35 Sterile Manufacturing Jobs - Page 2

For Production (Injectable): Exposure pertaining to Groninger vial filling, Groninger Bottle fiiling, Fedegari Autoclave, NKP vial Filling machine, lyophilizer, Spray dryer, Aseptic process, complex manufacturing, Exposure to CIP/ SIP, SKID manufacturing, pre-fill syringe, QMS is required For Production (OSD): Exposure of granulation, compression and coating process, BMR, Change control, CAPA, For Engineering: Exposure of maintenance of Sterile Manufacturing Plant, maintenance of Autoclave, Filling machine - Vial, Ampoule, Ophthalmic, Lyophilizer, Freeze dryer machine, BFS machine is required Job Location: Sun Pharmaceutical Medicare Limited (Baska) : Nr. Hotel Sarvottam, Survey NO 22 & 24 ,...

We are for Production Dept for multiple Position. Interested Candidate can apply to for this position. 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 and one photographs. If any queries call us on: 080-27839033, 34 & 38 MICROBIOLOGY: 1. Position: Asst. Manager (Only for male candidates) Qualification: B.Sc/ M.Sc- Microbiology/ BioTech Experience: 8-14 years experience in Sterile Manufacturing facility. Job Profile: Reviewer and secti...

Your role at PCI as part of the Batch File Review Team will involve compiling and reviewing batch documents across various process types such as OSD, Sterile, Biologics, Cell Therapy, and Gene Therapy. You will collaborate closely with internal and external stakeholders, preparing documentation for Quality Person (QP) review, coordinating corrections, and ensuring compliance with regulatory requirements. This position offers a diverse range of responsibilities and serves as an ideal foundation for those considering a future career as a QP. Key Responsibilities: - Compile and review batch documents, ensuring accuracy and completeness prior to QP review. - Collaborate with site personnel to ad...

As a Manufacturing Supervisor, your role involves ensuring efficient line clearance activities, preventive maintenance of machines, cleaning and sanitizing visual inspection and packing areas, operating machines, and maintaining logs as per SOPs. You are also expected to uphold cGMP, GDP standards, and enforce discipline within the department to ensure uniform compliance among all employees. Key Responsibilities: - Perform line clearance activities before commencing operations - Follow the preventive maintenance schedule of machines - Clean and sanitize visual inspection and packing areas - Operate machines and maintain logs according to SOP - Ensure adherence to cGMP, GDP, and discipline st...

As a Manufacturing Specialist in our company, your responsibilities will include: - Performing line clearance activities before commencing operations to ensure a clean and sanitized visual inspection and Packing area - Following the preventive maintenance schedule of machines - Operating the machines efficiently and filling the log of general areas as per SOP and work execution - Adhering to cGMP, GDP, and maintaining discipline in the department - Ensuring that all employees comply with the same standards Your role will also involve: - Ensuring that all equipment and production lines are in validated and calibrated status - Preparing daily production reports based on achieved targets - Crea...

We are seeking a motivated and detail-oriented Injectable Plant Compliance Manager to join our team. The ideal candidate will be responsible for ensuring compliance with all regulatory requirements and industry standards specific to the production of injectable pharmaceutical products. This role will serve as a key leader in maintaining quality assurance, overseeing audits, and implementing compliance systems to ensure the safety and efficacy of our products.

You will be responsible for conducting In-Process Quality Assurance (IPQA) activities on the shop floor throughout the various stages of sterile manufacturing and packing process. This includes performing sampling at each stage or when necessary during product manufacturing, filling, and packaging activities. Your duties will also involve conducting in-process checks of manufacturing, filling, and packaging processes. You will be required to perform Acceptable Quality Level (AQL) checks after completing visual inspection of products. Additionally, you will need to carry out audit trail and electronic data reviews batch-wise and as per the designated schedule. Furthermore, you will be tasked ...

As an Autoclave Operator, you will be responsible for operating and maintaining autoclave machines used to sterilize equipment and materials in injectable pharmaceutical production, ensuring compliance with GMP and safety standards. Your key responsibilities will include operating high-pressure autoclaves to sterilize vials, tools, and equipment, monitoring and recording temperature, pressure, and time settings, loading and unloading materials with correct placement and cycle selection, performing routine maintenance and safety checks, documenting sterilization cycles, reporting malfunctions, cleaning and disinfecting autoclave units following SOPs, and adhering to all regulatory and safety ...

You will be responsible for preparing and reviewing the master documents of sterile manufacturing for the parenteral facility. Additionally, you will prepare and review protocols and reports based on the specified requirements. Document management and preparation tasks such as BMRs, BPRs, and master SOPs will also fall under your responsibilities. Handling change control, deviations, CAPA, investigations, and providing training to subordinates, technicians, and operators within the department are key aspects of this role. You will also be accountable for audit and compliance on the manufacturing shop floor. The ideal candidate for this position should hold a B.Pharm/M.Pharm degree and posses...

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...