1426 Gc Jobs - Page 7

Company Description At TAPI, we're not just a companywe're a community committed to advancing health from the core. As the world's leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we're shaping the future of health worldwide. Our strength lies in our peoplea team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that t...

Job Description Summary Come Join Our Software Integration Team!! Our main activity consists in setting up GE Vernova software in different environments for internal and external customers, supporting project activities and providing expertise in tailoring the components based on requirements. We have a hybrid work environment as we work from home, the office and travel to customer sites as needed. The integration engineer is a key member in all projects, being engaged throughout the full lifecycle (Development, Factory Acceptance Tests, Site Acceptance Tests, Cutover, Support). GE Vernova allows us to bring a significant contribution to the Worldwide Electrical Energy context. Delivering on...

HPLC, GC, UV, Polarimeter, Karl Fisher, Raw Material, Inprocess material and Finished Product Testing. Having good knowledge of GMP and GLP.

Role Overview: As a Chemical Testing Analyst at the company, your primary responsibility will be reviewing and conducting chemical testing of various products, including raw materials, finished products, cosmetics, Ayurveda, Sidha & Unani products. You will play a crucial role in ensuring the accuracy of test results entered into the LIMS software. Furthermore, you will be tasked with handling advanced instruments such as HPLC, GC, FTIR, Dissolution, etc. Another significant aspect of your role will involve preparing technical documentation that adheres to FDA, CDSCO, and Ayush standards for audits. Key Responsibilities: - Review and conduct chemical testing of raw materials, finished produc...

As a 2024 batch MSc. (Chemistry) candidate interested in pursuing a career in Quality Control (QC) within a pharmaceutical Active Pharmaceutical Ingredients (API) manufacturing company situated in the Attibele Industrial Area near Hotel Ramee Guestline in Hosur, Tamil Nadu, you are encouraged to apply for the following opportunity. Role Overview: You will be expected to work in rotational shifts, making male candidates preferred for this role. Your responsibilities will include operating various equipment such as HPLC, GC, TLC, and conducting titrations. Strong English communication skills are a must-have requirement for this position. Key Responsibilities: - Perform quality control tests us...

As a Review Analyst at Piramal Pharma Solutions (PPS) located in Digwal, your role will involve reviewing analytical reports and handling investigation incidents. You will be responsible for the following key responsibilities: - Review in-process analytical data before release - Review intermediates, stability batches, and finished products analytical data - Knowledge on analytical method validations and method transfers - Review system audit trails for all types of instruments in QC - Review calibration data of instruments on a daily basis - Verify SOPs compliance on the shop floor - Conduct audits for laboratory system compliances as required - Investigate incidents, OOS, OOT, and root cau...

Job Title: Senior Business Development Manager (IT Consulting & Staffing Services) Employment Type: Full-time About the Role We are seeking a highly driven Senior Business Development Manager (BDM) with a strong background in IT Consulting and Staffing Services sales. This role is designed for a true sales hunter who thrives on building new client relationships, acquiring new logos, and generating revenue growth. The ideal candidate will bring a proven track record of exceeding sales targets, a stable career history, and the ability to work independently while partnering effectively with delivery teams. Key Responsibilities Develop and execute strategies to acquire new clients and expand mar...

Hands on experience in HPLC/GC including method development, routine analysis and method validations along with good documentation practices. Responsible to perform the Analytical method validation, method verification and method transfer activities.

Job Description Summary Come Join Our Software Integration Team!! Our main activity consists in setting up GE Vernova software in different environments for internal and external customers, supporting project activities and providing expertise in tailoring the components based on requirements. We have a hybrid work environment as we work from home, the office and travel to customer sites as needed. The integration engineer is a key member in all projects, being engaged throughout the full lifecycle (Development, Factory Acceptance Tests, Site Acceptance Tests, Cutover, Support). Job Description GE Vernova allows us to bring a significant contribution to the Worldwide Electrical Energy contex...

Description: We are seeking a highly skilled and experienced Senior Simulation Engineer to join our team. In this role, you will be responsible for conducting advanced thermal, power integrity, and mechanical vibration simulations for Printed Circuit Boards (PCBs) and electronic systems. Requirements: We are seeking a highly skilled and experienced Senior Simulation Engineer to join our team. In this role, you will be responsible for conducting advanced thermal, power integrity, and mechanical vibration simulations for Printed Circuit Boards (PCBs) and electronic systems. 4+ years of work experience in the following areas: Ansys PCB thermal simulation PCB power density analysis Mechanical vi...

