3421 Hplc Jobs - Page 7

Responsibilities: * Conduct quality control tests using HPLC (mandatory), GC (Mandatory), UV, Karl Fischer, PH Meter, and UV Spectrometer. * Ensure compliance with industry standards and customer requirements. Office cab/shuttle Provident fund

As a QC & R&D Chemist (Biological) at Sikandrabad, Uttar Pradesh, your role involves conducting various testing procedures and research activities related to biological formulations. **Key Responsibilities:** - Conduct chemical, microbiological, and biological testing of raw materials, in-process samples, and finished products. - Ensure adherence to quality standards, regulatory requirements, and specifications for biological formulations. - Perform stability testing and prepare detailed reports on product shelf-life and efficacy. - Maintain documentation and lab records as per regulatory and internal compliance guidelines. - Calibrate and maintain laboratory instruments and equipment. - Inv...

In your role at Dr. Reddys Laboratories Ltd., you will be responsible for ensuring safety, quality, and good laboratory practices at all times in the QC laboratory. Your key responsibilities will include: - Following good documentation practices in the laboratory. - Ensuring the cleanliness of the laboratory. - Managing sample receipt, issuance, analysis, reconciliation, and disposition. - Conducting analysis of In-process samples, Finished product, Stability samples, Swab samples, and Market complain samples. - Demonstrating expertise in chromatography (Waters & Agilent HPLC / UPLC/ GC) and Dissolution analysis. - Utilizing Lab ware LIMS, Empower3, and other 21CFR lab applications effective...

In this role at ZRC BIOTECH, you will be responsible for various tasks within different groups as outlined below: **Analytical Group:** - Design, perform, and review HPLC\UPLC, structural, and mass spectrometry based experiments. - Develop, qualify analytical methods, and transfer technology. - Prepare STP, SOP, and TTD documentation. - Perform routine calibration of instruments. - Maintain day-to-day compliance of the laboratory. - Manage samples including procurement of materials required for lab activities. **Formulation Development Group:** - Prepare technology transfer documents and collaborate cross-functionally with different teams. - Develop packaging for late phase batches, clinical...

About The Role Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : SAP S/4HANA Group Reporting Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Lead, you will lead the effort to design, build, and configure applications, acting as the primary point of contact. Your typical day will involve collaborating with various teams to ensure that application requirements are met, overseeing the development process, and providing guidance to team members. You will also engage...

About The Role Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : SAP S/4HANA Group Reporting Good to have skills : NA Minimum 7.5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Lead, you will lead the effort to design, build, and configure applications, acting as the primary point of contact. Your typical day will involve collaborating with various teams to ensure that application development aligns with business objectives, overseeing project timelines, and providing guidance to team members to...

About The Role Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : SAP S/4HANA Group Reporting Good to have skills : NA Minimum 7.5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Lead, you will lead the effort to design, build, and configure applications, acting as the primary point of contact. Your typical day will involve collaborating with various teams to ensure that application development aligns with business objectives, overseeing project timelines, and providing guidance to team members to...

Key Responsibilities Responsible for review of stability protocol & report. Responsible for Preparation of Annual Product Quality Review. Responsible for review of Master Packing Card & Master Formula Card. Responsible for preparation and review of Process validation Protocols and reports. Responsible for review of Batch Manufacturing and Batch Packing records Responsible for preparation of batch release certificate and ensuring batch release process performed as per the SOP. Responsible for issuance of Formats, Logbooks, Register, protocol, reports, BMRs and BPRs as per respective procedure. Responsible for review of QC documents such as Specifications and Standard Testing Procedure (RM, bu...

Responsibilities: * Maintain equipment and records * Prepare samples for analysis * Collaborate with team on method development * Operate HPLC & GC instruments * Report results accurately Thanks RIGHTCHOICE Provident fund Annual bonus

working experience in chemical lab in chemical company hplc,gc, etc....

Company: Strides Pharma Science Ltd Department: Quality Control (QC) Position: Executive Job Location: Bangalore Qualification: M.Sc. (Chemistry), B-Pharm, M-Pharm Experience: 2 to 5 Years Skills required: Experience on Raw material, In-process, Finished product, Stability and Microbiological testing. Work experience on FDA regulatory plants Flexible to work in shifts Regards, Srinidhi S s.srinidhi@arcolab.com

NOTE: Only Male & Candidates from AP & Telangana Preferred. Kindly Understand the JD It's not for the Clinical Trails Department Masters degree level in Chemistry,M pharmacy & B pharmacy 2023,24,25 passed outs. 2Years Bond & Need to Submit your 10th Original Mark list with us during the Bond Period. Bio-analytical: Role and responsibility: In process quality control of ongoing studies. Review of raw data, chromatograms and reports of the method validations and studies. Checking of all the instruments and equipments for the calibration status and appropriate labeling. Checking and monitoring of the day-to-day activities in the lab for compliance to SOPs and GLP principles. Checking of the con...

