13 Api Pharma Jobs

Urgent job opening of Senior Production for API Pharma Company at Dombivali. Experience: 5 years an above Job profile: 1) Manage entire range of activities of a cGMP compliant Plant. 2) Lead and motivate production team to achieve production and quality targets while manufacturing variousA PIs. 3) Review and ensure compliance of safety and cGMP norms forprocesses,equipment and operations. 4) Coordinate with Export, Purchase and Stores, plantmonthly production develop schedules and undertake manufacturing operations. 5) Establish production, quality assurance systems,standard Operating Procedures and Conditions (SOPs&SOCs) and ensure their continued compliance. 6) Monitor and assur equality a...

Urgent job opening of Senior Production for API Pharma Company at Dombivali. Experience: 5 years an above Job profile: 1) Manage entire range of activities of a cGMP compliant Plant. 2) Lead and motivate production team to achieve production and quality targets while manufacturing various APIs. 3) Review and ensure compliance of safety and cGMP norms for processes, equipment and operations. 4) Coordinate with Export, Purchase and Stores, plant monthly production develop schedules and undertake manufacturing operations. 5) Establish production, quality assurance systems, standard Operating Procedures and Conditions (SOP s & SOC s) and ensure their continued compliance. 6) Monitor and assure q...

As a Senior QA Officer, your role will involve various responsibilities to ensure quality assurance within the API pharma industry. You will be tasked with issuing Batch Manufacturing Records, equipment cleaning records, logbooks, and analytical reports for raw materials, finished products, and packing materials. Additionally, you will assist in the preparation of SOPs for different departments and conduct plant rounds to verify documents according to cGMP and GLP norms. Line clearance activities for manufacturing and packaging, issuing deviation forms, change control forms, and handling customer complaints will also be part of your duties. You will review and verify analytical and Batch Man...

API Pharmaceutical Company Required QC/Quality Control Officer Education: B.Sc., M.Sc. Location: Boisar (Palghar), Maharashtra Experience: 3 to 4 Years

As a Senior Executive in the Engineering and Maintenance department at Syngene International Ltd., located in Mangaluru, your primary role will be to serve as an experienced mechanical maintenance engineer with API Pharma experience. With a minimum of 3 to 8 years of experience in shift maintenance with API process equipment, you will play a crucial role in ensuring the proper functioning and maintenance of various process-related equipment such as Reactors, Centrifuges, Dryers, Filters, and more. Your educational background should include a BE/B.TECH in Mechanical Engineering to qualify for this position. Your technical skills will be put to the test as you contribute to the development of ...

You are an experienced mechanical maintenance engineer with API Pharma experience. You hold a BE/B.TECH degree in Mechanical engineering and possess a minimum of 3 to 8 years of shift maintenance experience with API process equipment. Your role involves ensuring overall adherence to safe practices and procedures, contributing to the development of procedures that ensure safe operations, and compliance with integrity and quality standards. You are responsible for driving a corporate culture that promotes environment, health, and safety (EHS) mindset, and operational discipline at the workplace. It is essential for you to ensure safety by adhering to safety protocols and following environment,...

1 to 2 years in Api pharma Responsible for analysis such as Microbial limit test and Bacterial Endotoxin test as per existing specification and test method. Responsible for calibration, and proper documentation.

Responsible for preparing work instruction for Production and manufacturing activities Carry out production activities as per production plan Responsible for monitoring batch process Maintaining equipments and area cleanliness

8 to 15 years in API Pharma Maintain the documents as per systems related to cGMP for various statutory & regulatory audits & inspections Review SOPs as per the QMS guideline Handling of external audits along with QA department

Experience in API pharma Perform all QC activity as per defined SOP and document it on time. To assist the Head QC in investigation of OOS results. To maintain the stability chamber for temperature, humidity, and recording.

1 to 2 years in Api pharma Responsible for analysis such as Microbial limit test and Bacterial Endotoxin test as per existing specification and test method. Responsible for calibration, and proper documentation.

Responsible for preparing work instruction for Production and manufacturing activities Carry out production activities as per production plan Responsible for monitoring batch process Maintaining equipments and area cleanliness

Candidate must have perfection in English communication. Knowledge of all regulated Guideline & Pharmacopoeia. Must have Knowledge all documentation of QA 18 to 20 Years in API Pharma Industry Experience