58 Syrup Jobs

Perform electrochemical tests (CV, EIS, CA) Develop materials for batteries, fuel cells, electrolyzer Fabricate electrodes and assemble cells Operate and maintain lab instruments Analyze data, document results, follow safety SOPs

Job Purpose To lead and manage end-to-end manufacturing operations for Liquid Oral and Topical formulations, ensuring timely production, compliance with GMP, quality standards, and optimal utilization of resources. Key Responsibilities Manufacturing & Operations Lead complete manufacturing operations for Liquid Oral and Topical dosage forms. Ensure execution of production plans as per approved schedules and business requirements. Monitor day-to-day production activities to meet output, quality, and efficiency targets. Team Management Manage, guide, and develop production teams to achieve departmental objectives. Ensure adequate manpower planning, training, and skill development. Promote a cu...

Develop and manage new business opportunities in IV fluids and generic formulations. Build strong relationships with hospitals, nursing homes, distributors, and stockists. Conduct field visits, territory mapping, and customer engagement activities. Identify and appoint new distributors/channel partners in assigned regions. Monitor market trends, competitor strategies, and pricing. Achieve monthly, quarterly, and annual sales targets. Coordinate with internal teams for supply chain, dispatch, pricing, and customer service. Preferred candidate profile

Job Title: Production Manager Pharmaceutical Company We are looking for an experienced Production Manager from the pharmaceutical industry to manage our production operations. Key Responsibilities: Manage complete production floor operations and ensure smooth daily activities. Handle manpower planning, allocation, and supervision on the production floor. Plan and execute daily, weekly, and monthly production targets . Prepare, review, and maintain BMR and BPR as per GMP requirements. Ensure strict compliance with GMP, SOPs, and QMS . Handle deviations, CAPA, and coordination with QA/QC teams. Monitor productivity, yield, and process efficiency. Ensure timely batch completion and proper docum...

Purpose/Objective Engineer - Automation and Instrumentation (Liquid Terminal) is responsible for the effective management and maintenance of automation and control systems specific to liquid terminal operations. This role is crucial for ensuring accurate and efficient handling of liquid cargo, maintaining safety standards, and optimizing the performance of liquid terminal facilities. Key Responsibilities of Role System Maintenance and Optimization: Conduct regular maintenance, troubleshooting, and optimization of automation and instrumentation systems to ensure uninterrupted liquid terminal operations. Technical Support: Provide expert support for automation systems, including programmable l...

1.Experience in Regulated Market (US, Europe) 2.Candidate should perform literature search 3.Should have some basic understanding of patent and generic formulation development. 4.Characterization of marketed product wrt market requirements Required Candidate profile 5.Knowledge of ICH stability conditions and compilation of analytical data 6.Preparation of various documents like PDR, stability protocol, development report writing FDR/PDR

Job Description Strong expertise in formulation development of sterile liquid injectable dosage forms, including end-to-end development and troubleshooting. Hands-on experience in drug device combination product development, with good understanding of device compatibility, functionality, and regulatory expectations. Proven experience in developing and handling lyophilized drug products (peptides, proteins, and small molecules), including cycle development and optimization.

Sakar Healthcares research-driven API-integrated EU GMP approved oncology oral and injection manufacturing units providing differentiated Oncology Product looking for Oncology F&D & Product Development Tablet, Capsule, Liquid Oral, Injectable and complex Injectable. Responsible for the entire operations of manufacturing Oral Liquid plant. Shall be well aware of entire Pharmalab line (Glass/Pet Bottles, Washing, filling, capping, inspection, labelling) Responsible for entire manufacturing process of all of oral liquid product formulations. This includes the management & coordination of daily activities to ensure high performance and production at all times To Coordination with senior manageme...

