418 Sterile Jobs

shift schedule, routine visit of plant machineries. Attending breakdowns, breakdown analysis of equipment/ machinery and documentation. Process maintenance - Vial Filling & Ophthalmic Filling lines. Up keeping of utility, microbiology, QC, packing.

Preparing shift schedule, routine visit of plant machineries operation. Attending breakdowns, breakdown analysis of equipment/ machinery and documentation as in their respective shifts. Required Candidate profile Process maintenance experience in Vial Filling lines and Ophthalmic Filling lines. Up keeping of production, utility, microbiology, QC and packing equipment and work related to facility maintenance

1. Perform analysis of raw materials, in-process, finished, and stability samples using HPLC. 2. Operate, review, and manage analytical data using Empower software. 3. Handle testing of sterile pharmaceutical products as per cGMP requirements.

Exp. of handling of manpower and shift Hands on exp of on line filled BMR & Log books Responsible for daily machine output as per machine speeds Required Candidate profile Must be from sterile Production only Knowledge of Raw material & Packing materials for Sterile packing having knowledge of sterilisations

Sr. Officer - QALL: Work Location - Baddi, Baroda & Navsari Ensure GMP/GLP compliance at Contract Manufacturing sitesand third party sites and provide registration documents and required support for registration from site. Ensure availability of current valid masterdocuments like raw material /packing material /finished product specificationsbatch manufacturing record /batch packing record at site and retrieval ofobsolete documents. To check and find non compliances at Contract Manufacturing /Third Party location and ensure corrective and preventive action. To execute, ensure and monitor processvalidation / Technology Transfer activities, Unit Operation, QMS Compliance atsite and arrange for...

Position :- Head - RA (Regulatory Affairs) We are seeking a strategic and experienced Regulatory Affairs leader with deep technical expertise in medical devices and/or pharmaceutical sterile injectable formulations . This role will act as the primary liaison with global regulatory bodies , including CDSCO, and will lead all compliance initiatives for domestic as well as international markets. Key Responsibilities :- Regulatory Strategy & Submissions Develop global regulatory strategies and lead dossier submissions. Manage interactions with USFDA, EMA, CDSCO, PMDA, TGA, KFDA, MDSAP markets. Ensure timely approvals and lifecycle management. Compliance & Quality Ensure compliance with EU-MDR, P...

Lead the formulation development of sterile, nutraceutical products, and new dosage forms. Plan, execute, and monitor development activities from concept to scale-up and technology transfer Required Candidate profile Proven expertise in injectable manufacturing processes, lyophilization & formulation techniques Strong documentation, project management & team-handling skills. Knowledge of regulatory guidelines

Walk In Drive For FR&D - Tech Transfer In Formulation Division @ Kothur Department:- FR&D - Tech Transfer Qualification :- M Pharmacy Division :- Formulation Interview Date: 20-12-2025 (Saturday) Interview Time :- 9.00AM TO 3.00PM Work Location:- MSN Formulations- Unit-II, Kothur | MSNF Unit-V, RK Puram Venue Location :- Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded ...

Walk In Drive For FR&D - Tech Transfer In Formulation Division @ Kothur Department:- FR&D - Tech Transfer Qualification :- M Pharmacy Division :- Formulation Interview Date: 20-12-2025 (Saturday) Interview Time :- 9.00AM TO 3.00PM Work Location:- MSN Formulations- Unit-II, Kothur | MSNF Unit-V, RK Puram Venue Location :- Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded ...

At Steribio Lifesciences, we dont just manufacture IV fluids we deliver lifelines. Born from a vision to transform patient care, our story is rooted in passion, precision, and purpose. At Steribio Lifesciences, we dont just manufacture IV fluids we deliver lifelines. Born from a vision to transform patient care, our story is rooted in passion, precision, and purpose. Because at Steribio, every drop saves a life and every life deserves the best. Position: QA Manager Location: Patas Experience: 8 to 10 years Industry: Pharmaceutical (LVP formulations Injectables) Roles & Responsibilities Quality Policies and Procedures: Establish and enforce quality assurance policies, procedures, and guidelin...

Role & responsibilities To maintain shift schedule time to time as per instructions provided by immediate supervisor. To follow good hygienic practices, safety rules and respective gowning procedure. To follow c-GMP practices. To participate in following activities with almost care of respective requirements. General area (CNC) daily routine activity. General area cleaning and sanitization supervision. Classified area daily, weekly and monthly activity. Clean area related activates. Garment washing area related activities. Handling of EDMS, LMS, Track wise, BRMS & QMS related activity. Department Training program as DTC. 5. To co-ordinate with other supervisor of area and of other department...

Amneal Pharma Walk-in Drive @ Pharma-SEZ, Matoda, Ahmedabad, (Gujrat) for Production/Packing department (Injectable/ Sterile) on 14th December 2025 (Sunday) We are looking for suitable candidates for injectable/ sterile manufacturing-Packing units for Ahmedabad location. Interview Details: Date: 14th November, 2025 (Sunday), Time: 09:00 AM to 04:00 PM Interview Venue : Amneal Pharmaceuticals Pvt Ltd Plot No 15, 16, 17 Pharmez | Village: Matoda | Sarkhej Bavla Road | Ahmedabad | Gujrat Office- (079) 2714677531 JOB LOCATION: Ahmedabad (SEZ Matoda) REQUIREMENT FOR INJECTABLE MANUFACTURING/ PRODUCTION/PACKING DEPARTMENT Designation : Operator/ Officer/ Sr. Officer /Executive/ Sr. Executive Depar...

vial washing/ manufacturing

Roles and Responsibilities : Design, develop, and implement sterile processing systems for pharmaceutical products. Collaborate with cross-functional teams to ensure compliance with regulatory requirements and industry standards. Conduct risk assessments and implement controls to prevent contamination or defects in the manufacturing process. Develop and maintain documentation for sterile processes, including protocols, procedures, and reports. Job Requirements : 8-20 years of experience in process engineering or a related field within the pharmaceutical industry. Strong understanding of API (Active Pharmaceutical Ingredient) production processes and regulations. Experience with project engin...

