2096 Hplc Jobs - Page 10

The ideal candidate will be responsible for method development and validation, as well as routine and stability analysis utilising a variety of analytical techniques, including HPLC, GC, Dissolution testing, and Karl Fischer titration.

Job Track Description: Requires relevant expertise in a professional, sales, or technical area through formal education. Performs technical-based activities. Contributes to and manages projects. Uses deductive reasoning to solve problems and make recommendations. Interfaces with and influences key stakeholders. Leverages previous knowledge and expertise to achieve results with teams and can complete work self-guided. College or university degree required. General Profile Requires knowledge and experience in own field. Will acquire on-the-job knowledge and skills. Develops an understanding of the company, processes, and customers. Uses existing procedures to solve routine or standard problems. Receives moderate guidance and direction from others. Functional Knowledge Requires expanded conceptual understanding of theories, practices, and procedures. Business Expertise Uses an understanding of key business drivers to accomplish work. Impact Impacts team through quality of service and information provided. Follows standardized procedures and practices to achieve objectives and meet deadlines. Leadership No supervisory responsibilities. Provides informal guidance to new team members. Problem Solving Uses existing procedures and technical experience to solve problems. Interpersonal Skills Exchanges complex information and ideas effectively. Responsibility Statements Tracks and reports business-critical project and people metrics for client operations. Finalizes the intercompany reconciliation process. Liaises with AP and the business. Prepares monthly and quarterly balance justifications and documentation. Prepares customized reports and dashboards. Keeps updated data readily available for presentations or reporting. Performs other duties as assigned. Complies with all policies and standards.

The role in Pharma Solution's Quality Control department based in Lexington requires you to perform complex testing of raw materials, in-process and finished products while ensuring the calibration and maintenance of analytical instruments in compliance with cGMP standards. This night shift position directly reports to the AQC Group Lead. Your key responsibilities will include conducting routine/non-routine testing using wet chemistry and instrumental analysis methods, testing various samples such as raw materials, APIs, finished products, stability samples, and cleaning verification samples. Proficiency in HPLC/GC analysis is essential along with documenting laboratory work following GDP, cGMPs, and SOPs. Troubleshooting, calibrating, and maintaining instruments, preparing laboratory reagents, and writing SOPs and reports are also part of your duties. You will be required to initiate and resolve laboratory investigations, train entry-level QC personnel, and ensure compliance with safety procedures and regulations. To qualify for this role, you should hold a Bachelor of Science in Chemistry, Pharmaceutical Science, or a related field, with a minimum of 3+ years of hands-on experience in quality control within a laboratory setting. Proficiency in HPLC/GC analysis, previous experience working with cGMP guidelines, and familiarity with potent materials and parenteral drug products are preferred. You must demonstrate a high level of proficiency in operating Microsoft Office applications, possess excellent communication skills, attention to detail, and organizational abilities. Being able to work effectively in a team environment, along with problem-solving and interpersonal skills, is crucial. Following written instructions and maintaining an organized laboratory are key aspects of this role. Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) providing end-to-end solutions for drug development and manufacturing. The company operates globally with facilities in North America, Europe, and Asia, offering services including drug discovery, pharmaceutical development, clinical trial supplies, and commercial API supply. PPS specializes in highly potent APIs, antibody-drug conjugations, sterile fill/finish, and biologic development and manufacturing services. This is a full-time position with job identification 7804 in the Analytical QC category, posted on 02/26/2025. The location is 1500 BULL LEA ROAD, Lexington, KY, 40511, US.,

B.Sc. or M.sc Diploma Pharmacy Fresher & Exp Location :Surat / Navsari / Bharuch / Ahmedabad Salary : 15000 to 35000 Chemical handling and disposal Analyze retrieved data and prepare reports for laboratory management HETAL : 90816 99400 Required Candidate profile Lab work to develop and improve both new and existing chemical product Assist with testing and calibrating lab equipment in preparation for specific tasks Maintaining lab and operating lab equipment

