123 Ftir Jobs - Page 5

We are seeking a highly skilled Quality Control Chemist to join our team in Ahmedabad. The ideal candidate will be responsible for testing and analyzing raw materials, in-process samples, and finished cosmetic and skin care products to ensure compliance with regulatory and company quality standards. This role requires strong analytical skills, hands-on experience with laboratory equipment, and a keen understanding of cosmetic formulations and Good Manufacturing Practices (GMP). Key Responsibilities: Conduct quality control tests on raw materials, bulk formulations, and finished cosmetic and skincare products. Perform instrumental analysis using HPLC, GC, FTIR, UV Spectrophotometry, and other laboratory equipment. Ensure compliance with GMP, ISO, and FDA guidelines for cosmetics and personal care products. Maintain stability study programs and analyze product performance over time. Conduct microbiological and physicochemical testing to verify product safety and efficacy. Develop, validate, and execute Standard Operating Procedures (SOPs) and analytical test methods. Identify and troubleshoot any quality deviations or formulation inconsistencies. Assist in the development of new formulations and improvement of existing cosmetic products. Collaborate with R&D, production, and regulatory teams to ensure overall product quality. Prepare and maintain detailed reports, documentation, and quality records for audits. Required Technical Skills & Qualifications: Education: B.Sc./M.Sc. in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field. Experience: 2-5 years of experience in a cosmetic, skin care, or personal care manufacturing QC lab. Strong knowledge of analytical chemistry techniques and laboratory best practices. Hands-on experience with analytical instruments such as HPLC, GC, UV, and FTIR. Familiarity with regulatory requirements (GMP, FDA, BIS, ISO 22716) for cosmetics and personal care products. Ability to analyze and interpret test results, batch records, and quality data. Proficiency in MS Office (Excel, Word, PowerPoint) for documentation and reporting. Strong problem-solving skills and attention to detail. Effective communication and team collaboration skills. Preferred Qualifications: Experience with microbiological testing and contamination control in cosmetics. Knowledge of stability testing protocols for skincare and personal care products. Understanding of color, fragrance, and texture analysis in cosmetic formulations. Ability to work in a fast-paced manufacturing environment and meet deadlines. Salary & Benefits: Competitive salary based on experience and qualifications. Performance-based incentives. Opportunities for professional growth and training. Health and wellness benefits.

