98 Gdp Jobs

The Quality Assurance (QA) Executive API (Bulk Drugs) role based in Savli, Gujarat requires a candidate with 2-5 years of experience and a qualification of B.Sc / M.Sc. As a QA Executive, your responsibilities will involve ensuring compliance with cGMP, ICH, and regulatory guidelines in API (bulk drug) manufacturing. You will be responsible for preparing, reviewing, and controlling SOPs, BMRs, BPRs, change controls, deviations, and CAPAs. In addition, conducting in-process checks for manufacturing and packaging activities, handling investigations for deviations, OOS/OOT results, and supporting root cause analysis are key components of this role. You will also be involved in participating in internal audits, regulatory audits (USFDA, EU, WHO, etc.), and vendor audits. Maintaining documentation for batch release, validation protocols, and quality systems, ensuring adherence to data integrity and good documentation practices (GDP), and supporting qualification and validation activities are crucial aspects of this position. Collaboration with cross-functional teams such as Production, QC, and R&D is essential for ensuring smooth operations. This is a full-time, permanent position with benefits including health insurance and Provident Fund. The work schedule is day shift with additional perks such as performance bonus and yearly bonus. The work location is in person.,

As a Store Manager at our pharmaceutical manufacturing unit in Nadiad, you will be responsible for overseeing and managing the inventory and warehousing operations. With 7-10 years of experience in pharmaceutical warehousing, you will utilize your expertise in GMP and GDP to maintain compliance with regulatory guidelines. Your role will involve managing day-to-day store operations, ensuring proper storage conditions, and monitoring inventory levels to prevent stock-outs or overstocking. You will lead a team of store assistants, operators, and forklift drivers, while collaborating with various departments to ensure seamless operations. Your responsibilities will include overseeing material handling, maintaining accurate documentation, and preparing for internal and external audits. Proficiency in ERP systems such as SAP or Oracle will be essential for managing inventory and generating reports for management. To qualify for this role, you should hold a Bachelor's degree in Pharmacy, Science, or a related field, with a diploma in Materials Management or Supply Chain being an added advantage. Strong knowledge of pharmaceutical regulations, GMP, GDP, and experience in handling APIs, excipients, and hazardous materials are required. Key skills such as leadership, analytical thinking, communication, and audit preparedness will be crucial for success in this position. Preferred certifications in GDP/GMP training, ISO standards, and relevant ERP systems will further enhance your candidacy for this role. Join us in ensuring efficient warehouse management and maintaining high standards of quality and compliance in our pharmaceutical manufacturing facility.,

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 SOC verification to ensure the reliability and functionality of integrated circuits. SystemVerilog (SV) and UVM Proficiency Demonstrate a strong understanding of SystemVerilog and Universal Verification Methodology for efficient verification processes. CDP, GDP, DFT DV Expertise Possess expertise in Compressed Data Pattern (CDP) and Generic Data Pattern (GDP) methodologies. Proficiency in Design for Test in Design Verification (DFT DV) techniques, including JTAG, MBIST, SCAN, PG, and PM. Qualifications: Bachelor’s or Master’s degree in Electrical Engineering, Computer Engineering, or a related field. 5 to 12 years of relevant industry experience in IP and SOC verification. Strong knowledge of SystemVerilog (SV) and Universal Verification Methodology (UVM). Expertise in CDP (Compressed Data Pattern), GDP (Generic Data Pattern), and DFT DV (Design for Test in Design Verification) methods, including JTAG, MBIST, SCAN, PG, and PM. If you are a talented Design Verification Engineer with a deep understanding of IP and SOC verification, as well as specialized expertise in CDP, GDP, and DFT DV methodologies, we encourage you to apply. Join our dynamic team and contribute to the advancement of cutting-edge technology. Job Category VLSI (Silicon engineering) Job Type Full Time Job Location IndiaBangalore

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 CDP, GDP, USB4, PG, and PM components. Testbench Development: Create and maintain advanced testbenches, including constrained-random and assertion-based methodologies, to thoroughly verify design functionality. Functional and Coverage Testing: Execute functional tests and track coverage metrics to ensure exhaustive testing of design features. Protocol Verification: Verify compliance with industry-standard protocols, including USB4, and identify and address protocol violations. Bug Reporting and Debugging: Document and report issues, and work closely with design teams to resolve bugs in a timely manner. Performance Verification: Assess and verify the performance of data path components, ensuring they meet specified requirements. Power Verification: Verify power management and power gating strategies to optimize power consumption. Scripting and Automation: Develop and use scripting languages and automation tools to streamline verification processes. Documentation: Prepare detailed verification plans, test reports, and documentation. Qualifications: Bachelor’s or Master’s degree in Electrical Engineering, Computer Science, or a related field. 4 to 7+ years of experience in design verification. Strong knowledge of CDP, GDP, USB4, PG, and PM domains. Experience with industry-standard verification methodologies and tools. Excellent problem-solving skills and attention to detail. Strong communication and teamwork skills. If you are a highly motivated and detail-oriented Design Verification Engineer with a passion for ensuring the quality and reliability of complex designs, we encourage you to apply. Join our team to work on cutting-edge technologies and contribute to the success of our projects. Job Category VLSI (Silicon engineering) Job Type Full Time Job Location IndiaBangalore

