315 Sterile Jobs - Page 6

"We are looking to hire Research Ops Interns - Pharma & Biotech who will work closely with our US-based Business Development team to identify industry trends, conduct pipeline analysis, and benchmark companies in the Pharmaceuticals, Vaccines, and Medical Devices space. Roles & Responsibilities include the following : Conduct clinical pipeline analysis, clinical trial analysis, medical conference tracking, and draw appropriate insights Create insights on the company's performance and benchmarking with competition to identify areas of competitive advantage, differentiation, and growth, areas that need improvement Understand competing platforms, technologies, capabilities and contextualize the...

"We are looking to hire Research Ops Interns - Pharma & Biotech who will work closely with our US-based Business Development team to identify industry trends, conduct pipeline analysis, and benchmark companies in the Pharmaceuticals, Vaccines, and Medical Devices space. Roles & Responsibilities include the following : Conduct clinical pipeline analysis, clinical trial analysis, medical conference tracking, and draw appropriate insights Create insights on the company's performance and benchmarking with competition to identify areas of competitive advantage, differentiation, and growth, areas that need improvement Understand competing platforms, technologies, capabilities and contextualize the...

We are looking to hire Research Ops Interns - Pharma & Biotech who will work closely with our US-based Business Development team to identify industry trends, conduct pipeline analysis, and benchmark companies in the Pharmaceuticals, Vaccines, and Medical Devices space. Roles & Responsibilities include the following : Conduct clinical pipeline analysis, clinical trial analysis, medical conference tracking, and draw appropriate insights Create insights on the company's performance and benchmarking with competition to identify areas of competitive advantage, differentiation, and growth, areas that need improvement Understand competing platforms, technologies, capabilities and contextualize them...

We are looking to hire Research Ops Interns - Pharma & Biotech who will work closely with our US-based Business Development team to identify industry trends, conduct pipeline analysis, and benchmark companies in the Pharmaceuticals, Vaccines, and Medical Devices space. Roles & Responsibilities include the following : Conduct clinical pipeline analysis, clinical trial analysis, medical conference tracking, and draw appropriate insights Create insights on the company's performance and benchmarking with competition to identify areas of competitive advantage, differentiation, and growth, areas that need improvement Understand competing platforms, technologies, capabilities and contextualize them...

Position Purpose Provide a brief description of the overall purpose of the position, why this position exists and how it will contribute in achieving the teams goal. - Support to oversee the smooth functioning of the department and ensuring consistent provision - Support To manage and motivate all departmental staff - Ensure the financial reporting to Head Office - Accounting production and statutory accounts Responsibilities - Oversee Preparation of the financial reporting sent on a monthly basis to the Head Office: P&L, balance sheet, off balance sheet, annexes, tax book, regulatory reporting schedules - Manage Prepare ad hoc Financial Reportings for Head office upon request - Contribute t...

KWALITY PHARMACEUTICALS LTD. 6 , MILE STONE, VILL. NAG KALAN, TH MAJITHA ROAD, AMRITSAR , PUNJAB 143601 (INDIA) About Our Organisation : Kwality Pharmaceuticals Ltd. is a manufacturer of finished pharmaceutical formulations in a dosage form. The company was incorporated on May 4 1983, and is ever progressing in Domestic and International markets. Kwality Pharma was Incorporated on May 4th 1983 by Mr. Ramesh Arora ( Founder ) of the company . Our company is based on its commitment to high quality and timely supplies. Kwality Pharmaceuticals Ltd are leading manufacturer & exporters of pharmaceutical formulations in Liquid Orals, Powder for Oral Suspension, Tablets, Capsules, Sterile Powder for...

Key Responsibilities: Formulation Development: Design and develop formulations for injectable products such as solutions, suspensions, emulsions, lyophilized products, and pre-filled syringes. Conduct pre-formulation studies, compatibility studies, and stability testing. Process Optimization: Define and optimize manufacturing processes for sterile products. Work on scale-up and validation batches for tech transfer. Documentation & Compliance: Prepare and maintain development reports, batch manufacturing records (BMR), and related documentation as per cGMP. Ensure compliance with ICH, USFDA, EMA, and other regulatory guidelines. Technology Transfer: Support technology transfer activities from...

