39 Dissolution Apparatus Jobs

Masters of Science M.Sc (Chemistry) or B.Pharm degree. A minimum of 4-5 years related experience in QC pharmaceutical manufacturing company. Job Profile : A Quality Control Officer is a professional who is Responsible for the Raw materials. in process and finished product and also stabling samples analysis and had knowledge of handling instruments like HPLC , UV-visible spectrophotometer , Dissolution Apparatus, pH meter , viscometer , KF, Polarimeter , Refractometer, Friabilator, D.T. Apparatus etc. Roles & Responsibilities: Responsible for in-process and finished product analysis and also analysis of stability samples. Handling instrument like HPLC, UV-visible spectrophotometer, Dissolutio...

To perform analysis of finished Products and in-process samples. Proficiency in using analytical instruments such as UV/VISIBLE and IR, HPLC Handling of laboratory incidents and deviation. Extensive knowledge of GMP regulations in cGMP Manufacturing Environment. Chemical and Instrumental analysis of In process and finished products. To perform analysis of stability samples. To perform the calibration of instruments like HPLC, Dissolution tester, UV Spectrophotometer. Analysis of OOS/OOT

Analysis of FP/Stability Samples on instruments like HPLC/UV/GC/Dissolution apparatus Exposure on QMS system Required Candidate profile Educational qualification: M.Sc or B.Pharm Experience : Minimum 1 years with HPLC operation and dissolution apparatus--Quality control send resume to sunil@flamingopharma.com,hr@flamingopharma.com

About Apotex Inc. Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to patients in more than 75 countries globally. Through vertical integration, the Apotex group is focused on the development and sale of generic, biosimilar and specialty products. For more information visit: www.apotex.com . Job Summary Planning and executing various analytical method development, validation for new products, comprehensive testing of API and finished dosages with all established regulatory and compli...

As an Analyst for testing of finished product analysis, you will be responsible for the following key responsibilities: - Perform finished product analysis, including expertise in handling HPLC, GC, and Dissolution apparatus - Conduct injectables analysis focusing on physical parameters using HPLC and GC techniques - Utilize instruments such as HPLC, GC, Auto titrator, IR for analysis and troubleshooting of HPLC/GC instruments - Participate in audits from regulatory bodies like USFDA, MHRA, TGA - Demonstrate strong communication skills for effective documentation and uphold the concept of data integrity The qualifications required for this position are: - Prior experience in finished product...

As a Formulations Specialist at our company based in Hyderabad, India, you will be responsible for the following key tasks: - Designing and executing pre-formulation experiments such as solubility, pKa, log P, dissolution, intrinsic dissolution, bulk density, flow indices, solid-state assessment, excipient compatibility, and more. - Conducting preclinical formulations to support lead identification, lead optimization, and clinical candidate selection, including solutions, suspensions, powders for constitution, compounds in capsules, and basic tablet abilities. - Utilizing solid-state equipment like PXRD, MDSC, TG, DVS, Polarizing and Hot-stage Microscopy, and dynamic image analysis technique...

You will be responsible for planning and executing various analytical method development and validation for new products, as well as conducting comprehensive testing of API and finished dosages while ensuring compliance with all established regulatory and safety requirements. You will review laboratory data, instrument logbooks, and reports as needed. Additionally, you will initiate departmental Corrective and Preventive Actions (CCRs) and track progress through the Quality Management System (QMS) for executing proposed changes. Furthermore, you will prepare Transfer of Analytical Procedures (TAP) protocols and reports for various sites, procure samples and impurities, and execute assigned T...

As a member of Apotex Inc., a Canadian-based global health company, your role will involve planning and executing various analytical method development and validation for new products. You will be responsible for comprehensive testing of API and finished dosages while ensuring adherence to all established regulatory and compliance requirements. Your key responsibilities will include: - Preparing working plans and timelines for assigned projects - Developing stability indicative analytical methods for drug substance and finished product - Ensuring all activities in Analytical Development are in compliance with cGLP and departmental quality systems - Applying AQbD approach to analytical method...

