35 Sterile Manufacturing Jobs

Role Overview: As an Analyst - Quality Assurance (Analytical Quality Assurance) at Immuneel, you will be responsible for in-process and batch QC activities. You will collaborate with internal QA, manufacturing, quality control, facilities operations, environmental health safety, and regulatory departments to ensure Analytical QA requirements are met and compliant with cGMP standards. Key Responsibilities: - Conduct Analytical Quality Assurance and development quality assurance tasks. - Review specifications, STP & ATR of raw material, packaging/consumable material, in-process, DS, DP finished product, and stability samples. - Review Certificates of Analysis (CoA) for various materials and pr...

Operate Aseptic Area processes including Lyophilizer, Autoclave, Vial Filling, Washing, and Sealing. Support sterile manufacturing activities as per safety and GMP guidelines.

Role Overview: As a member of the team, you will be responsible for performing line clearance activities before commencing operations, ensuring a clean and sanitized visual inspection and Packing area, and following the preventive maintenance schedule of machines. Operating the machines efficiently and filling the log of general areas as per SOP and work execution will also be part of your responsibilities. It is essential to adhere to cGMP, GDP, and maintain discipline in the department while ensuring that all employees comply with the same standards. Key Responsibilities: - Ensure that all equipment and production lines are in validated and calibrated status - Prepare daily production repo...

As a Machine Operator at our company, your responsibilities will include: - Following the preventive maintenance schedule of machines. - Checking the UAF working in the area. - Informing the concern supervisor immediately for any observations/disturbances related to documents and machines found in the area. - Filling the logs, BMRs, and documents of the area as per SOP and work execution. - Operating the machines and vessels of the area as per SOP. - Cleaning and sanitizing the area as per SOP. - Conducting line clearance activity before commencing operations as per SOP. - Attending training as per the schedule and ensuring training as per TNI. - Handling all packing related activities. - Cl...

Key Responsibilities Operate sterilization autoclaves and monitor sterilization cycles. Maintain records, load patterns, and routine validation checks. Ensure compliance with aseptic procedures. Desired Candidate Profile Experience in autoclave handling in sterile manufacturing. Knowledge of sterilization parameters and GMP standards.

Role Overview: You will be responsible for various activities including line clearance before operations, maintenance of machines as per schedule, cleaning and sanitizing the inspection and packing area, operating machines, and maintaining logs as per SOP. Your role will also involve ensuring compliance with cGMP, GDP, and enforcing discipline within the department to uphold standards. Key Responsibilities: - Conduct line clearance activities before commencing operations - Follow preventive maintenance schedule of machines - Clean and sanitize visual inspection and packing area - Operate machines and maintain logs according to SOP - Ensure all employees adhere to cGMP and GDP standards - Val...

Role Overview: As a member of the Batch File Review Team at PCI, you will be responsible for compiling and reviewing batch documents related to various process types such as OSD, Sterile, Biologics, Cell Therapy, and Gene Therapy. Your role will involve close collaboration with internal and external stakeholders to ensure documentation accuracy and compliance with regulatory standards. This position offers a diverse range of responsibilities and serves as an ideal foundation for individuals aspiring to pursue a career as a Quality Person (QP). Key Responsibilities: - Compile and review batch documents to ensure accuracy and completeness before QP review. - Collaborate with site personnel to ...

Operate Machine Sterile and Non-Sterile formulation area. IWK Machine Operator, Sterile manufacturing and knowledge of IWK filling machine, familiar with glopos system. Required Candidate profile Sterile and Non-Sterile Production Experience

Job Description: As a member of the team, you will be responsible for the following key responsibilities: - Responsible for preparation & review of the master documents of sterile manufacturing for parenteral facility. - Responsible for preparation and review of protocols and reports based on the requirements. - Responsible for document management and preparation like BMRs, BPRs, master SOPs etc. - Responsible for the handling of change control, deviations, CAPA, investigation etc. - Responsible to give training to all the subordinates, technicians and operators of the department. - Responsible for Audit and compliance on manufacturing shopfloor. - Knowledge of kaizen and continuous improvem...

