227 Dissolution Jobs

Key Responsibilities: 1. Stability Study Design & Planning Define study protocols, including time points, conditions (temperature, humidity, light exposure), and container types. Collaborate with formulation scientists and regulatory affairs teams to ensure studies align with regulatory guidelines (e.g., ICH, FDA). Plan long-term and accelerated stability testing for new and existing products 2. Compliance & Documentation Document study protocols, deviations, results, and reports. Maintain comprehensive stability study records for internal reference and regulatory submissions. Prepare stability data for inclusion in regulatory filings, ensuring compliance with ICH, FDA, or other relevant guidelines. Ensure that all documents are stored according to GMP and are easily retrievable during audits. 3. Equipment & Process Management Well-versed with Chromeleon Software Performing a Dissolution Test Well-versed with QC lab Instruments 4. Cross-functional Coordination Work closely with Production, QA, Engineering, and Warehouse teams to ensure smooth operations. Support QMS activities 5. Safety & Hygiene Compliance Ensure adherence to aseptic techniques and environmental monitoring standards in cleanrooms. Follow safety protocols for handling hazardous chemicals and sterilization processes. Train production staff on GMP, hygiene, and workplace safety standards. Required Qualifications & Skills: Education: B.Pharm / M.Pharm / M.Sc Experience: 2-7 years of experience in QC Stability Section for Formulation (preferably injectables) Technical Skills: Well-versed with Chameleon Software Performing a Dissolution Test Familiarity with cGMP, USFDA, EU-GMP, and WHO-GMP guidelines. Soft Skills: Strong problem-solving abilities, teamwork, attention to detail, and adaptability.

We are seeking a detail-oriented and proactive professional to manage monthly MIS reporting, critical issue tracking, and management approvals across multiple business units. This role requires strong analytical, coordination, and communication skills to ensure timely and accurate reporting for senior leadership. Role & responsibilities Prepare and consolidate Monthly MIS Reports for the multiple departments: Track and report critical issues and ensure timely escalation to management. Coordinate with department heads for data collection, validation, and approvals. Maintain dashboards and ensure accuracy of all reports submitted to senior management. Support in preparing presentations and summaries for management meetings. Ensure compliance with internal reporting standards and timelines. Preferred candidate profile Required Skills & Qualifications Bachelors degree in Finance, Business Administration, or related field. 3–5 years of experience in MIS reporting, data analysis, or similar roles. Strong proficiency in MS Excel, PowerPoint, and reporting tools. Excellent communication and coordination skills. Ability to work under tight deadlines and manage multiple stakeholders. Preferred Skills Experience in corporate governance, compliance, or legal reporting. Knowledge of ERP systems and data visualization tools (e.g., Power BI). Why Join Us? Opportunity to work across diverse business units. Exposure to senior management and strategic decision-making processes.

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation

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

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Saturday 20-09-2025. Requirement for Executive - FAR&D - Formulation Analytical Research & Development(FAR&D) Undertake method development, troubleshooting and method validation to GMP and ICH. Investigation of non-conforming samples, CAPAs, data evaluation and reporting. Write cGMP Quality documents including Standard Operating Procedures, laboratory equipment procedures and investigational protocols. Excellent, enthusiastic, clear communication skills, both written and verbal, with a diverse audience are critical to the success of this position. Proven ability to interact with cross - functional and cross - cultural teams. Previous experience of running analytical techniques such as HPLC, Dissolution, KF, IC with the ability to extract and prep various samples in a variety of forms. As this role involves liaising with other departments on a regular basis, you will need good communication skills and the ability to work effectively as part of a team. Note : Formulation Quality Control Candidates also eligible. Interview Date : 20-09-2025 Department : Formulation Analytical Research & Development(FAR&D) Experience : 1 to 6 Years Qualification : M. Pharmacy / M.Sc. / B Pharm Position: Executive Work Location : MSN R&D Center, Pashamylaram, Hyderabad Interview Venue Details MSN Laboratories, R&D Center,Pashamylaram, Hyderabad

Conduct chemical synthesis of new and existing agrochemical compounds in the lab. Develop and optimize synthetic routes and reaction conditions to improve yield, purity, and cost-effectiveness.

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation.

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation.

As an experienced candidate with 03-05 years in pharmaceutical manufacturing machine maintenance, your key responsibilities in this role will include: - Sampling and Testing of raw material - Testing of Finished product & semi finished products - Knowledge of HPLC/ GC Empower software - Knowledge of Operation of instruments like Dissolution/ FTIR / HPLC / GC / Polarimeter - Knowledge about basic QMS in QC like Incidence / OOS etc. - Handling of Instrument related software - Awareness about instrument calibration You are required to have a qualification of M.Sc / B. Pharm / M.Pharm to be eligible for this position.,

Develop, optimize, and validate analytical methods for raw materials, in-process samples, and finished products.Perform analytical testing using techniques such as HPLC, GC, UV-Vis, FTIR, titration, dissolution, and others.

