18 Wet Chemistry Jobs

As a Quality Control Technician III at Teva Pharmaceuticals, you will play a crucial role in ensuring the quality and safety of our products. With TAPI being the leading international supplier of active pharmaceutical ingredients (APIs), your responsibilities will include maintaining 24/7 audit readiness, utilizing experience in Wet Chemistry, and working in different shifts as needed. You will participate in internal, external, and regulatory audits, ensuring 100% participation in trainings against Corrective and Preventive Actions (CAPAs). Additionally, you will be responsible for initiating and investigating LIR, OOS, OOT, and borderline results, reporting them to the designated in-charge, and sharing necessary documents from Quality Control to Regulatory Affairs or other departments as required. In this role, you will determine team priorities in alignment with the plant's needs, coordinate with the team leader/manager, and uphold housekeeping, cGMP, GLP, and safety guidelines in the laboratory. Your duties will also involve sampling and analyzing raw materials, finished goods, intermediates, and cleaning samples, performing analytical tests following SOPs and monographs, and calibrating and verifying instruments. Maintaining the reserved samples room, chambers, autoclaves, and incubators, as well as helping in the preparation of department-related documents such as Standard Testing Procedures (STPs) and Standard Operating Procedures (SOPs), will be part of your responsibilities. You will ensure the sampling of finished products, raw materials, and intermediates for external analysis and timely labeling of approved and rejected samples. Additionally, you will be accountable for managing chemical stock records and reconciliation of standards. To qualify for this role, you should hold a Bachelor's or Master's degree in Chemistry and have a minimum of 3 years of relevant experience. Your attention to detail, adherence to safety and quality standards, and ability to collaborate effectively with team members and leaders will be critical to your success in this role. At Teva Pharmaceuticals, we are committed to Equal Employment Opportunity, including individuals with disabilities and veterans. Join us in our mission to uphold the highest standards of quality and integrity in pharmaceutical manufacturing.,

As a Quality Control Technician III at TAPI, you will be an integral part of the leading international supplier of active pharmaceutical ingredients (APIs). TAPI boasts the industry's broadest portfolio, which includes over 350 API products. With a rich history spanning over 80 years, we are recognized as one of the most trusted API suppliers globally, catering to 80 PERCENT of the top 50 pharmaceutical companies. At TAPI, our commitment to excellence is driven by our experience, expertise, cutting-edge technologies, and unwavering dedication to exceptional customer service. Your primary responsibilities will include maintaining 24/7 audit readiness, possessing expertise in Wet Chemistry, and being flexible to work in different shifts. You will actively participate in internal, external, and regulatory audits, ensuring full compliance with CAPA trainings. Additionally, you will be responsible for initiating and investigating LIR, OOS, OOT, and borderline results, promptly reporting them to the designated authority. Collaborating with various departments, you will facilitate the sharing of necessary documents from Quality Control to Regulatory Affairs and other relevant areas. In your role, you will play a crucial part in determining team priorities aligned with the plant's requirements, while coordinating effectively with team leaders and managers. Upholding stringent quality standards, you will adhere to housekeeping practices, cGMP, GLP, and Safety Guidelines within the laboratory. Your duties will encompass sampling and analyzing raw materials, finished goods, intermediates, and cleaning samples as per specific requirements, meticulously documenting results in analytical sheets, QA forms, LIMS, and online systems to ensure data integrity. Furthermore, you will conduct analytical tests following established monographs and SOPs, oversee the calibration and verification of instruments, and manage the reserved samples room along with chambers, autoclaves, and incubators. Your support will also be essential in preparing department-related documents such as STPs, SOPs, and more. Ensuring the timely sampling, approval, and rejection of labels for various products and maintaining accurate stock records of chemicals will be among your key responsibilities. To excel in this role, you should hold a Bachelor's or Master's degree in Chemistry and possess a minimum of 3 years of relevant experience in a similar capacity. Your dedication to upholding Teva's Equal Employment Opportunity commitment, which includes supporting diversity and providing equal opportunities to individuals with disabilities and veterans, is paramount in our inclusive work environment.,

