46 Analytical Testing Jobs - Page 2

Role & responsibilities An experienced customer service professional for a role that includes technical knowledge in mechanical and chemical/analytical testing. Customer-facing strengths with enough domain understanding to engage clients confidently, solve problems, and identify business opportunities. Preferred candidate profile Qualifications: Essential: B.Sc./Diploma/B.tech in textile/Graduation Desirable: Good communication skills Experience Profile : Minimum Years : 3 Years ; Maximum Years : 15 Years Industry/ Sector: Textile Testing Scope of job /Activities handled: Customer Services Key Results Areas ( KRAs) & Key Deliverables : Handle day to day operations in a timely, complete and proper manner Responsible to review the orders prior to sample registration and clear the queries with the customer beforehand. Select the correct package / tests to register the sample. Ensure that samples are booked correctly as per the request. Follow up, monitor and report on all pending activities to the customer Prepare and send quotations within set deadlines (when requested). Responsible for the timely delivery of the test reports and emailing the soft copy to the right contact. Constantly strive to deliver outstanding services Listen to and anticipate the clients needs to offer the most suitable solution Always act in a friendly and reliable manner Prepare regular job status report and communicate to CS Manager Act upon client feedback Manage timely trouble shooting and assist customers as necessary Ensure availability to customers Build and foster collaboration with internal teams involved in service delivery Go beyond regular service level and provide extra-mile support Abreast of SGS new products and services and propose them to customers as appropriate Ask for more business while interacting with customers Go beyond clients' core business to identify new opportunities Act upon or forward business opportunities beyond sphere of influence to the sales team Promote a positive image of SGS Interested candidate can mail the resume along with below details to preetika.rolston@sgs.com or call on +91 9026338996 Current CTC Expected CTC Total Experience Highest Qualification Current Compnay Notice Period

Experience: 4-8 Year Experience in manufacturing (API) as per Pharma Manufacturing GMP requirements. Responsibilities for Internal Candidates Key Roles & Responsibilities 1. Capable to handle independent projects 2. Analytical testing support to PDG synthetic group. 3. Coordinate with QA regarding method transfer, CCF and investigation reports. 4. Experience of handling of HPLC, GC, Potentiometer, Polarimeter instruments. 5. API Stability knowledge. 6. Capable to handle analytical method development, Implementation, Validation as per requirement. 7. Should have experience of Analytical method transfer to QC. 8. Experience of making documents like method transfer protocol & report, method validation protocol & report, method development report, specification, standard test procedure etc. 9. Should aware about GLP practices and 21 CFR part-11. 10. Keep the work area clean and the laboratory under controlled temperature. 11. Calibrate the instruments according to the master calibration schedule and follow GLP and SOPs. 12. Understand the safety and environmental aspect. 13. Maintain the reagents and standardize the volumetric solutions as per schedule. 14. Maintain the laboratory journals and instrument log books online. 15. Ensure compliance to Hazardous waste and chemical management. Responsibilities Qualifications Qualification : M.Sc (Analytical Chemistry), (Chemistry) & (Organic Chemistry)

Should able to perform and supervise following routine tests of general chemical nature:- To perform all tests on water i.e. pH, TDS, TSS, harnesses, alkalinity, BOD, COD etc. Pigment testing, Chemical Testing, application, analytical testing

Should be able to guide chemists and supervisor of the Laboratory to carry out Analytical tests and Application tests for Pigments. Analytical Testing Application Testing Pilot and R&D Testing Required Candidate profile Minimum 20 years’ experience in a Phthalocyanine Pigment Industry manufacturing Alpha, Beta Blues and Green Pigments.

As a QC Chemist, your primary role is to ensure the quality and integrity of raw materials, intermediates, and finished products in a chemical manufacturing setting. You'll be responsible for performing various analytical tests, interpreting results.

