119 Wet Analysis Jobs

Role & responsibilities Sample testing Documentation equipment calibration Preferred candidate profile Qualification -MSc in chemistry is must . Must have experience in Pharma - API industry or Testing laboratory . Must be have having good experience in HPLC , GC ,Wet analysis , Stability , Finished products ,Raw - Material .

Urgent Requirement in PHARMA Industry... Fresher's & Experience persons wanted in QUALITY CONTROL(Wet Analysis / HPLC / GC) AND RESEARCH & DEVELOPMENT (R&D) Department in Pharma Industry, Candidate should have good working experience in Pharma Manufacturing Units.. Roles and Responsibilities: FOR QC DEPARTMENT In the pharmaceutical industry, the Quality Control (QC) department is responsible for testing and analyzing raw materials, in-process materials, and finished drug products to ensure they meet safety, purity, and efficacy standards. QC Wet Analysis Department (or Wet Chemistry Lab) is responsible for performing traditional, bench-top chemical tests on raw materials, in-process samples, and finished products to ensure they meet quality specifications and regulatory standards. Gas Chromatography (GC) is a critical analytical technique used within the QC department to: analyze the chemical components of drugs, determine the purity of ingredients, and verify that the final product meets specifications for release. In the pharmaceutical industry, the Quality Control (QC) HPLC department uses High-Performance Liquid Chromatography (HPLC) to analyze raw materials, intermediate products, and final drug products, ensuring their identity, purity, potency, and stability. Roles and Responsibilities: For R&D DEPARTMENT The pharmaceutical R&D department is responsible for the entire lifecycle of new drugs, from discovering and developing them, through preclinical and clinical trials, to regulatory approval, manufacturing, and post-market surveillance. Key responsibilities include, conducting scientific research, designing experiments, analyzing data, managing clinical trials, ensuring regulatory compliance, and fostering innovation to bring safe and effective new treatments to patients. Qualification: B.SC(CHEMISTRY) / M.SC(CHEMISTRY) Experience: 0-5Years Salary: 15-30K Location : Jeedimetla ,Bollaram Hyderabad. Note : Only Male Persons Required. Contact: 8977333658.

The role based in Hyderabad, India, within the Chemistry Solutions department involves supporting the chemistry services team in delivering final compounds to clients by ensuring the testing and enhancing of purity levels as per requirements. This is achieved through effective coordination with a team of analysts. The main responsibilities of this role include building lasting internal client relationships by engaging in technical discussions with clients to understand project requirements. It also involves supporting team members in closing identified gaps to enhance client satisfaction. Additionally, ensuring seamless project execution through effective lab support and planning is crucial. This includes estimating lab requirements, monitoring instrument calibration, reviewing SOPs, and allocating resources based on daily work plans. Efficiency and quality in delivery are paramount, involving the evaluation of solvents/samples for analytical test suitability, approving analytical methods, and ensuring timely delivery of final reports to clients. The role also includes resolving method development issues, coordinating with R&D scientists for analytical queries, and interacting with external clients as needed. Maintaining safety at work is a key aspect, ensuring compliance with lab management practices, safe handling of chemicals and instruments, and successful implementation of new analytical techniques. Upholding data integrity and IP confidentiality is essential, along with developing the morale and skill set of the team through talent selection, knowledge enhancement, mentoring, and coaching. The candidate should possess knowledge of analytical tools and techniques, operational understanding of analytical instruments, documentation processes, safety protocols, IP confidentiality, and data integrity. Additionally, the ability to conduct cost-benefit analyses and optimize solvent usage is required. The ideal candidate will hold a postgraduate degree in Analytical Chemistry or Organic Chemistry with 9-12 years of relevant experience, or a Ph.D. in Analytical Chemistry or Organic Chemistry, or an M. Pharm in Pharmaceutical Analysis with 7-10 years of relevant experience. Advanced knowledge of MS Office and basic knowledge of ChemDraw are preferred. The additional responsibilities, educational qualifications, certifications, and key performance indicators will be discussed during the interview process. The work environment details, specific requirements, and other miscellaneous details will also be communicated accordingly.,