You will be joining our analytical team as a Junior Chemist, where your passion for chemical testing, wet chemistry, and spectrometry of metals and industrial materials will be utilized effectively. Your key responsibilities will include conducting chemical testing (both wet and instrumental) on metals, alloys, and chemicals, as well as operating and maintaining spectrometers, muffle furnaces, and other lab equipment. Additionally, you will be responsible for preparing reagents, managing chemical inventory, ensuring test accuracy, and submitting reports in a timely manner. It is crucial for you to adhere to laboratory quality and safety protocols at all times. To qualify for this role, you should hold a B.Sc. or M.Sc. degree in Chemistry, with at least 1-3 years of experience in a chemical or metallurgical lab being preferred. Familiarity with ICP/OES or Atomic Absorption Spectrometry would be considered a plus. Attention to detail and the ability to precisely follow procedures are essential qualities we are looking for in the ideal candidate. This is a full-time position suitable for both freshers and experienced candidates. In return, you will receive commuter assistance as part of the benefits package. The work schedule will consist of day shifts on a fixed rotation basis. Additionally, you will have the opportunity to earn performance bonuses and yearly bonuses based on your contributions to the team. Please note that the work location is in Navi Mumbai, Maharashtra. You should be able to reliably commute to this location or be willing to relocate before starting work. This is an in-person position that requires your physical presence at the workplace.,

About Apotex Inc. Apotex Inc. is a Canadian-based global health company dedicated to producing high-quality, affordable medicines for patients worldwide. With a workforce of almost 7,200 employees engaged in manufacturing, research and development, and commercial operations, Apotex medicines are available to patients in over 75 countries. The company's focus on generic, biosimilar, and specialty products is supported by vertical integration. Job Summary As a member of the ARD-Test Centre team, you will work under the guidance of a Supervisor or senior chemist. Your responsibilities will include conducting method validation for new products, performing full testing of API, in-process and finished dosages, and preparing regulatory submission documentation. You will also play a key role in project working teams. Job Responsibilities - Conduct validation of analytical testing procedures for drug substances and drug products. - Perform initial testing, stability sample testing, in-process testing, and raw material testing according to specifications. - Carry out additional tests required for dosage submissions. - Document and report results following established Standard Operating Procedures (SOPs). - Provide technical support to other departments in responding to deficiency letters from regulatory agencies. - Work collaboratively and safely as part of a team to achieve desired outcomes. - Exhibit behaviors aligned with organizational Values: Collaboration, Courage, Perseverance, and Passion. - Adhere to all compliance programs, including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety, Health and Environment policies, and HR policies. - Collaborate with peers in R&D solid dosage to enhance expertise and address their needs. - Refer complex issues, along with recommendations, to the Supervisor. - Ensure all work is carried out in compliance with regulatory, compliance, and safety requirements. - Provide compliant advice to internal contacts and make complex decisions in alignment with regulations. - Perform any other relevant duties as assigned. Job Requirements Education: A graduate/postgraduate degree in Chemistry/Pharmacy from a recognized school/university. Knowledge, Skills, and Abilities: - Proficiency in wet chemistry, analytical bench techniques, and Window-based software. - Familiarity with automated data acquisition systems is advantageous. - Experience with Auto/Manual dissolution tests and GC is beneficial. - Strong written and verbal communication skills in English. Experience: BSc with 5 years or MSc with 3-4 years of experience in a pharmaceutical lab within an R&D environment. Apotex is dedicated to creating an inclusive and accessible work environment where all employees are valued, respected, and supported. Accommodations are available for applicants with disabilities during the recruitment process. If you require accommodation for an interview or testing, please inform us.,

Assist in lab reactions & NPD under Sr. Chemists. Support experiments, sampling, data recording & literature search. Maintain SOP compliance, perform material balance, handle lab equipment & ensure safety. Document data for scale-up.

Hi Jobseeker, Greetings from Laurus Labs Ltd! Please find the below current openings at Laurus Labs Ltd- Visakhapatnam (Atchutapuram OSD Formulation Unit-2) Department : Quality Control-OSD Formulations Designation : Asst.Manager/Manager Section : Wet Chemistry & Dissolution Interested candidates can send their resume to seetaram.y@lauruslabs.com and please send the below details for further process. Total Exp : Current CTC : Expected CTC : Notice Period :