You will be responsible for performing In-Process Quality Assurance (IPQA) activities at the shop floor during various stages of sterile manufacturing and packing. This includes conducting sampling at each stage or when necessary during product manufacturing, filling, and packaging processes. Additionally, you will be required to perform in-process checks of manufacturing, filling, and packaging activities. After the visual inspection of products, you will conduct Acceptable Quality Level (AQL) inspections. It will also be part of your duties to carry out audit trails, electronic data reviews batch-wise and as per the schedule. You will manage control samples and stability samples. Moreover,...

Prepare, review of Annual Product Quality Review trend data, report. Handling of Change Control proposal. Validation batches monitoring, sampling Co-ordination Internal Audit and Non schedule Audit. QA Analysis of sterile pharma products. Required Candidate profile 1. Candidate must have min 4 yrs of experience at managerial level 2. Candidate must have sterile manufacturing experience.

Role Summary: The MQA Upstream Associate Manager is responsible for ensuring Solution/Emulsion preparation, Vial/Ampoule washing, Depyrogenation, Filling, Capping and Collection areas of production & monitor process for compliance to cGMP (current Good Manufacturing Practices) standards. The MQA Upstream Associate Manager is directly responsible for managing and coordinating all quality functions within the area. Capping and Collection Roles and Responsibilities: Responsible for ensuring operating state of cGMP compliance in Solution/Emulsion preparation, vial/ampoule washing, Depyrogenation, Filling, Capping and Collection operations. Maintain regulatory compliance in accordance with cGMP p...

Role Overview: As the QC Head, you will be responsible for leading the Quality Control function in medical device manufacturing to ensure that products meet global regulatory, safety, and performance standards. Your role will involve overseeing raw material testing, in-process quality checks, stability studies, validation protocols, and final product release in compliance with applicable regulatory guidelines. Key Responsibilities: - Establish, implement, and maintain QC protocols, SOPs, testing procedures, and specifications. - Ensure batch-wise testing, documentation, and release of raw materials, intermediates, and finished products. - Oversee microbiological and biochemical testing for s...

Role Summary The QC Head will lead the Quality Control function for medical device manufacturing ensuring products meet global regulatory, safety, and performance standards. The role involves oversight of raw material testing, in-process quality checks, stability studies, validation protocols, and final product release as per applicable regulatory guidelines. Key Responsibilities 1. Quality Control Management Establish, implement, and maintain QC protocols, SOPs, testing procedures, and specifications. Ensure batch-wise testing, documentation, and release of raw materials, intermediates, and finished products. Oversee microbiological and biochemical testing relevant to sterile and non-steril...

As a Supervisor in the Sterile manufacturing department, your role involves preparing, reviewing, revising, controlling, and implementing standard operating procedures related to activities such as Change control and CAPA. You will be responsible for ensuring the smooth functioning of the department. Your key responsibilities will include: - Preparation, review, revision, control, and implementation of standard operating procedures for the Sterile manufacturing department - Document preparation for activities like CCF, SOP, Investigation, Risk Assessment, Protocol, etc. Qualifications required for this role: - M.Sc in Pharmacy or M.Pharm - Minimum 8 to 11 years of relevant experience in the ...

The Engineering Manager will lead the engineering and maintenance functions for the Oncology Manufacturing Facility, ensuring reliability, compliance, and operational excellence. The role requires deep expertise in sterile and injectable pharmaceutical environments, with a strong focus on equipment performance, utilities management, and team leadership. Key Responsibilities: 1. Maintenance and Reliability Management Oversee maintenance operations to ensure optimal performance of production equipment, including lyophilizers, injectable filling lines, and rapid mixer grinders. Develop and execute preventive maintenance programs to minimize downtime and ensure uninterrupted manufacturing. Monit...

