876 Injectables Jobs - Page 4

Hiring for f&D Location- Baddi Experience- 4-7 years Salary Range- 40-50 k Industry - Pharma (injectable) interested candidates share resume on 9041666549

Please find below details of the job opportunity: Department: Production (Sterile Manufacturing) Designation: Operator - Assistant / Associate Qualification: Diploma / B.Sc/ Any Graduate Total Experience: 02 to 7 years (Pharma experience only) Job Locations: SEZ- Matoda (PHARMEZ), Ahmedabad Job Responsibility: Area: Aseptic & Controlled area operation (Filling, Sealing, filtration, Autoclave, Batch Manufacturing, terminal sterilization, Tunnel Operations, Visual Inspection testing/ VIT, packing etc.) Line: PFS, Lyophilizer and Vial, Bag Line, Emulsion Line Machine Exposure: Filling machine (Groninger / Optima), Dyno Truking, filling and sealing machine, Bosch filling machine, Steam sterilize...

Dear Candidate, We are seeking a skilled and detail-oriented LCMS Scientist to join our Analytical Characterization Team, focusing on peptide-based products as well as other technology-driven formulations. Position: Assistant Manager Department: Analytical Characterization Required Exp : 3-10years Qualification: Ph.D/M.Sc/M.Pharmacy Role & Responsibilities: Perform intact mass analysis and primary structure characterization of peptides. Conduct advanced studies including: - Disulfide bond mapping - Sequence confirmation - D/L isomer differentiation Develop and validate LCMS/MS methods for peptide analysis. Conduct impurity profiling for peptide-related impurities using LC-HRMS. Identify unkn...

Dear Candidate, Greetings from Intas Pharmaceuticals Ltd.! Intas Pharmaceuticals is a leading, vertically integrated global pharmaceutical company headquartered in Ahmedabad, India, with a strong presence in over 85 countries. Driven by innovation and quality, Intas is committed to developing and manufacturing affordable medicines that improve lives across the world. We are pleased to announce a Walk-In Drive for our SEZ Plant for professionals experienced in Injectable/Parenteral Manufacturing operations including Manufacturing Sterile Aseptic Clean Area Experience Required: - 3 to 12 Years Qualification Required: - Diploma / ITI Walk-In Drive Details: - Date: Sunday, 30th November 2025 Tim...

Job Summary The role involves executing and supervising packing operations for sterile injectable products , ensuring compliance with cGMP standards, regulatory guidelines, and company quality systems. The candidate will be responsible for line clearance, equipment handling, documentation, and maintaining aseptic practices during injectable packing. Key Responsibilities 1. Packing Operations Perform packing activities for injectable products (vials, ampoules, pre-filled syringes, cartridges). Operate and monitor packing equipment: Visual inspection machines (manual/semi-auto/auto) Labeling machines Cartoning machines Blister/strip packing machines (if applicable) Ensure correct batch coding,...

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...

As an Assistant Manager in Drug Regulatory Affairs (DRA), you will be responsible for managing activities with a focus on global regulatory strategy. Your key responsibilities will include: - Preparation, review, and submission of documents to SRA and other regulatory authorities. - Ensuring compliance with regulatory procedures and work practices. - Supporting clinical and non-clinical development by preparing IND and CTA filings. Qualifications Required: - Bachelor in Pharmacy - Master in Pharmacy - 3-7 years of work experience in a relevant field - Master's degree in a relevant scientific discipline or B Pharma/M Pharma with at least 3 years of experience in Regulatory Affairs of injectab...

Role & responsibilities Assist in maintenance and repair of pharmaceutical machinery (e.g., Blenders, Compressors, Granulators, Packing Machines, HVAC, Utility equipment). Perform routine preventive maintenance under supervision. Support in installation, alignment, and troubleshooting of mechanical equipment. Follow SOPs and safety guidelines while performing maintenance activities. Maintain tools, equipment, and work area in good condition. Record maintenance activities in logbooks as per GMP requirements. Assist senior technicians/engineers in breakdown maintenance. Identify minor mechanical issues and report them promptly. Ensure compliance with GMP, safety, and engineering standards. Sen...

Role & responsibilities Perform routine analysis of raw materials, in-process samples, and finished products. Conduct testing using instruments such as HPLC, UV, FTIR, pH meter, Dissolution apparatus, etc. (training will be provided). Prepare and maintain analytical test reports and documentation as per GMP guidelines. Follow SOPs, Good Laboratory Practices (GLP), and data integrity requirements. Assist in calibration and maintenance of laboratory instruments. Ensure proper sample management and labeling. Support stability studies by performing required testing. Report any deviations, OOS (Out of Specification), or abnormalities to seniors. Maintain a clean, safe, and compliant working envir...

Job Summary The Senior Research Associate will be responsible for end-to-end formulation and development of injectable products, including solutions, suspensions, emulsions, and lyophilized formulations. The role requires expertise in pre-formulation studies, formulation optimization, process development, and technology transfer while ensuring compliance with regulatory standards. Key Responsibilities 1. Pre-Formulation & Formulation Development Conduct pre-formulation studies: solubility, pH, compatibility, excipient screening. Develop sterile injectable formulations (IV, IM, SC, intrathecal, depot, etc.). Optimize formulations for stability, manufacturability, and regulatory requirements. ...

