592 Gc Jobs - Page 6

Role & responsibilities Responsible for sampling of Raw material, Packaging material and Finished product. Responsible for analysis of Raw material, Packaging material, Utility Raw material, In-process, Half finished product and Finished product. Preparation of reagents, solutions and standardization. Calibration and testing of instrument/equipment as per schedule. Handling of wet chemical analysis instruments Responsible to identify Out of specification results, Out of trend result and to inform the respective person then carry out investigation according to Head QC instruction. Responsible for analysis of tests in Stability study. Work as per the work instructions and follow all the safety standards. Responsible for sampling and analysis of Demineralized water, condensate water, reverse osmosis, raw water and ETP water. Establish and maintain effective working relationships with co-workers and with colleagues of other departments. Responsible for line Clearance of the critical process equipment during product change over cleaning in the production Orient, impart training to trainees and instruct them to carry out their duties efficiently and ensure that they follow all the safety instructions on their duties. Duties & responsibilities would include the above but not limited to and would be responsible to carry out any other duties & responsibilities assigned by the HODs / reporting head. Preferred candidate profile Good Knowledge in cGMP and Analytical chemistry Immediate joiner preferred

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Saturday 19-07-2025. Requirement for Executive - FAR&D - Formulation Analytical Research & Development(FAR&D) Undertake method development, troubleshooting and method validation to GMP and ICH. Investigation of non-conforming samples, CAPAs, data evaluation and reporting. Write cGMP Quality documents including Standard Operating Procedures, laboratory equipment procedures and investigational protocols. Excellent, enthusiastic, clear communication skills, both written and verbal, with a diverse audience are critical to the success of this position. Proven ability to interact with cross - functional and cross - cultural teams. Previous experience of running analytical techniques such as HPLC, Dissolution, KF, IC with the ability to extract and prep various samples in a variety of forms. As this role involves liaising with other departments on a regular basis, you will need good communication skills and the ability to work effectively as part of a team. Note : Formulation Quality Control Candidates also eligible. Interview Date : 19-07-2025 Department : Formulation Analytical Research & Development(FAR&D) Experience : 1 to 6 Years Qualification : M. Pharmacy / M.Sc. / B Pharm Position: Executive Work Location : MSN R&D Center, Pashamylaram, Hyderabad Interview Venue Details MSN Laboratories, R&D Center,Pashamylaram, Hyderabad

Hiring For QC Manager in Jhagadia MSC Chemistry / PhD / BE Chemical 15 to 20 Years Up to 18.0 LPA Budget Experience in Pthalic Anhydride must Send CV on sdpbharuch@gmail.com with Subject: QC Manager Jhagadia No Charges Share with your Friends Required Candidate profile Share Job with Your Friends Interview Venue: SDP HR Solution, Sixth Floor, 610, Golden Square, Beside Dmart, Near ABC Circle, Bholav, Bharuch Best Job Placement Consultancy in Gujarat

You will be joining our ARD team in Udaipur as an ARD Chemist / Scientist. Your main responsibilities will include method development and validation, impurity profiling, and instrumental analysis to assist our Synthesis R&D and quality operations. Your key responsibilities will include developing HPLC, GC, and LC-MS analytical methods for monitoring in-process reaction samples, validating HPLC methods suitable for AMV, performing impurity profiling of APIs and intermediates, identifying and characterizing impurities using advanced techniques like mass spectrometry, ensuring all analytical instruments are well-maintained, performing regular calibration and documentation of analytical instruments, maintaining proper records as per regulatory and internal quality standards, and supporting the preparation of SOPs, protocols, and technical reports. To excel in this role, you should possess a strong knowledge of HPLC, GC, and LC-MS techniques, have experience in method development and impurity profiling, be familiar with ICH guidelines and regulatory requirements, be proficient in analytical software like Empower/Chromeleon, and have good documentation and communication skills.,

