590 Gc Jobs - Page 5

End-to-end formulation and development of injectable dosage forms (Liquid, Lyophilized, Emulsion, etc.) Handling of scale-up, exhibit batches, and tech transfer Cross-functional coordination with ADL, RA, QA, and Manufacturing

Planning and executing assay-runs for cell based assays and ELISA as part of Method Development and Method Qualification studies Analysis of the data using parallel line analysis and equivalence testing Writing protocols and reports for Method development and Method qualification studies Maintenance of the cell lines, preparation of cell banks Review of raw data and data recording sheets and to ensure good documentation practices. Planning of day-to-day activities independently. Trouble shooting of the issues (if any) aroused during execution of assay-run. Involving in documents preparation for SOP, STP, MOA.

1) Development of mass spectrometry based methods for analysis of various molecules for pivotal studies such as biosimilarity, comparability etc.. 2)operation and maintenance of mass spectrometry instrument and performing troubleshooting activities 3)developing and carrying out multiple assays aimed at characterization of protein based therapeutics across various stage of the project 4) participate in design, development and implementation of methods for CQA/impurity characterization of molecules. Interpret results,and draw conclusions from multiple stage experiments 5) Author technical documents such as SOP,MoA,study protocol and reports for method and product development

1) Preparationof Analytical method validation Protocols and reports for the relatedsubstances and Assay by HPLC and residual solvents by GC 2) Preparation of Analytical methodvalidation Protocols and reports for the Identification analysis by HPLC,GC andparticle size analyzer and performing the analytical method validations for theIdentification, content and purity analysis by HPLC,GC and Particle sizeanalyzer. 3) Performing the Analytical methodvalidations by HPLC and GC. 4) R esponsible to follow and ensure strict compliance to GLP practices in the laboratory to meet the organizational goal which in line with procedural references. 5) Maintenance of log books and Calibration records as per procedural references. 6) Preparation of Analytical method validation Protocols and report for the Elemental Impurities analysis by ICP-MS and Perform the analytical method validations for elemental impurities by ICP-MS.

The Junior Analyst/Executive in Analytical Research and Development (ARD) Injectables plays a vital support role in the development and evaluation of sterile pharmaceutical products This position involves performing routine analytical testing of injectable dosage forms such as solutions, lyophilized powders, emulsions, and suspensions using instruments like HPLC, UV-Vis, FTIR, pH meter, and more Under the guidance of senior scientists, the junior analyst assists in method development, validation, and stability studies, ensuring that data is accurate and meets regulatory and internal quality standards Responsibilities include sample preparation, instrument handling, maintaining laboratory notebooks, and following Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) The role also includes preparing reagents, calibrating instruments, and maintaining documentation for analytical procedures and observations Junior analysts support data compilation for regulatory submissions and assist in investigations related to analytical deviations or out-of-specification results They collaborate with cross-functional teams such as Formulation RD, QA, and Regulatory Affairs to ensure timely and compliant development activities This position requires attention to detail, a willingness to learn, and the ability to follow procedures precisely Ideal candidates should hold a Pharm, MPharm (Pharmaceutical Analysis or Pharmaceutics

The candidate would be developing various analytical method (such as CD, Fluorescence spectrscopy ,CE UH/HPLC etc..)for CQA to support biosimilarity and analytical studies. Qualify method for biosimilarity and analytical studies. Responsible for performing biosimilarity, characterization and analytical studies for various molecules across lifecycle . Evaluation, interpretation and graphical representation of the measurement data as well as presentation of the results obtained from multiple experiments. Author technical documents such as MoA,MQR,SOP,study protocol and report.