5+ years of sales experience in sterile process technology or hygienic systems for pharmaceutical manufacturing. Record of excellence in value-based sales Established network in pharmaceutical manufacturing , consultancy firms , and EPC contractors .

Greetings from Continental Hospital Hiring CSSD Technician Experience : 1 to 3 In hospitals, the Central Sterile Supply Department (CSSD) is responsible for ensuring the cleanliness, sterilization, and distribution of medical equipment and supplies . It plays a crucial role in preventing hospital-acquired infections and maintaining patient safety. Here's a breakdown of CSSD functions: 1. Cleaning and Decontamination: CSSD personnel receive soiled items from various departments and disassemble them. They utilize automatic washers and ultrasonic cleaners to ensure thorough cleaning and disinfection, following established protocols. Inspections are conducted to confirm that items are free of de...

Greetings! We are looking for Formulation Research & Development Scientist - Injectables for a leading Pharmaceutical company based at Hosur location. Responsibility: 1. Develop robust formulations and processes for general products to various markets such as Regulatory, Semi-regulatory, ROW, and Domestic with application on QbD as needed. 2. Monitoring and supporting the formulation team for the completion of allocated projects within the timelines by trouble shooting the concerns involved. 3. Scale-up and optimization of manufacturing process; execution of pre-exhibit and exhibit batches; scale up and technology transfer from R&D to production to meet timeIines. 4. Plan and contribute to p...

We are seeking a dynamic and experienced candidate to lead and manage the overall operations of our sterile injectable manufacturing plant. The ideal candidate will be responsible for ensuring seamless plant operations, regulatory compliance, quality standards, and people management while driving productivity and efficiency. About the Responsibilities Strategic Leadership: Lead the end-to-end operations of the sterile injectable plant, including production, quality, engineering, supply chain, and EHS functions. Regulatory Compliance: Ensure full compliance with internal and external regulatory standards (e.g., EU-GMP, WHO-GMP) and corporate SOPs. Operational Excellence: Drive continuous impr...

Greetings!!! We are looking for RA Executive - Formulation Injectable for a leading pharma company at Chennai Key Responsibilities: Preparation & review of regulatory documents, technical dossiers, and official communications. eCTD filing for submissions across various regulatory authorities. Handling applications/renewals for Import & Test Licenses. Coordinating with QA, QC, AR&D, and other teams for submissions. Reviewing registration dossiers for accuracy & compliance. Preparing & filing ANDA and ROW market submissions. Desired Skills: Strong documentation & communication skills. Attention to detail, ability to manage multiple submissions. Experience in injectables regulatory affairs pref...

Key Responsibilities: Oversee daily QA operations in SVP manufacturing and ensure compliance with cGMP and regulatory guidelines. Perform and supervise IPQA activities in production areas including line clearance, in-process checks, aseptic practices, and documentation verification. Review and approve batch manufacturing records, quality control data, deviations, change controls, and CAPAs. Ensure timely investigation and closure of deviations, incidents, and OOS results. Monitor and review environmental monitoring and microbiological trends, ensuring compliance with aseptic standards. Actively participate in media fill and aseptic process validation oversight. Participate in internal audits...

If you interested, please share you CV on below details. Email : renu.kumari@adecco.com WhatsApp : 6364920532 Operator / Technician Role - Aseptic Area Manufacturing Skill - operation of filling machine, sealing machine , ALUS operation , storage vessel operation and cleaning Qualification Diploma Eng/ITI Category Operator Staff / Officer Aseptic Area Manufacturing Skill operation and supervising of filling machine, sealing machine , ALUS operation , storage vessel operation and cleaning Qualification B. Pharm/M. Pharm Category Staff

Walk In Drive For Production Injectables In Formulation Division @ Kothur Department:- Production Injectables Qualification :- ITI | Diploma | B Sc | B. Tech | B Pharmacy Experience :- 2 to 4 Years Skills :- Operators :- Filling | Production Injectables Packing / Blister | Lyo | PFS Operators | QMS | ALUS | Vial filling | Stoppering | Sealing Machine | Autoclave Division :- Formulation Interview Date:23-08-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- Unit-II, Kothur| MSNF-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 , In...

