234 Gdp Jobs - Page 6

Job Title: Quality Engineer. Experience: 4 to 10 years Location: Mysuru Notice Period: immediate to 15 days Mandatory Skill: QMS, Capa, GMP/Gdp/ GLP, Change Control, Deviation, Sop Preparation JD : Good understanding of Pharmaceutical GMP/GLP/GDP practices. *Experience in Pharma QMS activities like, handling Change Controls, Deviations, vendor qualifications and SOP updates. *Understanding of Internal Audits and CAPA closures. *Supporting for Quality metrics program. *Proficient experience with MS-office is required. *Strong written and verbal communication skills are essential *Experience working with virtual teams • Understanding of ISO 9001:2015 is required. *Strong communication, teamwor...

Responsibilities: Manage CSV projects from start to finish. Ensure compliance with GAMP, GDP, CapA, GXP, IT Compliance & LIMS standards. Collaborate with cross-functional teams on system validation. Free meal Cafeteria Food allowance Shift allowance Over time allowance Travel allowance Sales incentives Annual bonus Performance bonus Marriage & childbirth gifts

Oversees QC activities, staff training, SOPs, calibrations, GLP compliance, audits, records, and lab investigations (OOS/OOT) and aligns QC goals with production and ensures lab standards (candidates having approval from Raj. FDA will be preferred).

Role & responsibilities Review and approve Finished Goods and corresponding Certificates of Analysis (COA). Maintain detailed records of received samples in an organized manner. Ensure proper allocation and storage of approved COAS in the shared drive. Verify and confirm drug product permissions as per regulatory requirements. Oversee the finalization of packing materials in coordination with relevant departments. Conduct audits of new vendors, ensuring compliance with quality standards. Ensure proper implementation of Corrective and Preventive Actions (CAPA) for any deviations or complaints. Visit manufacturing sites to address and investigate market complaints effectively. Coordinate with ...

Role & responsibilities Review and approve Finished Goods and corresponding Certificates of Analysis (COA). Maintain detailed records of received samples in an organized manner. Ensure proper allocation and storage of approved COAS in the shared drive. Verify and confirm drug product permissions as per regulatory requirements. Oversee the finalization of packing materials in coordination with relevant departments. Conduct audits of new vendors, ensuring compliance with quality standards. Ensure proper implementation of Corrective and Preventive Actions (CAPA) for any deviations or complaints. Visit manufacturing sites to address and investigate market complaints effectively. Coordinate with ...

Experience: 5 to 12 years Location: Bangalore : We are seeking a highly experienced Design Verification Engineer to join our team in Bangalore. The ideal candidate will have 5 to 12 years of experience in IP and SOC verification, with a strong foundation in SystemVerilog (SV) and Universal Verification Methodology (UVM). In addition to standard verification skills, this role requires expertise in CDP (Compressed Data Pattern), GDP (Generic Data Pattern), and DFT DV (Design for Test in Design Verification) methods, including JTAG, MBIST (Memory Built-In Self-Test), SCAN, PG (Pattern Generator), and PM (Pattern Memory). Key Responsibilities: IP and SOC Verification Perform comprehensive IP and...

Number of Open Positions: 7 Location: Bangalore Experience: 4 to 7+ years : We are currently seeking talented and experienced Design Verification Engineers to join our team in Bangalore. As a Design Verification Engineer, you will be responsible for ensuring the functionality, performance, and reliability of our complex designs, with a focus on Core Data Path (CDP), Graphics Data Path (GDP), USB4 (USB 4.0), Power Gating (PG), and Power Management (PM) domains. We are looking for candidates with 4 to 7+ years of relevant experience in design verification. Key Responsibilities: Verification Planning: Collaborate with design and architecture teams to develop comprehensive verification plans for...

Strong understanding of pharmaceutical warehousing & distribution systems Leadership skills with experience in team management and performance development Expertise in SAP (MM/WM/SD modules preferred) knowledge of GST invoicing & E-way bill processes Required Candidate profile 10+ years of hands-on experience in a pharmaceutical warehouse or distribution center. Experience in managing operations involving multiple dispatch destinations across India.

