94 Karl Fischer Jobs

Our plant is in Sihor, Bhavnagar and we have a requirement of QC Chemist. If you are comfortable to shift to Sihor, Bhavnagar, do share your CV on khushbushah@jenburkt.com We are looking for candidates who have completed MSC. Overall: Fresher to 1 yr. of experience. CTC : Can be discussed on the call. Kind Regards, Khushbu

Perform the testing of Raw Material/Finished goods/In process materials & report the results. Handle the analytical instruments like HPLC, UPLC, GC, ICP, DSC, XRD, PSA

Candidate must have strong knowledge in Core PHP, Laravel, MYSQL, jQuery, AJAX, HTML and CSS. Must have a work experience of 1-2 years on PHP & Laravel Framework. Web-based software application development and maintenance on PHP

Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis of raw materials

analytical lifecycle: specs with RA, method validation, testing of RM/PM/IP/FP, water & environmental monitoring, stability programs.data integrity (ALCOA+), LIMS audit trails chromatography governance (integration, SST, system suitability).

1 Perform the testing of Raw Material/Finished goods/Inprocess materials and report the results. 2 Handle the analytical instruments like HPLC, UPLC, GC, ICP, DSC, XRD, PSAetc 3 Calibration of the Analytical instruments

1 Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures. (qualitative and quantitative chemical and collect/physical analysis of raw materials, finished products and/or stability samples)

Perform the testing of Raw Material/Finished goods/In process materials & report the results. Handle the analytical instruments like HPLC, UPLC, GC, ICP, DSC, XRD, PSA Calibration of the Analytical instruments as per the master calibration

Job description Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures. (qualitative and quantitative chemical and collect/physical analysis of raw materials,

Preparing test solutions, compounds,and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis

Responsible for conducting various chemical analyses, ensuring the safety and compliance of waste handling procedures, and contributing to the optimization of waste management processes. Exp: 2 to 5 years Salary : 5-7LPA Location : Baddi/Nalaghare

Job Opportunity at Natco Pharma Limited (Formulation Unit) Department: Quality Control Position: Chemist / Officer / Executive Qualification: B. Pharmacy / M. Pharmacy / M. Sc Experience: 3 to 5 Years Location: Kothur, Telangana Key Responsibilities: Analysis of finished products, raw materials, and in-process samples Operation and troubleshooting of instruments such as HPLC, UV, KF, IR, and Dissolution Apparatus Testing of Packing Materials Adherence to GLP, GDP, cGMP, and ALCOA+ standards Assay and dissolution testing using HPLC Regulatory exposure in formulation is mandatory Interested candidates may share their CVs at jaganmohan.p@natcopharma.co.in

Test chemical samples for quality control Sample preparation and analysis Perform variety of laboratory testing Analyzing and reporting test result Preparing chemical solutions Writing technical reports of test result Maintain laboratory equipment

Should have 1-2 Years of experience in Quality Control department

Responsible for Analysis of RM/ inprocess/ FP/PM Samples, Instrument Calibration, Instrument Qualification Protocols & perform Qualification activity(OQ/PQ), analytical record, analytical cleaning method validation of the API, Online SAP Activity etc Required Candidate profile M.Sc./B.Sc. with 4 to 8 yrs exp in QC of cGMP, USFDA, MHRA approved Bulk drug/API unit. Sound exp & knowledge of handling GC, HPLC, KF, pH meter, Spectrophotometer, Auto Titrator, MP/BP etc.is must. Perks and benefits Negotiable

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.

Responsibilities: * Conduct quality control tests using HPLC, GC, UV, Karl Fischer, Potentiometer methods * Hands on experience on QC instruments such as GC and HPLC and Titration and potentiometry is must Provident fund Annual bonus