About Company: Reveille Technologies is seeking a dynamic and experienced US IT Recruiter to join our team at our Tidel Park, Tharamani, Chennai location. As a US IT Recruiter, you will be responsible for sourcing, screening, and recruiting top-tier IT talent for clients across the United States. The ideal candidate should have hands-on experience in IT recruitment, a strong understanding of US employment practices, and the ability to manage multiple recruitment processes. Key Responsibilities : Sourcing Candidates : Utilize a variety of platforms including job boards, LinkedIn, social media, and professional networks to find top IT talent across the United States. Screening and Interviewing : Conduct initial screenings, technical assessments, and interviews to evaluate candidates qualifications, skills, and cultural fit. Client Collaboration : Work closely with hiring managers to understand job requirements and develop recruitment strategies to meet staffing needs. Candidate Management : Maintain a strong pipeline of qualified candidates and manage the recruitment process from the first point of contact to job offer. Offer Negotiation : Assist with negotiating job offers, including salary, benefits, and start dates in coordination with the hiring team. Compliance : Ensure all recruitment processes are compliant with US labor laws, immigration policies, and visa regulations. Reporting : Provide regular status reports to management and clients regarding candidate pipelines and recruitment activities. Qualifications : Proven experience as a US IT Recruiter or in a similar technical recruitment role. Strong understanding of the US IT market and recruitment trends. Proficiency in sourcing techniques , including using job boards Dice, Monster, LinkedIn . Familiarity with Applicant Tracking Systems (ATS) and recruitment software. Excellent communication and interpersonal skills, with the ability to negotiate and manage client relationships. Ability to work in a fast-paced environment and meet deadlines. Strong attention to detail and organizational skills. Knowledge of US visa regulations H1B, TN, L1 . How to Apply: Send your updated resume to sathish.s@reveilletechnologies.com

Technical Skill : Routine Operation & Analysis API Products HPLC, WET Lab Analysis

1.Routine Operation & Analysis API Products 2.HPLC, WET Lab Analysis

Maintain H1B petitions including annual H-1B CAP, extensions of current visas and transfer petitions for new employees. Prepare in-house documents and petitions for other visas including but not limited to F-1, L1, and dependent visas (H4, L2 etc). Have ability to lead immigration process from start to finish, working with non-immigrant & immigrant Visa applications and processes (H1-B, H-4, L-1, TN, and EB non-immigrant petitions, RFE, etc.), EAD renewals of employees and dependents. Maintain Public Access Files ensuring compliance, documentation and execution of immigration policies and procedures. Experience of handling FDNS site visits, PAF, DOL audits. Consultation: Assessing employees eligibility for Intra-Company Transfers (ICT) and other work permits in Canada. Providing initial consultations to clients regarding their options for bringing employees to Canada through ICT and other programs. Intra-Company Transfers (ICT): Managing the process of transferring employees from a foreign office to a Canadian office of the same company. Advising employees on the requirements and documentation needed for ICT applications. Assisting with the preparation and submission of ICT applications to Immigration, Refugees and Citizenship Canada (IRCC). Labour Market Impact Assessments (LMIA): Assisting in obtaining LMIA approval to hire foreign workers for positions where there are no qualified Canadian workers available. Advising on the LMIA application process, including advertising requirements and application submission. Assisting with the preparation and submission of LMIA applications to Employment and Social Development Canada (ESDC). Work Permits: Assisting clients in obtaining work permits for foreign workers in Canada, including open work permits and employer-specific ICT work permit. Advising clients on the eligibility criteria, documentation requirements, and application process for various types of work permits. Document Preparation and Review: Assisting employees in preparing and reviewing required immigration documents, including work permit applications, LMIA applications, and supporting documentation. Ensuring that all required documents are accurately completed and submitted in a timely manner. Case Management: Managing multiple immigration cases simultaneously, particularly those related to ICT, LMIA, and work permits. Keeping stakeholders informed about the progress of their applications and any changes in immigration laws or policies that may affect their case. Legal Research: Staying up-to-date with changes in Canadian immigration laws, policies, and procedures related to ICT, LMIA, and work permits. Conducting legal research to support immigration cases in these specific areas. Compliance: Ensuring that all immigration activities comply with Canadian immigration laws and regulations, particularly those related to ICT, LMIA, and work permits. Maintaining confidentiality and privacy of client information. Administrative Tasks: Maintaining accurate records of client interactions and case details, particularly those related to ICT, LMIA, and work permits. Handling administrative tasks related to client files, such as organizing documents and correspondence.

Candidate should have knowledge of handling and troubleshooting the sophisticated Analytical Instruments like HPLC, GC, IR, UV, KF ETC . Also He should be able to work, adopt and guide subordinates in following Good Laboratory Practices. He should be well versed with various regulatory & Statutory requirements. Candidate Profile: Should have minimum Four years experience. He should be able to work with the team and be willing to take initiative & challenge for completing the task assigned.

