85 Dissolution Jobs - Page 4

a. Should be well versed with IVIVC concepts b. Should have excellent knowledge on product development and clinical studies. c. Should have hands on experience on operating various simulation tools necessary for IVIVC. d. Excellent communication skills are must.

Role: Officer / Executive - Quality Control Job Location: Nashik At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.Viatris empowers people worldwide to live healthier at every stage of life.We do so via: Access Providing high quality trusted medicines regardless of geography or circumstance; Leadership Advancing sustainable operations and innovative solutions to improve patient health; and Partnership Leveraging our collective expertise to connect people to products and services. Every day, we rise to the challenge to make a difference and here's how this role, will make an impact: Role Purpose Seeking for candidates (Male/Female) with sound qualification background to ensure the testing of drug product in Quality control lab and to ensure every product is of the highest quality. They shall be concerned with sampling, specifications, testing, documentation, release procedures which ensure that the necessary and relevant tests are carried out under the norms of cGMP. Role & responsibilities Candidate must have relevant experience in Quality control OSD and QMS and able to operate & maintain laboratory equipment/instruments (HPLC, GC, Malvern Particle sizer, dissolution apparatus etc.) as per procedure. To maintain documents as per GLP requirements. To ensure the calibration status of laboratory equipment & instruments. To report and involve in incidence/Deviation/OOS/OOT investigations. Candidate must have sound exposure in the Quality Control Laboratory to supervise and maintain documents and retention of records as per GMP requirements. To ensure the review of QC documents like analytical reports SOPS, Qualification, Logbooks, Raw data sheet, analytical records, calibration and ensuring compliance to observations with proper root cause and justifications. Candidates participate in initiation, review, and closure of OOS/OOT and monitor the CAPA with implementation in Track wise. To ensure the compliance of the Corrective and Preventive Actions (CAPA) necessitated through various activities such as Regulatory Audits, Market Complaints, and Product Recall & Annual Product Review in the QC if applicable. To support Quality Assurance / Compliance /Regulatory Systems, Processes and ensure Monitoring, Execution, Initiation of the Quality Management Systems in Quality Control laboratory. Qualification & Experience Candidate must be B. Pharm/ M. Pharma/ M. Sc In Chemistry Experience- Candidate must have 2 to 6 years experience in a reputed pharma industry. Candidates must be willing to work in shifts Candidate who have faced regulatory Audits like FDA & MHRA Audit will be preferred.

QC Testing,HPLC,RP, Stability,GLP

Key Responsibilities Quality Strategy & Planning Develop and implement quality control standards, procedures, and policies. Define inspection criteria and quality benchmarks. Team Management Lead and supervise a team of quality inspectors or analysts. Provide training and guidance to QC staff. Manage and supervise QC laboratory activities Use effective negotiation skills to drive alignment and resolve conflict Inspection & Testing Oversee routine inspections and testing of raw materials, in-process, and finished products. Ensure compliance with internal and external specifications and regulations. Documentation & Reporting Maintain detailed records of quality control activities. Analyze QC data and generate reports to identify trends and areas for improvement. Compliance & Audits Ensure compliance with ISO, GMP, or other industry-specific standards. Coordinate and support internal and external audits. Problem Solving Investigate product quality issues and customer complaints. Implement corrective and preventive actions (CAPA).

2 VACACNCIES IN ADL - STABILITY TEAM 1) Stability - Team lead/Manager- Investigational analysis - ADL DEPARTMENT with 10 to 18 yrs of experience in Regulated and Emerging markets. 2) Executive / Scientist - ADL Stability with 6 to 9 yrs of experience in Regulated and Emerging markets. Educational qualification : M.Sc Analytical chemistry Dosage forms : Oral solids, Liquid orals, Opthalmic and injectable products Job description for AD: 1) Will be responsible and accountable for the trouble shooting and investigational analysis of R&D stability samples 2) Sound technical and scientific knowledge for investigation of anomalies. 3) Root cause identification and CAPA for OOT and OOS for developmental stability samples 4) Online review of HPLC and UV raw data of stability 5) Well versed with operation of Empower 3.0 and Chromeleon 7.2 software 6) Has experience in handling a team of 4 to 5 members 7) Should have exposure to Assay, Dissolution, preservative content and related substances testing Candidates with prior experience in investigational and trouble shooting analysis is preferable.