Position : Executive - Quality Education: M. Sc (Chemistry, Industrial Chemistry) Experience: Minimum 5 - 7 years of experience in QA of Polymer/Chemical plant. Job Location: Dahej Role & responsibilities: A. Purpose /Role of the job /: Describe in 1 phrase what contribution the job is expected to Make to the organisations objectives Quality Assurance of Finished Goods (SAN/ABS/ASA/PS) through inspection & testing of RMs, Additives, Packing bags, In-process intermediates, Final Product and Utilities/WWTP in shifts. Analysis of internal rejections and customer complaints to recommend preventive and corrective actions. B. Environment/Context/Complexity of the job: Describe the most important i...

Gaining an understanding of the client's needs and requirements and communicating them and the quality standards to the production teams. Devising ways to improve the manufacturing process to ensure higher-quality goods. Required Candidate profile Strong attention to detail, observation, organizational, and leadership skills. Knowledge of quality control procedures and legal standards. Good technical and IT skills. Perks and benefits Bonuses Flexible Work Arrangements Paid Time Off

Job Description At Publicis Sapient, we re at the forefront of revolutionizing the future of product engineering with state-of-the-art, scalable innovations If you re Associate Software Development Engineer seeking your next transformative challenge, we have an incredible opportunity for you: Our team utilizes advanced artificial intelligence and machine learning methodologies to design and implement intelligent, adaptive solutions that tackle complex real-world challenges, Your Impact: You will work in the spirit of agile & a product engineering mindset delivering the sprint outcomes, iteratively & incrementally, following the agile ceremonies Youre expected to write clean, modular, product...

You will be responsible for conducting WET, GC, and HPLC analysis as an Expert in the field. Your role will involve ensuring compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), Good Documentation Practices (GDP), and ALCOA+ guidelines. Key Responsibilities: - Conduct WET, GC, and HPLC analysis - Ensure compliance with GMP, GLP, GDP, and ALCOA+ guidelines Qualification Required: - M.Sc. in Chemistry - 3 to 5 years of experience - Good knowledge of GMP, GLP, GDP, ALCOA+ - Expertise in WET, GC, HPLC Analysis,

Roles and Responsibility Enterprise Architect with atleast 12+yrs exp with non-compromising Integration experience Java, RESTful APIs, Sprint Boot, Micro Services Lead PSR initiatives to enhance system efficiency and resiliency. Optimize Java applications for low latency, high throughput, and minimal resource consumption. Implement distributed microservices, ensure fault tolerance, reliability engineering best practices. Drive cloud migration strategies using AWS/Azure/GCP and serverless architectures. Architect and design high-performance, Java-based enterprise solutions Core Java & Backend Development: Java 8/11/17, Spring Boot, Spring Cloud, Microservices Architecture. RESTful APIs, Graph...

Role & responsibilities Handle end-to-end recruitment from understanding client requirements to candidate onboarding. Source qualified candidates using job boards such as Dice, Monster, CareerBuilder, LinkedIn, Indeed , and through networking or referrals. Screen and evaluate candidates based on technical skills, experience, and cultural fit. Negotiate salary rates, employment terms, and finalize job offers. Work closely with Account Managers and Delivery Leads to ensure timely submissions and successful placements. Maintain strong relationships with candidates for future opportunities. Ensure accurate documentation and compliance with US employment and visa regulations . Update and manage a...

As a Senior Executive QC in the Pharma and Herbal industry, you will be responsible for managing the QC laboratory and ensuring compliance with cGMP and GLP requirements. Your role will involve supervising QC analysts to maintain seamless laboratory operations and overseeing the testing of incoming raw materials, bulk, semi-finished, and finished products. You must have a minimum of 5-8 years of experience and demonstrate proficiency in operating HPLC, GC, UV, and other instruments used in QC analysis. Key Responsibilities: - Manage the QC laboratory in compliance with cGMP and GLP requirements - Supervise QC analysts to ensure seamless laboratory operations - Oversee regular testing of inco...

You will be joining Piramal Critical Care (PCC), a subsidiary of Piramal Enterprises Limited, as a Quality Control professional. PCC is a global player in hospital generics and the third largest producer of Inhaled Anaesthetics. Your role will be crucial in ensuring the quality and safety of the products manufactured by PCC for patients and healthcare providers worldwide. **Key Responsibilities:** - Conduct quality control tests on raw materials, intermediates, and finished products to ensure compliance with regulatory standards. - Perform analytical testing using techniques such as HPLC, GC, IR, and UV-Vis spectroscopy. - Document and report test results accurately, maintaining detailed rec...

