Be the First to Apply DivisionPiramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a
Job Title- Production Manager Location- Goa. Main Responsibilities- Planning and scheduling: Production Planning and Scheduling. Receive products requirement plan from supply chain, plan, execute, interact with cross functional departments for communicating requirement for completion of plan,
To follow the safety rules in the premises according to the company norms. •Monitoring of DP, RH and temperature in their Component preparation and sterilization area (Autoclave area). •Responsible for Maintenance and cleaning of Component preparation
To follow the safety rules in the premises according to the company norms •Timely completion of SOPs training and On the job trainings related to visual inspection and packing area. •Monitoring of DP, RH and temperature
QA Executive LOCATION: Ahmedabad REPORTS TO: Senior Quality Specialist DIRECT REPORTS: None GRADE: As Per Company Standards WORKPLACE TYPE: Onsite at All Manufacturing Sites within India Company Background: Ingredion is a Fortune 500 provider of ingredient
Be the First to Apply DivisionPiramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a
Job Title: Executive Business Unit: Sun Global Operations Job Grade G12A Location : Baska At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step,
To operate the necessary equipment such as cartridge washing, Filling, sealing, Autoclave, Auto Visual Inspection & batch manufacturing operation. To ensure compliance with cGMP. Maintain online documents related to production activities like BMR, e -log entries, calibration
Description: Operate and monitor manufacturing equipment and Instrument used in various stages of API production, such as reactors, Centrifuge, Dryer, Miller, sifter etc. Maintaining accurate records and documentation of production activities, including batch Manufacturing Record (BMR), Batch
Description: Operate and monitor manufacturing equipment and Instrument used in various stages of API production, such as reactors, Centrifuge, Dryer, Miller, sifter etc. Maintaining accurate records and documentation of production activities, including batch Manufacturing Record (BMR), Batch
Job Description Responsible for achieving API production targets while ensuring compliance, safety, quality, cost control, manpower management, and continuous improvement initiatives across manufacturing operations. Production Operations Plan, organize, and monitor daily API manufacturing activities. Ensure adherence
Be the First to Apply DivisionPiramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a
Be the First to Apply DivisionPiramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a
Job Title: Executive - Portfolio Program Qualification: Graduate / Post Graduate in Pharmacy with 3-6 years of experience in Pharmaceutical Quality Assurance or Production Candidate having sound experience in documentation as well as execution of oral
Job title: Executive Packing Location: Goa Site, Verna Industrial Estate, Salcete, Goa, India. About the job Our Team: We are the team (Production) of about 250 permanent employees and having state-of-the-art manufacturing facility for tablet/Capsule manufacturing.
1 cGMP and compliance review in the GMP area as per cGMP guideline. 2 Machine and area clearance. 3 Sampling of blend, intermediate stages, AQL finished product, ANSI sample, reserve sample, stability sample and In-process checks
Responsible for line clearance activity before commencing the different operations like dispensing, manufacturing, filling, inspection, sealing, labelling, and packing. Responsible to perform the environment monitoring activities Responsible for Process validation, cleaning validation/verification, hold time study, media
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Description: The role is responsible for ensuring day-to-day compliance with global GMP (Good Manufacturing Practices) during manufacturing, packing, and dispensing activities at the site. The role provides on-floor quality assurance support, ensuring operations are performed as
Job Purpose To support and execute qualification and validation activities related to production equipment, utilities, and processes in an Oral Solid Dosage (OSD) manufacturing facility, ensuring compliance with USFDA, cGMP, and regulatory requirements. Key Responsibilities Qualification