The QC Analyst II position at Piramal Pharma Solutions involves performing analytical chemistry examination testing on raw materials, finished products, or stability samples following approved Standard Operating Procedures (SOPs) and valid methods. This role, which operates during 2nd shift hours, is crucial for ensuring product quality and compliance with regulatory standards. Key responsibilities of the QC Analyst II include conducting chemical or physical testing analysis, documenting and submitting all raw data and results in LIMS, preparing reagents for chemical analysis, and ensuring compliance with compendial (USP/EU) testing requirements as per FDA 21 CFR. Moreover, the incumbent is expected to possess a good understanding of laboratory safety practices, cGMP, good documentation practices, and compendial testing requirements. The ideal candidate for this role should hold a Bachelor's degree in chemistry, biology, microbiology, or a related science field with relevant laboratory coursework. Additionally, a minimum of 2 years of laboratory experience, preferably in a GMP environment, is required. Proficiency in a range of analytical techniques such as Wet Chemistry testing, Balance, Dissolution, FTIR, KFM, UV/Vis, Titrations, Viscosity, PSD testing, pH, and conductivity is essential. The successful candidate should demonstrate strong written, verbal, and interpersonal communication skills, as well as proficiency with computer software like MS Word, Excel, or PowerPoint. As part of the Piramal Group, Piramal Pharma Solutions is committed to inclusive growth, ethical practices, and equal employment opportunity, ensuring that all applicants and employees are treated fairly in all personnel matters. Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. With a global network of facilities, PPS provides services ranging from drug discovery solutions to commercial supply of APIs and finished dosage forms. The organization's expertise covers a wide range of technologies, making it a preferred partner for innovators and generic companies worldwide. If you are passionate about quality control and analytical chemistry, and meet the qualifications mentioned above, we encourage you to apply for the QC Analyst II position at Piramal Pharma Solutions.,

M.Sc/B.Sc Chemistry Experience - 3 + yrs from Aroma/Chemical/Pharma analytical chemistry, handle lab instruments independently, knowledge of analytical, Must GC,HPLC, karl Fisher,chemistry, handle lab instruments independently, good grasping,

Job Description 1. Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report. 2. To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc. 3. Ensuring data integrity policy, GDP and its effectiveness up to compliance 4. To maintain the stability chamber and tracker. 5. To maintain the stability chamber and tracker. 6. To ensure charging and withdrawal of stability samples as per approved protocols. Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience :- 2 to 4 yrs. Education Others Competencies

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.

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).

Job Summary: We are looking for a skilled QC Chemist to join our QC team. The candidate will be responsible for conducting routine analysis of raw materials,intermediates and finished products,ensuring compliance with internal specifications. Provident fund

As a skilled Analytical Chemist, you will be responsible for various tasks related to method development, validation, and query response for finished products. Your duties will include preparing analytical method development reports, Certificates of Analysis (COA), and performing analysis of in-process samples, finished goods, and stability samples in accordance with cGMP requirements. It will be your responsibility to monitor the general laboratory and ensure its maintenance as needed. Your role will involve routine analysis and stability testing of finished products for parameters such as assay, related substances, dissolution, residual solvent, etc. Additionally, you will be required to review analytical data, calibration data, and qualification data. Troubleshooting and maintenance of analytical instruments like HPLC, GC, UV/Visible, and spectrophotometer will also be part of your tasks. Calibrating analytical instruments such as Analytical Balance, pH meter, UV spectrophotometer, and Karl Fischer Potentiometer according to the schedule will be essential. Compliance with in-house systems and procedures to uphold cGMP practices and regulatory requirements is crucial. You will also be responsible for maintaining reference standards, working standards, and coordinating activities in Chemical and Instrumentation departments. Handling troubleshooting and updating instrument log book entries will be part of your routine activities. Desired Skills: - Previous experience in formulation testing within reputable pharmaceutical organizations. - Proficiency in handling instruments like HPLC, GC, UV, UPLC, Dissolution tester, KF, and FTIR. - Strong knowledge of Microsoft Word, Excel, and PowerPoint. - Excellent communication and problem-solving abilities. - Assertive, proactive, and self-driven attitude. - Willingness to work in a dynamic work environment. Pedigree: - Bachelor of Science (B.Sc) in Chemistry, Master of Science (M.Sc) in Chemistry. - 1-3 years of relevant work experience.,

Hiring for QC Job Location - Jammu (sambha) Interview Location - Chandigarh Salary Bracket -4LPA to 5.5LPA Industry prefernce - Pharma (API) only Interested one share resume on meenakshikandpal@tdsjobs.com 9815675900