Candidate should be from API industry having knowledge of handling & troubleshooting of sophisticated Analytical Instruments. like HPLC, GC, IR, UV, KF ETC He should be able to work, adopt and guide subordinates and juniors in following Good Laboratory Practices. He should be well versed with various regulatory & Statutory requirements should be able to face regulatory and customer audits independently. Candidate Profile: Should have minimum 10 years experience including minimum 3 years as Deputy Manager. He should be able to guide the team for completing the task assigned. Also should be able to complete task timely assigned by the management

The responsibilities of this role include performing analysis of raw materials, intermediates, and finished products of Active Pharmaceutical Ingredients (APIs) according to approved specifications and Standard Operating Procedures (SOPs). You will be responsible for operating and maintaining analytical instruments such as HPLC, GC, UV-Vis Spectrophotometer, FTIR, Karl Fischer, Melting Point Apparatus, etc. Additionally, you will review and verify analytical data, ensuring proper documentation in accordance with cGMP and GLP guidelines. Preparation and standardization of volumetric solutions and reagents, carrying out stability studies as per ICH guidelines, and ensuring timely calibration of laboratory instruments are also key responsibilities. Method validation/transfer activities as per regulatory and internal requirements, participation in investigations related to OOS/OOT/Deviations and CAPA implementation, and coordination with QA, Production, and R&D departments for smooth workflow are essential tasks. Compliance with safety protocols and maintaining a clean and organized lab environment are also part of the role. The ideal candidate should have hands-on experience in analytical techniques, especially HPLC/GC. A good understanding of regulatory guidelines such as ICH, WHO, USFDA, etc., is required. Strong documentation and communication skills are essential, and experience in a regulated API manufacturing unit is preferred. This position falls under the Pharmaceutical & Life Sciences industry, specifically in the Corporate Quality Control department. It is a Full Time, Permanent role.,

As an ARD Chemist / Scientist at our Udaipur location, you will be a key member of our ARD team, responsible for method development and validation, impurity profiling, and instrumental analysis to support our Synthesis R&D and quality operations. Your primary responsibilities will include developing and validating HPLC, GC, and LC-MS analytical methods for monitoring in-process reaction samples, as well as developing HPLC methods suitable for Analytical Method Validation (AMV) and transfer to QC. You will also be tasked with performing impurity profiling of APIs and intermediates, identifying and characterizing impurities using advanced techniques like mass spectrometry, and ensuring that all analytical instruments are maintained in optimal working condition through regular calibration and documentation. In addition, you will play a crucial role in maintaining proper records as per regulatory and internal quality standards, supporting the preparation of SOPs, protocols, and technical reports, and ensuring compliance with ICH guidelines and regulatory requirements. To excel in this role, you must possess a strong knowledge of HPLC, GC, and LC-MS techniques, along with experience in method development and impurity profiling. Familiarity with analytical software such as Empower/Chromeleon, good documentation, and communication skills are also essential for success in this position.,

Do you want to be a part of the fascinating story of over 500 iconic brands spanning across more than 100 countries Being the best beer company starts with finding the best people. While we have big brands, we have bigger opportunities as well. AB InBev India is looking to hire a Senior Manager - Quality Analyst for its supply team based out of Aurangabad, Maharashtra. As a Senior Manager - Quality Analyst, you will be responsible for handling instruments like GC, Alcolyser, DMA, Sodium Meter, pH Meter, and Gas Generators. Your role will involve the calibration and maintenance of all BQA instruments while strictly following BQA SOPs. You will be analyzing in-process samples, highlighting deviations, and examining incoming brewing raw materials. Adhering to SOP's for all analysis, you will ensure reliable and accurate data is supplied through the use of BWC and control charting. Maintenance of all records and updating the AB datasheet regularly will be part of your duties. Additionally, you will conduct PRP audits and 5S Audits at regular intervals, maintaining 5S in the lab, and serving as a subject matter expert on instruments like GC's, Alcolyser, DMA, Sodium Meter, pH meter, Generators, centrifuge, sonicator, hot water bath, and Mash Bath. As a Senior Manager - Quality Analyst, you will play a crucial role as an enthusiastic team player in the Environmental Pillar, a qualified taster, and a trainer of new Brewing Quality Analysts. Your responsibilities will include brewing quality improvement analysis, developing and implementing process checklists and audits, as well as conducting and tracking CAR of brewery PRP audits. You will ensure all BQA lab consumables and inventory are maintained, adhere to safety requirements, and review daily data, control charts, calibration, and maintenance logs. Key dimensions of this role include being accountable for the Director (Supply & Logistics) KPI, Brewery Sensory Score, Regional BOP KPI, and VPO Implementation Department-specific KPI such as BPI & Plant Micro Index. Above all, a passion for beer is essential to excel in this role. Quench your thirst for success by joining AB InBev India as a Senior Manager - Quality Analyst. Come, sit at the tab and be a part of our dynamic team in Aurangabad, Maharashtra.,