Role & responsibilities Setup and Operation of Equipment : Operating aseptic filling equipment such as filling machines, capping machines, and sterilization units autoclaving in accordance with standard operating procedures (SOPs) and regulatory guidelines. Sterilization and Sanitization : Ensuring all equipment and materials used in the filling process are properly sterilized and sanitized to maintain aseptic conditions and prevent contamination. Quality Assurance : Conducting in-process checks and inspections to verify product integrity, including visual inspections, measurement checks, and sampling for microbiological testing. Documentation and Record Keeping : Maintaining accurate record...

Walk-in @ BADDI 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. Injectable Manufacturing & Packing & Visual Inspection (Executive/Senior Officer / Officer / Associate) Experience - 01 to 07 Years Qualification - B. Pharmacy/ M. Pharmacy / M. Sc /B. Sc / Diploma ENGINEERING (Instrumentation / Plant Maintenance / QMS) (Senior Executive / Executive / Senior Officer) Experience - 02 to 10 Years Qualification BE / B Tech QUALITY ASSURANCE Validation and Qualification / IPQA (injectable...

Experienced in microbiological practices, media prep, GPT, MLT, culture suspension, and water analysis. Skilled in reviewing activities, equipment calibration, and documentation for compliance. Relevant Exposure-Pharma/Biotech/Food

You will be working as a Production Chemist with a focus on knowledge of BRM, BPR, and exposure to GDP, GMP. Your role will involve experience in Sterile and Sterilization processes. As a Production Chemist, your responsibilities will include Batch Planning and Batch Manufacturing. The qualifications required for this position include relevant education details. The required skills for this role are a strong knowledge of BRM, BPR, exposure to GDP, GMP, and experience in Sterile and Sterilization processes. Preferred skills include proficiency in Batch Planning and Batch Manufacturing. Our company is committed to diversity and inclusivity, promoting an equal opportunity environment for all em...

As a Senior Manager in the Global Actions Management sub-function of Corporate Quality Compliance at Sunpharma, your main responsibility will be to ensure the assessment and derivation of global actions based on regulatory inspection citations, 483s, warning letters, and internal learnings. This will involve tasks such as reviewing regulatory guidance, existing site practices, drafting global action recommendations, preparing reference procedures, and finalizing recommendations in collaboration with the global action committee and stakeholders. You will also be responsible for issuing and approving global actions in Trackwise, coordinating with sites for implementation, reviewing site action...

Position - CSSD Technician (Female Candidates Only) - Mumbai Experience: 0 – 1 Year (Freshers are welcome; training will be provided) B.Sc in Chemistry or Biology Interested? Share your CV shubha@hireindians.com OR Call/WhatsApp at +918178223314 Required Candidate profile If you're a recent graduate looking to start your career in the healthcare sector, this is a great chance to gain hands-on experience in a reputed hospital setting.

Roles and Responsibilities Manage daily operations of the CSSD department, ensuring compliance with hospital policies and procedures. Oversee sterilization processes using autoclaves and other equipment to maintain high standards of sterility. Supervise a team of technicians and support staff, providing guidance on best practices and quality control measures. Develop and implement effective training programs for new employees, promoting knowledge sharing among team members. Collaborate with other departments to resolve issues related to inventory management, supply chain logistics, and patient care. Contact Number Mail ID: hodhr@kmchihsr.edu.in Land Line Number: 0422-680-6170/6171 Mobile Num...

Immediate requirement of CSSD Senior Technician Position - CSSD Technician Experience - Min. 10 Years of experience Qualification - Diploma Interested candidate can share their resume on :- Gaurav Bisla- 7838858533 (Whatsapp/Call)

Immediate requirement of CSSD Technician Position - CSSD Technician Experience - 1-4 Years Qualification - Diploma Interested candidate can share their resume on :- Gaurav Bisla- 7838858533 (Whatsapp/Call)

Responsible for leading production operations, coordinating production staff and equipment, ensuring product quality and profitability, and overseeing and managing the production operations involved in injectable products.