Formulation development and optimization for liquids and tablets Execute lab/pilot/commercial batches with complete documentation Perform stability studies and analytical/physical testing Troubleshoot formulation and manufacturing issues to improve product quality Support technology transfer and scale-up to production Ensure compliance with cGMP / WHO-GMP / regulatory requirements Maintain BMR, BPR, SOPs and technical reports Coordinate with QA/QC/Production/Regulatory for smooth execution of projects

Literature review of Raw materials. Procuring input materials and intermediates for F & D New product development. Improvement in quality of existing products. Documentation of entire product development cycle. Required Candidate profile Technology transfer Complaint handling & investigation Getting in touch with marketing department for new product/improved product feedback Technology transfer from F & D to Pilot or commercial batch

Responsibilities: Conduct routine and non-routine chemical and instrumental analysis of raw materials, in-process samples, and finished products. Ensure compliance with cGMP, GLP, and regulatory guidelines. Review and approve analytical documents, test reports, and batch manufacturing records. Maintain accurate laboratory documentation and ensure timely reporting. Oversee calibration, validation, and proper functioning of lab instruments (HPLC, UV, FTIR, etc.). Coordinate with the Quality Assurance and Production teams for smooth operations. Participate in audits and inspections conducted by regulatory authorities. Provide technical guidance and training to junior chemists and lab staff. Ens...

1. Sales and Marketing of our Small volume and Large volume parantels & Tablets & capsules & Sy and pharma products within Karnataka. 2. Visit Hospitals, customers and build and maintain relationships with doctors, hospitals, pharmacies, and other healthcare stakeholders. 3. Product Knowledge: Stay updated on product information, features, and benefits to communicate with healthcare professionals effectively. 4. Market Insights: Gather market information, competitor activity, and customer feedback. 6. Product Training will be given from time to time 7. Medical representatives/Marketing executives with 1-4 years may apply Male candidates only need to apply Salary 20000,30000/- per month. Pref...

Company: Aurobindo Pharma APL HC-4 (Naidupeta Location) Work Location: Naidupeta (Plant) | Walk-in Venue: Jadcherla, Telangana Interview Date & Time: Sunday, 16 November 2025 | 10:00 AM 03:00 PM Open Positions Production OSD (Granulation/Compression/Coating/Capsule Filling) • Executive/Sr. Executive: B.Pharm/M.Pharm, 2–6 years • TA/Sr. TA: ITI/Diploma/Degree, 2–8 years Production – Oral Liquid / Nasal Spray • Executive/Sr. Executive: B.Pharm/M.Pharm, 2–6 years • TA/Sr. TA: ITI/Diploma/Degree, 2–8 years Packing – OSD (Blister/Bottle) • TA/Sr. TA: ITI/Diploma, 2–8 years QC – IP/FP, Stability, Nasal • Executive/Sr. Executive: B.Pharm/M.Pharm/M.Sc, 2–6 years QA – IPQA, QMS, Validation, Market Co...

JD for Production Chemist @ Production planning & oversight Process optimization Quality control Troubleshooting Compliance Documentation Collaboration Subsidized Sharing Accommodation, Meals & Transport from company All Saturdays will be Half day

Must-have beverages experience in at least one area: 1. Filling & Packaging (PET/Glass/Can fillers, cappers, labellers, shrink/packer, palletizer) 2. Utilities (Boilers, Compressors, Ammonia/Chiller, Air & Water systems) 3. Process (Syrup Room/Blending/CIP) • Quality (in-process checks, HACCP, GMP) • ETP/WTP. Key responsibilities (select those that fit each sub-role): 1. Operate and maintain high-speed packaging lines (Krones/Sidel/KHS or similar). 2. Changeovers, basic troubleshooting, minor repairs, and line efficiency (OEE) improvement. 3. Adhere to GMP, 5S, HACCP, safety lock-out/tag-out. 4. Utilities: start-up/shutdown, routine checks, parameter logs, and preventive maintenance. 5. Proc...

JD for Production Chemist @ Production planning & oversight Process optimization Quality control Troubleshooting Compliance Documentation Collaboration Subsidized Sharing Accommodation, Meals & Transport from company All Saturdays will be Half day

Role & responsibilities 1*Batch Manufacturing: Oversee batch production, including setup, operation, and cleaning of equipment of EB & commercial. 2.*Regulatory Compliance: * Ensure that all formulations comply with relevant regulatory requirements, including FDA and ICH guidelines. Familiarity with regulatory inspections and compliance. 3.*Innovation: * Drive innovation for new technologies and approaches to improve product performance. 4. *Project Management: * Manage multiple projects simultaneously, prioritizing tasks, allocating resources to meet project timelines and understanding associated safety protocols. 5.*Collaboration: * Collaborate with cross-functional teams, including analyt...