Role and Responsibility: Technical Support: Provide expert technical support to customers and field personnel on HPLC troubleshooting, and resolving application issues. Application Development: Develop and optimize analytical methods and applications using HPLC for various industries, including pharmaceuticals, industrial, environmental, food, and life sciences. Customer Training: Conduct customer training sessions, webinars, and workshops to enhance user proficiency and satisfaction. Collaboration : Work closely with the sales and marketing teams to identify customer needs and develop tailored solutions. Collaborate with R&D to provide feedback on product performance and enhancements. Documentation: Prepare and maintain application notes, technical documents, and reports to support customer applications and product development. Innovation: Stay updated with the latest advancements in HPLC and contribute to the development of new applications and methodologies. Aware of calibration and operation procedure for instruments ( balance, K.F, HPLC. UV, refractometer and viscometer etc,) Experience of QC software like Empower, LIMS, Tiamo 3.0, Lab solution, SCM etc. Preparation of documents ( SOP, protocol etc) related to Quality control.Role & responsibilities Preferred candidate profile Qualification : B.Sc (chemistry)./ B.Pharma candidates only. Experience: 4-10 years experience working with HPLC/wet finish/Sampling is compulsory. Interested candidates can sent their CV to jagpal.dewal @ipca.com

Role & responsibilities Collect, prepare, and analyze ferro alloy samples using standard laboratory methods. Perform physical and chemical testing of raw materials, in-process, and finished products. Operate and maintain laboratory equipment (e.g., spectrometer, chemical balances, furnaces, etc.). Ensure test results meet defined quality standards and customer specifications. Record, maintain, and report laboratory data in accurate formats. Support production and quality teams with technical inputs on material testing. Follow safety protocols and maintain cleanliness in the laboratory. Calibrate instruments periodically and ensure proper documentation. Assist in developing and implementing quality improvement measures. Preferred candidate profile Diploma / B.Sc. (Chemistry / Metallurgy) or equivalent. 24 years of relevant experience in Ferro Alloys / Metallurgical / Chemical industry laboratory. Hands-on knowledge of ferro alloy testing and quality standards. Familiarity with spectrometry, wet analysis, and related equipment. Strong attention to detail, accuracy, and analytical skills. Good knowledge of laboratory practices and safety standards. Ability to work independently and in a team. Strong record-keeping and reporting skills. Basic computer knowledge (MS Office, data entry).

The job involves preparing and analyzing samples from various sources in order to provide information on compounds or quantities of compounds present. This includes using analytical techniques and instrumentation such as gas chromatography (GC), high performance liquid chromatography (HPLC), and spectroscopy (ultraviolet) to investigate chemical compositions. Additionally, wet analysis will be performed. The responsibilities also include interpreting data, reviewing and evaluating experiments and analyses, and presenting scientific results to relevant teams. The role requires the development of new HPLC and GC methods, as well as collaborating with cross-functional teams. Staying up to date with the latest scientific and technical trends is essential, as well as validating methods and equipment. This is a full-time position that offers a performance bonus and yearly bonus. The work location is in person.,