Development and validation of analytical methods for injectable dosage forms Stability study execution and data interpretation Support for formulation development and regulatory submissions (US/EU) Instrument handling: HPLC, GC, UV, KF, etc. Preparation of method validation reports, protocols, and SOPs

1. Responsible for review of specifications, STPs, GTPs and analytical test data sheets. 2. Review of analytical reports of raw material, packing materials, water samples, product samples, OOT, water trends and ensuring compliance. 3. Responsible to attend the training programs. 4. Responsible for monitoring of quality control Lab (Daily calibration, PMP, Instruments back up data, Excel work sheets lock, user log books). 6. Responsible for handling technology transfer documents. 7. Responsible for review of stability protocols, stability analytical data and summary reports. 8. Responsible for handling of change controls, OOS, OOT, Incidents and investigations. 9. Responsible for compliance of GLP in Lab. 10. Responsible for review and approval of LIMS related activities. 11. Approval and issuance of configured COA in LIMS. 12. Responsible for audit trail verification for QC lab instruments.

Eligibility : M.Sc / M.tech (Life Sciences / Biotechnology) Technical Skills : Various Extraction Techniques Purification techniques Phytochemical Activity (Qualitative quantitative) HPLC CG AAS FTIR UV-Vis Spectrophotometer General Skills : Complete knowledge of MS Office Standardisation of SOP Sample flow management English (Reading and Writing) Candidate must have a personal Laptop

Job Title: Quality Control Head Industry: API / Pharma Manufacturing Job Location: Ankleshwar, Gujarat Experience Required: 15 to 20 years of relevant experience in Quality Control within the API pharma industry Salary: 12.0 LPA to ?15.0 LPA Education: M.Sc. / B.Sc. (Chemistry) or M.Pharm / B.Pharm or equivalent Key Skills Required: Strong knowledge of data integrity principles Hands-on experience with instruments like HPLC, GC, and UV Experience in cleaning validation and microbiological testing Familiarity with incident investigations and regulatory compliance About the Company: A leading API pharma manufacturing group known for its strong global presence and commitment to quality and innovation. Job Responsibilities: Lead and manage the Quality Control (QC) department to ensure quality at every stage of manufacturing and testing. Oversee sampling, inspection, and testing of raw materials, packaging materials, in-process, and finished products. Ensure timely release or rejection of batches based on quality data. Handle stability chamber management, testing, and shelf-life evaluations as per protocol. Conduct microbiological analysis for raw materials, finished goods, water, and environmental monitoring. Review trends in physicochemical and microbiological test data for compliance. Manage out-of-specification (OOS), deviation investigations, and analytical support for product recalls and complaints. Coordinate with QA and R&D on specifications, analytical procedures, and validations. Ensure equipment/instrument qualification, calibration, and preventive maintenance. Maintain and audit QC records, reference/working standards, and ensure data integrity systems are in place. Supervise glassware cleaning, protocol validation, and implementation of cleaning procedures. Plan and execute internal audits and ensure compliance with GLP and GMP standards. Review and validate SOPs, protocols, and test methods (pharmacopeial & in-house). Support employee training in alignment with cGLP and cGMP practices. Evaluate change control proposals, failure investigations, market complaints, and implement improvements in QC systems. Ensure all activities follow company reporting systems and regulatory expectations.

1) Experience in preparing and reviewing of Method Development Report. 2) Knowledge of ICH Guidelines. 3) Strategic planning and performing Validation studies, Solubility Studies, Impurity and Standard Qualification. 4) Exposure of working on HPLC, LCMS, GC, UV and other equipment. 5) Ability to perform an analysis of related substances, assays and purity by using HPLC, IC. 6) Ability to perform analysis of residual solvents by using gas Chromatography. 7) Preparation and Review of development and validation/ method transfers/ protocols and reports based on R&D qualifications or monographs. 8) Ability to work in a team and contribute towards collective goals.

