206 Parenteral Jobs - Page 2

Role & responsibilities 1. Candidate will be based at Pharma R&D Center at Thane and will Analytical Research and Development for Regulated & Row Market with focus on Injectable Dosage. 2. Candidate should have expertise in Analytical Method Validation and Method Development, Routine, Stability for Injectables for Regulated/ROW Market. 3. Experienced and responsible analytical development to develop and Validate new analytical methods for analysis of formulations Injectable dosage forms as per ICH guidelines. 4. Candidate have to support and troubleshooting in the development and validation of analytical methods working across the technical teams. (Routine, Stability, Method Development and ...

Role & responsibilities An IPQA (In-Process Quality Assurance) Lead is responsible for overseeing and guiding the IPQA team to ensure all manufacturing and packaging operations comply with cGMP and regulatory standards. Preferred candidate profile Core responsibilities Supervision and leadership: Lead and guide the IPQA team to ensure all in-process quality activities are performed correctly and efficiently. Process monitoring: Conduct real-time monitoring of manufacturing and packaging processes to ensure compliance with standard operating procedures (SOPs) and Good Manufacturing Practices (GMP). Documentation and review: Review and approve batch manufacturing and packing records, logbooks,...

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 Engineering - (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification BE / B Tech QUALITY ASSURANCE IPQA (injectable) / IPQA (OSD) / Documentation (Officer / Senior Officer / Executive/Senior Executive) Experience - 02 to 09 Years Qualification - B. Pharmacy/ M Pharmacy / M.Sc. / B.Sc. MICROBIOLOGY (Officer / ...

• Communicate and collaborate with subordinates on goals. • Ensure complete strategy/system implementations as per directives • Induct new employee as per companys policy, ensuring no deviation while practicing policies and code of conduct • Guide team members to resolve issues, dealing with stockist & chemist. • Prepare and submit the tour programme for self and team as per the guidelines • Monthly analysis of Primary/ Secondary sales, customer coverage etc • Build business relationships with key customers • Brief sub-ordinates on the incentive scheme • Ensure Annual target Achievement of all HQ • Ensure achievement of all New Launches If Interested and have relevant experience, requesting ...

• Communicate and collaborate with subordinates on goals. • Ensure complete strategy/system implementations as per directives • Induct new employee as per companys policy, ensuring no deviation while practicing policies and code of conduct • Guide team members to resolve issues, dealing with stockist & chemist. • Prepare and submit the tour programme for self and team as per the guidelines • Monthly analysis of Primary/ Secondary sales, customer coverage etc • Build business relationships with key customers • Brief sub-ordinates on the incentive scheme • Ensure Annual target Achievement of all HQ • Ensure achievement of all New Launches If Interested and have relevant experience, requesting ...

Requirement of B.com/m.com Fresher's for Accounts & Warehouse Department

Role : Executive Small Volume Parenteral Manufacturing Location: Ahmedabad Department: Injectable / Sterile Production Key Responsibilities: Production Operations: Plan, organize, and execute the manufacturing batches of small volume injectable products. Operate / supervise key equipment: vial/ampoule washing, sterilization (autoclave, filtration), filling, sealing, capping, tunnel sterilizer, lyophilizer (if applicable) etc. Ensure line readiness, material dispensing, line clearance before/after operations. Aseptic Process & Sterility Assurance: Maintain cleanroom operations, gowning, environmental monitoring, microbial monitoring. Ensure correct operation of aseptic filling / sterile filtr...

Greetings from Kashiv Biosciences!!!! We are looking for Qualification, Validation and QMS Engineer for our Engineering Team in our Biosimilar Manufacturing facility based out of Ahmedabad. Below are the roles and Responsibilities. Roles and Responsibilities: Responsible for Engineering compliance , Equipment Qualification, Validation and QMS activity. Timely escalation of any challenge bottle necks pertaining to engineering compliance to the management (site leadership team) to ensure proper planning and solutions. Representing as a Subject Matter Export of Engineering department in front of regulatory auditors. Responsible for engineering investigations pertaining to equipment failures and...

Medcare Hospitals Medical Centres is looking for Technician - CSSD to join our dynamic team and embark on a rewarding career journey. Sterilize and maintain medical instruments and equipment. Ensure proper inventory of sterile supplies and their distribution. Monitor adherence to infection control protocols. Maintain detailed records of sterilization activities. Disclaimer : This job description has been sourced from a public domain and may have been modified by Naukri. com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

Medcare Hospitals Medical Centres is looking for Junior Technician - CSSD to join our dynamic team and embark on a rewarding career journey. A Junior Technician - CSSD (Central Sterile Supply Department) is responsible for assisting with the cleaning, sterilization, and distribution of medical equipment and supplies used in healthcare facilities. Their tasks may include inspecting and assembling surgical instrument sets, operating sterilization equipment, maintaining accurate records of inventory and usage, and ensuring compliance with infection control protocols. They should have knowledge of sterilization techniques and equipment. Loading the materials for sterilizationReceiving, checking ...

Role & responsibilities Manufacturing area:- Line clearance before start of batch processing and after cleaning. In-process checks during manufacturing stages Verification of machines settings, process parameters and yield reconciliatoin Sampling of in-process materials for testing. Monitoring of environmental conditions and compliance during production Verification of online entries in BMR Packing area: Line clearance before start of packing and after product/pack change over. Monitoring batch coding, overprinting, labeling, and packaging operations Performaning in-process checks - correct packing components, label reconciliation, and proper sealing. Monitoring controlled area discipline, g...