Hello Candidates, Greetings from Hungry Bird IT Consulting Services Pvt. Ltd We are hiring for QC Chemist HPLC/Premix Formulator/Biochemist for one of our client. Job Title: QC Chemist HPLC/Premix Formulator/Biochemist Location: Sanghi Nagar Hyderabad Department: Quality Control / R&D Reports To: QC Manager / R&D Manager Employment Type: Full-Time Job Summary: We are seeking a detail-oriented and innovative QC Chemist with expertise in HPLC, UV-Vis Spectroscopy, and Karl Fischer titration to perform analytical testing, ensure batch consistency, and contribute to the development of new premix formulations. The ideal candidate will have a strong background in quality control, formulation science, and regulatory compliance, particularly in the food or feed industry. Key Responsibilities: Analytical Testing: Perform qualitative and quantitative analysis using HPLC, UV-Vis spectroscopy, and Karl Fischer titration . Evaluate raw materials, intermediates, and finished premix products for compliance and stability. Quality Control: Conduct routine QC checks to ensure consistency, safety, and regulatory compliance across batches. Troubleshoot deviations and assist in root cause analysis. Documentation & Compliance: Prepare and maintain Standard Operating Procedures (SOPs) , Certificates of Analysis (COAs) , and batch documentation. Ensure lab practices comply with internal and external regulatory standards (e.g., FSSAI , ISO, etc.). Cross-functional Collaboration: Work with R&D and production teams during pilot batches and scale-up processes. Provide input on formulation improvements and new product development. Instrument Maintenance: Maintain, calibrate, and troubleshoot laboratory instruments as per schedules and SOPs. Formulation Development: Develop and optimize nutritional and functional premix formulations to meet evolving customer and market needs. Stay current with trends in ingredient technology and food/feed safety. Key Skills & Abilities: Proficient in HPLC , UV-Vis spectroscopy , and Karl Fischer titration . Strong understanding of quality control procedures and regulatory standards. Ability to develop and optimize formulations based on scientific and commercial criteria. Experience or familiarity with FSSAI regulations and other relevant certifications is a plus. Excellent skills in technical writing, documentation, and reporting . Strong analytical mindset with excellent data interpretation and problem-solving abilities. Flexible and adaptive to new technologies, trends, and regulatory changes. Qualifications: Bachelors or Masters degree in Biochemistry, Chemistry, Food Technology , or a related field. 1 - 5 years of relevant experience in QC, formulation , or analytical testing , ideally in nutraceuticals , food/feed , or pharma sectors. (Interested candidates can share their CV to aradhana@hungrybird.in or call on 9959417171.) Please furnish the below-mentioned details that would help us expedite the process. PLEASE MENTION THE RELEVANT POSITION IN THE SUBJECT LINE OF THE EMAIL. Example: KRISHNA, HR MANAGER, 7 YEARS, 20 DAYS NOTICE Name: Position applying for: Total experience: Notice period: Current Salary: Expected Salary: Thanks and Regards Aradhana, +91 9959417171

Hi Jobseeker, Greetings from Laurus Labs! Please find the below positions of current openings at Laurus Labs - Visakhapatnam (Atchutapuram OSD Formulation Unit) Department : Quality Control-OSD Formulations Designation : Associate/Executive Section : Wet Chemistry & LC-MS/GC-MS Interested candidates can send their resume to seetaram.y@lauruslabs.com and please send the below details for further process. Total Exp : Current CTC : Expected CTC : Notice Period :

Key Responsibilities: Perform analytical testing and analysis of raw materials, intermediates, and finished pharmaceutical products. Conduct instrumental and wet chemistry techniques, including HPLC, GC, UV-Vis, FTIR, and titrations. Develop and validate analytical methods for new and existing pharmaceutical formulations. Conduct stability studies and ensure proper documentation of results. Maintain and calibrate laboratory instruments and equipment. Prepare and review standard operating procedures (SOPs) for analytical testing and instrument operation. Ensure compliance with cGMP (current Good Manufacturing Practices), ICH guidelines, and other relevant regulatory standards. Support analytical troubleshooting and provide solutions for any issues that arise during testing. Review and interpret data, providing detailed reports and documentation for regulatory submissions. Collaborate with cross-functional teams, including R&D, production, and regulatory affairs. Conduct investigations and root cause analysis in case of product quality deviations. Maintain accurate records of all laboratory activities and ensure data integrity. Stay updated with new analytical techniques, instruments, and industry trends.