Manager/Sr. Manager (Injectable): Should have experience in following area; Having exposure of team leading in area of Analytical method development for various type of Injectable products (i.e. liquid, Lyophilized, Peptide & Complex injectable) Exposure of R&D analysis support for routine, development, in process and stability samples and data trending/interpretation etc. Having exposure of timely completion of calibration of various analytical instruments such as HPLC, GC, Dissolution app., IC, KF & Viscometer etc., Exposure in Dissolution method development for complex injectable on Type IV dissolution apparatus Pharmacopeia method updation & impact assessment on products Perform pre-validation of various analytical methods/technics Troubleshooting of Analytical methods & Plant queries Training to fresher s for proper handling of Instruments/activities

Manager/Sr. Manager (Injectable): Should have experience in following area; Having exposure of team leading in area of Analytical method development for various type of Injectable products (i.e. liquid, Lyophilized, Peptide & Complex injectable) Exposure of R&D analysis support for routine, development, in process and stability samples and data trending/interpretation etc. Having exposure of timely completion of calibration of various analytical instruments such as HPLC, GC, Dissolution app., IC, KF & Viscometer etc., Exposure in Dissolution method development for complex injectable on Type IV dissolution apparatus Pharmacopeia method updation & impact assessment on products Perform pre-validation of various analytical methods/technics Troubleshooting of Analytical methods & Plant queries Training to fresher s for proper handling of Instruments/activities

Scientist (Topical): Should have experience in following area; Analytical method development for various type of Topical products (i.e. cream, gel & ointment) + Reverse Engineering development work R&D analysis support for routine, development, in process and stability samples Calibration of various analytical instruments such as HPLC, GC, Dissolution app., IC, KF & Viscometer etc., IVRT study Solubility studies & Excipient Compatibility Study Pharmacopeia method updation & impact assessment on products Perform pre-validation of various analytical methods/technics Troubleshooting of Analytical methods & Plant queries Training to fresher s for proper handling of Instruments/activities

Do you want to be a part of the fascinating story of over 500 iconic brands spanning across more than 100 countries Being the best beer company starts with finding the best people. While we have big brands, we have bigger opportunities as well. AB InBev India is looking to hire a Senior Manager - Quality Analyst for its supply team based out of Aurangabad, Maharashtra. The responsibilities of this role include handling instruments like GC, Alcolyser, DMA, Sodium Meter, pH Meter, and Gas Generators. Calibration and maintenance of all BQA instruments are essential, strictly following BQA SOPs. You will be responsible for the analysis of In-Process Samples, highlighting deviations, and analyzing incoming brewing raw materials while adhering to SOPs for all analyses. Ensuring reliable and accurate data is supplied through the use of BWC and control charting is a key aspect of this role. Maintenance of all records, updating AB data sheets regularly, conducting PRP audits and 5S Audits at regular intervals, and maintaining 5S in the lab are part of the responsibilities. As a subject matter expert in instruments such as GC's, Alcolyser, DMA, Sodium Meter, pH meter, Generators, centrifuge, sonicator, hot water bath, and Mash Bath, you will be responsible for instrument management. Being an enthusiastic team player in the Environmental Pillar, a qualified Taster, and setting up daily Taste panels are additional responsibilities. You will also train new Brewing Quality Analysts, conduct brewing quality improvement analysis, develop and implement process checklists and audits, and track CAR of brewery PRP audits. Ensuring all BQA lab consumables and inventory are maintained, adhering to safety requirements, and reviewing daily data, control charts, calibration, and maintenance logs are crucial tasks. Other responsibilities include maintenance of Data Transfer Sheets and KPIs related to BQA, 5S maintenance in the BQA lab, UT sample arrangement for Tasting, updating Monthly KPIs, and keeping the QC manager and shift brewers updated on daily brewing quality issues. Training as a microbiologist Relief is also part of the role. Key dimensions include accountability for the Director (Supply & Logistics) KPI, Brewery Sensory Score, Regional BOP KPI, and VPO Implementation Department-specific KPIs such as BPI & Plant Micro Index. An undying love for beer is the driving force behind all these responsibilities. Quench your thirst for success and come be a part of this dynamic team!,