B.Sc. or M.sc Chemist / Chemical / MIcro. Location :Surat / Navsari / Bharuch / Ahmedabad/ Vadodara Salary : 15000 to 25000 Living + Travel Free Chemical handling and disposal Analyze retrieved data and prepare reports for laboratory management Required Candidate profile Lab work to develop and improve both new and existing chemical product Mo No : +91 90816 99400 / +91 90816 88100 / 90816 99600

Looking for a skilled Quality Control Analyst to join our team in Bangalore. The ideal candidate will have 3-5 years of experience in coding and quality control, with a strong background in healthcare management services. Roles and Responsibility Monitor and evaluate the quality of coding processes to ensure compliance with industry standards. Develop and implement quality control procedures to identify areas for improvement. Collaborate with cross-functional teams to resolve quality-related issues and enhance overall process efficiency. Analyze data and trends to identify opportunities for quality improvement and optimize processes. Develop and maintain quality control documentation and reports. Ensure all quality control activities align with organizational goals and objectives. Job Requirements Minimum 3 years of experience in coding and quality control, preferably in healthcare management services. Strong knowledge of quality control principles and practices, including Six Sigma and Lean methodologies. Experience with coding systems and software, such as Epic Systems or Cerner. Excellent analytical and problem-solving skills, with attention to detail and the ability to interpret complex data. Strong communication and collaboration skills, with the ability to work effectively with cross-functional teams. Ability to work in a fast-paced environment and adapt to changing priorities and deadlines.

B.Sc. or M.sc Chemist / Chemical / MIcro. Location :Surat / Navsari / Bharuch / Ahmedabad/ Vadodara Salary : 15000 to 25000 Living + Travel Free Chemical handling and disposal Analyze retrieved data and prepare reports for laboratory management Required Candidate profile Lab work to develop and improve both new and existing chemical product Mo No : +91 90816 99400 / +91 90816 88100 / 90816 99600

JOB DESCRIPTION Job Title: Instrumentation Engineer Job Location: Syngene International Limited, Bengaluru About Syngene: Syngene ( www. syngeneintl. com ) is an innovation- led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self. Compliance to Syngene s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Core Purpose of the Role: This is an exciting opportunity to play a role in the Quality control department of Syngene. The role will provide several responsibilities of Instrument management, Breakdowns, Preventive maintenance, documentation, Lab safety requirements, Compliance as per Syngene policy and EHSS requirement. It provides an opportunity to handle overall instrument management activities. Role Accountabilities Coordinate with vendors/service engineers for scheduled preventive maintenance, calibration activities and breakdown resolution Address and resolve all types of instrument- related issues and queries. Support and maintenance of all Chromeleon client systems. Regularly review firmware and ICF driver versions and participate in version upgrade migrations. Collaborate with IT, infrastructure, and database teams to resolve third- party application issues. Involve in the installation and qualification activities of analytical instruments. Initiation and closure of Change control, CAPA, Deviation, LIR in the Trackwise system. Handling of the labware LIMS application for the Work process initiation, Review and approval of analytical activities. Involve in work allocation of the calibration activities to team in LIMS. Preparation of calibration and Preventive maintenance schedule for the instruments. Coordinate with E&M and IT teams for maintenance and software- related issues. Any other job allocated by Head QC / Group Leader /Section Head. Adherence to Good Laboratory Practice and Good documentation practices. Individuals working in the GMP environment are responsible for documenting/record the activities contemporaneously and accurately as per Good documentation practices. Handling of LMS, LIMS, ELN, TrackWise and EDMS Softwares for routine activities as applicable. Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience Demonstrated Capability Education Experience: 6- 9 years Skills and Capabilities Expertise in handling breakdowns, preventive maintenance and qualification activities of laboratory Instruments/ equipment like HPLC, GC, Dissolution tester, KF Autotitrator, coulometer etc. Capable of thinking scientifically to address complex problems and develop solutions. Work as a team and have a collaborative mindset. Good communication skills. Education: MSC/ B. tech Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

To perform analysis of finished Products and in-process samples. Proficiency in using analytical instruments such as UV/VISIBLE and IR, HPLC Handling of laboratory incidents and deviation. Extensive knowledge of GMP regulations in cGMP Manufacturing Environment. Chemical and Instrumental analysis of In process and finished products. To perform analysis of stability samples. To perform the calibration of instruments like HPLC, Dissolution tester, UV Spectrophotometer. Analysis of OOS/OOT