WALK IN Interview - SUNDAY 7th Sep 2025 - Quality Control - Unison Pharmaceuticals Pvt Ltd Ahmedabad About us : Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality and affordable medicines across the nation. With more than 4 decades of medical service to society, Unison is today one of the fastest-growing companies in Gujarat State. In addition to this, the company is ranked 82 among the top companies of India (Rupee wise sales) MAT March 2020. This makes Unison a distinguished company across the pharma industry. We are expanding!! You are invited to join one of the fastest growing pharma companies in India!! Department: Quality Control Section: HPLC Analysis & Chemical Analysis/ QC QMS Experience: 2-7 years Designation: Officer / Sr. Officer / Executive Location: Moraiya, Ahmedabad. No. of Openings: HPLC Analysts: 5 Physico Chemical Analysts: 5 QC QMS: 2 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 & experience, we encourage you to apply for this position. Please walk in to the interview on SUNDAY 7th Sep 2025 b/w 10:00 AM to 3:00 PM at below mentioned venue. Venue: Unison Pharmaceuticals Pvt. Ltd. Unit III- 7, 8, 9 Steel Town, Opposite Nova Petrochemicals, Village- Moraiya, Taluka- Sanand, District- Ahmedabad- 382213 Regards, HR Team Unison Pharmaceuticals Pvt Ltd

Roles and Responsibilities Conduct quality analysis of raw materials, in-process samples, finished products, and stability studies using various lab instruments such as UV Spectrophotometer, Polarimeter, Viscometer, pH Meter, Conductivity Meter, etc. Prepare documentation for laboratory activities including test reports, protocols, SOPs etc. according to company standards. Maintain a clean and organized work environment. Collaborate with cross-functional teams to resolve issues related to product development and manufacturing. Knowledge in 5'S

Post- Lab Technician Location - Pune Urlikanchan Factory Contact - 9356395439 Education: A post-secondary education (degree and/or diploma) in a science-related field (e.g., Chemistry, Geology, Mining Engineering) is often preferred. 2 -aboratory Experience: Prior experience in a laboratory setting, sample preparation and analysis techniques, is highly desirable. 3 -Sample Handling and Preparation: Sampling, sorting, and labeling samples. Crushing, pulverizing, splitting, and sieving samples according to established procedures. Preparing samples for analysis using various techniques (Wet analysis).

Department - Quality Control Experience - 2 to 5 years Qualification - M.Sc chemistry (Full time) Section - HPLC / GC / Wet lab To ensure that training is acquired for each activity/instrument prior to its execution/operation and that it is as per respective TNI. To perform Analysis (Chemical)of raw material/packaging material/in-process samples /intermediate /bulk & finished products/ process validation samples/ stability samples/ cleaning validation/method transfer sample, PD lab sample etc. To ensure that all tests carried out in the laboratory are documented contemporaneously in an appropriate authorized and controlled worksheet/ bound book. To make entries in the sample inward register / LIMS as required for assigning analytical reference number and to store at recommended storage condition until completion of the analysis. To operate and maintain laboratory equipment/instrument as per analyst qualification program. To ensure that entries in log books are made where ever instruments are used in the analysis. To perform all associated activities (bench reagents, indicators, volumetric solution preparation, factor determination etc.) required for sample testing by following the approved procedures. To perform analysis (Chemical) to qualify working standards against reference standard /certified standard/ primary standards. To ensure all primary standards/working standards/certified standards/reference standards are stored as per the storage conditions specified and documented. To check the availability of analytical resources like chemicals/reagents / standards etc. before start of the analysis. To take online print and perform data punching in the LIMS. To monitor temperature of laboratory daily. To send those samples to outside laboratory for analysis for tests not able to be carried out in laboratory. To maintain and ensure controlled laboratory practice in the quality control department. To document the raw data as per current GDP. To follow the SOPs of Quality control department and related area. To follow Specification, STP, GTP and protocol during analysis. To use applicable PPEs (personal protective equipment) while performing testing in the laboratory / during handling hazardous solvents/chemicals. To keep himself updated with current regulatory requirements and train the subordinates and colleagues for day to day activities as well as regulatory. To keep the things and his work area clean and tidy and get involved for the routine trouble shooting (if any). To ensure up-keeping of the instrument/equipment. To ensure laboratory inventory management. To inform section head any incident/ OOS/ OOT/ OOC on its immediate occurrence and for day to day activities. To investigate incident/ OOS/ OOT/ OOC (if any) under consultation with the department head/section head. To perform the analysis of stability samples as per the analyst qualification, requirements and respective procedure. To perform the calibration of instrument as per the planner and / or as and when required. To manage all standards for issuance and its usage. To co-ordinate with in-house service engineers and / or external service engineers as and when required. To ensure the destruction of remnant samples after analysis as per applicable procedure. To perform analysis at CHL inter locations whenever required. Responsible for implementing company quality ethics policy for data integrity and inform management and responsible data integrity compliance head on any data integrity issues as per corporate data governance policy. To escalate any issues related to discipline, availability of manpower, hygiene, contamination, cross contamination, Incidents or deviations, malfunctioning of equipments, any unusual observations, any safety risk or quality risk to next level or in absence further up. To perform any other activities as assigned by HOD after completion of the necessary trainings as applicable.