- Conduct the experiment as per planning - Calculate reagent quantities, yields, etc. - Enter the experimental observations in Electronic Lab Notebook (ELN) - Conduct chemical reactions in batch and photochemical reactors - Handle the chemistries such as photochemistry, alkylation, oxidation, nitration, diazotization, chlorination, fluorination, vapourphase chemistry, etc - Conduct various purification techiques like fractional distillations, column chromatography and extractions - Prepare reports and documents as per product development element review methodology - Maintain the inventory of the reactors as per the laboratory management element - Interpret the GC, HPLC and wet chemistry results

Support/assist the lab supervisors/chemists by performing routine and non-routine laboratory analysis/wet chemistry on product and in-process samples, to support plant operations for the purpose of quality assurance/control. Perform calibration and maintenance of test equipment. Prepare samples and ensure accurate data generation and records, in accordance with the standard operating procedures. Utilize analytical instruments to address quality assurance/control issues. Prepare chemical stock solutions and reagents, as well as set preparation standards. We are recruiting a Laboratory Technicianto join one of our leading multinational clients and their expanding team. This position is based in Bangalore and offers an excellent opportunity for experienced proposal management professionals in theConventional Energysector. Graduate with the background in Chemical/Process/Technical Engineering. Computer-literate. Preferable experience in quality control systems. Experience -0-5 years Perform various activities in lab operations to prepare sample with processing techniques and conduct testing on various products in compliance with company policy.

Job Description: We are hiring a Quality Control Executive for our API manufacturing unit. The ideal candidate must have hands-on experience in HPLC/GC , a sound understanding of GMP/GLP , and should be able to manage end-to-end QC activities as per regulatory and organizational requirements. Key Responsibilities: Sampling of raw materials, packaging materials, water, in-process samples, validation samples, stability samples, finished products, process aids , and equipment cleaning samples . Perform analysis of samples using appropriate techniques and instruments (HPLC/GC), based on qualification and training. Perform upkeep and calibration of laboratory instruments and equipment . Responsible for maintenance and upkeep of laboratory chemicals, analytical standards, and glassware . Maintain and monitor the upkeep of reagents, indicators, and volumetric solutions . Oversee the reserve/control sample room and stability chambers . Monitor temperature and humidity of laboratory working areas. Adhere to Good Laboratory Practices (GLP) , Good Documentation Practices (GDP) , and companys Code of Conduct . Ensure proper management of QC documents and data integrity. Report any discrepancies, incidents, OOS (Out of Specification), OOT (Out of Trend) , or non-conformities to the supervisor. Follow all safety precautions during analysis and lab operations.

Opportunity with SGS India for the position of Chemist (Wet Chemistry) | Location - Ahmedabad Note: This position would be on 3rd Party Payroll. Company Profile: Established in 1878, SGS transformed grain trading in Europe by offering innovative agricultural inspection services. SGS is the world's leading inspection, verification, testing and certification MNC. We are recognized as the global benchmark for quality and integrity. With more than 96,000 employees, we operate a network of more than 2,700 offices and laboratories around the world. We cater quality services to 9 Businesses in India like Consumer & Retail Services, Oil & Gas, Industrial services, AFL, Minerals etc. Kindly visit our Global Website: www.sgs.com India Website: www.sgsgroup.in Experience - Fresher to 1-2 Years Education - M. Sc in Chemistry Walkin Details - 12th June and 13th June Time - 9:30 am - 4:30 pm Location - Ahmedabad, Gujarat Following is the Job Description for Chemist (Wet Chemistry): To perform sample preparation by using appropriate method. Assist Section In-charge for new method development and method validation to upgrade lab capability. Handling of CRM and stability check of CRM. Development, modification, verification and validation of methods Result entry in SLIM. Internal verification of equipment and equipment maintenance. Responsible for method validation To assist QAC and Section In-charges to maintain calibration status and their records. Verify Instrument maintenance and Calibration of Chemical and instrument lab area. Ensure compliance with mandatory local and other laws pertaining to health safety environment protection, within the lab and outside surroundings, compliance to SGS OI procedures Interested Candidates please share your updated CVs on fleur.dsouza@sgs.com

Qualification- M.sc & B.sc (Major) Lab Experience is preferable Both Male and female can apply Compute Knowledge is Must. Prior experience is preferable Salary is negotiable as per experience