Role & responsibilities Method development : HPLC/GC Stability study Wet chemistry analysis (UV, IR, SOR, Titration...etc) Reaction monitor Routine support GLP awareness

We are looking for skilled Analysts with expertise in HPLC and GC techniques for immediate joining. The candidate will conduct analytical testing to ensure pharmaceutical product quality, develop and validate analytical methods, and contribute to continuous laboratory improvement initiatives. Key Responsibilities: Perform analytical testing using HPLC, GC, UV-Vis, ICP-MS, and LC-MS techniques to assess product quality and purity. Develop, validate, and optimize analytical methods in compliance with cGMP guidelines. Collaborate with cross-functional teams to troubleshoot and resolve method validation and analytical issues. Maintain detailed and accurate records of test results, instrument calibrations, and maintenance schedules. Participate in continuous improvement projects to enhance laboratory efficiency and accuracy. Required Qualifications: Bachelors degree in Pharmacy (B.Pharma) or equivalent. Postgraduate qualifications such as M.Pharma, MS/M.Sc in Pharmacology, Food Technology, Biotechnology, Biochemistry, Biology, or Microbiology are preferred. 2-7 years of relevant experience in pharmaceutical analytical laboratories. Strong knowledge and hands-on experience with HPLC, GC, UV-Vis, ICP-MS, and LC-MS instruments. Familiarity with cGMP guidelines and pharmaceutical quality standards. Excellent documentation and analytical skills. Preferred Skills: Experience in method development and validation. Good understanding of pharmaceutical regulatory requirements. Ability to work effectively in a team-oriented environment.

Job Summary: The Lab Technician is responsible for performing routine and specialized laboratory tests, preparing samples, maintaining lab equipment, and ensuring the accuracy and reliability of test results. This role supports research, development, quality control, or clinical analysis activities within the laboratory. Key Responsibilities: Collect, prepare, and analyze samples according to standard operating procedures (SOPs). Perform routine laboratory tests and record results accurately. Calibrate, maintain, and clean laboratory equipment and instruments. Maintain laboratory inventory, including reagents, supplies, and equipment. Ensure adherence to safety protocols and maintain a clean and organized workspace. Assist in documenting test procedures and results for reports. Troubleshoot and report any technical issues or discrepancies. Support research and development projects by providing technical assistance. Follow quality control and quality assurance procedures to maintain lab standards. Comply with all relevant regulatory and safety standards.

Roles and Responsibilities: Develop analytical methods for biochemistry samples using GC-MS, LCMS, and other relevant techniques. Conduct method validation, optimization, and transfer to ensure accuracy and reliability of results. Collaborate with cross-functional teams to resolve method-related issues and improve overall efficiency. Maintain accurate records of experiments, data analysis, and reporting in accordance with regulatory requirements. Stay up-to-date with industry developments in mass spectrometry technologies and apply this knowledge to improve laboratory operations. Desired Candidate Profile: 2-7 years of experience in Analytical Method Development & Validation (GC-MS & LCMS). MS/M.Sc(Science) degree in Bio-Chemistry or Chemistry from a recognized university. Strong understanding of chromatography principles, including HPLC/UPLC systems. Proficiency in developing analytical methods for biochemistry samples using various instruments such as GC-MS/MS.