The ideal candidate should possess strong communication skills and be well-versed in analytical techniques such as HPLC, GC, IR, UV, and Wet analysis.,

Long Description 1. Perform characterization of peptides , nucleic acids-based (oligonucleotides) or other injectable drug products using High Resolution Mass Spectrometry (LC-HRMS) . Experience with QToF/Orbitrap instruments and Ion Mobility will be preferred. Additional experience in Fluorescence, particle size analysis (DLS), and other relevant techniques (e.g. SEC-MALS) are desirable. 2. Analyze and interpret LC-MS and MS/MS data for impurity profiling and characterization. Solve problems and implement new research methods through literature search, coordinate with cross-functional teams (formulation, QA, QC, regulatory, etc.), application specialists, etc. to complete analytical tasks. 3. Prepare, review and share LC-MS data and documentation (SOP, STP, Test Reports, etc.) in a timely manner for regulatory submissions. Follow good laboratory practices (GLP) , manage samples (collection, storage, and disposal), deviations and incidences as per established procedures. 4. Undertake routine maintenance & calibration of the analytical instruments, troubleshoot equipment malfunction often in coordination with service engineers, etc. Assist in the maintenance of the laboratory, inventory of R&D consumables, & other lab management activities from time to time Competencies Education Masters in Pharmacy or Applied Chemistry Doctorate in Pharmaceutical Technology or Analytical Chemistry Work Experience 5 – 7 years (with MPharm) or NIL (with PhD)

Work with Us. Change the World. At AECOM, we're delivering a better world. Whether improving your commute, keeping the lights on, providing access to clean water, or transforming skylines, our work helps people and communities thrive. We are the world's trusted infrastructure consulting firm, partnering with clients to solve the world’s most complex challenges and build legacies for future generations. There has never been a better time to be at AECOM. With accelerating infrastructure investment worldwide, our services are in great demand. We invite you to bring your bold ideas and big dreams and become part of a global team of over 50,000 planners, designers, engineers, scientists, digital innovators, program and construction managers and other professionals delivering projects that create a positive and tangible impact around the world. We're one global team driven by our common purpose to deliver a better world. Join us. Serves as lead engineer on mid- to large size projects. Provides specialized technical input to studies and design for staff's specific area of expertise. Approves and signs off on work. Provides technical expertise for studies and design efforts. Presents complex technical solutions to clients. Performs quality control reviews of work developed by others. Participates in development of technical proposals. Provides estimates for the engineering budget and schedule to meet requirements on large projects. Additional Information

Aforeserve Technologies Pvt Ltd (XtraCover) is looking for Quality Control Executive (QC) to join our dynamic team and embark on a rewarding career journey Assist in quality control tasks and activities. Develop and implement quality control policies and procedures. Monitor and report on quality control performance metrics. Collaborate with quality control teams and stakeholders. Ensure compliance with quality control standards and regulations.

QC Role & responsibilities : Handling of QC instruments, Such as HPLC, GC, UV, FTIR, Dissolution Apparatus, Melting point, Karl Fischer apparatus, Auto titration, Analytical weighing Balance, Polari meter, Disintegration Apparatus, pH Meter etc. Analysis of In process, validation, Hold time study, finished products and stability samples according to related specifications Daily as well as monthly calibration of analytical balance of instrumentation section To maintain the daily logs adhering to the Good Laboratory Practices. Daily standardization of Karl Fischer reagent. Daily temp recording of instrumentation room, chemical room & refrigerator. Daily preparation of 0.4% NaoH for discarded penicillin sample deactivation. Regular, online analysis of cleaning (Rinse & swab) samples. QA Role & responsibilities : Execute and review Equipment Qualification protocols (IQ, OQ, PQ) in compliance with regulatory requirements. Prepare, execute, and review Cleaning Validation protocols and reports. Participate in the design, execution, and documentation of Computer System Validation (CSV) as per GAMP 5 guidelines. Coordinate and support Process Validation activities, including preparation and review of protocols, execution, and final reporting. Ensure that all validation activities are compliant with cGMP, regulatory guidelines, and internal SOPs. Perform gap assessments, risk assessments, and deviation handling related to validation. Collaborate with cross-functional teams including production, engineering, QC, and IT for validation planning and execution. Assist in internal audits, regulatory inspections, and prepare responses to audit observations. Maintain and update validation master plans and SOPs regularly.