Role Overview: As a Pet Care Food Lab Analyst, you will be responsible for analyzing pet food products to ensure they meet quality standards and regulatory requirements. You will work closely with the product development and quality assurance teams to conduct tests, evaluate ingredient quality, and provide insights that enhance product formulations. Key Responsibilities: Conduct laboratory tests on pet food samples, including nutritional analysis, and ingredient quality assessments. Ensure compliance with industry regulations and standards (e.g., BIS, AAFCO, FDA). Document test results accurately and prepare detailed reports. Collaborate with product development teams to optimize formulations based on lab findings. Monitor and maintain laboratory equipment to ensure accurate and reliable testing. Stay current with industry trends, research, and advancements in pet nutrition. Assist in troubleshooting quality issues and contribute to corrective action plans. Participate in training sessions and workshops to enhance lab techniques and methodologies. Qualifications: MSc in Chemistry /food science or a related field; Masters degree preferred. Experience: 3-5 years of experience in laboratory setting, preferably in food testing or pet nutrition.

Maintenance and use of GC FID To test and analyze proximate parameters like UV parameters, Analysis of Fatty acids Maintaining samples before and after analysis Maintaining the CRM Method verification & validation SOP preparation Interpretation of the results. Qualifications 6-8 years experience of working in food testing laboratory. Proficient in analytical techniques of wet chemistry, proximate analysis, watr analysis, Allergen testing, Meaurement of Uncertanity calculation. Greaduate Bsc/Msc in Chemistry Additional Information Good interpersonal and communication skills. Energetic, flexible and innovative. Able to work independently and to coordinate several activities simultaneously. Good in communication, read and write in English and local language. Acts quickly and decisively. Knowledge in Microsoft Office (such asMicrosoft Word, Excel, Power Point, & etc.),

Responsible to develop, implement and be responsible for the production plan for their respective departments. To deliver timely and accurate analysis of samples to meet customer commitments. Be responsible for record control, measurement traceability and testing results review and approve the testing reports. Maintenance of Standard Reference Materials, Chemicals, Reagents, and Glassware used in the laboratory. To support the installation of additional analytical equipment, methods for the analysis of all kinds of food/feed/water matrices based on the transfer of existing methods and knowledge form the Eurofins Group Preparation of standard operating procedures. Validation of non-standard test methods and non-routine test methods. Be responsible for skill training, reviewing, and appraising the laboratory staff. Be responsible for configuring and monitoring the instrument, equipment, and its environment conditions. Organize and supervise confirmation and verification of the testing methods. Estimation of measurement uncertainty for test parameters Scope preparation for new parameters Be responsible for control of nonconformity work, complaint, Retest request etc Reliable, independent, and service oriented approach to work Qualifications 8-10 years experience of working in food testing laboratory. Strong understanding of ISO 17025 implementation and accreditation process. Proficient in analytical techniques of wet chemistry, proximate analysis, heavy metals analysis. Should have strong leadership skills to handle team of analysts, allotting and supervising the task to team and also monitoring and evaluating the work done. Preferrably a food analyst Graduate in B.Sc / M.Sc in Chemistry Additional Information Good interpersonal and communication skills. Energetic, flexible and innovative. Able to work independently and to coordinate several activities simultaneously. Good in communication, read and write in English and local language. Acts quickly and decisively. Knowledge in Microsoft Office (such asMicrosoft Word, Excel, Power Point, & etc.),

Role & responsibilities: Sampling of packed finished goods. Sampling of Bulk raw materials. Approval of Raw Material and Finished products as per specification Working in SAP to enter analysis results of FG & RM Collect the products batch samples and report. Testing of RAW material & Finish Good as per their specifications Maintain and ensure the housekeeping activities at QC laboratory Data management Sampling of packed finished goods. Sampling of Bulk raw materials.C, Ft IR etc.) Preferred candidate profile: 1. Wet chemistry analysis, Routine Product analysis, RM and FG analysis 2. Communication and Team Work 3. Ready to relocate at Rasal, Pali (near Raigad at plant) 4. Ready to work in shifts 5. Male Candidate required Preferred Location: Khopoli, Raigad, Sudhagad, Pali, Mahad, Roha, Pen, Khalapur, Panvel, Navi Mumbai Job Location: Rasal (Pali-Raigad)