Should have 1-2 Years of experience in Quality Control department

JOB DESCRIPTION Designation: Method validation Expert Job Location: Bangalore Department: Analytical Method Validation and Special Instrumentation About Syngene About Syngene At Syngene, Safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and sops, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements always in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards always Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Planning and allocation of Routine and non-routine activities for the entire team member. Investigation of QMS Elements and Report Generation, Approval and co-ordination with QA and Maintaining a QMS/TAT/TPA matrix. Key Responsibilities: Planning and allocation of Routine and non-routine activities for the entire team member. Interaction with production, ADL, R&D, QA and other department for QC related functions. Interaction with client and Project team for the smooth functioning of project related activities. To review the In-process, cleaning, intermediate and finished product specification. Initiate the change control and taking approval from analytical QA. Planning and allocation of Documentation preparation. Review of routine/non-routine validation reports. Review of method verification and method validation protocol. Review of standard qualification protocol forced degradation protocol and method transfer protocol. Ensuring, verifying and reviewing the instrument usage log periodically and accordingly checking the labels as per SOP. To maintain the sampling packing area Investigate and close for planned and unplanned deviations. Review of Certificate of analysis. Approval of specification of Non-technical batches. Responsible for Ensuring that the Good Laboratories Practices are followed while working in QC Laboratory. Responsible for Ensuring the Use of required safety apparels while sampling, analysis and working in Laboratory. Responsible for taking any other job allocated by Head of the Department. To ensure safety compliance as per Syngene policy and EHSS requirements. Educational Qualification: M Sc / M Pharma (Analytical/General chemistry) Technical/Functional Skills: Should be well versed with the latest analytical techniques like HPLC/GC, KF/KFC, IR/UV, LC-MS, GC-MS, IC, ICP-OES/ICP-MS, DSC, TGA, etc. . . Being well-versed in the Chromeleon data management application and LIMS will be advantageous. Experience: 9 - 12 years Behavioural Skills: Should be an adaptive learner. Should demonstrate effective Communication skills. Organization and ability to balance work and Life. Should possess good Time Management abilities. Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status about public assistance, veteran status, or any other characteristic protected by applicable legislation or local law.

Role & responsibilities Solid Oral - Production & Packing Officer - Executive and Plant Operator - Technical Assistant : Tablet/ Capsule - Granulation, Compression, Coating, Inspection, Capsule Filling and Wurster coater. Tablet/ Capsule - Blister Line (BQS), CVC Bottle Line Warehouse (Supervisor / Machine Operator): Officer Senior Executive and Plant Operator - Technical Assistant: RM, PM, FG, Dispensing, Dispatch , Documentation Engineering Executive/Sr. Executive: Process Equipment (Mechanical/Electrical/Instrumentation) of OSD Plant like preventive maintenance and breakdown related activities of equipment of OSD plant such as FBD, FBP, RMG, coating, compression, capsule, Packing machine etc. Technician: Process equipment's- Fitter/Electrician/ Instrumentation: Handling preventive maintenance and breakdown of equipment of OSD Plant such as FBD, FBP, RMG, coating, compression, capsule, sifter, stirrer, Wurster coater, packing machine etc. HVAC Operator - Operation and maintenance of AHU, Cooling tower, BMS, Chiller Quality Assurance (IPQA) Officer / Senior Executive: IPQA in process (Mfg. and Pkg.) Quality Control (Analyst) Officer / Sr. Executive: HPLC / GC / IR / UV / Dissolution and other QC Equipment/ QC Method Validation and Transfer.

Responsibilities: * Conduct chemical research in life sciences industry using chromatography techniques. * Develop new products through R&D processes with focus on liquid chromatography methods. Over time allowance Provident fund

You will be responsible for maintaining quality results, ensuring regulatory compliance, and improving existing systems to prevent non-conformance. This includes operating, calibrating, and maintaining various instruments such as HPLC, Dissolution, Analytical Balance, UV Spectrophotometer, Viscometer, GC, etc. You will also be required to record and maintain online entries in the instrument usage log book and follow good laboratory and documentation practices. Your responsibilities will also include performing analysis as per test request forms, following correct test procedures for analytical validations/verifications, routine analysis, and stability studies. Basic knowledge of method development and validation, as well as experience in drug product analysis, will be advantageous. To be considered for this role, you should have an M.Sc. in Organic/Analytical Chemistry and be able to join as soon as possible. A good technical knowledge and understanding of the mentioned instruments and procedures will be required to excel in this position. If you meet the qualifications and are looking to contribute to a dynamic team focused on maintaining high quality and compliance standards, we encourage you to drop your resume at recruitment@cironpharma.com or contact (EXT-250).,