Sr. Executive / Executive based in Kadi, Mehsana District, Gujarat. The ideal candidate brings 5-8 Years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Additional info: Key Skills: HPLC, GC Analysis, Method Validation, Wet Analysis, Water Sampling, Report Compilation Qualification: M.Pharm / B.Pharm / M.Sc Experience: 5 to 8 years Must demonstrate strong ownership, attention to detail, and the ability to work in a fast-paced, inspection-ready environment. Familiarity with ICH, WHO TRS, ISPE, and data integrity principles is expected; hands-on with spreadsheets/ERP/LIMS is a plus.

Candidate should have hands-on chemical analysis of food products in a laboratory, Performing proximate analysis to determine the moisture, ash, crude fat, crude fiber,crude protein content of samples. Conducting a wide range of wet chemistry tests. Required Candidate profile Bachelor's or Master's degree in Chemistry, Food Science, or a related field.1-2 years of proven experience in a food testing lab, with a primary focus on proximate and wet chemistry techniques.

Candidate should have hands-on chemical analysis of food products in a laboratory, Performing proximate analysis to determine the moisture, ash, crude fat, crude fiber,crude protein content of samples. Conducting a wide range of wet chemistry tests. Required Candidate profile Bachelor's or Master's degree in Chemistry, Food Science, with a primary focus on proximate and wet chemistry techniques.

Role & responsibilities Perform the calibration and preventive maintenance of the instruments as per the respective schedules. Analysis of raw material / finished products / stability samples / Dissolution profiling for R&D/ Plant support. Analytical Method Development /Verification Assay, Related substances, Dissolution etc . Perform the determination of KF factor, Daily verification of Balances, pH meter, Milli-Q water system, Hot Air Oven, Refrigerator temperature monitoring. Develop/ optimize the analytical methods by Chemical/ instrument analysis Verify/ validate the analytical methods by Chemical/ instrument analysis Preparation / Revision of Specification and Method of analysis for Raw materials / Finished Product / Inactive / Excipients etc Appropriate documentation of results and calculations, preparation of SOPs, specifications and test methods. Interpret results, evaluate data, draw relevant conclusions and give timely feedback to concerned Departments. Analytical Technology transfer of analytical methods by Chemical/ instrument analysis Perform the Impurity standard/ working standard/ primary reference standards. Receiving and filling controlled copy of specifications / method of analysis / SOP / STP etc Operation of various software like Oasis LIMS, Q Edge TMS, Chromeleon etc Preferred candidate profile Qualification: B. Pharm / M.Pharm / M. Sc Experience: Minimum 2 years in HPLC Analysis Development and Validation Perks and benefits Mediclaim

The role involves handling various responsibilities related to Wet Analysis, Specification Preparation, CCF Handling, and Instrumentation such as HPLC and GC Analysis. The ideal candidate for this position should have a qualification of M.Sc. in Chemistry, B. Pharmacy, or M. Pharmacy.,

