103 Kf Jobs

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).

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 standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngenes quality standards always Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Job Description Analysis of Raw material/ In process / intermediate and finished product Handling of HPLC/GC/UV/KF /FTIR and other analytical instruments Sampling of Raw material / Intermediate/ Finished product Handling QMS activities Instrument calibration and qualification Maintained the Lab as per GMP requirements. Reserve sample management Experience : 1- 4 years Education M.Sc in general or organic chemistry Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status regarding public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities Show more Show less

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 instruments like GLC, HPLC, UV-Visible, FTIR, ICP, K/F, Melting point, and should be able to coordinate with QC staff, R&D, Commercial, and Production for quality and dispatch related activities. The Assistant Manager - QC will also be responsible for troubleshooting related to QC activities, training subordinates on 21 CFR Part 211, 111 with data integrity (Part-11) compliance in the lab, and maintaining awareness about responsible care (Environment, Health, Safety, and Security). The ideal candidate should have an M.Sc. in Chemistry with 8-12 years of experience. Competencies required include being responsible for implementation and compliances of various regulatory standards, hands-on experience as a reviewer of electronic data and hybrid systems in regulatory environments like US-FDA, WHO, and knowledge about 21 CFR Part 211, 111 with data integrity (Part-11). This role reports to the QC Head and will have 2-3 reportees. The Assistant Manager - QC will work closely with the Site Quality Head, CQA & RA Head, and Unit HR Head.,

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 systems that ensures safe operations and compliance to companys integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements always in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngenes quality standards always Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Job Description: Performing analytical method validations and related documentation, as well as analysis of RM, PM, Intermediates, API, and Finished products. Key Responsibilities Following Good Laboratory Practices while working in the QC Laboratory. To maintain and clean responsibility allotted for individual instruments. Use of required safety apparel while sampling, analyzing, and working in the laboratory. Carry out the analysis of validation samples as per the protocol. Initiation of laboratory incidents and deviation. Preparation of calculation sheets and making draft reports. Disposal of sample for analysis after use. Taking any other job allocated by HOD or Section Head. Analysis of Intermediate, finished product, and working standard qualification as per the specification. Ensure that the instrument usage log is verified and reviewed periodically, and check the labels accordingly as per SOP. Preparation of protocols and Observation data sheets. Should be well versed with the latest analytical techniques like HPLC/GC, KF/KFC, IR/UV, LC-MS, GC-MS, IC, and ICP-OES/ICP-MS, etc... Being well-versed in the Chromeleon data management application and LIMS will be advantageous. To ensure safety compliance as per Syngene policy and EHSS requirements. Educational Qualification: M Sc / M Pharma (Analytical/General chemistry Technical/Functional Skills Should be well versed with the latest analytical techniques like HPLC/GC, KF/KFC, IR/UV, LC-MS, GC-MS, IC, ICP-OES/ICP-MS, DSC, TGA, etc... Being well-versed in the Chromeleon data management application and LIMS will be advantageous. Experience: 1- 4 years Behavioral Skills Should be an adaptive learner. Should demonstrate effective Communication skills. Organization and ability to balance work and Life. Should possess good Time Management abilities. Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status about public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. Show more Show less

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, Balance, among others. This is an entry-level position that offers a great opportunity for learning and growth in the field of Quality Control. If you are passionate about QC, eager to learn, and looking to kickstart your career in the pharmaceutical industry, this role is perfect for you. Join us in our mission to maintain high-quality standards and contribute to the success of our organization.,

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 / 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.

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 initiation to completion, ensuring adherence to timelines and budget constraints Develop project plans, allocate resources, and monitor progress to achieve project objectives Identify and mitigate risks to project success, implementing appropriate solutions as needed Operational Efficiency:Streamline processes and procedures to improve operational efficiency and effectiveness Identify opportunities for automation or technological enhancements to optimize workflow and productivity Collaborate with cross-functional teams to implement process improvements and best practices Data Analysis and Reporting:Analyze data to identify trends, patterns, and insights relevant to the organization's objectives Generate reports and presentations to communicate findings and recommendations to key stakeholders Utilize data-driven insights to inform decision-making and drive continuous improvement initiatives Stakeholder Engagement:Build and maintain relationships with internal and external stakeholders, including clients, partners, and vendors Collaborate with stakeholders to understand their needs and requirements, ensuring alignment with organizational objectives Effectively communicate project updates, issues, and resolutions to stakeholders, fostering transparency and trust Compliance and Risk Management:Ensure compliance with relevant laws, regulations, and internal policies and procedures Proactively identify and address potential risks and compliance issues, implementing appropriate controls and safeguards Keep abreast of industry developments and best practices to inform risk management strategies

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.

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 of 4 to 6 years of relevant experience in the Quality Control and Compliance (QCC) Department is required. Candidates applying for internal job postings should have completed at least 2 years in their current role. If you meet the qualifications and are looking to contribute your expertise in analytical instrumentation and quality control, we encourage you to apply for this rewarding opportunity.,

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.