers or the sales team. - Prepare formulations to meet product specifications and guide the R&D team in preparing samples. - Provide samples/prototypes to meet customer requi...

As a Production and Quality Executive at our company, you will play a crucial role in managing production processes within the beverage industry. Your responsibilities will include overseeing plant operations, maintaining product quality, and guiding production teams to achieve company objectives effectively. Here is an overview of what you can expect in this role: **Role Overview:** You will be responsible for overseeing production processes, ensuring seamless operations, and addressing quality issues in collaboration with the production team. Your role will involve production planning, quality control processes, managing inventory, developing QC procedures, and leading the QC team of manuf...

Job Purpose: To operate and monitor granulation equipment and processes in compliance with cGMP, SOPs, and safety standards, ensuring consistent production of high-quality pharmaceutical granules for tablet or capsule formulation. Key Responsibilities: Operate granulation equipment such as high-shear mixers, fluid bed dryers, oscillating mills, and blenders. Weigh, dispense, and mix raw materials as per batch manufacturing records (BMR). Monitor granulation parameters and adjust settings to maintain product quality. Perform in-process checks (e.g., moisture content, granule size) and document results accurately. Clean and maintain equipment and work areas as per SOPs. Execute machine changeo...

Manual Preparation and Amendments of existing Policies. Forms & Formats Modifications for case sheets and various departments. Formulation of New committees and Quality Indicators. Check NABH standards and GAP Analysis in system Verification of Annual calendar activities for Branches. Preparation of training schedule for Quality Staff. Department training for Quality Staff Implementation of clinical Audits in the units. Conduct facility Rounds with Branch safety team Verification of Quality Indicators Raw Data Verification of Committees functioning Verification of Audit Reports Verification of Outsource facility Audit Reports. Risk Management analysis like Incidents Management, Hazmat manage...

Overseeing the daily operations of existing & upcoming manufacturing plants. Developing and executing business strategies. Ensure efficient supply chain management. Work closely with CMD, operational excellence, and strategic business execution Required Candidate profile Must have experience to Handle Plant operations, coordination with PPIC, Supply Chain and Marketing team for smooth functioning. Experience in Pharmaceutical Contract Manufacturing Industry only.

Dear All, We are seeking a highly motivated and talented Analytical R&D Scientist(Injectables) to join our innovative team. The ideal candidate will have a strong foundation in Analytical development and you will play a crucial role in developing new and improved formulations, ensuring product quality, and meeting regulatory requirements. Location: Hyderabad(Dulapally) Required Experience: 5-7 Years Job Responsibilities: 1. To follow the departmental SOPs 2. To ensure the error free and online documentation. 3. To ensure only calibrated instrument /equipment's are used for analysis. 4. To coordinate with supervisor in developing the methods for dissolution, assay by UV/HPLC and RS by HPLC. 5...

Preferred candidate profile 1. Production Chemist - Fresher ( B.Pharm/M.Pharm) 2. Production Chemist - Should have experience in manufacturing of dry powder injections(B.Pharm/M.Pharma/Msc) Exp- 2 to 10yrs 3.Blister Operators-(2 to 5yrs) Should have experience in handling blister packing machines for tablets/injectables 4.Operators Injectables-(2 to 5yrs) Sterilisation Tunnel Powder filling machine-Ambica/NKP Labelling Machine Auto Cartonators 5. Dry syrup line-(2 to 5yrs) Must have relevant exp in dry syrup filling line 6. Capsule Filling-(2 to 5yrs) Must have relevent exp in capsules filling lines 7. Blister Packing-(1 to 5yrs) Must have relevent exp in Blister packing,preferable person ha...

Role & responsibilities : Production Planning: Manage daily manufacturing activities, manpower, and ensure timely, quality production as per schedule. Documentation & Compliance: Complete and review BMRs, follow SOPs, and ensure all work meets cGMP and regulatory standards. Coordination: Work with QA, QC, Stores, and Maintenance teams for smooth production and equipment upkeep. Team Management: Guide, train, and motivate team members to follow company policies and good manufacturing practices. Safety & EHS: Maintain a safe work environment, ensure PPE usage, report incidents, and follow all EHS rules. Process Improvement: Support productivity enhancement, cost-saving ideas, and new technolog...