You will be responsible for performing quality control activities in the Fill and Finish department. Your key responsibilities will include: - Conducting testing using HPLC, GC, Dissolution apparatus, and UV Visible Spectrometer - Performing weight analysis and stability studies - Working with Injectable dosage forms Qualifications required for this role: - B.Pharm/B.Sc/M.Sc. degree - 2 to 6 years of hands-on experience with HPLC, GC, Dissolution apparatus, and UV Visible Spectrometer,

About Apotex Inc. Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to patients in more than 75 countries globally. Through vertical integration, the Apotex group is focused on the development and sale of generic, biosimilar and specialty products. For more information visit: www.apotex.com. Job Summary Planning and executing various analytical method development, validation for new products, comprehensive testing of API and finished dosages with all established regulatory and complia...

As the Quality Control Head at Celogen Pharma Pvt. Ltd., you will be responsible for directing all laboratory operations related to testing of raw materials, packaging materials, in-process materials, and finished pharmaceutical products. Your role will involve ensuring strict compliance with current Good Laboratory Practices (GLP) and all applicable national and international regulatory standards to provide high-quality, timely analytical support for manufacturing and product release. **Key Responsibilities:** - **Analytical Testing:** - Perform routine and non-routine analytical testing using various techniques such as HPLC, KF, Dissolution, Titration, and Physical testing. - Ensure testin...

Responsible for in-process and finished product analysis and also analysis of stability samples. Handling instrument like HPLC, UV-visible spectrophotometer, Dissolution Apparatus, pH meter, viscometer, KF, Polarimeter, Refractometer, Friabilator, D.T. Apparatus etc. Analysis of finished product, stability product and raw material. Preparation of SOP for related to instrument and system. Preparation of protocol, worksheet for raw material and finish product. Documentation like ATP, Development report, Validation protocol, Validation report, STP preparation. Performing sample based check, monitor transactions provide feedback on quality. Sampling of Raw material, entry, packaging and labeling...

About Apotex Inc. Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to patients in more than 75 countries globally. Through vertical integration, the Apotex group is focused on the development and sale of generic, biosimilar and specialty products. For more information visit: www.apotex.com . Job Summary Planning and executing various analytical method development, validation for new products, comprehensive testing of API and finished dosages with all established regulatory and compli...

Job Title: Executive – Analytical Development Business Unit: R&D1 Regulatory Affairs Job Grade G12A Location Baroda At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Job Description To work as per cGMP and ensure its...

You will be responsible for ensuring the quality control, warehouse operations, engineering, and production activities in the Fill and Finish department. **Quality Control:** - As an Operator, you should have ITI qualification with 1 to 5 years of experience in handling samples, chemicals, reagents, and SAP procurement. - As an Analyst- Chemical, you should hold a B.Pharm/B.Sc/M.Sc. degree with 2 to 8 years of experience in HPLC, GC, Dissolution apparatus, and UV Visible Spectrometer. Knowledge of weight analysis and stability studies for Injectable dosage forms is required. **Warehouse:** - The Shift In charge role requires Any Graduate/Postgraduate with 6 to 10 years of experience in wareh...

As an Officer in the Research & Development-Analytical Development Laboratory, your role will involve performing various analytical tasks. Your key responsibilities will include: - Performing Analysis on HPLC - Operating Dissolution apparatus - Conducting Related substance Analysis - Working on Analytical method development and Validation To qualify for this position, you should have: - Minimum 1 year of experience - M.Sc or B. Pharm degree Please note that no additional details about the company were provided in the job description.,

You will be responsible for testing finished products and analyzing them using instruments such as HPLC, GC, and Dissolution apparatus. Your key responsibilities will include: - Conducting finished product analysis - Performing injectables analysis, focusing on physical parameters using HPLC and GC - Operating instruments like HPLC, GC, Auto titrator, IR, and troubleshooting HPLC/GC issues - Participating in audits by regulatory bodies like USFDA, MHRA, TGA It is essential that you possess good communication and documentation skills, as well as an understanding of data integrity concepts.,

Role Overview: You will be responsible for planning and executing various analytical method development and validation for new products, comprehensive testing of API and finished dosages while ensuring compliance with regulatory and safety requirements. You will review laboratory data, instrument logbooks, and reports when necessary. Additionally, you will initiate departmental change control requests and oversee the progress through the QMS system. Your role will involve preparing Transfer of Analytical Procedures (TAP) protocols and reports for various sites, along with procurement of samples and impurities as required. Key Responsibilities: - Prepare working plans for assigned projects an...