Role & responsibilities Operate and maintain QC instruments, including HPLC, GC, UV, FTIR, Dissolution Apparatus, Melting Point Apparatus, Karl Fischer Apparatus, Auto Titration, Analytical Weighing Balance, Polarimeter, Disintegration Apparatus, pH Meter, etc. Perform analysis of in-process samples, validation, hold-time study, finished products, and stability samples as per relevant specifications. Conduct daily and monthly calibration of analytical balances in the instrumentation section. Maintain daily logs and ensure adherence to Good Laboratory Practices (GLP). Perform daily standardization of Karl Fischer reagent. Monitor and record daily temperature readings of the instrumentation room, chemical room, and refrigerator. Prepare 0.4% NaOH solution daily for the deactivation of discarded penicillin samples. Conduct regular and online analysis of cleaning (rinse & swab) samples Preferred candidate profile Hands-on experience with laboratory instruments and analytical techniques. Knowledge of GLP, GMP, and regulatory guidelines. Strong documentation and record-keeping skills. Ability to work in a fast-paced, compliance-driven environment. Attention to detail and problem-solving skills.

We are seeking a highly motivated and experienced Study Director to oversee chemical characterization studies within our research and development team. The ideal candidate will have a strong background in analytical chemistry, extensive knowledge of chemical characterization techniques, and a proven track record in managing complex projects. This position offers a competitive salary and benefits package, along with opportunities for professional growth and development. If you are passionate about advancing scientific research and thrive in a collaborative environment, we encourage you to apply. Roles and Responsibilities 1. Oversee and manage chemical characterization studies from initiation to completion, ensuring adherence to regulatory standards and internal protocols. 2. Design study plans and methodologies that are scientifically sound and aligned with project objectives, including the selection of appropriate analytical techniques and equipment. 3. Coordinate with cross-functional teams, including project managers, chemists, and quality assurance personnel, to ensure effective study execution and communication. 4. Review and approve study protocols, analytical methods, and reports to ensure accuracy, compliance, and scientific integrity. 5. Provide technical expertise and guidance related to chemical characterization, including the interpretation of analytical data and results. 6. Ensure that all studies are conducted in compliance with Good Laboratory Practice (GLP) and other relevant regulations. 7. Manage study budgets and timelines, identifying potential risks and implementing mitigation strategies to ensure successful project delivery. 8. Train and mentor staff on appropriate methodologies and regulatory requirements related to chemical characterization studies. 9. Participate in project meetings, presenting study findings and progress updates to stakeholders, and incorporating feedback into study design and implementation. 10. Maintain up-to-date knowledge of industry trends, emerging technologies, and regulatory changes affecting chemical characterization and related fields. 11. Facilitate communication with regulatory agencies as needed, providing data and documentation to support submissions and inquiries. 12. Contribute to the continuous improvement of departmental processes and methodologies, ensuring best practices are followed in study design and execution.

Urgent opening for QC Officer-Sr. Officer in Dahej, Bharuch. Note: Walk In Interview at Ahmedabad Date & Time: 20th July, 2025 at 09:00 AM Onwards Job Location: Dahej, Bharuch Experience: 2 to 7 years in API Qualification: M.Sc./B.Pharm/M. Pharm Required Candidate profile Roles and Responsibilities: -Experience in Section LCMS / PSD / HPLC / GC /Method Validation -Candidate preferred from Pharma API (Active Pharmaceutical Ingredient).

