149 Kf Jobs - Page 3

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.

Location: Panoli (Ankleshwar) Industry: Pharmaceutical Manufacturing Qualification: Msc Chemistry Experience: Minimum 3+ Years ( Pharma Background) CTC: Up to 7 LPA Call: Riya Placement Pvt. Ltd. Call: 7621044256 Email: recruitment@riyaplacement.com Perks and benefits Bonus & Incentives PF & ESIC Paid Leaves

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

Conduct final inspection and testing of finished products to ensure compliance with quality standards and customer specifications. Hands-on experience in testing of Finished products Instruments must be handled like HPLC, GC, KF, IR, DT, and Dissolution. Hands-on experience like software like Empower and LIMS. Qualification M.SC/B.Pharma 3 to 6 years Additional Information

Date: 1 Sept 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Development Services Job Title: Analyst Job Description At Syngene, Safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and sops, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to companys integrity & quality standa...

The Assistant Manager - QC position at Bharuch SEZ requires a candidate with complete experience in API/Bulk/Intermediates industries as per global regulatory requirements. The individual will be responsible for the implementation and compliances of 21CFR-Part11, ICH-Q7A, cGMP, WHO-GMP, ISO9001, FSSC, HACCP, and other global QMS requirements at the SEZ site. Key responsibilities include regularizing QC activities as per cGMP requirements, ensuring regulatory and pharmacopeia compliance in the lab, reviewing hybrid and electronic data for IPQC and FG analysis, conducting analytical method validation, OOS, and OOT. The candidate should have knowledge about IMS system, analytical skills for QC ...

Date: 1 Sept 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Development Services Job Description Designation: Analyst Special Instrumentation and Method validation Job Location: Bangalore About Syngene At Syngene, Safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and sops, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and syst...

As a Trainee - API QC at Dishman Carbogen Amcis Limited, located in Bavla, Gujarat, India, your primary responsibility will be to handle QC instruments and their documentation during routine activities for various tests such as IR, LOD, KF, Polarimeter, UV, Balance, etc. Your role will involve working in the Quality Control department, specifically focusing on maintaining the quality standards of the products. You will be responsible for conducting tests using various instruments and ensuring accurate documentation of the results. The ideal candidate for this position should have a strong understanding of QC procedures and possess knowledge of instruments like IR, LOD, KF, Polarimeter, UV, B...

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

Conduct final inspection and testing of finished products to ensure compliance with quality standards and customer specifications. Hands-on experience in testing of Finished products Instruments must be handled like HPLC, GC, KF, IR, DT, and Dissolution. Hands-on experience like software like Empower and LIMS. Qualification M.SC/B.Pharma 3 to 6 years Additional Information

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 ...

Hikal Ltd is looking for Officer to join our dynamic team and embark on a rewarding career journey The Senior Officer plays a crucial role in the organization, responsible for overseeing and executing various tasks and projects to ensure the smooth functioning of operations This role requires strong leadership, analytical skills, and the ability to collaborate effectively with team members and stakeholders Key Responsibilities: Leadership:Provide leadership and guidance to team members, fostering a positive work environment Lead by example, demonstrating professionalism, integrity, and dedication to the organization's goals and values Project Management:Manage and coordinate projects from in...

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, dis...

Skill Required 3 to 4 year Pharma background experience for FP , In process and PV samples. Roles and Responsibilites To analyze the samples of in process/FP/Process validation as per work allotted by section in charge/Designee. Preparation of report and submission of reports along with raw data to section in charge/Designee within time. Immediate reporting of any odd observation, incident, OOT and OOS result during analysis to section in charge/Designee. Qualification Required M.sc/B.pharm Relevant skills / Industry experience Should have 2 to 4 year experience. Relevant professional / Educational background M.sc/B.pharm

Conduct final inspection and testing of finished products to ensure compliance with quality standards and customer specifications. Hands-on experience in testing of Finished products Instruments must be handled like HPLC, GC, KF, IR, DT, and Dissolution. Hands-on experience like software like Empower and LIMS. Qualification M.SC/B.Pharma 3 to 6 years Additional Information

As an Analyst, you will be required to have knowledge of instruments such as HPLC, UV, FTIR, GC, Polarimeter, KF, Autotitratior, etc. Your primary responsibilities will include sampling, testing, and releasing raw material, packing material, and miscellaneous material samples. It will be your duty to maintain reserve samples as per standard operating procedures (SOP). You will also be responsible for reviewing instrument logbooks, raw data of raw materials, packing materials, miscellaneous materials, in-process and finished products, as well as water analysis. To be considered for this position, you must possess a Bachelor's or Master's degree in a scientific field. Additionally, a minimum o...

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: Kn...

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

Walk In Drive For Quality Control In Formulation Division @ MSN Formulation Unit -II , Kothur . Department :- Quality Control Formulations Experience:- 2 to 8 Years Skills :- Formulation QC - HPLC | GC | GC MS | LIMS | LCMS | ICPMS | Dissolution | IP/FP | Stability | Method Validation | Method Development | Method Transfer | E&L | | Proficiency with Equipment | Method Development & Optimization | Understanding of Regulations | Data Analysis | Testing and Inspection | Process Improvement | Regulatory Compliance | Equipment Maintenance | Training and Support | Root-cause analysis | Method development and validation | (OSD & Injectables) | USFDA | Regulatory Approvals Division :- Formulation In...

We are seeking a skilled Analyst with hands-on experience in FTIR/Disso/UV/KF/HPLC techniques(Multiple requirements). The candidate should be well versed with Method Development, Method Validation and routine analysis. Required Candidate profile It is on the rolls of Cotecna Life Sciences India Pvt Ltd(Erstwhile Geochem Laboratories) If interested please share profiles on nilesh.kadam@geochem.net.in No walk-in interviews on 27-Aug-25

Eurofins is the world leading Food Testing laboratory group, deploying a comprehensive range of state-of-the-art analytical techniques in order to support its clients' increasingly stringent quality and safety standards. We are present in India as Eurofins Analytical Services India Pvt Ltd and provide a comprehensive and one-stop testing service to businesses and organizations involved in food and feed processing, Agro products, Export, Hospitality and Retail chains. About The Role 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...