As a member of the Analytical Development team at Apotex Inc., you will be responsible for planning and executing various analytical method development and validation activities for new products, ensuring compliance with regulatory and safety requirements. You will review laboratory data, instrument logbooks, and reports, and initiate departmental Corrective and Preventive Actions (CCR) to track progress through the Quality Management System (QMS). Your key responsibilities will include: - Preparing working plans and timelines for assigned projects - Developing stability indicative analytical methods for drug substances and finished products - Ensuring compliance with cGLP, documentation, an...

Job Summary We are seeking a skilled Analytical Scientist to join our Analytical Research and Development team. The successful candidate will be responsible for routine testing of development/in process and stability samples. Apt knowledge in method development, method validations, and analysis of API and excipients as per pharmacopeial requirements is expected. This role will involve extensive use of chromatography techniques and adherence to regulatory standards. The ideal candidate should have a strong background in analytical chemistry, data analysis and keen eye for detail and a commitment to ensuring the highest quality standards. Roles & Responsibilities You will be responsible to per...

Perform analytical testing of raw materials, intermediates, and final products using instruments such as HPLC, and dissolution testers. Assist in the development, optimization, and validation of analytical methods. Record and analyze data accurately.

Role & responsibilities for Biopharmaceutics Scientist Method development, Validation and method transfer for API, complex generics products like long acting injectables, nasal sprays, topical products, peptide injections, peptide OSDs, etc using various analytical technique. Expertly in peptide characterization. Expertly in clinically relevant dissolution method development and establishing IVIVC/IVIVR. Closely working with CRO/CDMO/CTL to develop and validate analytical method using various technique. Review of development, validation and other analytical documents. High technical knowledge and hands on experience on various analytical techniques. Well versed with USP/EP/BP/IP and various ...

As a Fill and Finish QC at our company, you will play a crucial role in ensuring the quality of our pharmaceutical products. Your responsibilities will include: - Performing quality control tests using equipment such as HPLC, GC, Dissolution apparatus, and UV Visible Spectrometer. - Conducting weight analysis and stability studies for Injectable dosage forms. To excel in this role, you should possess the following qualifications: - B.Pharm/B.Sc/M.Sc. degree. - 2 to 6 years of hands-on experience in a similar role. - Proficiency in using HPLC, GC, Dissolution apparatus, and UV Visible Spectrometer. Join our team and contribute to the production of high-quality pharmaceutical products.,

i. Experienced in independent instrumental analysis of raw material, in process samples, finished product and stability samples of pharmaceutical products. ii. Well versed in analysis of Tablets, capsules, liquids samples, for common test as Assay, Related substances, Dissolution and preservative content analysis as per controlled specification and method of analysis. iii. Should able to operate, calibrate and maintain instruments like HPLC, GC, Dissolution apparatus, UV and FTIR etc. iv. Experience of Empower, Lab solution software shall be recommended. v. Exposure to perform AMV or development shall be preferred. vi. Aware about on line & good documentation practices. vii. Should have know...

The ADL Research Associate role at our organization in Vadodara requires 1-3 years of experience and a qualification of BSc/MSc Chemistry. As an ADL Research Associate, you will be responsible for developing, validating, and implementing analytical methods to support pharmaceutical product development. Your expertise in analytical instrumentation and regulatory guidelines will ensure compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Collaborating closely with R&D, Quality Assurance (QA), and Regulatory Affairs teams, you will contribute to formulation development, stability studies, and technology transfers. Your key responsibilities will include develop...