27 Dissolution Apparatus Jobs

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...

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

You are invited to join Zydus LifeSciences Ltd. at their Injectable manufacturing plant in Ahmedabad. We are currently looking to fill the following positions: 1. Production: - Staff positions ranging from Executive to Assistant Manager require candidates with a B. Pharm / M. Pharm/ B.E background and 4 to 10 years of experience in Supervising and Controlling Production areas such as Isolator, Aseptic Filling, Vial Washing, Autoclave, Lyophilizer, and Visual Inspection. Knowledge of QMS activities is a plus. - Plant Operator and Technical Assistant roles require candidates with a Diploma or ITI qualification and 3 to 6 years of relevant experience in operating production machines like Isolat...

Job Description 1. Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report. 2. To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc. 3. Ensuring data integrity policy, GDP and its effectiveness up to compliance 4. To maintain the stability chamber and tracker. 5. To maintain the stability chamber and tracker. 6. To ensure charging and withdrawal of stability samples as per approved protocols. Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience :- 2 to 4 yrs. Education Others Competencies

We are #hiring Quality Control - Executive for our manufacturing units VPL Chemicals and Symbio Unit 2 located in Dabaspet and Tumkur respectively. Job Description 1. Testing of raw materials, in-process samples, finished products as per SOP/STP. 2. Calibration of QC Lab instruments. 3. Identifying the chemicals testing requirements for testing of samples on regular basis plan for procurement of chemicals, standards and glassware. 4. Preparation qualification of in-house working standards and review of validity of reference standards and impurities as per Pharmacopoeia. 5. Upkeep of calibration records, working standards records and timely completion of log books in line with audit requireme...

Job Description Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report. Having analytical knowledge of Nasal/Derma products. 3. To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc. 4. Ensuring data integrity policy, GDP and its effectiveness up to compliance 5. To maintain the stability chamber and tracker. 6. To maintain the stability chamber and tracker. 7. To ensure charging and withdrawal of stability samples as per approved protocols. Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience...

GLP Compliance. Analysis of API, Finish product, Excipient and development stability Samples. Routine support in product development. Dissolution profiling. Analytical method development for Assay, Related compound, Residual solvent and Dissolution. Partial Validation for analytical method. Preparation of SOPs. Review of analytical Data. Operation and calibration of sophisticated instruments like Dissolution apparatus, HPLC, UPLC, GC and et

Role & responsibilities Operate and maintain QC instruments, including HPLC, GC, UV, FTIR, Dissolution Apparatus, Melting Point Apparatus, Karl Fischer Apparatus, Auto Titration, Analytical Weighing Balance, Polarimeter, Disintegration Apparatus, pH Meter, etc. Perform analysis of in-process samples, validation, hold-time study, finished products, and stability samples as per relevant specifications. Conduct daily and monthly calibration of analytical balances in the instrumentation section. Maintain daily logs and ensure adherence to Good Laboratory Practices (GLP). Perform daily standardization of Karl Fischer reagent. Monitor and record daily temperature readings of the instrumentation ro...

Role & responsibilities Preferred candidate profile Perks and benefits

Knowledge of analytical method development, Validation and stability analysis of Oral and Injectable dosage forms. Handling of Tablets, Capsules, Oral Liquids and Oral Suspensions. Handling of dissolution apparatus for Tablets, Capsules, Oral Liquids and Oral Suspensions.USP Type-I, USP Type-II & USP Type-IV. Knowledge about the handling of analytical instruments like HPLC,GC, UV,SOR,IR,Particle size analyser,Osmometer,viscometer etc. Knowledge about the calibration of HPLC,GC,UV,SOR,IR,Particle size analyser,Osmometer,viscometer etc. Knowledge about regulatory guidelines and requirements. Knowledge about method transfer activities. Knowledge about the safety aspects. Knowledge about GLP and...

Role & responsibilities :- Job overview :- The role requires strong analytical data review skills and experience with various QC instruments . The position involves supporting their North American sites , Potentially requiring the candidate to work according to US time zone. Key Responsibilities & Required Experience: Strong exposure to Analytical Data Review and electronic data review from QC instruments such as HPLC, GC, Dissolution Apparatus, and Malvern 3000 Thorough understanding of Quality Control investigations, including Lab Incidents, OOS, and OOT Preparation and Review of Method validation, Method Transfer, Method Verification and Equivalency documents, etc Review of Analytical raw...

Hiring: Operators & Officers for OSD Production & Packing (Onco & Non-Onco) | Sterile Production | Quality Control | Microbiology Interview Location: Elite Hotel, Jadcherla Walk-in / Immediate Joiners Preferred 1. Operators & Officers for OSD Production & Packing (Onco & Non-Onco) Experience: 2 to 6 Years Qualifications: I.T.I / Diploma / D. Pharmacy / B. Pharmacy Job Responsibilities: Operation of equipment: Granulation, Compression, Coating, Capsule Filling, Blister & Bottle Packing Supervision of Granulation, Compression, Coating, and Packing lines (Blister/Bottle) 2. Officers & Operators for Sterile Production (Onco) Experience: 2 to 6 Years Qualifications: Diploma / B. Sc / D. Pharmacy ...

Long Description 1. Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report. 2. To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc. 3. Ensuring data integrity policy, GDP and its effectiveness up to compliance 4. To maintain the stability chamber and tracker. 5. To maintain the stability chamber and tracker. 6. To ensure charging and withdrawal of stability samples as per approved protocols. Competencies Education Others Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience :- 2 to 4 yrs.