As a Technical Perfumer Fine Fragrances with the global fragrance house in Andheri, you will play a crucial role in developing and matching fine fragrance compositions using analytical data derived from GC-MS reports. Your responsibilities will include: - **Fragrance Matching & Development:** - Analyse GC and GC-MS reports to identify key raw materials, structure, and balance of fine fragrance compositions. - Develop accurate fragrance matches and recreate market references or client benchmarks. - Modify or improve existing fragrance formulas for performance, stability, and cost optimization. - **Analytical Interpretation & Raw Material Identification:** - Interpret chromatographic data to d...

Global Data Insights and Analytics ( GDI&A ) navigates Ford Motor Company through the disruptions of the information age, unleashing the power of Data, Advanced Analytics, and AI to drive value and help transform Ford Motor Company through proactive, actionable, evidence-based decision making. GDI&A delivers data-driven platforms, advanced analytics, and AI/ML solutions to support Ford s Industrial System, Sales, Service, Marketing, Strategy, Finance, and Ford Credit. We are seeking an initiative-taking and experienced candidate to lead and mentor a multi-skilled product team comprising of data scientists, machine learning engineers, product designers, and software engineers through the enti...

Walk-In Interview Date : 02nd November 2025 (Sunday) Timing : 9.00 AM to 2.00 PM Venue : Umedica Laboratories Pvt, Ltd. Plot No 221,221/1 II Phase GIDC Nr Morarji Circle, Vapi 396195. 1. Tablet Manufacturing Department: Ability to handle process like Dispensing, Granulation, Compression, Coating, SOPs preparation, well versed with ALCOA & GDP principles. QMS Manufacturing investigation (OOS/OOT/Deviation/CAPA),Training.) Position: Officer to Sr. Executive Qualification: M.Sc. / B.Pharm / M.Pharm No. of Vacant Position: 10 Experience: 2 to 8 years To Operate Granulation lines (RMG/FBD/FBP/Roll Compactor), Automatic Compression Machine (PLC/SCADA based Cadmach & Fluid Pack), Coating (Kevin & G...

Spearheaded the execution and analysis of a broad range of technical tests for detergent bars, powders soaps, ensuring process optimization and superior product quality Independently conducted consumer research, technical studies, and performance

Key Responsibilities: 1. Production Operations: Execute and supervise daily Softgel manufacturing operations including gelatin mass preparation, encapsulation, drying, and inspection . Ensure all activities are carried out as per BMR, SOP, and cGMP requirements. Coordinate with QA and QC for in-process checks and line clearance. Maintain process parameters (temperature, humidity, viscosity, machine settings, etc.) within specified limits. 2. Documentation & Compliance: Prepare and maintain Batch Manufacturing Records (BMR) , logbooks, and equipment usage logs. Ensure timely completion and accuracy of documentation as per Good Documentation Practices (GDP) . Adhere to data integrity and regul...

Develop and optimize innovative oral care flavors (toothpaste, mouthwash, gum). Collaborate cross-functionally, manage flavor library, ensure regulatory compliance, conduct lab tests, sensory analysis, and partner with suppliers for flavor innovation Required Candidate profile ICT Mumbai – M.Tech: Deep chemical/engineering base in flavour & perfumery. IGMPI – PG/Exec Diploma: Flexible, industryfocused. FFDC – Diploma: Short, practical aroma training. MU – M.Tech:

Position: Executive - Project Management (CMO Formulations) Location: Hyderabad(Dulapally) E xperience Required: 1-3 years of relevant experience as a Project Manager in CMO Formulations Aizant Drug Research Solutions Pvt Ltd is on the lookout for a dynamic and talented Project Manager to join our innovative Formulation CMO Team ! If you have a passion for pharmaceutical excellence and thrive in a fast-paced environment, this opportunity is for you. Key Responsibilities: This role is crucial for ensuring the smooth and efficient progression of both Technology Transfer and Commercial Production projects. The ideal candidate will have 2-3 years of experience, a strong background in project man...