To offer consultation & patient diagnosis at Kaya Skin Clinics, perform/supervise all medical procedures to be carried out in clinic, ensuring efficacy, safety & high professional standards of medical procedures carried out under your supervision. Required Candidate profile Presentable & Good Communication Candidate must be MBBS with MD or DVD or DDV or DNB Must be committed to work for minimum 2 years 6days working (Week Off in weekday) Contact- 8247551800/7022617038 Perks and benefits Leaves & Incentives as per company policy

Role & responsibilities : Execution support in formulation development for liquid/lyophilized protein formulation Execution of Lyophilization cycle development Execution of Product and process development studies (product contact part compatibility, hold time, freeze thaw, thermal cycling study, agitation study, Photostability study, temperature excursion study, In-use study, reconstitution solution stability study, preservative efficacy) Execution of Product and process characterization studies Preparation of scientific documents like protocol, report, BMR, TTD, MOA Execution of subvisible particles testing using different techniques (MFI, HIAC) Execution of functional performance testing u...

Biological E. Limited invites experienced applicants to join in the below departments for our Vaccine Facility in Hyderabad with 2- 10 years experience for Manufacturing - Antigens Department & Engineering Department. Educational Qualifications: M. Sc, B. Tech (EIE, EEE), Diploma (Lifesciences), B. Sc (Lifesciences), ITI(with relevant experience) Roles and Responsibilities: 1. Production Bulk Manufacturing (Drug Substance / Antigens) To perform Upstream and Downstream activities of bacterial & viral antigens (Vaccines) Execution of upstream and downstream production batches. Focus on timely execution, to ensure that the process is carried out as per cGMP compliance and batch timelines Execut...

1. Manufacturing- Experience Operators Any Diploma / B. Sc with 2 to 12 years of relevant Experience in manufacturing injectables Operate production equipment such as Injectable , Sterile , Parenteral machines, Vial / Ampoule filling , Capping , Compounding , Washing ,Sealing, Terminal sterilization, Stopper process. Monitor and control the production process to ensure quality products are produced within specified parameters. Maintain accurate records of production data and perform routine maintenance tasks on equipment as required. Collaborate with other team members to resolve issues and improve overall efficiency. Ensure adherence to Good Manufacturing Practices (GMP) guidelines. Must ha...

Job Description: You will be responsible for the production and quality control of injectables and ophthalmic products. Your main duties will include: - Overseeing the manufacturing process of injectables and ophthalmic products - Ensuring compliance with regulatory standards and guidelines - Conducting quality control checks to maintain product quality - Troubleshooting any issues that arise during the production process Qualification Required: - M.Pharm in Pharmaceutics Please note that this is a summary description of the job role.,

Role & responsibilities Key Responsibilities: • Environmental Monitoring in sterile areas (viable & non-viable) • Monitoring Grade A/B/C/D cleanrooms & aseptic zones • Settle plates, contact plates, swab sampling, active air sampling • Non-viable particle monitoring in critical areas • Documentation as per ALCOA+ principles • Handling EM deviations, excursions & CAPA support • Operation of EM instruments (air samplers, particle counters) • Support during WHO, EU-GMP & regulatory audits

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...

Work Location : Ankleshwar Organization : Chiron Behring Vaccines Private Limited Role & responsibilities Sterile Formulation Activities Prepare buffers, solutions, and bulk formulations as per BMR/BPR. Handle antigen/protein/thawing, compounding, and blending operations. Perform sterile filtration using 0.22/0.45 m filters and validate filter integrity tests. Operate formulation vessels, mixing tanks, transfer pumps, and CIP/SIP systems. Maintain strict aseptic practices and environmental compliance during all activities. Conduct in-process sampling and support stability studies. Aseptic Filling Operations Operate vial/ampoule/syringe filling machines, isolators, and RABS systems. Perform f...

role and responsibility of production qms in sterile formulations (injectables opthalmics ointments) USFDA.

Role and responsibility of PRODUCTION QMS reporting to production head and QA, Sterile production QMS exposure must.

Plant Maintenance (Mechanical) - Parental, Injectables

To respond CSV schedule to ensure all quality, manufacturing and engineering systems remain qualified to current GxP and GAMP5 requirements. Injectables exposure is must. Planning and performing(CSV). CSV-related deviations, change control documents. Required Candidate profile Exp of US FDA 21 CFR Part 11, EU Annex 11 & GAMP 5, Software testing requirements for SCADA, MES, is MUST. Develop CFR Part 11 CSV plans, traceability matrices, reports, IQ/OQ protocols.

Responsibilities: 1. Lead QMS initiatives, ensuring compliance with regulatory standards. 2. Manage deviations, change controls, investigations, cleaning validations. 3. OSD / Injectable QMS 4. Audit Compliances, cGMP, ICH, 21 CFR Knowledge Health insurance Provident fund

Role & responsibilities : Aseptic Area Manufacturing Operate and monitor aseptic filling and sealing machines Handle and clean storage vessels Perform operations such as Automated Loading and Unloading Systems (ALUS) Carry out line clearance, changeovers, and batch-wise documentation Handling Sterile Manufacturing Operating and monitoring equipment like autoclaves, lyophilizers, filling machines, and compounding vessels. This also involves performing and documenting routine cleaning, sterilization-in-place (SIP), and clean-in-place (CIP) procedures. Performing manufacturing and filling processes while strictly adhering to aseptic techniques to ensure product sterility. This includes gowning ...

Robust Packaging Design for Drug Device Combination products (Complex Generics Injectable Products) for regulated markets. Literature research & identifying the right devices for Drug Device Combination Products. Innovator samples analysis / characterization of packaging components. Define strategy for Drug Device Combination Products (DDCP) & align all functions of organization. Coordinate with Manufacturer & develop and execute end to end packaging solutions across all formats of devices including Pen Injectors, Auto-Injector, Syringes and etc. Ensuring compliance of device regulations as per 21 CFR 820, ISO 11608, 14971, FMEAs, Risk Management/control. Develop, validate & Implement variou...