You will be working as an Officer/Sr. Officer/Executive/Sr. Executive with 2-8 years of experience in injectable Manufacturing. Your role will involve following instructions and procedures outlined in the Entry-Exit SOP for Grade C and Grade B areas, as well as ensuring proper functioning and behavior in the aseptic area. You will be responsible for adhering to personnel hygiene practices within the factory premises, following Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) as per SOP guidelines, and monitoring temperature, relative humidity, and differential pressure. Additionally, you will be tasked with overseeing the handling of material movement in the producti...

You will be responsible for performing commissioning and qualification of Pharmaceutical equipment, specifically systems for Oral Solid Dosage, Injectables, and Fill/Finish. This includes a variety of equipments such as RMG, CoMil, Tablet press, Coating Machine, blister packing machine, Vial Filling Line, PFS Line, Isolators (Negative & Positive), RABs (Open and Closed), GL Reactors, Dryer, Nutsche Filters, Centrifuges, Lyophilizers, etc. Your responsibilities will include developing CQMP, VMP, FRA, cGMP review sheet, interdependencies, System boundary, URS, SCA/SLIA, CLIA, DQR, SRA/QRA, SAT protocol, commissioning protocol, IQ protocol, OQ protocol, PQ protocol, process validation, and clea...

You have an exciting opportunity to join as a Deputy Manager in Stores within the pharmaceutical sector located in Surendranagar, Gujarat, India. With over 10 years of experience in pharmaceutical warehouse operations, you will play a vital role in ensuring efficient and compliant warehouse management. Your main responsibilities will include overseeing warehouse operations, such as the receipt, verification, storage, and dispatch of raw materials, packaging materials, and finished goods while adhering to cGMP and GDP standards. You will be responsible for maintaining accurate inventory records through physical stock counts and reconciliation with SAP/ERP systems to minimize waste and identif...

Shall have good knowledge on operation of Purified water system. 2. Shall have good knowledge on operation of Pure steam generator system. 3. Shall have good knowledge on operation of WFI system. 4. Shall have good knowledge on GMP and GDP.

1. Shall have good knowledge on operation of Purified water system. 2. Shall have good knowledge on operation of Pure steam generator system. 3. Shall have good knowledge on operation of WFI system. 4. Shall have good knowledge on GMP and GDP.

1. Shall have good knowledge on operation of Purified water system. 2. Shall have good knowledge on operation of Pure steam generator system. 3. Shall have good knowledge on operation of WFI system. 4. Shall have good knowledge on GMP and GDP.

Roles and Responsibilities Operate formulation machines such as FBC, blender, coating, and dryers. Ensure compliance with Good Manufacturing Practices (GMP) and Good Documentation Practice (GDP). Monitor machine performance and troubleshoot issues to minimize downtime. Maintain accurate records of production runs and quality control tests. Collaborate with team members to achieve production targets. Desired Candidate Profile 2-6 years of experience in pharmaceutical manufacturing operations or related field. Strong understanding of GMP/GDP regulations and industry standards. Proficiency in operating various types of machinery including dryers, mills, etc.

As an ETL Developer for the Data and Analytics team, at Guidewire you will participate and collaborate with our customers and SI Partners who are adopting our Guidewire Data Platform as the centerpiece of their data foundation. You will facilitate and be an active developer when necessary to operationalize the realization of the agreed upon ETL Architecture goals of our customers adhering to Guidewire best practices and standards. You will work with our customers, partners, and other Guidewire team members to deliver successful data transformation initiatives. You will utilize best practices for design, development, and delivery of customer projects. You will share knowledge with the wider G...