Position is responsible for the Quality Control Program. Team Lead will work in the Analytical/Chemical lab & will ensure Input material, WIP & Finished goods are sampled, tested & approved timely and in compliance to CP Standards/guidelines & applicable local regulatory requirements. He is also responsible for qualification & maintenance of lab equipment. He will drive continuous improvement in the areas of Quality, Good Manufacturing Practices, Good laboratory Practices ,EOHS & FP&R. Job Context: TL quality has to follow and ensure compliance for physical and chemical sampling/ testing program for Raw materials, Work-in-process (WIP) & Finished products at the facility based on Quality Standard expectations & local regulatory requirements. Ensures Lab equipment/instruments Qualification (DQ,IQ,OQ,PQ), Calibration Verification & Maintenance Program as per the defined procedures & protocols. Understands equipment Basic Operation & performance evaluation & assists in equipment breakdowns & trouble shooting. Understands Hazards associated with Lab Equipment, Lab Chemicals, Lab Operations. Implements an effective & efficient lab safety program. Partners with site EOHS program & drives key aspects of Site EOHS program applicable to laboratories. Participates in Internal audits and External audits (Contract manufacturers and Labs, Suppliers, etc.) Functions as part of the Plant GMP and Quality Team. The Team Leader is an effective and valuable member of the Management team to ensure delivery of business results in his area. This position requires having high degree of collaborate with Making, Finishing and Materials. Drive continuous improvement using Data Analytics tools. Key Accountabilities: Ensuring RP/PM Quality , WIP & FG : To follow physical and chemical sampling and testing program for raw materials, work-in-process (WIP) & finished products at the facility. This must be in compliance to QS 024 and local regulatory requirements. Timely testing and release of RM/WIP/FG to support plant critical metrics of AU & UPDT. Ensure use of corporate lab methods IQ/OQ/PQ of Lab equipments Calibration Documentation Ensures all testing is performed according to corporate methods, laboratory requirements, applicable regulatory requirements, and policy. Maintain laboratory quality assurance system that covers analyst qualification as well as equipment IQ/OQ/PQ, calibration, maintenance and use of analytical reference standards. Ensures that the reporting of data and maintenance of records is detailed. Also, that the interpretation of the data is accurate and that the results are effectively communicated to appropriate individuals including management. Participates in internal audits and external audits (contract manufacturers and labs, suppliers, etc.) Functions as part of the Plant GMP and Quality Team. Continuous improvements Integrates and applies CI tools to drive critical metric improvements Exploits data and information to identify and measure potential improvements FP&R & EOHS Understanding the technical requirements of EOHS, Product Safety, Regulatory, and Quality and Microbiology in factories, laboratories, and research facilities. Takes corrective actions in a timely manner to mitigate potential EOHS or Quality incidents Abides by facility safety and GMP requirements and sets the example Proactive in self-assessing against corporate EOHS and Quality standards and governmental regulations Follow FP&R laid down standards applicable to area. Compliances Adherence to policies & procedures of the company, production processes and systems/SOP s & regulatory requirements. Cost Reduction Identify, recommend and implement a manufacturing cost reduction program, and implement new technology in the area. Communication Mentoring & Feedback, DBS Competencies Required Functional Competencies Product Safety, Regulatory and Quality (Quality Orientation) Innovation Manufacturing Management (Safety Awareness) Leadership Competencies Effective Execution (Driving Execution) Planning/Priority Setting (Leading Work) Self - Awareness / Personal Impact (Continuous Learning) What you will need.. Minimum of 7 years of laboratory experience in a regulated environment, having good skills on analytical instruments HPLC, GC, AAS, FTIR, UV-VIS spectrophotometer, NIR, NMR, pH meter etc. Adequate communication & presentation skills required. Qualification of Master degree or equivalent experience in Chemistry.

Urgent hiring!!!!! Location: Sikkim Department: Quality Control Designation: Officer/Sr. Officer Preferred candidate - Having 3 - 5 yrs. of experience in Quality control - FG/RM section Must have hands on experience in QC instrument i.e. HPLC, UV Spectrophotometer, FTIR, K.F apparatus, Analytical balance, pH meter, Water Activity Analyzer. Candidate from OSD only. Interested candidate may apply at hr.plant@zuventus.com Preference will be given to early joiner.

Provides technical & application services & support to Agilent customers. This includes timely and cost-effective problem resolution with the objective to enhance our customer experience and meet Agilent contractual agreements. Leverage post sales interactions with customers to probe and qualify further revenue opportunities and provides highly qualified leads to sales. Performs a set of required admin tasks to ensure flawless customer service for contract and trade customers. Job Roles & Responsibilities Responsibilities of this position include but are not limited to; Responsible for providing technical & application support for Agilent analytical instruments to existing & new customers in markets of Biopharma / Proteomics / Pharma / Food etc. at identified locations at PAN India level. Deliver customer education courses on-site as well at COE labs Cost & time effective application method deployment on Agilent instruments Promptly troubleshoot method/technology transfers issues from one instrument to another. Lead projects requiring coordination with other functions & customers. Deliver product seminars for customers, prospects, and employees. Training of internal & external team and provide technical support. Respond promptly to related customer queries & help in prompt resolution of customer escalations. Participate in programs to stimulate demand for all Agilent range of products/services and ensure timely and proper execution of those programs. Perform Installations, Preventive Maintenance, Repair, software & hardware IQ OQ on Agilent products as required. Co-ordinate internally with all the field sales team and Managers to ensure that the key customers are delighted. Must be willing to travel extensively Qualifications Master s Degree in Chemistry/Analytical Chemistry / Instrumentation / Pharmacy / Biotechnology or equivalent Relevant basic/theoretical knowledge of analytical instruments like HPLC, LCMS, LC-QTOF, GPC, GC, GCMS, ICPMS, ICPOES, AAS, UV, FTIR etc. (preferably LCMS, LCQTOF) Biopharma exposer will be added advantage Experience more then 4 years Candidate should enjoy travelling and visiting customers. Excellent numerical, verbal and written communication, troubleshooting and problem-solving skills along with good organizational & negotiation skills.