VACANCY FOR TEAM LEADER - ANALYTICAL METHOD DEVELOPMENT (FORMULATIONS) - REGULATED MARKET Experience: 10 to 15 years Designation : Asst. Manager/ManagerEducational qualification : M.Sc Job profile : Need to work independently and should have handled a team of 6 to 8 members for method development and routine testing To guide and mentor analysts with practical training for developing analytical methods. SOP training and Analyst certification for new joinees within the team. Work allocation and planning of daily activities for the team subordinates Monitoring of routine analysis and trouble shooting To support site for critical trouble shooting and investigation Review of raw data , LNB and filing of routine analysis SOP preparation and training Pharmacopoeia & DMF Review Interaction with cross functional teams Review of calibration data of analytical instruments Review and check file note/deviation with investigation and CAPA for the same.

Qualification : M. Pharmacy (Analytical)/M.Sc.(Analytical) Experience : 2-3 yrs. (Formulation Experience) Location : Balnagar (Hyderabad) Skills Required: Sound knowledge of Dissolution, Analytical method development for tablets, capsules, oral solutions, ICH stability testing, Water HPLC, UV-Visible Spectrophotometer, KF Auto tiltrotor, Analytical method validations, transfer and verifications as per ICH guidelines and USP/BP guidelines, Analysis of in-process, stability & protocol driven samples. Reports, Protocols and STP, SOPs Preparation. GLP Activities. Chromatographic software like Empower. Prefer Male people & Immediate Joiners.

Experience - 2 Years + In Formulation QC * QC - Finish Product - GC/HPLC/ Dissolution/AAS/UV * QC- In process- HPLC/UV/Dissolution/GC * QC - Validation- HPLC/UV/GC/Dissolution * RM - HPLC * Stability HPLC GC UV Dissolution * RM Reviewer

Job summary We are seeking an individual to perform the Preventive Maintenance and Break Down Maintenance of Analytical Equipment's present in Quality Control . Roles & Responsibilities To perform the preventive and breakdown maintenance of analytical equipment's or Instruments like HPLC, UPLC, GC-HSS, Dissolution Test Appratus, Titrators, FTIR, UV-VIS Spectrophotometer,.... To update the preventive maintenance plan whenever addition of instruments or match the calibration schedule. To prepare the task lists for all analytical equipment's and update them in SAP. To perform the preventive maintenance as per the PM schedule. To make sure of closing the generated PM orders in SAP after performing the PM. To ensure that the instruments / equipment are used with utmost care and as instructed in the relevant SOP. To attend the breakdown's and close notification or order of the instrument /equipment after the Completion of breakdown maintenance. To be a part of investigating the incidence related to instrument Responsible for the maintaining of required spares for all instruments in warehouse. To get the quotations for the required spares and services for the maintenance of the instruments. To generate the purchase requisitions for the required spares and services. To perform the PM in the given frequency within the given period. Adhering to the allotted shift schedule with right time. If any changes prior permission shall be taken from Group leader. Qualification Educational qualification: An B.Tech. or any Degree in Instrumentation, Mechanical, Electronics, Electrical. Required Work experience : 3 to 6 years Skills & attributes: Technical Skills • Hands-on Experience on maintenance of Waters HPLC (Arc, e2695), Agilent HPLC (1200, 1260 Infinity), Agilent GC-HSS (7890, 8890, 7897, G1888), Dissolution Testers (Electrolab, Sotax), Metrohm Titrators. • Working experience in a cGMP (Current Good Manufacturing Practice) environment, with a special emphasis on Good Documentation Practices (GDP). • Basic knowledge in SAP usage Behavioural skills • Prioritizes effective communication and demonstrates a performance-oriented mind-set. • Effective verbal and written communication skills. • Performance-oriented approach, consistently striving for high standards. • Demonstrates flexibility in working shifts and a clear understanding of team dynamics. Additional Information About the Department Quality Control Formulations For more details, please visit our career website at https://careers.drreddys.com/#!/

The position is one of a leadership role. Work experience of at least 10 years in the Indian BFSI, real estate and infrastructure domain, of which at least 6 years should be in leading a team of 8 to 10 members wherein the candidate should have worked on and be centrally involved in project management and driving research and consulting engagements with or within banks, HFCs, NBFCs and corporates. Ability to drive business development and acquisition efforts in the above sectors is also critical.