To Strengthening our QA/QC Team, we are looking for young, intelligent, dynamic, energetic & highly motivated person believing in long term professional relation for the post of QA/QC - Chemist for our factory location at Dahej GIDC, Dist: Bharuch in Gujarat. Job Profile:- QA/QC Chemist (0-2 Years) - B.Sc / M.Sc Ensure products meet customer expectations and demand. Awareness about the standard operating procedure of QC department. Update and maintain inspection and quality records and databases to monitor and document compliance with company standards. Root Cause Analysis, Problem solving Techniques. Knowledge of ISO - QMS - Environment & Safety. Execute audits of work processes and measure quality data for review to ensure finished product complies with quality standards prior to shipment. Manage inventory, create lot numbers, and ensure all products have proper documentation Inspection of dispatch of finished product and preparation of certificate of analysis. Solution preparation and its normality determination. Good instrument handling and calibrations knowledge like HPLC, GC, GPC, Viscometer etc. Sampling and analysis of raw material, Finished product and in-process sample and reporting. Manage during the production product mole ratio and quality of work and products.

WALK IN Interview - SUNDAY 7th Sep 2025 - Quality Control - Unison Pharmaceuticals Pvt Ltd Ahmedabad About us : Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality and affordable medicines across the nation. With more than 4 decades of medical service to society, Unison is today one of the fastest-growing companies in Gujarat State. In addition to this, the company is ranked 82 among the top companies of India (Rupee wise sales) MAT March 2020. This makes Unison a distinguished company across the pharma industry. We are expanding!! You are invited to join one of the fastest growing pharma companies in India!! Department: Quality Control Section: HPLC Analysis & Chemical Analysis/ QC QMS Experience: 2-7 years Designation: Officer / Sr. Officer / Executive Location: Moraiya, Ahmedabad. No. of Openings: HPLC Analysts: 5 Physico Chemical Analysts: 5 QC QMS: 2 Perks & Benefits: Dynamic work environment Career development opportunities Work-life balance Free transportation Canteen Facility Free insurance coverage for self, spouse, and kids Range of learning opportunities to help employees grow and thrive If you are passionate about continuing to work in the pharmaceutical industry and possess the required skills & experience, we encourage you to apply for this position. Please walk in to the interview on SUNDAY 7th Sep 2025 b/w 10:00 AM to 3:00 PM at below mentioned venue. Venue: Unison Pharmaceuticals Pvt. Ltd. Unit III- 7, 8, 9 Steel Town, Opposite Nova Petrochemicals, Village- Moraiya, Taluka- Sanand, District- Ahmedabad- 382213 Regards, HR Team Unison Pharmaceuticals Pvt Ltd