At SCIEX, our work at one of Danaher's 15 operating companies plays a vital role in saving lives. We are driven by a shared commitment to innovate for real-world impact. As a global leader in mass spectrometry, SCIEX provides cutting-edge solutions for precise detection. With a history spanning over 50 years, SCIEX has been at the forefront of developing revolutionary technologies and solutions in mass spectrometry and capillary electrophoresis. Our products empower customers to swiftly address environmental threats, gain deeper insights into disease-related biomarkers, enhance patient care in clinical settings, expedite the introduction of relevant drugs to the market, and ensure the safety and healthiness of food. Joining SCIEX means embarking on a fulfilling role that magnifies your contribution to the world and enables you to unlock the potential of life. SCIEX, a part of Danaher's 10 Life Sciences companies, collaborates to expedite the exploration, advancement, and delivery of solutions that protect and enhance human health. **Field Service Engineer** As a Field Service Engineer within the Western Service Team based in Pune, you will be reporting to the Service Manager in Mumbai. This role is completely remote. **Responsibilities** The Field Service Engineer will have the following key responsibilities: - Successfully completing assigned training tasks on designated products and duties. - Conducting top-notch installations, repairs, and maintenance on mass spectrometry instruments and managing escalation calls. - Addressing critical calls and prioritizing customer satisfaction. **Essential Requirements** The essential requirements for this position include: - A Bachelor's Degree in Engineering. - A minimum of 3 years of experience with instruments such as GC, HPLC, and Mass Spectrometer. - Profound expertise in analytical instrumentation in Service, particularly in the realm of mass spectrometry, and relevant experience in Mass Spec and HPLC. - Proficiency in computer operation and MS Office. - Proficient in English (both written and verbal). **Travel, Motor Vehicle Record & Physical/Environment Requirements:** - Willingness and ability to travel, including overnight or outstation calls on short notice, if necessary. - Capability to handle, transport, or carry equipment as needed. **Preferred Qualifications** Having prior experience in the following areas would be advantageous: - Chromatography - Mass Spectrometry Join our exceptional team today. Together, we will expedite the practical impact of future science and technology. We collaborate with customers worldwide to help them surmount their most intricate challenges by crafting solutions that bring the force of science to life. To learn more, please visit www.danaher.com. At Danaher, we cherish diversity and the presence of both similarities and differences, whether visible or not, within our workforce, workplace, and the markets we serve. Our team members, customers, and shareholders bring distinctive and diverse perspectives due to these varied attributes.,

You will be responsible for conducting lab testing and analysis in a Pharma Laboratory located in Gurugram. The ideal candidate should possess an MSc in Chemistry, B.Pharma, or a related field with 2 to 10 years of experience. Your main duties will include chemical testing of raw materials, finished products, cosmetics, Ayurveda, Sidha, and Unani products. You should also have knowledge and experience in handling instruments such as HPLC, GC, GC-MS/MS, ICP-MS, and Dissolution equipment. Additionally, you will be required to maintain documentation in accordance with NABL Audit standards. This role requires attention to detail, strong analytical skills, and the ability to work effectively in a laboratory setting.,

Post – Assistant Manager (QC) Location: Ahmedabad (Kathwada) Gender – Male Experience- HPLC, GC, KF Education – BSC Chemistry / BE, B. Tech (Chemical) Experience – 6 to 10 yrs Preference – Food / Pharma industry

Project Managers are responsible for overseeing the project/engagement/activity on a daily basis and are responsible for delivering high-quality results within the identified objectives and constraints, ensuring the effective use of the allocated resources. They are responsible for risk and issue management, project communication and stakeholder management. Project managers perform the activities of planning, organising, securing, monitoring and managing the resources and work necessary to deliver specific project goals and objectives in an effective and efficient way. - Grade Specific Senior Project Manager - Responsible for leading either a large project or a definable segment of a very large and complex project. Clients may be external or internal. PM are responsible for the translation of the client''s complex business requirements into formal agreements. For these, PM establish specific solutions, applications or processes which ultimately culminate in customer acceptance of the results. This includes working with client team members and executives to identify business requirements and subsequently working with, and leading others, in the initiating, planning, controlling, executing and closing the client''s solution. PM are responsible for a wide range of process activities beginning with the request for proposal through development, and final delivery. Skills (competencies) Accountability Active Listening Adaptability Analytical Thinking Business Acumen Business Partnering Business Transformation Change Management Coaching Confidentiality Collaboration Commercial Management Complex Engagement Management Contract Management Crisis Management Critical Thinking Cultural Awareness Customer Centricity Data-Driven Decision-Making e-Great e-KPI e-MMX e-Monitoring Emotional Intelligence e-skills Estimating Executive Presence Financial Analysis Financial Control Financial Reporting Influencing Lean Portfolio Management Managing Difficult Conversations Microsoft Project Negotiation Problem Solving Project Financial Planning Project Governance Project Management Project Planning Qwiz Relationship-Building Risk Assessment Risk Management Scope Management Scrum Stakeholder Management STAR Storytelling Strategic Thinking Teamwork Time Management Unified Project Management (UPM) Unified Service Management (USM) Verbal Communication Written Communication Agile (Software Development Framework) Delegation UPM (Methodology) USM (Methodology)