253 Stability Studies Jobs - Page 10

? Job Description: ? ? We are looking for a skilled and proactive QA/QC professional with 2 5 years of experience to join our quality team. The candidate will be responsible for executing and overseeing quality assurance and quality control activities in compliance with regulatory and company standards. ? ? Key Responsibilities: ? ? Quality Control? ? Perform analytical testing of raw materials, in-process samples, and finished products. ? ? Operate, calibrate, and troubleshoot instruments such as HPLC, UV-Vis, GC, FTIR, and KF. ? ? Prepare and review analytical documentation including test reports, COAs, and calibration records. ? ? Guide and Mentor QC Executives / Trainees for analytical t...

Role & responsibilities Independently design, plan and execute moderate to complex analytical method development experiments. Analyze the data, communicate results to clients and write technical protocols and reports Prepare method protocols, & technical reports for characterization of analytical methods based on separation techniques (HPLC, UPLC, GC), Spectro-analytical technique (Ultraviolet-Visible Spectrophotometry) and dissolution testing. Experience in developing pharmaceutical small molecules analytical chemistry methods for dissolution muti-media screening and analyzing data using compendial methods. Exposure in stability testing as per ICH guidelines. Preferred candidate profile Exp...

Oversee and execute analytical testing of raw materials, in-process samples, and finished products. Ensure compliance with cGMP, GLP, and regulatory guidelines. Review and approve analytical data, test results, and documentation. Troubleshoot analytical instruments like HPLC, GC, UV, and FTIR. Support method validation, stability studies, and regulatory audits. Implement quality improvement initiatives and ensure data integrity

Method development & Validation ( HPLC /GC/ UV/ Potentiometer etc..) for both Solid orals and Injectables & Handling of all analytical instruments/ Equipments, SOPs prepation, SPEC and STPs prepation/ review,Stability samples analysis .

For day to day sample extractions & instrument (LCMS/MS - GCMS/MS) sequencing Roles and Responsibilities Testing of various agriculture and food products for chemical and nutritional testing by standard and in-house methods Hands on expireance in Proximate Analysis Operating the lab instruments like pH meter, weighing balance, incubator, GCMS/MS & LCMS/MS, UPLC Preparation of standard solutions Daily maintenance of lab equipment. Following good laboratory practices Following disposal process for samples & solutions as per SOP. Accurate analysis and interpretation of test results Maintenance of laboratory documents and records Validation of methods and calibration/verification of instruments ...

Functional or Technical skills JOB DESCRIPTION Job Role : Analytical Chemistry-Analyst Department : Analytical - BGRC Job Location : Bangalore About Syngene : Syngene ( www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational disc...

Subject: P&G Requirement- Management Associate to be outsourced from M/s Ashkom A] Required No. of resources: 1 No B] Job Title/Description: Associate MPD Process AMA PHC, BB C] Responsibilities: Refer the highlighted below [ additionally, refer Screen shot shared earlier under - General : Key Accountabilities] 1) To raise Change control in Veeva GTRAQ QA system for MPD depts. in scope CCPs. Scope- CCPS to be raised for MPD teams located at different locations PAN India) 2) To maintain track of on-going/work in progress CCPs /closer of change controls 3) To keep track of timely completion of action items (In scope- CCPs raised by MPD )& to maintain action log of work completed/ongoing & pend...

Preferred candidate profile Year of experience : 4 - 6 yrs Must have exposure on Review of documents MFR, BMR, BPR, QC specification, process validation data, stability summary report. Having exposure in licensing, Knowledge of GMP & GDP. Candidate must have exposure in regulatory market. Interested candidate may share resume at hr.plant@zuventus.com

*Greetings*!! *We Are Hiring_Quality Control _ Chennai Location* *Education*- B.Sc / M.Sc *Experience* - 2 to 5 Years *Location* - Chennai *Preferable Candidate from only Pharmaceutical Manufacturing* Key Skills - handling HPLC , QMS , Raw materials and Wet Analysis For more details and to apply, please reach out at pna@softgelhealthcare.com or call 8608396077 References will be highly appreciated

The Analytical Science and Technology (AST) Expert is responsible for coordination and management of analytical activities of commercialized products as we'll as to provide scientific analytical support. About the Role: The Analytical Science and Technology (AST) Expert is responsible for coordination and management of analytical activities of commercialized products as we'll as to provide scientific analytical support. Key Responsibilities: Coordination and management of analytical method transfers and stability studies. Compilation of data reports. Compilation of Quality control monographs describing test procedure and specification setup. Scientific analytical support for quality control,...

Develop and optimize formulations for new and existing products Conduct pre-formulation studies, including solubility, stability, and compatibility tests Prepare laboratory-scale and pilot batches and analyze physical and chemical properties

Roles and Responsibilities Conduct stability studies, method validation, and analysis of finished products using techniques such as GC, HPLC, UV-Vis, KF, FTIR, and dissolution testing. Ensure compliance with GLP guidelines and maintain accurate records of all experiments and results. Collaborate with cross-functional teams to resolve issues related to product quality control and manufacturing processes. Develop and implement new methods for analyzing raw materials, intermediates, and finished products. Participate in method development activities to improve existing methods or develop new ones.