Long Description 1 Exposure to perform the testing of Inprocess, Finished product, Stability and Cleaning validation samples etc. 2 Having knowledge of Analytical Instruments to perform the testing by HPLC, GC, UV, IR, KARL FISCHER etc. 3 Having Analytical testing skills to perform the MDI/DPI Products test like Assay, APSD, DDU, RS, Spray Pattern, FPM and physical testing etc. 4 Exposure of Laboratory investigation like OOS, OOT, Incidence, Deviation. 5 Exposure of Stability sample management & Regulatory Audits. 6 Exposure of Analytical method transfer, Analytical method validation / Verification activity. 7 Knowledge of GLP and Good documentation Practices. Competencies Innovation & Creativity Result Orientation Collaboration Customer Centricity Developing Talent Stakeholder Management Strategic Agility Process Excellence Education Graduation in Pharmacy Work Experience 5 to 8 years

FSSAI Approved 1.Perform chemical analysis of food samples. 2.Operate instruments like HPLC,GC-MS. 3.Ensure compliance with FSSAI, NABL & ISO standards 4.Conduct method validation 5.Preapre test reports and audit documentation 6. Supervise lab staff

Eurofins Scientific is an international life sciences company that provides a wide range of analytical testing services to clients across multiple industries. From food and pharmaceuticals to environmental and cosmetic products, Eurofins ensures safety, authenticity, and accuracy. With a global presence and over 900 laboratories, Eurofins is a leader in food, environmental, pharmaceutical and cosmetic product testing, as well as in genomics, clinical studies support, and other specialized diagnostic testing. Support processing of incoming samples by accurate and timely entry and review of sample information in LIMS. Employee Responsibilities: Audit sample information, including the formal review of all protocols, specifications, methods, and other documents submitted by the client or used by the project within a LIMS system. Manage technical information within a LIMS system relating to Sample Management. Send entry instructions to the sample administration regarding incoming samples. Direct client interaction via email Communicate with Project Management, Inside/Outside Business Development, and Technical groups as necessary to complete assignments Communicate regular status updates to supervisor Qualifications M.Pharm/M.Sc Additional Information Experience level : 3 - 5 years in Bio/Pharmaceutical Analysis Key Candidate Attributes: Self-motivation; excellent quality of work and attention to detail Ability to communicate effectively with coworkers and internal/external clients Ability to learn new tasks quickly and to move easily from task to task Ability to handle prioritization and multiple tasks simultaneously Ability to use a personal computer and learn necessary programs Good communication skills (oral and written) Organizational ability and good judgement Science background/education and/or laboratory experience

- Having experience in manufacturing cosmetics related products such as Cream, Lotion, Shampoo, Face Wash, Cleaner, Skincare, Nailpolis etc. - Supervising in-process quality control and managing bulk approvals and finished goods (FG) release. Required Candidate profile - Hands-on experience in instrumental and analytical testing of raw materials (RMs). Maintaining comprehensive records of quality tests, inspections, and other related activities.

About the Role: Responsible for analytical testing, documentation, and lab operations as per GMP standards. Key Responsibilities: Conduct chemical and instrumental analysis (HPLC, GC, UV, etc.) Ensure compliance with SOPs and GLP Prepare COAs and maintain records Calibrate and maintain lab instruments Coordinate with QA and production teams Qualifications & Skills: B.Sc / M.Sc / B.Pharm / M.Pharm 23 years experience in QC lab (pharma/chemical) Proficiency in analytical instruments and documentation Application Process: Interested candidates can send their resume, current CTC, and expected CTC to omshrilabs.hr@gmail.com Email Subject Format: Role: QC Officer | Name: [Your Name] | Experience: [Years] Only shortlisted candidates will be contacted. This is a full-time, on-site position based in Kota, Rajasthan. Immediate joiners preferred.