- Testing of In-Process and Finished Goods Sample - Documentation of Quality Control related activities - Calibration and Maintenance of Lab Equipment - Preparation of required reports (Daily/Monthly) - TQM & 5S Required Candidate profile Ideal candidate must be a B.Sc/M.Sc in Polymer Science/ Diploma from CIPET with 3-6 years of experience in Quality Control of Polymer Products

1. Laboratory Quality Compliance: Ensure QC laboratory operations comply with GLP, GMP, and global regulatory standards. Implement and maintain laboratory quality systems, including data integrity controls and documentation practices. Review and approve laboratory investigations, Out-of-Specification (OOS) and Out-of-Trend (OOT) reports, and Corrective and Preventive Actions (CAPA). 2. Regulatory & Audit Compliance: Prepare and participate in regulatory inspections (USFDA, MHRA, WHO-GMP, etc.), customer audits, and internal audits. Ensure timely implementation of audit observations and compliance commitments. Maintain compliance with ALCOA+ (Attributable, Legible, Contemporaneous, Original, Accurate) principles for data integrity. 3. Documentation & SOP Management: Develop, review, and approve Standard Operating Procedures (SOPs) related to laboratory quality assurance. Oversee the review and approval of analytical reports, Certificates of Analysis (CoAs), and method validation protocols. Ensure proper documentation control and record-keeping for all QC lab activities. 4. Laboratory Investigations & Risk Management: Lead investigations related to laboratory deviations, instrument failures, and non-conformities. Identify root causes and implement corrective and preventive actions (CAPA). Monitor laboratory trends to proactively mitigate risks affecting product quality. 5. Training & Continuous Improvement: Conduct training sessions on GMP, GLP, data integrity, and regulatory updates for QC and QA personnel. Promote continuous improvement initiatives to enhance lab efficiency and compliance. Stay updated on changes in pharmaceutical regulations and implement necessary changes in lab QA practices. 6. Instrument Qualification & Method Validation: Oversee qualification and calibration of analytical instruments (HPLC, GC, FTIR, UV, etc.). Ensure compliance with method validation, verification, and transfer protocols. Collaborate with QC teams to ensure analytical methods are robust and compliant.

Roles and Responsibilities Operate laboratory equipment such as GC-MS, FTIR, HPLC, UV Spectrometer, Polarimeter, Viscometer, etc. to analyze samples and gather data. Develop new methods for analyzing complex chemical compounds using various analytical techniques like spectroscopy (FTIR), chromatography (HPLC), mass spectrometry (GC-MS). Collaborate with cross-functional teams to troubleshoot issues related to product quality control and process optimization. Desired Candidate Profile 1-2 years of experience in an R&D environment handling chemicals & performing analytical work. MS/M.Sc(Science) degree in Chemistry or equivalent qualification from a recognized university. Strong understanding of chemistry principles including organic chemistry, physical chemistry, biochemistry etc. .