You will be responsible for conducting routine tests on raw materials, in-process samples, and finished products to ensure they meet quality standards. Utilizing various analytical techniques and instruments, including wet analysis and instrumentation, will be essential in this role. It is crucial to accurately document all test results and laboratory activities in accordance with company protocols. Maintaining detailed and organized records for traceability and reporting purposes is a key aspect of the job. Adhering to company and regulatory procedures for testing and quality control is necessary to ensure compliance with ISO standards and other relevant regulations. Checking and calibrating laboratory equipment regularly to ensure proper functioning and reporting any malfunctions or issues to the appropriate personnel for timely resolution are important responsibilities. You will also be required to prepare samples and reagents for analysis, ensuring proper handling and storage while following standard operating procedures (SOPs) for sample preparation. Safety guidelines and protocols must be strictly followed while working in the laboratory, including the use of personal protective equipment (PPE) as required to promote a safe working environment. Assisting Senior QC Officers with various tasks and projects as needed, collaborating with team members to achieve departmental goals, and communicating test results and any issues or discrepancies to the QC Manager / Sr. QC Officers promptly are also part of the job responsibilities. Participation in regular meetings to discuss quality control findings and improvements is expected. The ideal candidate should have a Bachelor's degree in Chemistry or a related field, basic knowledge in wet analysis, instrumentation, and ISO standards, as well as a minimum of 1 year of experience in a relevant field. Strong verbal and written communication skills are essential, along with the ability to share information clearly and work well with others. Excellent problem-solving skills to identify and resolve issues efficiently are required. The job involves working in a laboratory setting with exposure to chemicals and testing equipment, standing for extended periods, and handling laboratory equipment. In addition to competitive market standard salaries, the benefits package includes comprehensive Medical Insurance Benefits up to 4L for family, Commute Assistance / Company travel to factory, TA / DA Allowance, paperless digital reimbursement of expenses, statutory benefits ESI/PF as per regulations, Worker Compensation Insurance Policy, and Travel Insurance. Key requirements for this position include proven ability in Customer Relationship Management, experience in achieving targeted sales outcomes, willingness to travel extensively to meet with customers, a background in industrial sales & marketing, fluent English language skills, experience in selling premium industrial capital goods (preferred), demonstrated success in industrial sales, particularly in welding products, strong analytical and strategic thinking abilities, excellent relationship management and communication skills.,

You are invited to join Global Calcium Pvt. Ltd., a prominent API manufacturing company located in Bangalore, India, specializing in speciality API's, benzodiazepines, ophthalmics, oncology, chelated minerals, and organic mineral salts. We are currently seeking talented individuals to fill various roles in the QC Department. Open Positions: - QC ICP-MS Analyst (2 openings) - QC DMF Support (2 openings) - QC Analytical Validation Support (2 openings) - QC Wet Analysis (2 openings) Qualifications: - B.Sc./M.Sc. in Chemistry or related fields - 1 to 4 years of relevant pharmaceutical QC experience - Familiarity with cGMP practices and regulatory compliance Responsibilities: - Perform routine and non-routine analyses using analytical techniques and instruments - Develop and validate analytical methods and protocols - Prepare and maintain detailed documentation and reports - Ensure adherence to regulatory guidelines and GMP standards - Collaborate with other departments for cross-functional projects - Participate actively in laboratory investigations and troubleshooting activities Walk-in Interview Details: - Venue: Global Calcium Pvt. Ltd., Unit III, 19 & 19B, Sipcot Industrial Complex, Phase - 1, Dharga, Hosur - Date: 14th June 2025 - Time: 9:30 AM to 11:00 AM Please note that only candidates with relevant experience in the pharmaceutical QC domain will be considered for these positions. Benefits and Perks: - As per industry standards If you possess the required skills and experience in DMF preparation, UV, regulatory documentation, elemental impurity analysis, cGMP practices, HPLC, GC, classical wet chemistry techniques, quality control, ICP-MS, wet analysis, and method validation techniques, we encourage you to attend the walk-in interview and become a part of our dynamic team at Global Calcium Pvt. Ltd.,