Role & responsibilities To perform microbial analysis of Raw Material, Water samples, In Process, Finished Product Samples and Stability Samples. To perform Media preparation, sterilization and Growth promotion testing. To perform hold times studies carried out in Microbiology department. To perform Preservative efficacy test. To perform Microbial Limit Test validation. Prepare Environment Monitoring and Water analysis Trend. Perform culture maintenance and purity of cultures.` To perform instrument calibration and qualification of Incubators, Autoclave. Responsible to adherence of GLP and Health, Safety Environment system in Laboratory. Should have good written and communication skill. Pref...

JD @ QC Executive will ensure that products meet quality standards & regulatory requirements with analyzing samples, conducting tests, maintaining documentation & more. Accommodation, Meals & Transport from company side Saturdays are Half day

Key Responsibilities: 1. Packing Operations: Supervise daily packing activities of Softgel capsules as per Batch Packing Records (BPR) and SOPs . Monitor operations such as blister packing, bottle packing, labeling, and cartoning . Ensure correct batch details, labeling, and packing material reconciliation. Coordinate with QA for line clearance before and after batch operations. 2. Documentation & Compliance: Prepare and maintain Batch Packing Records (BPR) , logbooks, and reconciliation sheets. Ensure all entries are accurate, legible, and completed in compliance with Good Documentation Practices (GDP) . Adhere to data integrity and cGMP requirements at every stage. 3. Material & Resource M...

Roles & Responsibility: To ensure proper Coordination and receive the production plan & arrangement of all resources accordingly. To ensure Testing and control as per documents to produce 100% safe products. To ensure compliance of Cleaning and Sanitation program as per matrix. To ensure that targets of Quality Measures are achieved. To ensure that the goals of FSSC and QMS are achieved. To ensure Calibration of lab and process measuring instrument as per defined frequency. To ensure the effective implementation of defined PRPs, OPRP and CCP. Initiate Effective corrective action against identified gaps in any external and internal audits. Monitor & achieve the target of Sugar, Concentrate, p...

OPEN POSITIONS Production Technical Assistant • Granulation, Compression, Coating, Capsule Filling • Liquid & Nasal Spray manufacturing Packing Technical Assistant • Bulk / Bottle packing, Labelling machine operation Quality Assurance Executive • QMS, IPQA, Market complaints, Training coordination Quality Control Executive • Nasal spray product analysis using LC-MS, HPLC, GC, UV, GC-MS, etc. EXPERIENCE RANGE 2 8 years (pharma formulation plants only) EDUCATIONAL QUALIFICATION • Production / Packing : ITI / Diploma / B.Sc. • Quality Control : M.Sc. (Chemistry) / B. Pharm • Quality Assurance : B. Pharm / M. Pharm WORK LOCATION APL Healthcare Ltd. Unit IV, Naidupeta, Tirupati District, Andhra P...

scientistsDepartment: Formulation Research and Development Duties and Responsibilities: The responsibilities of the Scientific Leader include Prepare and maintain a project tracker with date and schedule and scientists' activities Serve as the point of contact for RM procurement tracking directly with Purchase team, experiment planning, executions and updates in the India laboratory. Provide regular updates to Head of the Dept. on project technical status. Manage work schedule and appropriate human resouresourcesrce based on prioritized experiments with Head of Dept. Work with the scientific and admin team to track ordering and inventory status and maintain lab to maximum functioning efficie...

Responsibilities: * Manage production schedules & resources effectively * Oversee liquid oral, syrup & suspension formulations * Ensure GMP compliance at all times * Handle manpower efficiently

Topical Powder Manufacturing, Filling & Sec.Packing Activities oral Powder Manufacturing, Filling and Sec. Packing Activities Batch Initiation Manufacturing Secondary packing & tertiary Packing Share resume to hrd@stedmanpharma.com, Call - 7904827192 Required Candidate profile B.pharm Looking for candidate with Pharma formulation experience