As a Quality Chemist at the Water Treatment Plant (WTP) and Effluent Treatment Plant (ETP) team, your role will involve ensuring the quality of chemical processes and compliance with environmental standards. You will have the opportunity to contribute to the improvement of processes and resolution of quality issues. **Key Responsibilities:** - Conduct quality control tests on water treatment and effluent treatment processes. - Analyze chemical samples and interpret results to ensure compliance with standards. - Prepare reports and documentation on quality testing and findings. - Collaborate with engineering and production teams to improve processes and resolve quality issues. - Maintain labo...

You are required for a (Lab Analysis) residue lab with the following technical knowledge: - Proficiency in HPLC, GC, LC-MS, GC-MS, ICP-OES, and Instruments Handling. - Completing working tasks and reporting to the department head. - Coordinating with Lab chemists. Qualifications required: - B.Sc or M.Sc in Analytical Chemistry or M.Sc in Biochemistry. You will be working in the Animal Feed / Food industry with 4 to 8 years of experience. The salary offered is attractive and will be based on your experience. An age requirement is set above 25 years. The work location is in Nanjai Uthukuli, Erode. Your point of contact for this job position is K.Rajendran AGM HR (hr@skmpornafoods.com) with con...

Hiring for Fresher Bench Sales Recruiter and US IT Recruiter Location: ECIL, Hyderabad Exp: Freshers - (On-site) (Night shifts) Qualification: Any Graduation Notice Period: Immediate Job Description : * Must have good communication skills. * Willing to work for night shifts. * Candidate with good percentage in their graduation is required. ***Note : 1. Freshers you will have bond of 1.5 years and need to submit 10th original certificate on joining day. 2. Graduation is must, You need to have graduation results. 3. There is no Cab facility but food will be provided in office itself.

New Chemical Entity- Design & Development (Research & Development) 1. Design & Discover NCE molecules a. Literature search and design route of synthesis b. To help in designing patentable structures of pharmacophore (prodrug design) c. IPR clearance d. Design routes of synthesis e. Synthesis of NCE’s molecules to generate library 2. Synthesis process development and validation a. Development of non-infringing rout of synthesis for lead compound b. Feasibility study c. To finalize the route of synthesis. d. Experiment design according to final route of synthesis e. Development and optimization of synthesis process f. Process Validation 3. Interpretation of analytical data (HPLC, GC, SOR, etc)...

Role & responsibilities Job Title: Quality Control / Quality Assurance Executive (Fresher) Industry: Pharmaceuticals Manufacturing Department: Quality Control (QC) / Quality Assurance (QA) Company: Vivek Pharmaceuticals Pvt Ltd Location: Jammu Employment Type: Full Time Experience: 0 2 Years Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc (Chemistry, Microbiology, Biotechnology or related field) Job Summary: We are looking for passionate and detail-oriented candidates to join our Quality team. The selected candidates will be part of controlling product quality, compliance with regulatory requirements, and in all quality operations. Key Responsibilities: Quality Control (QC): Conduct routine t...

Role & responsibilities Complete Analysis of various raw materials, In-process, Drug substance and finished Products in line with Pharmacopeia method and in-house Specification and test procedures. Change Control, Deviation, Root Cause investigation, CAPA, OOS, OOT, Incidence Calibration of Instruments HPLC , UV-Visible Spectrophotometer, pH Meter,KF Titrator, weight balance. Working standard preparation as per SOP. Ensure the timely analysis of samples GLP, GMP, GDocP (With respect to Regulatory Guidelines) Function in details of various Section of QC/QA(Eg.Raw Material, Finished Product,Stability Study etc. Data Integrity 21 CFR Part 11 Qualification, Calibration, Validation. Maintaining t...

Role Overview: As a Lab Chemist at the phenolic resin plant, you will be responsible for conducting quality control tests, analyzing raw materials, monitoring product consistency, and ensuring compliance with industry standards. Your role will involve performing analytical testing, troubleshooting quality deviations, maintaining lab equipment, and supporting production with process optimizations. Key Responsibilities: - Conduct quality control tests to ensure product consistency - Analyze raw materials and finished products using analytical techniques such as FTIR, GC, HPLC, titration, and viscometry - Troubleshoot quality deviations and implement corrective actions - Maintain lab equipment ...