About the Role We are currently seeking a data-driven and detail-oriented Program Intern to join the Founder’s Office. This role will involve critical thinking, problem-solving, and analytical thinking to drive operational improvements and support strategic initiatives. The charter for this role will include Work closely with the founder/senior leaders to turn ideas into validated experiments. Dive into industry trends, discover competitor insights while also working on user research. Build a hypothesis to solve the different problem statements, execute, validate and scale the results Align with stakeholders across the org to drive the actionables; be a driving force in cross-functional teams Present findings, recommendations, and progress updates to leadership. Support key projects and initiatives, ensuring they are on track and aligned with the company's objectives Ideal Persona would Prior experience in building a start-up or interning at a start-up. Good communication and presentation skills, both written and verbal. Ability to work collaboratively and effectively with diverse teams and stakeholders. High on agency with first principle problem-solving approach Familiarity with analytical tools like Excel (advanced), SQL, Python, or other business intelligence software is a plus. Strong organizational skills and ability to manage multiple tasks simultaneously. A proactive mindset with a strong ability to identify potential problems and come up with creative solutions.

Analytical QA Reviewer - Officer: Looking for a candidate with 2 to 4 years of work experience as QC analyst / AQA reviewer in reputed pharma companies. Should have Knowledge of handling/ analytical data review of HPLC , FTIR , UV spectrophotometer , KF Autotitrator , Dissolution apparatus. Have Basic knowledge of CGMP , GDP , Data integrity . Should have Basic knowledge of OOS (Out of specification), OOT, OOC

Roles & Responsibilities 1. To perform In-process and Finished product tests for Assay, Related substance, Residual solvent, UOD, Dissolution, and Water content. 2. To perform Exhibit, Hold time and process validation samples analysis. 3. To Handle HPLC, GC, Dissolution, UV and KF systems and its maintenance. 4. To handle Empower software, sample sets loading and processing independently. 5. Good experience in chromatography. 6. Knowledge on Investigations, Deviations, OOT and OOS. 7. To handle SAP, LIMS and DCMS activities. 8. To follow good laboratory practices (GLP) and good documentation practices (GDP). Qualification Educational qualification: MSC chemistry, B-Pharm Minimum work experience: 5-7 years years in QC. Additional Information

- In this highly visible role, you will have the opportunity to make a significant impact on Apple Products, and leave a footprint for years to come. We have an opportunity for an accomplished PCBA DFM engineer to lead the development, and ramp for a next generation Apple product.- Our PCBA DFM engineering team enables the mass creation of impossible products as a partner in the development of Apples renowned designs.- Key responsibilities will include:- Attend development builds as required under direction of Operations Engineering Directly Responsible Individual (DRI).- May provide guidance and resources to contract manufacturing (CM) partner engineers.- Acts as project leader on a variety of complex projects.- Plans, develops and implements technically complex procedures for PCBA manufacturing process, rework, and testing.- Make recommendations for changes required in testing equipment (ICT and Functional test), manufacturing processes, and new testing requirements.- Designs and develops technically complex new processes to improve quality and efficiency.- Provides early manufacturing involvement to ensure new products are manufacturable. Activities include driving out costs in design/PCBA manufacturing tooling, influencing designs so that they are manufacturable, reducing complexity by using standard size packaging.- Interface with Apple Printed Circuit Board Assembly (PCBA) Subcontractor and manage technical aspects of Volume Manufacturing builds including rework processes, with direction as necessary from Operations Engineering DRI.- Ensure Apple PCBA Subcontractors/JDM partner adherence to Process Parameters and Procedures as well as approved Manufacturing and Test processes. Ensure maintenance of specified quality levels at PCBA Manufacturing sites- Travel domestically and internationally to supplier sites - 30% BS/MS in Mechanical, Electrical, Industrial, Chemical or Manufacturing Engineering with 5 to 6 years experience working in Printed circuit board assembly or with surface mount technology at a contract manufacturer or any related experience. 5+ years of experience in printed circuit assembly manufacturing processes. Surface mount technology process knowledge including stencil printing, pick and placement process, reflow process, hotbar, robotic/laser soldering and ACF process. Experience developing process quality plans, supplier quality audits, and driving corrective actions and failure analysis efforts. Preferred Qualifications Working knowledge of printed circuit board assembly (PCBA) reliability concepts, failure analysis techniques like EDX, SEM and FTIR. Experience with the development and evaluation of various SMT processes Project management experience and a deep understanding of problem solving tools including design of experiments, root cause analysis and statistical analytical tools Experience with any of the following: packaging technology, chip scale or wafer level chip scale packaging technology, molding process, System in package construction Effective communication skills with an ability to explain complex problems to a wide variety of technical and non-technical audiences Good team player with an ability to work with multiple x-functional teams Education & Experience Apple is an Equal Opportunity Employer that is committed to inclusion and diversity. We also take affirmative action to offer employment and advancement opportunities to all applicants, including minorities, women, protected veterans, and individuals with disabilities. Apple will not discriminate or retaliate against applicants who inquire about, disclose, or discuss their compensation or that of other applicants.Apple s most important resource, our soul, is our people. Apple benefits help further the well-being of our employees and their families in meaningful ways. No matter where you work at Apple, you can take advantage of our health and wellness resources and time-away programmes. We re proud to provide stock grants to employees at all levels of the company, and we also give employees the option to buy Apple stock at a discount both offer everyone at Apple the chance to share in the company s success. You ll discover many more benefits of working at Apple, such as programmes that match your charitable contributions, reimburse you for continuing your education and give you special employee pricing on Apple products.Apple benefits programmes vary by country and are subject to eligibility requirements.

