68 Analytical Testing Jobs - Page 3

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)

About The Role Position Summary: Ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations Essential Duties and Responsibilities Applies GMP/GLP in all areas of responsibility, as appropriate Demonstrate and promote the company vision Regular attendance and punctuality Read and understand analytical procedures Review documentation, generated data, calculated results, and final reports according to departmental, corporate, and client SOPs Gain a technical understanding of the techniques in which review is being performed Use MS Windows applications such as EXCEL, Word, Access, Outlook email Conducts all activities in a safe and efficient manner Performs other duties as assigned Qualifications Basic Minimum Qualifications: To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements below are representative of the knowledge, skill or ability required. Education/Experience: A masters degree in Pharmaceutical/Analytical Chemistry Experience level : 0"“2 years of Analytical testing of Pharmaceutical Raw Material (e.g. ROI, LOD, pH, KF, etc) and GMP experience preferred. Additional Information 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 Strong Math Skills Logical Thinking, Good Reasoning Ability Motivation to excel Coaching/mentoring of peers

Job Title: Quality Manager Location : Mundra (Gujarat), Chittorgarh (Rajasthan), Vadakkencherry (Kerala) Company: RamKripa International Job Type: Full-Time Qualification: Graduation Experience Required: 2-5 years of experience in quality control and Laboratory Salary Range: 18,000 - 25,000 per month About the Company- RamKripa International RamKripa International is a 100% export company specializing in minerals, agro-inputs, and industrial products. We deliver high-quality limestone, fertilizers, and related materials to global markets, with a strong commitment to quality, innovation, and customer satisfaction. Job Summary The Quality Manager will lead and supervise all quality control activities within the production process, ensuring that every product meets customer expectations, complies with industry benchmarks, and adheres to regulatory requirements. Key Responsibilities The role involves inspecting raw materials, monitoring the production process, and checking finished products. It also includes conducting audits and ensuring compliance with standards, maintaining quality documentation and reports, and identifying and resolving quality issues. Required Qualifications Applicants should have a graduation degree in Engineering, Science, or a related field and must possess knowledge of quality assurance methods and industry standards. Experience A minimum of two years in a quality control role in a manufacturing industry or Laboratory is required. Skills Required Sample testing . Salary Range 18,000 - 25,000 per month (Net)

At Umendra Life Sciences Pvt. Ltd. , we take quality seriously. Our products are trusted by consumers worldwide, and were looking for a Quality Control (QC) professional to ensure they meet the highest standards. If you're passionate about precision and excellence, this role is for you. Your Role: As part of our QC team , you'll focus on testing raw materials, in-process samples, and finished products to ensure they meet established specifications. Your job is to detect and prevent defects before products reach the market. Key Responsibilities: Conduct physical and chemical testing of raw materials and final products (pH, viscosity, stability, active ingredient analysis). Perform stability studies to ensure product consistency over its shelf life. Test emulsions, creams, lotions, gels, ointments, and serums for quality parameters like texture, fragrance, absorption, and spreadability . Verify the quality of packaging materials (bottles, tubes, jars, labels) to prevent contamination or leakage. Use analytical instruments like HPLC, GC, FTIR, and UV spectrophotometer to test active ingredients. Maintain batch release records and ensure compliance with international quality standards . Investigate batch failures, customer complaints, and product recalls , and suggest improvements. Knowledge of Validations, QMS, CVC, etc. Qualifications & Experience Required: Education: Bachelor's/Masters degree in Chemistry, Microbiology, Pharmacy, or a related field . Experience: 2-5 years in Quality Control within Personal Care, Cosmetics, or OTC Manufacturing . Skills: Strong knowledge of analytical testing, regulatory compliance, and quality verification techniques . Technical Expertise: Hands-on experience with HPLC, GC, FTIR, and UV spectrophotometer is preferred. Join us in delivering safe, effective, and high-quality personal care products that people trust. Note : Candidates from Ahmedabad, Varodara, ankleshwar,Surat,Bharuch, Mehsana, Dahej and Surendranager are Preferred.

Role & responsibilities Develop and implement quality control processes, procedures, and guidelines to ensure consistency, reliability, and compliance with quality standards and regulations. Conduct inspections and audits of production processes, materials, components, and finished products or services to identify quality issues, defects, or non-conformities. Review specifications, blueprints, and technical documents to understand quality requirements, tolerances, and acceptance criteria for products or services. Collect and analyze quality data, metrics, and performance indicators to evaluate process capabilities, identify trends, and drive continuous improvement initiatives. Monitor adherence to quality standards, work instructions, and regulatory requirements throughout the production process, ensuring compliance with ISO, FDA, or industry-specific quality standards. Train and educate production staff on quality control processes, procedures, and best practices, fostering a culture of quality awareness, accountability, and continuous improvements Preferred candidate profile Min 2 years experience of working in similar industries. Candidates having QC experience with critical instruments handling skill like GC, Spectrometer, Viscometer, pH meter, Conductivity meter, analytical testing with using volumetric solution etc. Having excellent skill in English speaking, computer knowledge in excel, word & ppt, SAP operating experience is must for QC job