160 Gdp Jobs - Page 3

Hiring - ADL (AMD) - Nagpur Location Location - Nagpur MH Company - Pharma (MNC) Core OSD Formulation + Method Validation Experience Msc or Mpharm /bpharma Responsibility - Sr. Role Description 1. Analytical Method Development New analytical method development and troubleshooting of existing method of different types of Oral solids dosage form (Granules, Tablets, Pellets, Capsules etc.) for Regulated market projects or as per business need. 1. Ensure robust & cost effective method development of product by considering the available facility & resources 2. Conduct Literature survey, different pharmacopoeia & pharmacopeia forum search and review & application of same in AMD. 3. Conduct Pre-formulation studies (API characterization and Drug-Excipients compatibility studies). 4. Operation and calibration of different analytical instruments. 5. Take into account existing QC facility while developing any product for successful method transfer. 6. Analytical method validation and method transfer activity. 7. Maintain the Good Laboratory practices, Good Documentation practice and Good hygiene practices. 8. Prepare for all type of internal and external audit/inspection. 2. Stability Studies of R&D Products 1. Responsible for stability studies of new R & D products for Regulated market projects. 2. Responsible for interpretation of stability data of the products related to analytical methods. 3. Observations of stability trend and discussion of same with formulation team. 4. Management of stability batches analysis and take the decision for stability studies of different batches as per requirement. 3. Routine Support to F&D Team 1. Responsible for providing routine support for the new product development for regulated market projects. 2. Planning and execution of routine batches analysis in minimum possible time. 3. Analytical data review and to provide the online results and observations to F&D Team. 4. GLP, GDP and Documentation Support 1. Responsible for maintaining the overall GLP and GDP in the Laboratory and providing overall GLP support during day to day activities. 2. Maintenance of working standards, Impurities and reference standards 3. Responsible for preparation, review and approvals of all the documents generating in the ARDL laboratory. 5. Team Building 1. Ensure continuous training and up-gradation of knowledge of the R&D team so that they are at the cutting edge of technology. 2. Set challenging goals for team members to ensure they deliver as per their true potential & as per the need of organization. 3. Identify & nurture the top talent of team. 4. Arrange a monthly interaction with team members to understand & resolve their performance bottle necks & also give them feedback for course correction. Performing any other responsibility as per the requirement, in the larger interest of organization. Interested!!!Please share your cv at Neetij@selectsourceintl.com Thanks & Regards

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, teamwork, data analysis, inductive reasoning and root cause analysis skills are required.

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 manufacturing partners for handling market and sample-related complaints. Perform joint analysis of complaint samples in collaboration with manufacturers to identify root causes. Maintain strict adherence to Good Documentation Practices (GDP). Possess sound knowledge of Schedule M, USFDA, MHRA and ensure compliance in relevant activities. Sound knowledge of IPQA (In-Process Quality Assurance) activities across different dosage forms (e.g., tablets, capsules, syrups, ointments, etc.) Sound knowledge of different types of SOPS (Standard Operating Procedures), including preparation, review, implementation, and compliance monitoring. Basic understanding of QMS (Quality Management System), including its elements and relevance in pharmaceutical operations.

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 manufacturing partners for handling market and sample-related complaints. Perform joint analysis of complaint samples in collaboration with manufacturers to identify root causes. Maintain strict adherence to Good Documentation Practices (GDP). Possess sound knowledge of Schedule M, USFDA, MHRA and ensure compliance in relevant activities. Sound knowledge of IPQA (In-Process Quality Assurance) activities across different dosage forms (e.g., tablets, capsules, syrups, ointments, etc.) Sound knowledge of different types of SOPS (Standard Operating Procedures), including preparation, review, implementation, and compliance monitoring. Basic understanding of QMS (Quality Management System), including its elements and relevance in pharmaceutical operations.

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

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 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.,

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.

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 Guidewire Data and Analytics team to enable predictable project outcomes and emerge as a leader in our thriving data practice. One of our principles is to have fun while we deliver, so this role will need to keep the delivery process fun and engaging for the team in collaboration with the broader organization. Given the dynamic nature of the work in the Data and Analytics team, we are looking for decisive, highly-skilled technical problem solvers who are self-motivated and take proactive actions for the benefit of our customers and ensure that they succeed in their journey to Guidewire Cloud Platform. You will collaborate closely with teams located around the world and adhere to our core values Integrity, Collegiality, and Rationality. Key Responsibilities: Build out technical processes from specifications provided in High Level Design and data specifications documents. Integrate test and validation processes and methods into every step of the development process Work with Lead Architects and provide inputs into defining user stories, scope, acceptance criteria and estimates. Systematic problem-solving approach, coupled with a sense of ownership and drive Ability to work independently in a fast-paced Agile environment Actively contribute to the knowledge base from every project you are assigned to. Qualifications: Bachelors or Master’s Degree in Computer Science, or equivalent level of demonstrable professional competency, and 3 - 5 years + in a technical capacity building out complex ETL Data Integration frameworks. 3+ years of Experience with data processing and ETL (Extract, Transform, Load) and ELT (Extract, Load, and Transform) concepts. Experience with ADF or AWS Glue, Spark/Scala, GDP, CDC, ETL Data Integration, Experience working with relational and/or NoSQL databases Experience working with different cloud platforms (such as AWS, Azure, Snowflake, Google Cloud, etc.) Ability to work independently and within a team. Nice to have: Insurance industry experience Experience with ADF or AWS Glue Experience with the Azure data factory, Spark/Scala Experience with the Guidewire Data Platform.

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