As a Materials Engineer/Expert FTIR Spectroscopist, you will take ownership for conducting Failure Analysis on cross-functional projects involving different internal and external partners and ensuring that they are planned, well-executed and on time. This is a great opportunity to be a technical leader.This position offers the opportunity to make a significant impact in innovative materials analysis within a dynamic and collaborative environment. If you bring technical expertise, intellectual curiosity, and a collaborative spirit, we encourage you to apply. Masters or PhD in Chemistry, Polymer Science, Materials Science, or a related field, or equivalent experience in FTIR spectroscopy and failure analysis. Extensive experience in FTIR analysis of organic materials, polymers, adhesives, films, and plastics, especially in failure investigation and material degradation studies. Strong expertise in polymer and adhesive science, with familiarity in consumer products and consumer electronics components and assemblies. Proficient in all types of IR analysis techniques, capable of performing nuanced, tool-based spectral interpretation with careful attention to accuracy. Develop and execute experimental plans that leverage FTIR spectroscopy to solve complex material challenges, ensuring detailed investigation and reliable results. Collaborate cross-functionally with other Material Scientists and engineers on the team to develop and execute multi-technique experimental plans to drive root cause. Background in consumer electronics materials, with knowledge of typical failure modes in polymers, adhesives, and plastic components. Excellent communication skills, able to convey sophisticated technical findings in an accessible manner to diverse stakeholders. Preferred Qualifications Lead FTIR-based failure analysis and characterization of adhesives, films, plastics, and polymer systems, specifically for organic and multi-component formulations. Conduct detailed characterizations of polymers, adhesives, and films, analyzing material properties, interactions, and potential degradation mechanisms to identify root causes of failure. Collaborate closely with company-wide engineers, technical teams, and requestors to ensure alignment on project goals and effective communication of findings. Utilize a broad range of IR analysis techniques (ATR, transmission, micro-spectroscopy) and perform skilled and insightful interpretation of spectra with minimal reliance on automated libraries, and avoiding over-interpretation. Engage with cross-functional team members and specialists as needed, recognizing when additional expertise is required to achieve the best outcomes. Contribute to the development of innovative FTIR and other molecular, optical and/or polymer analysis methodologies and best practices within the team, continuously advancing our analytical capabilities. Highly collaborative, with a natural curiosity and a creative, solution-driven approach to problem-solving. Ability to work independently while encouraging a collaborative environment, supporting knowledge sharing, and teamwork across projects.

