Injectable Plant Compliance Manager Hetero

13.0 - 18.0 years

13 - 16 Lacs

jadcherla

Work from Office

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.

Posted 5 days ago

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Associate Endo

2.0 - 6.0 years

0 Lacs

indore, madhya pradesh

On-site

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 with managing control samples and stability samples. Your role will also include participating in the qualification of master kit approval for visual inspection activities. You will be expected to review and approve all relevant documents related to the qualification of visual inspectors. Overall, your attention to detail and adherence to quality standards will be crucial in ensuring the production of high-quality sterile products.,

Posted 6 days ago

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Team Member-Production (Autoclave/Compounding) Dr. Reddy's Laboratories

2.0 - 6.0 years

0 Lacs

andhra pradesh

On-site

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 protocols. To qualify for this role, you should have a Diploma/B.Tech or equivalent, experience in sterile manufacturing or equipment operation is preferred, knowledge of autoclave operations and safety procedures, and physical ability to lift heavy items and stand for long periods.,

Posted 1 week ago

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Executive Manufacturing QMS and compliance Injectable Amneal Pharmaceuticals

3.0 - 7.0 years

0 Lacs

ahmedabad, gujarat

On-site

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 possess a minimum of 3-5 years of experience in manufacturing QMS, process review, and compliance. Knowledge of Kaizen and continuous improvement methodologies will be an advantage.,

Posted 2 weeks ago

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Associate Director Endo

5.0 - 9.0 years

0 Lacs

indore, madhya pradesh

On-site

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 of regulatory guidelines such as USFDA and EU standards. Hands-on experience with production equipment, QMS systems, and shop floor excellence tools is also desired. If you are ready to take on the challenge of leading a production block in a fast-paced, quality-driven environment, we are excited to hear from you.,

Posted 1 month ago

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