A dynamic and result-oriented Scientist R&D to lead the research and development activities of plant nutrition and bio stimulant products. The ideal candidate will be responsible for formulation development, innovation, process optimization, quality control, and regulatory compliance to bring next-generation products to market. Key Responsibilities: • Lead R&D projects on the development of bio stimulants, micronutrient formulations, specialty plant nutrition products and bio botanicals. • Identify and validate new active ingredients from natural sources. • Drive scientific innovation to improve product performance and process improvement of the existing products and new product development. Prioritize and manage multiple projects, ensuring timely progress, budgeting, and milestone achievements. • Prepare technical documentation including SOPs, and product dossiers. • Collaborate with agronomy, regulatory, and production teams for product concept, positioning, and scale-up. • Coordination with quality control department and production department to ensure product consistency and compliance. • Foster a culture of innovation, safety, and continuous learning. • Responsibility for patent drafting, scientific publications, and technical presentations. Job Specification: • Education: Ph.D. in Chemistry (Organic chemistry/ Analytical chemistry). • Experience: 1-3 years in Industrial R&D preferred. • Expertise in application of sophisticated analytical instruments like AAS, UV, IR, GC and HPLC for product characterisation and estimation of active molecules. Kindly drop your resume at hr@marisymbio.com / 8220342663

Role & responsibilities We are seeking a skilled and proactive Instrumentation Maintenance Engineer to manage the complete maintenance lifecycle of analytical instruments and lab equipment. The ideal candidate will ensure optimal performance, calibration, and compliance of instruments used in quality control and R&D labs. Preferred candidate profile

Ensuring the quality of APIs through testing, analysis, & documentation Sample & inspect raw materials Maintain an accurate & complete record of testing, analysis Investigate deviations from the quality standard Ensure compliance with GMP regulations Required Candidate profile Bachelor's degree in B.Sc/M.Sc Chemistry, B.Pharm/M.Pharm. Previous experience in QC in API pharma manufacturing Strong knowledge of analytical techniques & instrumentation, e.g., HPLC, GC, UV-Vis

• Site analytical testing , evaluation and Development • Implementation of Pharmacopeial Updates and Source Change Document. • Managing master data operations within the LIMS and SAP system. • Developing, Optimizing, Validating, Verifying and Method transfer of analytical methods. • Ensuring discipline in Track Wise by monitoring pending tasks and facilitating the closure of quality events. • Ensuring adherence to regulations and maintaining the completeness of relevant logbooks or registers.