- Develop analytical methods for OSD products using techniques such as UV, FTIR, Dissolution, HPLC, GC, Ion Chromatography, Wet Analysis etc. - Conduct method validation studies to ensure compliance with regulatory requirements. - Collaborate with cross-functional teams to resolve method-related issues and improve process efficiency. - Ensure timely completion of tasks assigned by supervisors while maintaining high-quality standards.

Openings for Residue analysis persons in Food Testing - Hyderabad , Navi Mumbai , Ahmedabad Designation : Junior / Senior Analyst Experience: 2- 10 Years Department : Residue Location : Hyderabad Qualification : M.Scs. (Organic Chemistry/Chemistry/Analytical chemistry) Industry : CRO & Testing Laboratory (Third party testing lab ) Roles and Responsibilities: Analysis of Pesticide residues of Food and Agriculture products as per SOPs, IS, AOAC, FSSAI. Method development, validation and report preparation. Operation and Calibration of equipment i.e., LC-MS/MS, GC-MS/MS, Analysis of Pesticide residues in Water samples. Analysis of Antibiotics in Aqua & Marine products, Feed, Milk & Milk products. Analysis of Pesticide Residues in Fruits and vegetables, Milk & Milk products, Feed & Feed Products and Miscellaneous samples. Mycotoxin analysis in Food & Agricultural products and feed samples. Use and calibration of instruments such as Micro Pipettes, Analytical Balance, Micro balance, Centrifuge, Turbo Evaporator, HPLC & GC. Analysis of Residue in food by LC MS/MS,GC MS/MS, method development and validation, food additives, contaminants analysis on HPLC,GC with different detectors, Worked in ISO 17025:2017 and FSSAI approved lab NABL audit will be added advantage. Regards, Priyanka Jajula

locationsMUMBAI, IND time typeFull time posted onPosted 4 Days Ago job requisition idR1147726 . Front ending the customer Driving CRAs to improve the efficiency Offers of employment are conditional upon passage of screening criteria applicable to the job.

Excellent Opportunity! Analysts required in the QC department at Unison Pharmaceuticals Pvt Ltd, Moraiya. Apply Now!!! Company: Unison Pharmaceuticals Pvt Ltd Experience: 1-8 Years Qualification: B.Pharma/M.sc/M. Pharma Location: Moriya, Ahmedabad Job Role : Physico Chemical (Analyst)- Friability / DT / Hardness / Thickness / UV Perform physical and chemical analysis for Raw material/ Inprocess / Finished Product based on the test requirements like UV, friability, DT, hardness, thickness, moisture, average weight, and uniformity weight. Prepare documents for each analysis performed and get those checked by the reviewer. 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, we encourage you to apply for this position. Please submit your resume to career@unisonpharmaceuticals.com to be considered for this role. Join our team at Unison Pharmaceuticals and take the first step towards a rewarding career!!! Regards Team HR Unison Pharmaceuticals Pvt. Ltd.