Job Responsibilities : Wet chemical analysis, KF titration, Potentiometric titration, pH measurements, Calibration of lab instruments, GLP, Execution of Calibrations and CSV. Work Location: Hetero Labs Limited-Unit-I, Survey No:10, I.D.L, Gaddapotharam(Vil), Jinnaram(Mndl), Sangareddy Dist, Telangana

Department : Quality control Open Position : ( HPLC, GC ,Wet Lab ) Work Location: Bidar Key Responsibilities Responsible to perform the HPLC / GC/Wet analysis of Raw material & intermediates, in process/cleaning, intermediate, finished product and stability samples as per the work allotment. method validation, protocols & preparation, review, data review and planning, troubleshooting worked on Empower Software. Good communication& Interpersonal skills. Check the Calibration, Preventive maintenance and status tag of the instruments prior to use. Operate and calibrate the instruments as per SOP. Print the ARDS from GMP Pro and enter the test results after completion of the analysis. Ensure the instrument log entries in GMP Pro after completion of each activity during the analysis. Send the samples for other laboratory testing (internal/external) as per the procedure. Maintenance and storage of all Chemicals, columns and Standards. Discard the samples as per the disposal procedure upon satisfactory verification of batch release status. Handover the solid and liquid waste to ETP for disposal as per the procedure. Check the validity of Chemicals, Reagents, Reference/Working Standards and instruments prior to use. To Co-ordinate with the supervisor in preparation of Investigation reports in the event of OOS, OOT and deviations. Report all the departmental activities to the immediate supervisor and HOD. Assisting the Head of the department for all QC related activities. Attend for the scheduled and unscheduled OJT/GMP trainings.

Excellent Opportunity! Analysts required in the QC department at Unison Pharmaceuticals Pvt Ltd, Moraiya. Apply Now!!! Company: Unison Pharmaceuticals Pvt Ltd Experience: 1-7 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/ In process / 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. HPLC Analyst: Carry out HPLC testing for assay, related substances, dissolution, and stability samples. Operate and maintain HPLC systems (Waters, Agilent, Shimadzu) with appropriate software (Empower/Chromeleon). Prepare standard and sample solutions as per SOPs and approved procedures. Document and report results with accuracy and clarity in analytical worksheets, logbooks, and LIMS (if applicable). Ensure compliance with GMP, GLP, and ALCOA+ data integrity principles. Perform regular calibration and maintenance of HPLC instruments. Support OOS/OOT investigation and participate in deviation handling and CAPA implementation. 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.

Role & responsibilities Should able to handle HPLC & GC,PH Meter, Knowledge on GMP&GLP Preferred candidate profile Familiarity with analytical testing techniques using HPLC/GC/FTIR/Dissolution/UV. Performing calibration of instrumentations Testing of finished product, raw materials, packaging and stability Perform analytical testing - HPLC, FTIR, UV

Job Description: 24 7 audit readiness. Participation in internal, external, regulatory audits. Ensure 100% participation in trainings against CAPAs. Responsible for initiation and investigation on LIR, OOS, OOT & boarder line results and reporting them to the in-charge. Supporting to share required documents from QC to RA/ other requirement. Determining team priorities in accordance with the plants needs, while coordinating with the team leader /Manger. Follow up the housekeeping, cGMP, GLP and Safety Guideline in laboratory. Sampling and analysis of RM / FG / intermediates / cleaning samples based on requirement and result entry in analytical sheet, QA form, LIMS and online documentation as per data integrity norms. Perform analytical test according to the monograph and SOP. Responsible for calibration and verification of instruments. Maintaining of reserved samples room and chambers / autoclaves / incubators. Responsible to work in shift as per requirement. Help to in charge in preparation of documents related to department (like STPs, SOP’s and etc.) Ensure the sampling of finished products, Raw material, Intermediate and sending sample to outside laboratory for analysis. Must be ensured sampled, approved and rejected labels timely as required. Responsible to maintain the stock record of chemicals and reconciliation of standards. Any other job assigned by the Manger -QC Manger or group leader-QC Qualifications: Preferred experience with Wet lab instruments/techniques including but not limited to KF Titrator, Auto-titrator, analytical balance, FTIR, Polarimeter, UV, X-ray Diffraction, etc. At least 5-years of relevant experience with Master of science (Chemistry).