Walk-In Interview: 14th December 2025 @ Sanand Job Location : Virochannagar Plant Venue : Hotel Veritas Grand, Sanand Vinayak Entice, Sanand - Viramgam Highway, Sanand, Ahmedabad - 382110 Time : 09:00 AM TO 03:00 PM Position: Technical Assistant / Executive Dept.: Quality Control (Formulation/Micro) Qual./ Exp.: B. Sc. / B. Pharm / M. Sc. / M. Pharm with 1 to 5 Years of relevant experience Area: Analysis /Qualification / Operations on HPLC/GC/FP/IP/RM/PM. Environment Monitoring, Media Preparation and Autoclaving, MLT, BET, Sterility Testing, Analytical Stability, Analytical method transfer Dept.: Quality Assurance (Formulation) Qual./ Exp.: B. Pharm / M. Pharm / M. Sc. with 1 to 5 Years of r...

Ensuring Timely execution of Green field/ brown field projects to facilitate smooth and safe site operations without impacting Cost and Quality norms. 3. Key Accountabilities Major Activities / Tasks I. Project charter / Concept note Proven working experience as a lead Project Engineer in Pharmaceutical (API) Green field & brown field projects. Assist in preparation of business case/ Project charter/ Concept note to User. Ensures the Equipment engineering support to different projects Tenders and job start-up. Develop plant layout and prepare plans for facilities and requirements. Estimation of cost for budgetary proposal which includes operational cost also. Introduction of New technologies...

Roles and Responsibilities : Lead the design, construction, and commissioning of green field projects in the pharmaceutical industry. Oversee brownfield projects to ensure successful implementation of new equipment installations and facility upgrades. Develop and manage project budgets, schedules, and resource allocation plans for multiple projects simultaneously. Collaborate with cross-functional teams to identify opportunities for process improvements and implement changes that meet regulatory requirements. Job Requirements : 8-19 years of experience in civil engineering or a related field within the pharmaceutical industry. Strong understanding of API (Active Pharmaceutical Ingredient) ma...

Ensuring Timely execution of Green field/ brown field projects to facilitate smooth and safe site operations without impacting Cost and Quality norms Project/ Planning/ Execution/ Monitoring/Communication/ Documentation and Handover Proven working experience as a lead Project Engineer in Pharmaceutical (API) Green field & brown field projects. Assist in preparation of business case/ Project charter/ Concept note to User. Ensures the Equipment engineering support to different projects Tenders and job start-up. Develop plant layout and prepare plans for facilities and requirements. Ensure statutory approval / Regulatory approval during each stage of project. Coordinates the evaluation of the d...

WALK-IN DRIVE @ HYDERABAD We are pleased to announce a walk-in drive for various positions at our Matoda manufacturing facility . If your experience aligns with any of the openings listed below, we invite you to attend with your updated resume. 1. ENGINEERING (Instrumentation / QMS / Plant Maintenance / Qualification) Roles: Senior Executive / Executive / Senior Officer Experience: 3 10 Years Qualification: BE / B. Tech 2. ANALYTICAL DEVELOPMENT FORMULATION Roles: Research Associate / Sr. Research Associate Experience: 3 8 Years Qualification: B. Pharmacy / M. Pharmacy / M.Sc. 3. FORMULATION DEVELOPMENT INJECTABLE & OSD Roles: Research Associate / Sr. Research Associate / Research Scientist ...

We have Multiple Job opening. below are the positions: Qa (Qualification & Validation) - Fresher QA (Documentation) - Fresher. Instrumentation Engineer - 3 years Mechanical Engineer - 3years Mechanical Officer - 2 Years Water System Technician/ Operator - 3 years HVAC Technician/ Operator - 3 year Utilities Technician/ Operator - years QC Micro Water Testing (Executive , Officer) - 3+ years QC Machine Operator - 3 years QC chemist - 3 years & Freshers QC Area Maintaining Technician/ Operator - 3 years Note: Sterile Injectables is mandatory for experienced candidates. Interested candidate can call on following numbers: Land Line. : (+91) 22 40659 259

Roles and Responsibilities Perform sterilization processes such as autoclave, vial washing, and lyophilization. Operate equipment including OT (Operation Theatre), tunnel, injectables, injection machines, USFDA compliant systems. Ensure proper cleaning and aseptic techniques are followed in ICU settings. Maintain accurate records of media fill testing results. Collaborate with team members to ensure smooth operation of CSSD department.

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.

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 Sterile Aseptic Clean Area Manufacturing Experience Required: - 3 to 12 Years Qualification Required: - Diploma / ITI Walk-In Drive Details: - Date: Sunday, 7nd December 2025 Time...

Manufacturing Compliances Roles: M. Pharmacy with 6 to 10 Years / B. Pharmacy with 8 to 12 Years of Experience in QMS (Quality Management System) like Risk Management, Change Control, Deviations, CAPA, investigation, Audit, inspections Compliance & Document control. Ensure adherence to Good Manufacturing Practices (GMP) guidelines. Must have experience in manufacturing injectables with USFDA regulatory environment & process.

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...