2053 Formulation Jobs - Page 49

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.

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.

Candidate having minimum 3 to 5 year experience in Granulation, Compression & Coating section in pharmaceutical industry. Interested candidate can call on this mobile no-+91-78310 31890, 9816336040 Food allowance Health insurance Annual bonus Provident fund

Division Manufacturing Department Formulation Sub Department 1 Engineering - Formulation Job Purpose The incumbent is a team member of Unit Engineering Maintenance & Reliability Team and carries overall responsibility to: 1.Execute the maintenance activities in the plant & ensure the minimum Instrumentation & Automation breakdown with maximum efficiency by following safety & GMP Standards 2.Support EM & R Senior Instrumentation Engineer in carrying out Functional EM&R Planning, Detailed Scheduling and Execution of CMP to- ensure continuity of availability of plant & equipment at optimal cost; achieve standard capacity; ensure overall plant & equipment integrity & reliability - in compliance ...

Job Title: Global Fabric Cleaning Powders Ecodesign R&D Associate Business Group: Home Care (R&D) Location: Bengaluru BUSINESS CONTEXT Fabric Cleaning Powders is the largest format by volume and turnover in the Home Care portfolio globally. As per the new Share that Matters strategy in Home Care, the focus in Powders is to grow share in selective Power Growth Cells in our key markets. This is achieved through Unmissable Brand Superiority by delivering Product Superiority against local and global competitors. Further, the business needs Fuel for Growth from scale formats like Powders. This is needed to drive disproportionate growth in new formats of the future. Globally, Powders have been con...

Technician Granulation 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. ...

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...

The primary role is to make direct contributions to the engagement team by assisting clients on Organization Readiness and Consolidation in a deal / M&A scenario. The primary responsibilities of current role may include: Organization readiness in a post deal integration: Understand the integration vision and strategy set out in the deal objective Work with C-suite executives, business and internal firm stakeholders to identify integration guiding principles Identify the target operating model, organization construct and governance model for the consolidated entity Evaluate the considerations for organization readiness for interim (Day 1 /100), desired end state Establish Day 1 / Day 100 chec...

Role & responsibilities Plan, execute, and review Validation Protocols and Reports (Process, Cleaning, Analytical Method, and Computer System Validation). Execute and review Equipment Qualification activities (IQ/OQ/PQ, Re-qualification). Support preparation and maintenance of Validation Master Plan (VMP) . Ensure compliance with cGMP, FDA, MHRA, WHO, and other international regulatory guidelines. Coordinate with cross-functional teams (Production, Engineering, QC, R&D) for smooth execution of validation activities. Conduct risk assessments and gap analysis for equipment, utilities, and processes. Review and maintain SOPs, protocols, and technical documentation related to validation. Handle ...

Role & responsibilities Operate and monitor tablet compression machines (e.g., Cadmach, Fette, Korsch, or equivalent). Set and adjust machine parameters (RPM, compression force, weight, thickness, hardness, etc.) as per BMR. Ensure proper tooling installation, changeover, and maintenance of punches & dies. Perform in-process checks (IPC) like weight, thickness, hardness, friability, and appearance. Record all operational activities in BMR, logbooks, and other documents as per GDP. Ensure line clearance, cleaning, and preventive maintenance of machines. Report deviations, breakdowns, and abnormalities to supervisors/engineering. Adhere strictly to cGMP, GDP, EHS, and safety guidelines during ...

Maintain and update quality documentation, COAs (Certificate of Analysis), MSDS, batch records, data records Coordinate with vendors and internal teams for quality-related queries and pending documents Coordinate with Sales Team for Specifications / Query Support internal and external audits and implement corrective actions Assist in customer complaint investigations and root cause analysis QC & QA Documentation Handling claims for all activities Knowledge of KOSHER, HALAL, MSDS, FSSAI Check verifies and update parameters of the products like Haz class, FEMA Nos Ensuring that products comply with relevant supporting quality standards, regulatory compliance (egFSSAI) Ensure compliance with ap...

Role & responsibilities Operate and monitor tablet coating machines (Auto Coater/Conventional Pan) as per batch manufacturing records (BMR). Perform coating processes (aqueous/organic) ensuring uniformity and quality standards. Set and monitor machine parameters (spray rate, pan speed, inlet/outlet temperature, atomizing pressure, etc.). Carry out equipment cleaning, calibration, and preventive maintenance. Record all operational details in BMR, logbooks, and related documents. Coordinate with QA/QC for in-process checks and ensure compliance. Report deviations, breakdowns, and abnormalities immediately. Maintain proper stock of coating materials and consumables. Follow cGMP, GDP, safety, an...

Manage quality audit program for vendors supplying APIs, Intermediates, Key raw materials, excipients and other raw materials, etc. To prepare periodic audit schedule/ plan for Asia, EU and US region vendors in coordination with commercial supply chain department. To allot scheduled vendor audits to the auditors and ensure execution of audits as per schedule and applicable regulatory requirements, company policies and standards. To ensure preparation of audit reports and its distribution to the vendors within defined timeline. To coordinate with commercial department for timely receipt of compliance/ response from audited vendors. To ensure that responses are reviewed and audits are closed w...