Develop, validate, and optimize analytical methods for qualitative and quantitative analysis of raw materials, intermediates,and finished products. Perform instrumental analysis using techniques such as HPLC,GC.

Setting strategy for evaluating and implementing new technologies within the Analytical Development department. Required Candidate profile with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc

R&D (Synthesis) -Agrochemical Industry-Saykha,Gujarat. Industry IT Software - Application Programming / Maintenance Qualification M.Sc Key Skills R&D Research & Development Executive UPLC HPLC GC Analytical Development

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

R & D (Analytical Development) - Agrochemical Industry-Saykha,Gujarat. Capital Placement Services 3 - 8 years Industry Pharma / R&D / Biotech Qualification M.Sc Key Skills R & D Analytical Development LAB Agrochemical UPLC Green Field Projects HPL

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

Officer - Quality Control: Qualification - M.Sc / B. Pharm / M.Pharm Experience - 03-05 years experience in pharmaceutical manufacturing machine maintenance Job Responsibility - 1. Sampling and Testing of raw material . 2. Testing of Finished product & semi finished products 3. Knowledge of HPLC/ GC Empower software 4. Knowledge of Operation of instruments like Dissolution/ FTIR / HPLC / GC / Polarimeter 5. Knowledge about basic QMS in QC like Incidence / OOS etc. 6. Handling of Instrument related software. 7. Awareness about instrument calibration.

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

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

Please walk in to the interview on SUNDAY 13th Sep 2025 b/w 10:00 AM to 3:00 PM at below mentioned venue. Venue: Unison Pharmaceuticals Pvt. Ltd. Block A, Office Number: 905,6,7,8 Safal Pegasus, 100 Feet Anand Nagar Rd, Chinar Bungalows, Prahlad Nagar, Ahmedabad, Gujarat 380015 Apply now to become a part of a growing team!! 1) Analyst: ADL - Routine Analysis Experience: 2 to 8 years Job Role: ADL - Sample Analyst Markets: Domestic & Regulatory Location: Moraiya, Ahmedabad (Transportation is available from specific routes of Ahmedabad) Designation: Officer / Sr. Officer No. of vacancies: 05 Roles and Responsibilities : Perform chemical, physicochemical and wet analysis as per product requirements. Routine In-process, Finished product (Initial & Stability samples) analysis. Data reporting with good documentation practice and presenting results in informative report format. 2 ) Analyst: - ADL - LCMS Experience: 2 to 8 years Job Role: ADL - LCMS Analyst Location: Moraiya, Ahmedabad (Transportation is available from specific routes of Ahmedabad) Designation: Officer / Sr. Officer No. of vacancies: 05 Roles and Responsibilities : Method development of nitrosamine impurities/NDSRI/genotoxic impurities on LCMS/MS with proper documentation and prepare Analytical test procedure & worksheet. Routine API & Finished product (Initial & Stability samples) analysis like Nitrosamine impurities, Genotoxic impurities, NDSRI, related substances Method validation for analytical method on LCMS/MS Responsible to Stability data compilation for finish product as per requirement. Follow GLP in the laboratory. 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 Regards, Team HR Unison Pharmaceuticals Pvt Ltd

About The Role Data Executive

Dear Applicants, Greetings from Biophore India !! We have opening for Formulation AR&D Department. Experience : 3 7 Years Qualification : B. Pharm /M. Pharm or M Sc Work Location: R&D Centre -Pashamylaram, Isnapur, Sanga Reddy. Job Description 1) Method Development and routine analysis of Assay, Dissolution, Related substances, Content Uniformity, Blend Uniformity. 2) Responsible for Analytical Method Validation activities for solid orals and injectables. 3) Responsible for Routine and Stability analysis activities for solid orals and injectables. 4)Responsible for the Review of documents generated in Method development activity. 5)Responsible for the Preparation and Review of Tentative method of analysis and Method development Reports. Please Carry below documents: 1. Updated resume. 2. Last 3 months pay slips or bank statement 3. Offer letter or Increment letter from the present employer,4. Photocopies of all Education certificates Ref to Friends or colleagues. Contact Person- Prasad- HR Interview Date: 13 -09-2025 (Saturday) Time:9:30AM 2:00 PM

Role: Officer - Quality Control / Quality Assurance 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 We have Openings in Both QC (Lab / Microbiology / CSV) and QA(IPQA / Documentation / QMS / AQA) . 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 1 to 4 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.