Roles & Responsibilities You will be responsible for end to end Formulation development of Injectable including development, execution, filing and approval. You will be responsible to co-ordinate closely with analytical team to devise effective Proof of Concept (POC) for developing generic equivalent of Reference Listed Drug (RLD)/generic Injections. You will be responsible to support in scale-up to pilot/plant scales for Injectable Products. You will be responsible to monitor the development for robust, effective and bioequivalent drug product in timely manner adhering to safety and quality standards. Also provide support in documentation for regulatory submissions. You will be responsible ...

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 d...

Job Band: Job Band 13 (JB13) Hiring Manager: Akhil Kodiyamtharappel Sadasivan Lead Recruiter: Tino Manimuthu Country: India Our ability to grow, develop new capabilities and serve even more patients around the world depends on associates like you, who are passionate about our mission. Thank you for considering this new opportunity to further unlock your potential. JOB SUMMARY: - Ontime completion of testing, analysis, and documentation with respect to regulatory guidelines. REPORTING: - Reports to Deputy Manager QC ESSENTIAL DUTIES: - Administration/Internal Communications: Responsible for completing testing as part of Chemical, Functional and incoming inspection. Responsible for Document Re...

Responsible and Accountable for the oversight of Quality operations and GMP compliance across the West and South EPD TPM s for, LL Systems & Contract Operations in India. Effectively monitoring the rating of TPM/LL sites Lead the implementation of quality strategy and plan in the above-mentioned sites including EQD policies implementation. Implement Quality Projects at identified TPM s from time to time. Ensure quality compliance to regulatory w.r.t. labelling, stability studies and documentation across the 4 business divisions to deliver acceptable quality products coming from LL and TPM sites to consumers on sustainable basis. Develop strategy on quality as per Abbott`s EPD requirements fo...

Key Responsibilities Perform analytical testing of raw materials, intermediates, and finished APIs using HPLC, GC, UV, and other analytical instruments. Execute analytical method validation, method transfer, and verification as per regulatory guidelines. Ensure compliance with cGMP, GLP, and regulatory standards (ICH, USFDA, EU, WHO) . Maintain accurate documentation, calibration logs, and test reports in compliance with company SOPs. Support investigations, OOS, OOT, and CAPA implementation . Coordinate with QA and Production teams for smooth project execution. Contribute to laboratory upkeep, safety practices, and audit readiness.

Candidates should have good hands on Experience on HPLC, GC, Stability, Wet Lab, RM Sampling & Analysis, Documentation, Standardization of Karl fisher Titrator. Responsible for Calibration of Instruments. Can handle QMS & AMV activities Required Candidate profile Preferred immediate Joiners. USFDA preferable. Interested candidate can share CV on sachin.kapte@enaltec.com Mob.8976826875

Role & Responsibilities: Upkeep the laboratory with respect to cleaning and discipline. To follow the GLP regulations within the laboratory. To perform the method development, in process and stability activity of drug product as per the plan and priority. To record and maintain daily temperature and humidity record of laboratory in logbooks. To follow relevant safety and regulatory norms. To follow all time compliance to company policies and values. To prepare analytical data sheets as per current version of specification and Method of Analysis. To conduct project related analytical activities at Quality Control laboratory. To calibrate the instruments as per the plan or as and when required...

Job Opening: QC Chemist – Executive Level Company: Dalas Biotech Limited Qualification: B.Sc. / M.Sc. in Chemistry or related field Experience: 2 to 7 Years Instrumental Analysis using HPLC, GC, KF, UV Spectrophotometry

Principal task: Analytical Method Development by HPLC for all Project. Review the analytical method development data, validation study data and method transfer protocol and reports. Calibration of HPLC system. To maintain GLP/GDP in working environment. Preparation of analytical data and submit for review. Analytical Method Development and Validation. Responsibilities: Calibration of HPLC’s as per SOP and maintenance of HPLC Systems. Maintaining record for all analytical reports by entering all the data in raw data note book and timely release of analytical reports. Preparation & Review of analytical method validation protocol and report as per the current regulatory requirement. As per Prot...

1. Develop, validate, and optimize analytical methods for raw materials, intermediates, and finished products. 2. Perform stability studies, impurity profiling, and release testing in line with ICH and regulatory guidelines. 3. Prepare comprehensive documentation, including method development reports and validation protocols. 4. Collaborate with formulation scientists to support product development and scale-up. 5. Troubleshoot analytical methods and instrumentation, ensuring efficient lab operations. 6. Ensure compliance with GMP, GLP, and regulatory standards within ADL.

HPLC, Stability test ,

Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, a...

13579 External Job Description Role Description Job Purpose To ensure that inspection and all related activities are carried out as per the defined quality system and only conforming product batches are released, in quick time, for packing. Daily Activities a) Getting the details about status of different batches in various Pug mills, Mixers, reactors, TSDs etc from the preceding shift Officer-Level I. b) Making a list of approved, pending batches, and obtaining any special instructions or communication regarding batches, processes, practices etc in the previous shift. c) Ensuring implementation of 5S activities on the shopfloor and QA lab. d) Ensuring the regular updation of various ledgers...