Walk-in Drive @ Ahmedabad on 18th May'25 (Sunday) for Quality Control Department We are looking for suitable candidates for OSD Quality Control for Ahmedabad location Unit Interview Venue Details: Date: 18th May 25 (Sunday), Time: - 9:00 AM to 1:00 PM Venue : Amneal Pharmaceuticals Pvt. Ltd Survey No. 634,637-641 Village: Rajoda Tal: Bavla Dist: Ahmedabad -Gujarat - 382220 1) REQUIREMENT FOR OSD QUALITY CONTROL DEPARTMENT Total Experience: 02 to 7 years (Pharma experience only) Qualification: B.Sc./ M.Sc/ B. Pharm/ M. Pharm Designation: Officer/ Sr. Officer /Executive/ Sr. Executive Department: Quality Control Desired Profile: Test RM, PM, in-process, finished & stability samples (various dosage forms i.e., tablet, Capsules, oral suspension/ ointment/powder etc) as per SOPs/pharmacopeia Operation of HPLC, GC, UV, FTIR, Dissolution, KF, wet & physical tests Troubleshoot basic issues Ensure ALCOA adherence in shift activities Candidate with good communication & interpersonal skills, computer knowledge, exposure to cGMP and understanding of regulatory requirement will be preferred. Note : Candidate should relevant experience in USFDA regulatory approved pharmaceuticals (Preferred 21 CFR compliant) organization. Kindly carry your updated CV along with copies of CTC proof, Appointment letter, Increment letter, last 3 months salary slips, Bank statement, Education certificates & Marksheets, Aadhar & PAN card and passport size photograph, at the interview venue. Disclaimer: Beware of fake job offers claiming to be from Amneal Pharmaceuticals Pvt. Ltd. or Companies under Amneal Group (collectively referred to as AMNEAL). Amneal neither send job offers from free email services like Gmail, Rediffmail, Yahoo mail, Hotmail, etc. nor charges any fees/security deposit from any job seekers. Amneal will not be responsible to anyone acting on an employment offer not directly made by Amneal. Stay vigilant and report any suspicious activity to Amneal.

Conduct Extractables & Leachable studies Operate LC-MS/MS, GC-MS/MS, UHPLC, GC-FID Method development, validation & data interpretation Ensure GLP, NABL, 21 CFR Part 11 compliance Exp. in PFAS, BPA, Nitrosamines preferred MSc/M.Pharm/Biotech required

Job Title - CAL- PRD + Level :Senior Manager + S&C- IMU Management Level:6- Senior Manager Location:Mumabi/ B'lore Must have skills: Account management Good to have skills:NA Experience: Minimum 11+ years of experience Educational Qualification: Graduation/ Post Graduation from a premier B School Roles & Responsibilities: Growing business: Contribute to expanding Accentures footprint and share of wallet in client/industry; accountable for portion of business results on the account (at a minimum.) Bring disruptive and innovative ideas to originate new opportunities (while also pursuing business-as-usual opportunities.) Leverage industry networks and partner with experienced CALs to understand the overall growth of the industry at Accenture and build industry mastery. Get involved in complex commercial problems and negotiations. Deepen Accenture acumen (e.g., organizational constructs/networks/offerings/ecosystem partners) to assess how to bring all of Accenture to the client. Lead/contribute to development of assets and offerings. Build long-standing, trust-based relationships Establish self as a trusted advisor with the client C-suite through an in-depth understanding of the client as well as industry Build networks at Accenture to be able to bring the best of Accenture to the client Professional & Technical Skills: Rich experience in the Consumer Goods industry with in-depth industry expertise including the industry/digital/technology trends Demonstrate sustained client relations management experience at a C-suite level or operated at a senior management level in the industry role Experience of 11+ years in consulting and account management experience; domestic consulting experience preferred. Experience of working in a consulting firm will be preferred Experience of working with C-level executives at the client organization. About Our Company | Accenture Qualifications Experience: Minimum 11+ years of experience Educational Qualification: Graduation/ Post Graduation from a premier B School

Ensure that the manufactured products consistently meet established standards, customer specifications, and industry regulations Optimize processes and drive continuous improvement initiatives Product Modification/ Development as per customer need Required Candidate profile B. Sc Chemistry with M. Sc Polymer Science mandatory 12+ years' experience in Quality Assurance & Control in a chemical/ polymer manufacturing company (preferably in polystyrene manufacturing)