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 production area, maintaining documentation as per GDP and cGMP standards, and ensuring day-to-day records are accurately maintained. You will also be responsible for providing training to new chemists, workers, and operators, conducting line clearance before operations, and planning manufacturing based on raw material availability. Your duties will include supervising the preparation and filtration of cleaning/disinfectant solutions, ensuring equipment readiness before batch manufacturing, and overseeing the operation and cleaning of various machinery and utilities. You will verify load cell handling, monitor non-viable particle count, record operation and cleaning details, and handle equipment like homogenizers, pH meters, and foggers. Furthermore, you will be involved in activities such as aseptic process stimulation, media fill cleaning, and sanitization, as well as general area cleaning and sanitization in grade C and D areas. You will also be responsible for data entry in the pharmacloud system, audit preparation and execution, periodic medical checkups, and reporting unsafe acts/conditions/incidents to supervisors. Overall, you will play a crucial role in ensuring the smooth functioning of manufacturing processes and maintaining high standards of cleanliness, documentation, and safety within the pharmaceutical production environment.,

A. Job Objective Monitor and review In Process quality control checks to meet the required quality compliance as per specifications. Strategic and planning Functional Core:- Review and provide decision based on the IQC sheet Online feedback to production for correction Daily plant round for ensuring compliance of SOPs, GDP, GMP guidelines etc. on the shop floor Refer ZMIC for special instruction during color change/ product change and guide the IQC operator for the same. Review the implementation of the same. Monitoring CAPA during shifts. Investigation of internal stranger/failure to identify the Root cause analysis and take corrective/preventive action for the same. Track instance of repeat failure from operators and take measures/set processes to avoid re-occurrence of the same and to ensure FTR. Line clearance of camera inspections, HCM, ATS, printing machines and Final Inspection System Ensuring document verification generated during shift on daily basis against defined standards Internal process Preparation of various reports Maintenance and verification of gauges to ensure proper calibration of these equipments on a regular basis in each shift Ensure verification of shade against master and Macbeth report Verification of daily profiles and online graphs Periodically conduct process, product and systems Audit. To provide data for annual product quality review & Participate in APQR and finalise the recommender's People development Ensure proper manning and shift handling, shift activities. Effective training to the operators with evaluation for compliance. Effective manning to utilization of available sources.

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 cleaning validation protocol. You will execute Commissioning, qualification, and validation activities for Pharma Process Equipments for API, Fill/Finish, and OSD. Additionally, you will review, analyze, and interpret system performance data, handle deviations/discrepancies, conduct investigations, CAPA, and ensure promotion of cGMP and regulatory compliance in assigned projects. Furthermore, you will exercise good judgment in selecting methods and techniques for obtaining solutions, maintain GDP, ALCOA practices, and have hands-on experience with Pharma Process Equipments. Drafting equipment operation SOPs will also be a part of your role. Qualifications & Other Requirements: - BS/MS in Engineering (Chemical, Pharma). - 4-10 years of experience in validation, quality systems, operations, engineering, or a combination thereof. - Experience in multiple GMP validation disciplines with advanced technical knowledge. - Knowledge of Validation Lifecycle approach, international regulatory requirements, and standards. - Experience with Documentum or Maximo is a plus. - Strong verbal and written communication skills, excellent organizational and time utilization skills. - Ability to work independently and within project teams. - Industry experience related to cGMP drug manufacturing, validation, and chemical process design. - Strong computer knowledge including Microsoft Office products.,

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 identify non-moving or expired materials. In addition, you will develop, review, and implement Standard Operating Procedures (SOPs) aligned with cGMP, GDP, and regulatory requirements, ensuring proper labelling, segregation, and documentation of materials for traceability and prevention of cross-contamination. Leading and mentoring warehouse staff to enhance compliance and continuous improvement will also be a key aspect of your role. Collaborating with various departments such as Quality Assurance, Quality Control, Procurement, Production Planning and Inventory Control, and Finance will be essential to streamline operations and resolve any discrepancies. Your expertise in SAP/ERP systems, knowledge of cGMP, GDP, and pharmaceutical warehousing regulations, along with strong leadership and communication skills, will be crucial for success in this role. Furthermore, you will be responsible for maintaining a safe and hygienic warehouse environment through monitoring cleaning, sanitization, and pest control measures, while ensuring compliance with Environmental, Health, and Safety (EHS) standards. Managing dispatch of finished goods, accurate preparation of dispatch-related documents, and handling rejected materials as per PPIC instructions will also fall under your purview. To qualify for this role, a Bachelor's degree in Pharmacy, Science, or a related field is required, with a Master's degree or MBA in Supply Chain Management being preferred. Proficiency in SAP/ERP systems for inventory and warehouse management, along with a deep understanding of cGMP, GDP, and pharmaceutical warehousing regulations will be necessary. Your strong leadership, communication, and interpersonal skills will be key assets in successfully fulfilling the responsibilities of this position.,

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.