ABOUT AGRATAS Agratas is a wholly owned subsidiary of Tata Sons. We design, develop and manufacture high-quality, high-performance, sustainable batteries applied to multiple use cases in the mobility and energy sectors, to match our customers requirements. Agratas is a scale-up business with a start-up mentality, driven by our pursuit of green growth and technological progress. We develop next-generation battery technologies at our state-of-the-art R&D Innovation Hubs in India and the UK. JOB SUMMARY The In-Process Quality Manager is crucial in ensuring the quality and reliability of EV battery cells throughout the manufacturing process. Reporting to the Site Quality Head, this role involves developing and implementing quality control procedures, managing in-process quality assurance, leading a team, and ensuring compliance with industry standards. The IPQC Manager will drive continuous improvement initiatives, manage lab operations and collaborating with various teams. The position also includes responsibilities for training, value stream mapping, and supporting critical deliverables. You will manage a team comprising Shift Supervisors, Quality engineers, SMEs. Your responsibilities will include active participation in collaborative efforts aimed at enhancing both product quality and manufacturing processes, This position is essential for maintaining high standards of quality in our production processes and ensuring the delivery of reliable and high-performance battery cells. RESPONSIBILITIES In-Process Quality Control and Assurance: Create and enforce in-process quality control procedures and standards, ensuring adherence to company and regulatory specifications. Track and analyse key performance indicators (KPIs) related to in-process quality. Implement corrective actions as necessary to address deviations. Perform regular Process verifications audit of manufacturing processes to verify compliance with quality standards and identify areas for improvement. Review quality data to detect trends and drive continuous improvement initiatives. Ensure that in-process materials and components meet required specifications before advancing to subsequent production stages. Keep accurate records of quality inspections, non-conformances, and corrective actions. Prepare and present quality performance reports to senior management. Engage in continuous improvement initiatives, contributing ideas to enhance manufacturing processes and product quality. Build and Maintain Value stream Maps: Develop and maintain value stream maps for in-process quality for E-Zone, A-Zone and B -Zone, ensuring efficient quality control processes and identification of areas for improvement. Lab Management: Oversee the in-process quality labs, ensuring accuracy and reliability in all analytical testing. Oversee Operations: Manage the operational efficiency and accuracy of testing within quality labs. Ensure that all tests are performed according to established procedures. Quality Control: Develop and enforce quality controls for in-process cells, resolving testing issues and ensuring timely, accurate lab work. Ensure standard operating procedures (SOPs) and testing methods to reflect best practices and regulatory requirements. Analyse abnormal data, providing actionable recommendations to relevant teams to address any issues and improve lab processes. Team Leadership: Manage Team: Lead and manage a team of quality engineers and technicians. Provide training, guidance, and performance management to ensure high-quality outputs. Training Programs: Develop and deliver comprehensive training programs for quality technicians, covering equipment operation, quality control methods, and safety protocols. Foster Communication: Promote teamwork and open communication within the team. Ensure lab staff are proficient and adhere to departmental policies and procedures. Supplier and Equipment Interaction: Collaborate with Suppliers: Work with equipment suppliers for demonstrations and support the procurement process for quality lab equipment. Monitor and maintain clean and dry room requirements for quality labs. Maintain Facilities: Ensure that lab facilities and equipment are well-maintained and meet operational requirements. Continuous Improvement and Regulatory Compliance: Lead Investigations: Investigate deviations, out-of-trend results, and test failures associated with production and testing processes. Implement corrective actions as needed. Drive Improvements: Lead continuous improvement initiatives to enhance laboratory quality and efficiency. Promote 5S and lean manufacturing principles. Ensure Compliance: Ensure adherence to relevant quality standards (e.g., ISO 9001, IATF 16949, ISO 14001). Conduct process audits to ensure SOPs and quality standards are followed. Performance Management and Communication: Set Targets: Define and manage quality targets and metrics. Develop and implement action plans to address any deviations from expected performance. Communicate Effectively: Clearly communicate priorities, expectations, and responsibilities to the team. Ensure alignment and understanding across the department. If Relevant experience, then mail your resume at Pooja.tiwari@agratas.com

Product Development/Product performance/Process Parameter Knowledge on modification of activated carbon structure Develop specialty carbons for gas phase potable waters Testing as per international testing procedures Establishment of Quality system Required Candidate profile Contact: 8939813208 Mail ID: finadsorbent@carbons.in

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

Candidate should do the UI/Functional/Integration testing; coordinate with team & client; follow quality standards; write/execute test cases; knowledge of test methods, MS Office; bonus: automation tools; strong analytical & communication skills.

Key Responsibilities Quality Strategy & Planning Develop and implement quality control standards, procedures, and policies. Define inspection criteria and quality benchmarks. Team Management Lead and supervise a team of quality inspectors or analysts. Provide training and guidance to QC staff. Manage and supervise QC laboratory activities Use effective negotiation skills to drive alignment and resolve conflict Inspection & Testing Oversee routine inspections and testing of raw materials, in-process, and finished products. Ensure compliance with internal and external specifications and regulations. Documentation & Reporting Maintain detailed records of quality control activities. Analyze QC data and generate reports to identify trends and areas for improvement. Compliance & Audits Ensure compliance with ISO, GMP, or other industry-specific standards. Coordinate and support internal and external audits. Problem Solving Investigate product quality issues and customer complaints. Implement corrective and preventive actions (CAPA).

To Lead and manage day to day activities at the Lab not limited to only recording data, maintaining equipment, including protecting the accuracy and efficiency of the experiments while keeping the lab organised. Contact : Hr.Apurva (8799969317)