We are hiring for Multiple position in Microbiology Department at Goa for Bangalore Location. Interested Candidates can walk in on 9th Nov 2025 or apply for this position Date & Time 09 th November ,2025 (Sunday). Time: 9.00 AM TO 5.00 PM. Note: Contact person Mr. Srinivasa M, those who are unable to attend the interview are requested to forward their resumes to email id: naveenkumarp@microlabs.in Candidates are requested to carry their copies of Resume, Mark Sheets,Experience Certificates, Latest salary certificate, pay slips of three months andone photographs. If any queries call us on: 080-27839033, 34 & 38 MICROBIOLOGY: 1. Position: Asst.Manager/ Manager (Only for male candidates) Qualif...

To perform Area cleaning. To perform Equipment operation and cleaning. To perform the visual inspection and packing activities. To perform the documentation as per Batch record and SOP. Responsible to maintain documents as per cGMP norms. Ensure the training completion before doing activity. Maintain personal hygiene.

We are looking for a dedicated and detail-oriented individual to support sterile injectable production operations. The role involves handling equipment, cleaning, sterilization processes, documentation, and adherence to cGMP standards within the pharmaceutical manufacturing unit. Key Responsibilities: Operate and clean HPHV steam sterilizers as per SOP. Handle and maintain vial washing machines and depyrogenation tunnels. Clean, assemble, and prepare machine parts and load patterns. Wash and prepare sterile garments for manufacturing zones. Prepare and filter disinfectants, IPA, and other cleaning solutions. Perform cleaning of equipment and rooms in the sterile processing areas. Execute bat...

To perform area cleaning. To perform equipment operation and cleaning. To perform the visual inspection and packing activities. To perform the documentation as per batch record and SOP. Responsible to maintain documents as per cGMP norms. Ensure the training completion before doing activity. Maintain personal hygiene. Reporting all the activities, incidents and problems to reporting officer.

To perform area cleaning. To perform equipment operation and cleaning. To perform the visual inspection and packing activities. To perform the documentation as per batch record and SOP. Responsible to maintain documents as per cGMP norms. Ensure the training completion before doing activity. Maintain personal hygiene. Reporting all the activities, incidents and problems to reporting officer.

Role Overview: - You will be responsible for the preparation and review of master documents for sterile manufacturing in the parenteral facility. - Your role will involve preparing and reviewing protocols and reports as per requirements. - You will handle document management and preparation of BMRs, BPRs, master SOPs, etc. - Managing change control, deviations, CAPA, investigations will also be part of your responsibilities. - Providing training to subordinates, technicians, and operators in the department will be your duty. - Ensuring audit and compliance on the manufacturing shop floor. - Utilizing knowledge of kaizen and continuous improvements. Key Responsibilities: - Prepare and review ...

This job is with Pfizer, an inclusive employer and a member of myGwork the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Use Your Power for Purpose As a Senior Associate, you will play a crucial role in improving patients lives while working at Pfizer. Your contributions will directly impact the development and delivery of innovative solutions that enhance the quality of life for patients worldwide. Join us in our mission to bring breakthroughs that change patients lives. What You Will Achieve In this role, you will: Handle Technology Transfer activities & New Product Introduction process Knowledge of validation and practices related...

You will be responsible for conducting audits and ensuring compliance at Sterile Manufacturing sites. This includes monitoring the site, overseeing batch release processes, performing joint analysis, and providing first pack approval. Additionally, you will be handling complaints related to manufacturing processes. **Key Responsibilities:** - Conduct audits and ensure compliance at Sterile Manufacturing sites - Monitor the site to ensure adherence to quality standards - Oversee batch release processes - Perform joint analysis with relevant teams - Provide first pack approval for manufactured products - Handle complaints related to manufacturing processes **Qualifications Required:** - Bachel...

You will be joining Lifecraft, a leading manufacturer of pharmaceutical process equipment known for delivering innovation and precision in sterile manufacturing. As a part of the dynamic marketing team, you will contribute to scaling new heights in the industry. Key Responsibilities: - Specialize in Injectable Process Equipment - Utilize Sterilization Technology effectively - Manage WFI & Pure Steam (STEM) Generation Systems - Oversee Sterile Manufacturing & Compounding Suites - Lead Team Development & Strategic Planning - Utilize PAN India Market Experience effectively Qualifications Required: - 5-8 years of relevant experience in pharmaceutical process equipment - Full-time availability - ...