The Opportunity: . Officer - Quality Control is responsible to perform Quality Control activities at AQAL. What we are looking for :- Responsible for Timely analysis of under test samples giving timely results Coordination with tollar for quality related issues and clarification Sampling and analysis for RM/Intermediate/Finished Goods. Ensure compliance of ATR. Assisting team in ISO implementation Knowledge of calibration, standard preparation, standardization and relevant documentation. Handling knowledge of HPLC,GC and wet analysis. B. Sc. / M. Sc. (Chemistry) 2-5 years of experience in Quality including cGMP, ISO and regulatory Audits Knowledge of Quality Control in Fine Chemicals and pharmaceutical company. Experience of cGMP Willingness to learn Team Player Good communication skills How you will thrive and create an impact :- Give timely reports to SAP for result recording. Fill and update all documents. Zero accidents in the Quality operations. Achieving batch wise timelines, quantity and quality. Will train & supervise the working of all operators working in his dept. Will monitor the waste generated during operation. Will be member of the Emergency response team and will guide & train other team members in case of Emergency. Maintain ISO 9001:2015, SAP, and other Quality system into department. Will maintain the analytical records / log sheets as per GMP & ISO guidelines. Disclaimer: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer. Why Avantor Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science. The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor. We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today! EEO Statement: We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law. If you need a reasonable accommodation for any part of the employment process, please contact us by email at and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address. 3rd party non-solicitation policy: By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation

The Opportunity: Officer - Quality Control is responsible to perform Quality Control activities at AQAL. What we are looking for :- Responsible for Timely analysis of under test samples giving timely results Coordination with tollar for quality related issues and clarification Sampling and analysis for RM/Intermediate/Finished Goods. Ensure compliance of ATR. Assisting team in ISO implementation Knowledge of calibration, standard preparation, standardization and relevant documentation. Handling knowledge of HPLC,GC and wet analysis. Education: B. Sc. M. Sc. (Chemistry) Experience: 2-5 years of experience in Quality including cGMP, ISO and regulatory Audits Preferred Skills/Qualifications: Knowledge of Quality Control in Fine Chemicals and pharmaceutical company. Experience of cGMP Skills/Competencies: Willingness to learn Team Player Good communication skills How you will thrive and create an impact :- Give timely reports to SAP for result recording. Fill and update all documents. Zero accidents in the Quality operations. Achieving batch wise timelines, quantity and quality. Will train & supervise the working of all operators working in his dept. Will monitor the waste generated during operation. Will be member of the Emergency response team and will guide & train other team members in case of Emergency. Maintain ISO 9001:2015, SAP, and other Quality system into department. Will maintain the analytical records log sheets as per GMP & ISO guidelines.

Post: Officer - QC Experience: 1-5 Years Qualification: M.Sc No. of Vacancy: 3 Nos. JOB RESPONSIBILITY :- Responsible for sampling and Instrumental/chemical analysis of RM, In-Process, Intermediate, Finished product, Cleaning samples, Validation samples, Market samples and Stability samples. Responsible to perform the calibration of instrument/equipment available in Quality Control laboratory. Maintain the laboratory as per GLP and GMP System. Sampling, Analysis, and review of raw material/packing material, Wet analysis i.e., water content, IR, UV, LOD, Assay by potentiometry, Sulphated ash etc, finished goods sampling, working on HPLC & GC instrument. Interested candidates can share CVs at jhelam.s@randstad.in