11 Terminal Sterilization Jobs

Job Description: You will be responsible for handling manufacturing activities including Dispensing, Compounding, Filling, Sealing, and Terminal Sterilization. Key Responsibilities: - Manage manufacturing activities such as Dispensing, Compounding, Filling, Sealing, and Terminal Sterilization. Qualifications Required: - Relevant experience in QA-IPQA department. - Knowledge of manufacturing processes. (Note: No additional details of the company are mentioned in the job description),

By clicking the Apply button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description: OBJECTIVES/PURPOSE : Manages technical topics related to the global manufacturing of Drug Product within the scope of VBU Manufacturing Science & Technology. Independently develops and implements continuous improvement activities for current and future manufacturing sites within the Takeda vaccines manufacturing network and drives cha...

Use Your Power for Purpose Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team. We rely on a team of dedicated and agile members who understand the importance and impact of their role in Pfizer's mission. You will help to ensure that patients and physicians have the medicines they need when they need them. The significance of your role cannot be overstated, as it directly influences the availability of essential medications. Your dedication and agility are crucial in maintaining the high standards of our manufacturing processes. By continuously striving for excellence, you contribute to the overall mission of delivering life-saving treat...

Job Description Job Responsibilities: Responsible for document management like BMR's, BPR's, master SOP's etc. Responsible for preparation & review of the master documents of production. Responsible to ensure UAF working in area. Responsible for the handling of change control, deviations, investigation & CAPA, etc Responsible to give training to all the subordinates, technicians and operators of the department. Activities other than defined in the job responsibility are to be done, as per the requirement of HOD, by following HOD's instruction and guidance. Responsible for line clearance activity before commencing the operations. Responsible to check that all the records and logbooks related ...

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...

As a Document Management Specialist, your role involves handling various responsibilities related to document management, production processes, and quality compliance. Your key responsibilities include: - Managing documents such as BMRs, BPRs, and master SOPs to ensure accuracy and completeness. - Preparing and reviewing master production documents to maintain quality standards. - Ensuring the proper functioning of the UAF in your designated area. - Handling change control, deviations, investigations, and CAPA processes efficiently. - Providing training to subordinates, technicians, and operators to enhance their skills and knowledge. - Conducting line clearance activities before starting pr...

Key Responsibilities JOB DESCRIPTION Sterile / Parenteral / Aseptic Filling, Sealing, Filtration, Production QMS Batch Manufacturing Autoclave Terminal Sterilization Packing & Visual Inspection Qualifications Qualification Requirement: B.Pharm / M.Sc Experience: 2-7 years

As a Production Manager in our company, your role will involve the following key responsibilities: - Responsible for document management including BMRs, BPRs, and master SOPs. - Preparation and review of master documents of production. - Ensuring UAF working in the area. - Handling change control, deviations, investigations, and CAPA. - Providing training to subordinates, technicians, and operators. - Performing line clearance activities before operations. - Checking records and logbooks related to aseptic manufacturing. - Preparation, review, revision, control, and implementation of standard operating procedures. - Ensuring cleaning and sanitization of General, Controlled & Aseptic areas. -...

You will be working in the Operations department of Pharma Solution business located in Lexington. Your role as a Manufacturing Operator will involve performing various production activities such as component preparation, filling, capping, autoclaving, terminal sterilization, compounding, and lyophilization production. You will report directly to the Manufacturing Supervisor. - Complying with all relevant policies and procedures - Performing line clearances and cleaning/sanitization - Operating and maintaining production equipment - Ensuring proper ingredients and quantities of batches - Executing validation protocols - Maintaining records - Following Good Manufacturing Practices - Reviewing...

Role Overview: You will be responsible for handling manufacturing activities such as Dispensing, Compounding, Filling, Sealing, and Terminal Sterilization in the QA-IPQA department. Key Responsibilities: - Perform quality assurance checks during manufacturing processes - Ensure compliance with established protocols and procedures - Identify and report any deviations or non-conformances - Participate in internal and external audits - Assist in the investigation of quality issues and implementation of corrective actions Qualifications Required: - Bachelor's degree in a related field - Prior experience in QA within a manufacturing environment - Strong attention to detail and analytical skills -...

The role we are offering is for a Block Head to lead a key production block within our injectable manufacturing facility. Your responsibilities will include overseeing end-to-end manufacturing operations, managing a team of production staff, driving process optimization, ensuring regulatory audit readiness, maintaining compliance with cGMP standards, implementing changes, overseeing equipment and maintenance, coordinating cross-functionally, and managing inventory and resources. You should have a degree in Pharmacy, Engineering, or a related field, along with proven experience in sterile/injectable manufacturing. Strong leadership and team management skills are required, as well as knowledge...