Roles and Responsibilities Perform breakdown maintenance, corrective maintenance, preventive maintenance, and sterile injectable equipment to ensure optimal performance. Ensure compliance with USFDA regulations during all manufacturing processes. Maintain accurate records of equipment calibration, cleaning validation, and batch production runs. Collaborate with cross-functional teams to resolve issues related to injectables manufacturing. Desired Candidate Profile 4-9 years of experience in pharmaceutical industry with expertise in breakdown maintenance, corrective/preventive maintenance, HPLC analysis, formulation development. B.Tech/B.E. degree in Electrical or equivalent qualification. St...

Responsibilities: Experience in Method Validation. Experience in Stability Study. Experience of review Electronic data review and backup systems. Expert in Qualification of analytical instruments like HPLC, GC, AAS, FTIR, UV etc. Expert in Calibration of analytical instruments like HPLC, GC, AAS, FTIR, UV etc. Must have minimum 3+ years of experience as a Reviewer. Must have an experience of reviewing all types of QC software. Must be familiar with cGMP/GLP practices and ICH and FDA Guidelines. Required Skills Must be excellent in written and spoken English; net savvy and adept at computer skills. Logical thinking. Organizing. Good in communication. Required Qualification: - B.Sc/M.Sc - Chem...

Responsibilities: Responsible for Documentation work in QC Department Candidate must have knowledge of HPLC & GC Responsible for manufacturing the batch as per MOM or BMR. Shall maintained all records related to manufacturing Overall looking after the complete filling, packing activities and Procurement of the packing material. To ensure the compliance of safety Requirement Cleanliness Hygiene and Environment in Working Areas. Responsible for Domestic / Export/ batch production & their Documents for their smooth Dispatch Activity. Required Skills: Must be excellent in written and spoken English; net savvy and adept at computer skills Attention for detail Team player Good in communication Req...

Review and analyze health data to ensure accuracy and compliance with regulatory requirements.Collaborate with cross-functional teams to identify and resolve data discrepancies.Develop/implement effective data review processes to improve quality Required Candidate profile Strong understanding of employment firms and recruitment services.Excellent analytical and problem-solving skills, with attention to detail and the ability to work independently.

Review and analyze health data to ensure accuracy and compliance with regulations.Identify trends and patterns in health data to inform business decisions.Collaborate with cross-functional teams to develop and implement data-driven solutions. Required Candidate profile Strong understanding of health data principles and regulations.Experience with data analysis and interpretation techniques.Excellent communication and collaboration skills.

Interested Candidate please share your resume to atull@harmanfinochem.com Job description Below are details for QC candidate to be recruited. Must have 3 to 6 yrs of experience in QC Should handle HPLC / GC instrument. M.Sc or B.Sc with experience also preferred. Should have worked in GLP /GMP environment Must have experience in API QC Shall have knowledge of 21 CFR / CSV / data integrity / validations Shall have knowledge of Method validation / Method transfer

Procurement Operations: Source and procure raw materials (APIs, excipients), packaging materials, and other pharma-related items. Evaluate purchase requisitions and coordinate with internal departments (production, QA/QC, R&D) to ensure timely procurement. Issue purchase orders (POs) and track their status until delivery and GRN. Vendor Management: Identify, evaluate, and develop new suppliers and maintain strong supplier relationships. Negotiate prices, payment terms, delivery schedules, and contracts. Monitor vendor performance based on quality, cost, delivery, and service. Inventory & Cost Control: Coordinate with the inventory team to maintain optimum stock levels. Analyze and control pr...

Manager - Quality Control (Formulations) 10 to 15 years of experience in Pharmaceutical Industry especially in Formulations Unit. Should have experience in successfully handling Quality Audits. Thorough knowledge in all types of Analytical instruments, analytical methods, HPLC, Method validation and method development etc., Should possess profound knowledge and skills in OSD/Formulations products. Total Quality Management (TQM), preparation and successful implementation of SOP's. Should lead a team in QC department and responsible for TQM. Sound working knowledge in MS Office and computer skills. Responsible for day-to-day and periodical MIS reports. Coordination with Production, QA and othe...

About The Role Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : SAP S/4HANA Group Reporting Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Lead, you will lead the effort to design, build, and configure applications, acting as the primary point of contact. Your typical day will involve collaborating with various teams to ensure that application requirements are met, overseeing the development process, and providing guidance to team members. You will also engage...

Conduct thorough reviews of ECR data to ensure accuracy and compliance with company standards.Identify and report any discrepancies or errors in the ECR system.Collaborate with cross-functional teams to resolve issues Required Candidate profile Strong understanding of ECR systems and data analysis principles. Excellent analytical and problem-solving skills with attention to detail.

Conduct thorough reviews of ECR data to ensure accuracy and compliance with company standards.Identify and report any discrepancies or errors in the ECR system.Collaborate with cross-functional teams to resolve issues Required Candidate profile Strong understanding of ECR systems and data review principles. Excellent analytical and problem-solving skills with attention to detail. Ability to work effectively in a fast-paced environment

Conducting Regular Analysis by HPLC Method Validation Method Development

Responsibilities: Hands-on experience in instrumental and analytical testing of raw materials (RMs). Maintaining comprehensive records of quality tests, inspections, and other related activities. Required Skills Must be excellent in written and spoken English; net savvy and adept at computer skills. Logical thinking. Organizing. Good in communication. Required Qualification:- B.Pharm/B.Tech/B.E/B.Sc/M.Sc - Chemistry/Chemical