Roles and Responsibilities Ensure compliance with cGMP guidelines during batch manufacturing of eye drops, injectables, parenteral products, and injections. Monitor production processes to ensure quality standards are met. Conduct regular audits to identify areas for improvement and implement corrective actions. Collaborate with cross-functional teams to resolve issues related to formulation development and process optimization. Develop and maintain documentation for batch records, SOPs, and other relevant documents. Desired Candidate Profile 8-12 years of experience in pharmaceutical industry with expertise in ophthalmic manufacturing. Bachelor's degree in Pharmacy (B.Pharma) or equivalent ...

Quality assurance, Change management, Change control, APQR's, Media fill, Microbiology Compliance and Documents handling in software

Title: Parenteral Line Manager Job Grade: G9 Senior Manager Educational Qualification: B.Pharm / M.Pharm Location: Baska, Gujarat Experience: Knowledge of parenteral manufacturing operations Understanding regulatory guidelines Leadership & Team Management Skills Problem Solving & Decision-Making Proficiency in handling production documentation & compliance Min. 15 years of experience working in sterile manufacturing plant or Block In-charge experience Position Summary Responsible for plant operations from material procurement to product dispatch along with operational activities, manufacturing actions, lean management, training, regulatory compliance, cross functional coordination, new produ...

Packing operations for products ensuring adherence to SOPs, GMP, and BPRs, monitor line clearance, Coordinate withQA, warehouse, maintenance teams, verify labeling, batch coding, and PM before use, conduct in-process checks and escalate deviations

Role & responsibilities : Equipment Qualification DPI liquid Injection Cleaning Validation Ampoule ,Vial Washing Media Fill Leak Test Line Clearance In Process Validation( Related to sampling ) Dental cartridge BMR/BPR

Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team i...

Investigate quality issues within manufacturing and quality laboratories Examine deviations, out-of-specification results, and atypical investigations Identify root causes and suggest effective corrective action plans Ensure all reports comply with regulatory requirements and company policies Contribute to moderately complex projects, managing your own time to meet targets Develop plans for short-term work activities within a collaborative team environment Apply skills and discipline knowledge to contribute to work within the Work Team Make decisions to resolve moderately complex problems in standard situations Work under general supervision, following established procedures and general inst...

• Communicate and collaborate with subordinates on goals. • Ensure complete strategy/system implementations as per directives • Induct new employee as per companys policy, ensuring no deviation while practicing policies and code of conduct • Guide team members to resolve issues, dealing with stockist & chemist. • Prepare and submit the tour programme for self and team as per the guidelines • Monthly analysis of Primary/ Secondary sales, customer coverage etc • Build business relationships with key customers • Brief sub-ordinates on the incentive scheme • Ensure Annual target Achievement of all HQ • Ensure achievement of all New Launches If Interested and have relevant experience, requesting ...

• Communicate and collaborate with subordinates on goals. • Ensure complete strategy/system implementations as per directives • Induct new employee as per companys policy, ensuring no deviation while practicing policies and code of conduct • Guide team members to resolve issues, dealing with stockist & chemist. • Prepare and submit the tour programme for self and team as per the guidelines • Monthly analysis of Primary/ Secondary sales, customer coverage etc • Build business relationships with key customers • Brief sub-ordinates on the incentive scheme • Ensure Annual target Achievement of all HQ • Ensure achievement of all New Launches If Interested and have relevant experience, requesting ...

• Communicate and collaborate with subordinates on goals. • Ensure complete strategy/system implementations as per directives • Induct new employee as per companys policy, ensuring no deviation while practicing policies and code of conduct • Guide team members to resolve issues, dealing with stockist & chemist. • Prepare and submit the tour programme for self and team as per the guidelines • Monthly analysis of Primary/ Secondary sales, customer coverage etc • Build business relationships with key customers • Brief sub-ordinates on the incentive scheme • Ensure Annual target Achievement of all HQ • Ensure achievement of all New Launches If Interested and have relevant experience, requesting ...

Reviewing submission related documents including Inactive Ingredient Evaluation, Q1/Q2, Product Development Report, Quality Plan, Product Manual, Trade dress, Specifications, Master Packaging Card and Validation Protocols/Reports etc. DMF Review for ANDA submissions. Outlining requirements for labelling, storage and packaging for FDA submission. Compilation of ANDA sections of US market for sterile dosage form. Review of manufacturing related documents such as BMR, BPR and Stability study Protocols /Reports etc. To draft response and timely submission for regulatory deficiencies. To coordinate with cross-functional teams for regulatory requirements. Keeping up to date with regulatory guideli...

Job Role : Block Head (Engineering) Grade : Senior Manager Location : Guwahati Experience : 15+ Years (experience in lyophilizer ) Qualification : BE. Instrumentation Overseeing the engineering functions of parenteral block. Coordination with production personnel, contractors & machine manufactures to sort out machine related problems, major and minor modifications for smooth running in process. Tracking and maintaining the critical spares required for preventive and routine maintenance Planning various maintenance schedules and lead the team of engineering to ensure implementation of the schedules with the help of junior sub-ordinates for improving the overall reliability of the equipments....

Job Title: CSSD Technician Company Name: Manipal Hospitals Job Description: The CSSD Technician will be responsible for the effective cleaning, sterilization, and management of surgical instruments and medical equipment in the Central Sterile Services Department (CSSD). This position requires adherence to strict sterilization protocols, ensuring all equipment is ready for surgical procedures, and maintaining compliance with health and safety standards. The technician will also assist in the organization and inventory of surgical instruments, while maintaining accurate records of sterilization processes. Key Responsibilities: - Perform cleaning, decontamination, and sterilization of surgical ...

Qualification: Diploma / B.Tech / B.Pharma Experience: 38 years in Cartridge/PFS Line filling. Must have hands-on experience with Bausch Strobel or Syntegon filling machines (should be clearly mentioned in the resume)