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 initiatives Preferred candidate profile Basic knowledge of sterile/aseptic manufacturing / pharma production equipment Interest in plant maintenance Willingness to work in shifts & controlled environment Good documentation and communication skills Attention to detail and compliance mindset Good observations and analytical skiils

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, coordinate with interfacing functions, and provide feedback to production line WIP for batch cut off. Maintaining efficient line operation by ensuring the availability of all necessary materials, communicating rejection analysis, and following SOPs, cGMP, and regulatory guidelines are essential aspects of your job. Additionally, you will be responsible for communicating CAPA or complaints to associates, implementing continuous improvement actions, and optimizing the consumption of consumables. People development and training play a significant role in this position, including multi-skilling operators, conducting contract training, and interviews. You will also be expected to review shift documents, plan and provide training on GDP, and ensure associates attend training on GMP & DI policy. Key Result Areas for this role include OTDIF, PML, AFOE Despatch, % reduction of complaints in Printing, packing & Camera, number of print defects, and % compliance (safety, regulatory). You will interact with internal interfaces such as production and quality teams, as well as external interfaces including vendors and customers. Competencies required for this role include troubleshooting, knowledge of printing technology, printing and camera operations, problem-solving, camera inspection, GDP and GMP, and familiarity with various methodologies like 5S, Kaizen, and 7QC Tools. Your ability to demonstrate values such as caring, collaborative, and progressive during discussions will be evaluated as part of the selection process.,

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 creating production plans on a monthly and daily basis according to material availability. Handling tasks such as change control, deviations, CAPA, investigations, and document management including BMRs, BPRs, and master SOPs will be part of your duties. You will also be involved in the preparation, review, revision, control, and implementation of standard operating procedures within the sterile manufacturing department. Conducting line clearance activities before commencing various operations such as manufacturing, sterilization, and filling, as well as checking and maintaining records and logbooks related to manufacturing processes, garment washing, drying, and equipment sterilization are key aspects of your role. Additionally, you will be required to perform any activities as instructed by the HOD, provide training to subordinates, technicians, and operators, and stay updated on self-hygiene practices. Attending training sessions as per the schedule and ensuring compliance with the Training Need Identification (TNI) will also be part of your responsibilities. Qualifications required for this role include M.Sc., B.Pharm, or M.Pharm degree.,

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 alignment with the DOA (Delegation of Authority) and Organogram. Prepare, review, and circulate meeting minutes, status reports, and internal action trackers. Support project managers and engineering teams in compiling and submitting vendor quotations and costing back-ups for CC. Liaise with Finance, Sales, Procurement, and Design teams to ensure accurate and timely documentation handoff. Schedule and follow up on internal project review and budget meetings. Ensure that the latest Organogram versions and project responsibilities are tracked and applied. Assist in preparing TAW dashboards, presentations, and compliance summaries for Steering Committees. Maintain version control and archival of all TAW documents in structured formats (digital + hard copy). Required Skills & Qualifications • Bachelor's Degree in Engineering (Mechanical/ Electrical), Business Administration, or a related field. • Fresh Engineering Graduate or 1 to 3 years of experience is preferred in project coordination, documentation, or technical admin roles. • Strong understanding of technical project workflows, preferably in pharma, HVAC, cleanroom, or EPC environments. • Excellent written and verbal communication skills. • Proficient in MS Oice (Excel, Word, PowerPoint) and SAP/ERP tools. • High attention to detail, organizational discipline, and multi-tasking ability. • Familiarity with ISO/GMP/GDP documentation standards is an added advantage.