Department: Pharma Standard - AD Required Qualification & Experience: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 5 Years of experience in the field of pharmaceutical industry/CRO setup. For Preparative: Experience on instruments like Preparative HPLC and SFC Expertise in Purification of peptides, impurity isolation. For Analytical: Expertise Analytical Method Development of peptides and oligoes. Regular sample analysis for supporting to synthesis team. Handling experience on DAC column packer and media packing will be advantageous. Department: Pharma Standard - Quality Control Required Qualification & Experience: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 5 Years of experience in the field of pharmaceutical industry/CRO setup. Theoretical knowledge and hands-on experience on instruments like Shimadzu HPLC with Lab solution software, Agilent HPLC, Balance, pH meter, TGA instrument, FTIR. CGMP,GMP, experience on LCMS is preferrable. Knowledge on Data Integrity, GDP, QMS. Department: Pharma Standard - Inventory Required Qualification & Experience: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 5 Years of experience in the field of pharmaceutical industry/CRO setup. Management of Inventory items, handling, weighing, dispatching of inventory materials. Hands-on experience on semi-microbalance, microbalance. Maintaining Real time stock updation of the inventory list in excel or SAP system and updating the stock quantities to the relevant stakeholders, whenever required. Basic understanding on Data Integrity, GDP and QMS Please bring your Updated CV along with last 3 Months Payslips, Recent Increment Letter, Aadhar Card/PAN Card: Date : Saturday, 10 May 2025 Time: 09:00 AM to 4:00 PM Walk-in Interview Location: Daicel Chiral Technologies (India) Pvt Ltd Genme Valley, IKP Knowledge Park, Survey No. 542/2, Koltur Village, Shamirpet Mandal, Medchal-Malkajgiri District, Hyderabad-500101 Note: Candidates who are unable to walk-In, May send their resume to hr@chiral.daice.com or whatsApp to 9000066897

Department: Pharma Standard - AD Required Qualification & Experience: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 5 Years of experience in the field of pharmaceutical industry/CRO setup. For Preparative: Experience on instruments like Preparative HPLC and SFC Expertise in Purification of peptides, impurity isolation. For Analytical: Expertise Analytical Method Development of peptides and oligoes. Regular sample analysis for supporting to synthesis team. Handling experience on DAC column packer and media packing will be advantageous. ************************************************************************************************** Department: Pharma Standard - Quality Control Required Qualification & Experience: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 5 Years of experience in the field of pharmaceutical industry/CRO setup. Theoretical knowledge and hands-on experience on instruments like Shimadzu HPLC with Lab solution software, Agilent HPLC, Balance, pH meter, TGA instrument, FTIR. CGMP,GMP, experience on LCMS is preferrable. Knowledge on Data Integrity, GDP, QMS. ************************************************************************************************** Department: Pharma Standard - Inventory Required Qualification & Experience: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 5 Years of experience in the field of pharmaceutical industry/CRO setup. Management of Inventory items, handling, weighing, dispatching of inventory materials. Hands-on experience on semi-microbalance, microbalance. Maintaining Real time stock updation of the inventory list in excel or SAP system and updating the stock quantities to the relevant stakeholders, whenever required. Basic understanding on Data Integrity, GDP and QMS Please bring your Updated CV along with last 3 Months Payslips, Recent Increment Letter, Aadhar Card/PAN Card: Date : Saturday, 10 May 2025 Time: 09:00 AM to 4:00 PM Walk-in Interview Location: Daicel Chiral Technologies (India) Pvt Ltd Genme Valley, IKP Knowledge Park, Survey No. 542/2, Koltur Village, Shamirpet Mandal, Medchal-Malkajgiri District, Hyderabad-500101 Note: Candidates who are unable to walk-In, May send their resume to hr@chiral.daice.com or whatsApp to 9000066897

Preferred candidate profile Looking for a candidate with 2 to 4 years of work experience as QC analyst /AQA reviewer in reputed pharma companies. Should have Knowledge of handling/analytical data review of HPLC, FTIR, UV spectrophotometer, KF Autotitrator, Dissolution apparatus. Have Basic knowledge of CGMP, GDP, Data integrity. Should have Basic knowledge of OOS (Out of specification), OOT (Out of rend), OOC (Out of calibration).