Role & responsibilities (Production): Assist in manufacturing operations of parenteral dosage forms (sterile injections) as per SOPs and GMP guidelines. Monitor and record process parameters during manufacturing and filling operations. Ensure compliance to cGMP, documentation and data integrity norms. Support continuous improvement initiatives in production efficiency and compliance. Role & responsibilities (Engineering): Assist in preventive maintenance and breakdown handling of production equipment Support engineering team in equipment qualification and calibration activities. Monitor Utility systems Maintain proper documentation as per GMP norms. Follow safety protocols and support new in...

As a Line Lead at ACG Associated Capsules Pvt. Ltd., your primary responsibilities include monitoring and verifying all shift activities, executing post-production planning, and preparing shift machine performance reports to support decision-making by the HOD/Incharge. You will be responsible for implementing quality corrections to minimize printing defects and achieve the target AFOE@Despatch. Ensuring that all requirements are in place for color change, monitoring ATS operation with production and quality, and checking line clearance of machines as per SOP are crucial tasks in this role. You will also be expected to supervise color changes with required cGMP and GDP requirements, coordinat...

Role & responsibilities Incharge for QMS activities, Preferred candidate profile Should have good knoledge about QMS, Validation, calibration , qualification, re-qualification, change control. CAPA, OOS, OOT & Investigation. Mainly for all Process equipments and Utility ( HVAC System, Purified System, Refrigerator System, Air Compressor System & Boiler ) Exposure with Regulatory Aduits.

Role & responsibilities 1) To perform the analysis by following cGMP, GLP, ALCO+, and safety compliance 2) To perform the sampling, testing of RM, PM, In-process, Intermediate and Finished product. 3) Participate in Investigation of deviation, Incident, OOS etc. 4) To perform all qualification activities of instrument and equipment in QC Lab. 5) Aware of calibration and operation procedure for instruments ( balance, K.F, GC. UV,refratometer and viscometer etc,) 6) Experience of QC software like Tiamo 3.0, Lab solution, SCM etc. 7) Preparation of documents ( SOP, protocol etc) related to Quality control. Kindly Send CV to mail ID, jagpal.dewal@ipca.com vishal.rankham@ipca.com

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. Your role will involve ensuring that all equipment and production lines are in validated and calibrated status, preparing daily production reports based on achieved targets, and cre...

Job Title: TAW Coordinator Technical Administration & Documentation Department: Technical Administrative Wing (TAW) Reports To: TAW Manager / Engineering Head / GM Projects Location: Kompally, Hyderabad. Required to travel to project sites on need based. Job Purpose: To coordinate, document, and monitor the end-to-end TAW workflow (QD CC CM BS), ensuring seamless communication between cross-functional teams, accurate records, and strict adherence to established processes and organograms. Key Responsibilities Coordinate and track TAW workflow stages: Quotation Document (QD) Confirm Contract (CC) Commencement Meeting (CM) Budget Sheet (BS) Maintain and update project-specific documentation in ...

Execute and monitor API production operations as per BMRs, SOPs, and production plans. Handle day-to-day operations of reactors, centrifuges, dryers, and other related equipment. Ensure compliance with cGMP, safety, and environmental guidelines. Required Candidate profile Coordinate with QA/QC, maintenance, and warehouse departments to ensure smooth workflow. Ensure line clearance, raw material availability, Immediate to 30 days preferred

WHO-GMP guidelines, pharmaceutical material handling, inventory systems (ERP/SAP) Material handling, storage, and movement comply with WHO-GMP Strong expertise in pharmaceutical warehousing, inventory control, regulatory compliance, cross-functional. Required Candidate profile Lead day-to-day warehouse operations receipt, storage, issuance, and dispatch of raw materials, packaging materials, intermediates, finished goods. Relevant experience in a pharmaceutical warehouse

The Executive - Production position at Dishman Carbogen Amcis Limited in Bavla, Gujarat, India, requires you to be proficient in Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP). You will also be responsible for participating in audit preparation for regulatory agencies. Additionally, knowledge of HAZOP study and process safety is essential for this role. This position falls under the Industrial, Law, Manufacturing, and Legal job segment.,