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.,

Role Overview Responsible for qualification & calibration activities for defined instruments and equipment as per schedule & procedures with QMS. Illustrative Responsibilities Ensure that qualification & calibration activities are planned and executed within time frame defined by the procedure and equipments are released on time as per the pre-defined schedule. Responsible for coordinating with lab supervisors / system owners for handling of any non-conformances or escalations Handling of QMS related activities like, Change control, CAPA and Deviation with its effectiveness check. Responsible for quality compliance activities for laboratory instruments qualification and calibration. Summarize, review, and report the analytical Instruments qualification and calibration for further approval. Ensure a disciplined work environment to provide expertise to subordinates colleagues in the proper performance of laboratory procedures. Ensure on time GDP in technical function with right first time (RFT) approach. Responsible for ensuring team compliance to EHS, Quality & Business policies Any other work given by management from time to time. Quality & Compliance Responsible for following GMP/GLP/ GDP/EHS policies by self as well as the team Required skills Technical expertise in Analytical instruments qualification, calibration, protocol preparation and QMS. Build cohesive team valuing team spirit Able to anticipate the implications and consequences of situations and take appropriate actions in the interest of Client as well as Cal Scientific without compromising quality. Clear thoughts and effective and crisp communication. Job requirement M.Sc specializing in Chemistry/ M. Pharma with proven experience of min. 8-10 yrs. in Instrument qualification and calibration. In depth experience in Chromatography (HPLC, UPLC, GC), Spectroscopy (MS, FTIR, UV), Thermal techniques (DSC, TGA) and Particle size measurements. Expertise in analytical instruments qualification and calibration, protocol preparation, CAPA, Investigations, Deviations (QMS) Good Knowledge of ICH guidelines and different global regulatory authorities. Job Location-Mulund

As a Senior Executive - Chemistry in the Quality Control department at Zydus Pfizer located in Ahmedabad, your role will require you to have a Bachelor's degree in Pharmacy or a Master's degree in Chemistry along with 2 to 4 years of relevant experience. Additionally, experience within Zydus for a minimum of 12 to 24 months is preferred. Your responsibilities will include hands-on experience with GMP/GLP/GDP/Data integrity ALCOA+ practices and the operation and calibration of various Wet chemistry techniques such as IR, UV, pH, KF, Polarimeter, and LPC. You will also be expected to handle operations, sample analysis, method validation, calibration, and troubleshooting of HPLC systems from Agilent and Shimadzu. Proficiency in basic computer applications like Word, Excel, and PowerPoint is essential for this role. In terms of behavioral skills, you should be self-motivated with basic problem-solving abilities. Your administrative skills should encompass being proactive, effective time management, and a collaborative approach towards working with team members. Excellent communication skills, both written and verbal, are crucial for this position to ensure seamless coordination within the team and across departments.,

Work location: Urse/Mann Pune warehouse Position - Officer/ Executive QA Experience: 5-7 years warehouse QA experience. JD: To perform quality inspection of finish product at warehouse end Monitoring of temperature sensitive products (Cold/Cool chain) Analytical/control sample collection & document verification of finish product & release in SAP system GDP/GSP inspection of warehouse. Imparting training to warehouse staff as per SOP’s. Monitoring of 100% inspection activity of finish product. If relevant and interested pls share your cv

We are currently seeking a Qualified Person (QP) to join a prominent pharmaceutical company situated in the Hertfordshire region. As the Qualified Person, you will play a crucial role in the organization by performing various responsibilities. Your primary duties will include conducting QP batch release activities, supporting the day-to-day functioning of the Quality Management System, and ensuring compliance with the QP Code of Practice and Eudralex Volume 4 GMP guidelines for QPs (Annex 16). Additionally, you will be responsible for undertaking routine product certification as a Qualified Person in alignment with relevant regulations and standards. Moreover, as a Qualified Person, you will contribute to the maintenance of GMP & GDP standards across all site operations. To excel in this role, you should possess a relevant degree in a scientific discipline, demonstrate proven industry experience in pharmaceutical quality assurance, and exhibit a solid understanding of GMP and GDP standards. Your expertise in these areas will be crucial in ensuring regulatory compliance and upholding quality standards within the organization. In conclusion, this position offers an exciting opportunity for a Qualified Person to make a significant impact within a leading pharmaceutical company. If you meet the specified requirements and are keen to advance your career in the STEM sectors, we encourage you to apply for this role at the earliest opportunity.,

Walk-in at Matoda Were currently recruiting for multiple positions at our SANAND manufacturing facility. If any role aligns with your experience, please bring your updated resume and walk in during the scheduled drive. Please find our current job requirements and venue details mentioned. Requirement : Injectable Manufacturing & Visual Inspection Aseptic operations/ QMS / SKID / Multi-vessel / SVP / Visual Inspector (Senior Officer / Officer / Associate) Experience - 01 to 05 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI Time and Venue : 12th June 2025, 09:30 Hrs to 14:00 Hrs SATURDAY ______________________________________________________ INTAS, Matoda facility Plot No. 457, 458 Sarkhej Bavla Highway, Matoda Village, Sanand, Taluka, Ahmedabad, Gujarat 382210 ______________________________________________________ We would be pleased if you forward or refer any of your colleagues matching the desired job roles. *Having relevant qualification only can attend the scheduled walk-in.