Dear Candidate, We are Inviting Applications for the positions in our Analytical Research & Development department. Job Description : Position Name: Research Chemist/Senior Research Chemist/Research Associate Experience: 1 to 5 years Qualification: M.Sc Analytical Chemistry/Organic Chemistry/M.pharm Work location: Uppal/Mallapur Key Skills and Competencies: High-Performance Liquid Chromatography (HPLC) Key Skills and Competencies: Operation and Maintenance : Proficiency in operating HPLC systems (e.g., Agilent, Waters, Shimadzu) and performing routine maintenance, calibration, and troubleshooting of equipment issues like pressure fluctuations or detector errors. Method Development and Validation : Ability to develop and optimize HPLC methods for analyzing small molecules, impurities, or degradation products, adhering to ICH guidelines (e.g., ICH Q2 for validation). Data Analysis : Expertise in interpreting chromatograms, quantifying analytes, and using software like Empower or ChemStation for data processing and reporting. Sample Preparation : Skilled in preparing samples (e.g., dissolution, extraction) for pharmaceutical or chemical analysis, ensuring reproducibility and accuracy. Regulatory Compliance : Knowledge of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) for documentation, method validation, and audit readiness. Troubleshooting : Ability to diagnose and resolve issues such as peak tailing, baseline drift, or column degradation. Experience Level (1-5 Years) : 1-2 years: Basic operation, routine analysis, and data interpretation under supervision. 3-5 years: Independent method development, validation, and troubleshooting with familiarity in handling complex matrices. Prep HPLC Key Skills and Competencies Operation and Maintenance Hands-on experience with Preparative HPLC systems (e.g., Agilent, Waters, Shimadzu, GE KTA). Proficiency in system setup, gradient programming, scale-up from analytical to preparative runs. Routine maintenance and calibration of pumps, fraction collectors, and detectors. Troubleshooting common issues such as pressure fluctuations, air bubbles, or pump leakage. Purification & Method Development Strong background in method development and optimization for preparative HPLC to isolate target compounds (APIs, impurities, natural products, metabolites, peptides). Experience in scaling up analytical methods to preparative scale while ensuring recovery, purity, and yield requirements. Knowledge of different stationary phases (C18, C8, size-exclusion, chiral) and selection of appropriate mobile phases. Sample Preparation & Fraction Collection Skilled in preparing crude samples (reaction mixtures, fermentation broths, plant extracts) for scalable purification. Competence in managing fraction collection strategies , solvent recovery, and sample lyophilization/drying. Ensuring high-quality isolation of compounds with reproducibility. Data Analysis & Reporting Ability to interpret chromatograms , verify purity and recovery using both analytical HPLC/UPLC and complementary techniques (LC-MS, NMR). Proficiency in software like ChemStation, Empower, Unicorn, or equivalent for processing preparative runs and reporting results. Documentation of purification workflows in compliance with client and regulatory requirements. Regulatory Compliance & CRO Environment Knowledge of Good Laboratory Practices (GLP) and CRO industry requirements for method documentation, record-keeping, and reproducibility. Familiarity with client-driven project timelines and requirements. Experience preparing project reports, tech-transfer documents, and audit-ready records. Troubleshooting & Continuous Improvement Expertise in diagnosing issues like sample overload, poor recovery, carry-over, baseline instability, or column degradation. Ability to suggest process improvements for higher throughput and purity levels. Experience Level (Typical Range: 1-5 Years) 1-2 years: Basic operation of preparative HPLC systems. Performing routine purification runs under supervision. Basic troubleshooting and hands-on sample preparation. 3-5 years: Independent purification and method development for wide compound classes. Competent in scale-up from analytical to preparative levels. Handling of challenging crude matrices and optimization of recovery/yield. Active participation in client projects , troubleshooting, and mentoring junior team members. Interested candidates can contact 6309995773 or share their profiles to saivardhan.kothuri@chemvedals.com

Role Purpose The purpose of the role is to source and hire the right talent against the requirements shared by the business and ensuring a positive employer brand experience for the candidate throughout the hiring process. Do 1. Hire the required talent from the different sourcing channels Understand business projections and urgency of talent requirements across order and cadre demands, skill type (type A/B/C), volume vs. niche etc. As per the talent requirements shared by the business, Create sourcing plan as per hiring channel mix and cost considerations Utilize job portals, consultants, employee referral to find the right fit from the industry/ within Wipro For the shortlisted candidates, facilitate the selection process with the technical panel As per the requirement by the business, facilitate different selection tests like technical programming language skills Conduct HR evaluation round and negotiate with the candidate(s) on the salary, position etc Take necessary approval from the tower lead/ head ensuring, hiring is strictly as per Wipros salary range, minimizing exceptions to meet average cost per candidate target Formally roll out the job offer to the selected candidate(s) and coordinate with him/ her for offer acceptance Motivate, engage and maintain relationship with the selected candidate(s) from time to time till their joining Coordinate with the HRSS team for background verification of the selected candidate Communicate with Business Teams and Managers to from time to time on the status of joining etc 2. Manage Candidate Experience throughout the recruitment process Conduct candidate connect and pre-hiring candidate engagement activities to ensure healthy joining ratio Adherence to Wipro guidelines, processes and protocols with respect to responsiveness, clarity, compensation structure, SLAs, quality and auditability in all candidate communication, and Zero valid escalation on hiring process Resolve candidate concerns and manage candidate escalations, turnaround slightest negative experience Daily maintain the data on the recruitment tool (Synergy) and upload all the candidate documents from time to time Ensure the weekly/ monthly/quarterly dashboards are updated and readily available for the management review Conduct meetings with WMG teams to update on the progress, risk and issues involved in hiring for a position and seek help if necessary Follow checks and balances placed by the recruitment team and conduct regular reviews with the management to ensure reliability, quality and integrity of recruitment data in the system boldest ambitions. To realize them, we need people inspired by reinvention. Of yourself, your career, and your skills. We want to see the constant evolution of our business and our industry. It has always been in our DNA - as the world around us changes, so do we. Join a business powered by purpose and a place that empowers you to design your own reinvention. Come to Wipro. Realize your ambitions. Applications from people with disabilities are explicitly welcome.