Role & responsibilities: - In-Process Quality Assurance Activities Documentation and Compliance Process & System Control cGMP Compliance & Audit Readiness Qualification Required: - B.Pharm / M.Pharm Experience Required: - 3 to 10 Years Walk-in Interview Details: - Interview Date: - 26th October, 2025 (Sunday) Interview Time: - 9:30 AM to 5:30 PM Interview Venue: - Pride Plaza Hotel , Judges Bungalow Rd, off Sarkhej - Gandhinagar Highway, Bodakdev, Ahmedabad, Gujarat 380054.

Job Description We are hiring Production Officers with hands-on experience in granulation operations for wet and dry formulations. The role involves operating key granulation equipment and ensuring smooth production activities as per GMP standards. Key Responsibilities Handle and operate RMG, FBD, FBP, Octagonal Blender, DC Blender. Execute wet and dry granulation processes as per BMR/SOPs. Ensure line clearance, hygiene & safety compliance. Maintain production documentation and perform IPC checks. Coordinate with QA, Maintenance & Warehouse for production continuity. Maintain equipment cleaning & preventive maintenance records. Desired Candidate Profile Qualification: B.Pharm / B.Sc / Diplo...

We are hiring Senior IT Officer is responsible for managing and supporting all aspects of IT infrastructure, systems, and applications within the pharmaceutical organization. This includes ensuring system security, data integrity, compliance with GxP and FDA regulations, and supporting technology initiatives that enhance operational efficiency. Key Responsibilities: 1. IT Compliance and Documentation Draft, review, and maintain IT Standard Operating Procedures (SOPs), protocols, and related documentation. Ensure all IT processes comply with GxP, GAMP 5, 21 CFR Part 11, EU Annex 11, and ALCOA++ principles. Participate in validation and periodic review of GxP computerized systems for Quality C...

Job Summary: We are seeking a dynamic and experienced professional to join our team as an Application Development Technical Specialist . The primary responsibility of this role is to work with customers and business teams to lead new applications, generate specifications, and replicate successful applications across local and global markets. In addition, the candidate will introduce new products to customers, work closely with the global team on grade translation, technology transfer, and knowledge building, and address customer processes and complaints. Responsibilities also include designing and developing demo tools, publishing technical bulletins on successful applications, conducting ap...

Production Executive for OSD pharma

Role & responsibilities Job responsibilities: 01 To plan and implement an effective Preventive Maintenance System so that the facility and all the equipment are always available for their intended use. 02 To Maintain the Utility services in utmost efficient condition so that production activities are never hampered. 03 To arrange for attending to breakdowns in the factory depts. Promptly so that productive time loss is minimum. 04 To ensure regular calibrations of all measuring and testing equipment in the factory. 05 To ensure that all the machinery are serviced and maintained as required by the quality system. 06 To maintain records of the maintenance and engineering activities as per the ...

JOB DESCRIPTION Position Title BOPP development Position Code U-FL-TC-NN-1148 Reporting To President Technical & New product Development ( Films) Function NPD & Technical Services Unit/ Location Films Division, Noida 1. JOB PURPOSE Responsible for Product development and process improvement w.r.t BOPP Films 2. PRINCIPAL ACCOUNTABILITIES Accountabilities Key Performance Indicators ( Accountabilities indicate your primary responsibilities) (Key Performance Indicators are the measurement parameters and target which define your accountabilities and responsibilities. Product Development & Application ( BOPP & CPP) Process Improvement Liaise with Technological consultants, Customers, Raw Material ...

Seeking an immediate joiner with 3–8 years’ regulatory experience B.Pharm/M.Pharm. Responsible for CTD/ACTD dossier prep,review,query response,team coordination,regulatory submissions,documentation. Strong R&D,research, communication skills required.

Role: Formulation Direct Reporting: Sr Director Formulation Function: Research & Development Job Purpose and Scope Responsible for product development across all divisions of research, such as delivery technologies, microencapsulation & nano encapsulation ,processes, fluid bed processes, spray drying and congealing process. Accountability Result Indicator Quality of formulation No. of stable formulations developed Internal stakeholder feedback Time taken to operationalize Compliance of product with regulations across geographies Key Accountabilities: Develop and commercialize of all research projects related to beadlets, Pellets and various microencapsulation technology. Prepare project mana...