Role Purpose The purpose of the role is to source and hire the right talent against the requirements shared by the business and ensuring a positive employer brand experience for the candidate throughout the hiring process. Do 1. Hire the required talent from the different sourcing channels Understand business projections and urgency of talent requirements across order and cadre demands, skill type (type A/B/C), volume vs. niche etc. As per the talent requirements shared by the business, Create sourcing plan as per hiring channel mix and cost considerations Utilize job portals, consultants, employee referral to find the right fit from the industry/ within Wipro For the shortlisted candidates, facilitate the selection process with the technical panel As per the requirement by the business, facilitate different selection tests like technical programming language skills Conduct HR evaluation round and negotiate with the candidate(s) on the salary, position etc Take necessary approval from the tower lead/ head ensuring, hiring is strictly as per Wipros salary range, minimizing exceptions to meet average cost per candidate target Formally roll out the job offer to the selected candidate(s) and coordinate with him/ her for offer acceptance Motivate, engage and maintain relationship with the selected candidate(s) from time to time till their joining Coordinate with the HRSS team for background verification of the selected candidate Communicate with Business Teams and Managers to from time to time on the status of joining etc 2. Manage Candidate Experience throughout the recruitment process Conduct candidate connect and pre-hiring candidate engagement activities to ensure healthy joining ratio Adherence to Wipro guidelines, processes and protocols with respect to responsiveness, clarity, compensation structure, SLAs, quality and auditability in all candidate communication, and deliver Zero valid escalation on hiring process Resolve candidate concerns and manage candidate escalations, turnaround slightest negative experience Daily maintain the data on the recruitment tool (Synergy) and upload all the candidate documents from time to time Ensure the weekly/ monthly/quarterly dashboards are updated and readily available for the management review Conduct meetings with WMG teams to update on the progress, risk and issues involved in hiring for a position and seek help if necessary Follow checks and balances placed by the recruitment team and conduct regular reviews with the management to ensure reliability, quality and integrity of recruitment data in the system Applications from people with disabilities are explicitly welcome.

Role & responsibilities Solid Oral - Production & Packing Officer - Executive and Plant Operator - Technical Assistant : Tablet/ Capsule - Granulation, Compression, Coating, Inspection, Capsule Filling and Wurster coater. Tablet/ Capsule - Blister Line (BQS), CVC Bottle Line Warehouse (Supervisor / Machine Operator): Officer Senior Executive and Plant Operator - Technical Assistant: RM, PM, FG, Dispensing, Dispatch , Documentation Engineering Executive/Sr. Executive: Process Equipment (Mechanical/Electrical/Instrumentation) of OSD Plant like preventive maintenance and breakdown related activities of equipment of OSD plant such as FBD, FBP, RMG, coating, compression, capsule, Packing machine etc. Technician: Process equipment's- Fitter/Electrician/ Instrumentation: Handling preventive maintenance and breakdown of equipment of OSD Plant such as FBD, FBP, RMG, coating, compression, capsule, sifter, stirrer, Wurster coater, packing machine etc. HVAC Operator - Operation and maintenance of AHU, Cooling tower, BMS, Chiller Quality Assurance (IPQA) Officer / Senior Executive: IPQA in process (Mfg. and Pkg.) Quality Control (Analyst) Officer / Sr. Executive: HPLC / GC / IR / UV / Dissolution and other QC Equipment/ QC Method Validation and Transfer.

0.6 - 4 years with In depth knowledge and skill set pertaining to Molecular Modelling, Docking, Molecular mechanics, Quantum Mechanism, Molecular Dynamics simulation and QM/MM simulations is must. Brief knowledge/ experience of protein structure, function, dynamics and engineering. Sound knowledge in programming and scripting languages like Fortran, C, C++, Perl and Python. Putting theory into practice Are you inquisitiveFinally looking for a place to put your expert skills in MD, QM, MM to solve real world problemsYou have arrived at the right place.