HPLC, GC, UV-Vis, FTIR, Karl Fischer Titration GMP, GLP, FDA compliance Quality Management Systems (QMS) Lab equipment calibration Analytical method development/validation Wet chemistry techniques Data analysis, LIMS Problem-solving, troubleshooting

The job requires a candidate with 2 to 7 years of experience in Analytical Chemistry for a position at a Chemical Manufacturing Company's Pharma Division in Ahmedabad. The salary ranges from Rs. 35,000 to Rs. 40,000 per month based on the candidate's knowledge. The responsibilities include handling analytical instruments such as HPLC, GC, UV, IR, performing instrument calibration, analyzing finished products and raw materials, and conducting wet lab analysis. The job type is full-time and requires in-person work at the specified location. Contact person for the position is Gopi (HR) reachable at 7777981971.,

You will be responsible for reviewing and conducting chemical testing of raw materials, finished products, cosmetics, Ayurveda, Sidha & Unani products. You will need to accurately enter the test results into the LIMS software. Additionally, you will be required to handle instruments like HPLC, GC, FTIR, Dissolution, etc. Technical documentation in compliance with FDA, CDSCO & Ayush standards for audits will also be part of your responsibilities. The position is based in Gurugram and requires a minimum qualification of B.Pharma, M.Pharma, MSc. Chemistry or a related field. The ideal candidate should have 2 to 15 years of relevant experience.,

Greetings from Avani Consulting. We are hiring QC Officer / Trainee and QC Associates for a leading Pharma API Company in Mysore. Positions: 1. QC Officer / Trainee : EXP: 2 to 3 year exp in Pharma Company. Salary : Up to 4LPA ( Take way home only . NO Parks & Benefits ) 2. Quality Control Associates - API : EXP: 5 to 9 year exp in Pharma API Industry. Salary : Up to 7.5LPA ( Including Parks & Benefits ) Preferred candidate profile Qualification : M.Sc. Chemistry Experience : Pharma -API Quality Control Role & responsibilities : Handling and troubleshooting of Analytical Equipment's like HPLC, GC-HS, FT-IR, UV, Potentiometry, Polarimeter, ICP and KF. Handling of Analytical Method development and Method Validations. Qualification of Equipments as per GLP requirements. Analysis of Inprocess, Stability and FG Samples as per the Specification. Operation, Maintenance and Calibration of HPLC and GC as per the schedule. Review of results and release of Analytical test report or Certificate of Analysis. Maintenance of minimum consumables in the Laboratory. Planning and coordination to release on time results delivery. Investigation of OOT/OOS in the laboratory. Sampling of Raw Material, Inprocess and Finished product samples. Basic knowledge on LIMS/SAP. Handling 21 CFR compliance. ***NOTE :: NO CHARGES Looking forward to know about your interest. Thanks & Regards Priyanka Palit [9518220852 | priyanka@avaniconsulting.com]

Experience in routine Analysis, Calibration, Analytical Method Development & Validation, Hands on experience over various analytical instruments like HPLC & GC, Documentation as per regulatory requirement.

Perform analysis of raw materials, in-process samples, and finished products using HPLC and GC as per approved specifications and methods. Operate, calibrate, and maintain analytical instruments like HPLC, GC, UV-Vis Spectrophotometer, FTIR, and Dissolution apparatus. Troubleshoot analytical instruments and coordinate with engineering or vendors for timely servicing when needed. Prepare and review analytical reports, SOPs, calibration records, and logbooks. Ensure all testing activities comply with cGMP, GLP Participate in internal audits, regulatory inspections, and support CAPA implementation where applicable. Manage sample receipt, labeling, storage, and disposal as per SOP. Ensure timely testing and release of materials and products. Participate in on-the-job training programs and ensure adherence to updated testing techniques and quality practices. Mentor junior analysts on analytical techniques and compliance requirements.

Position: Sr. US IT Bench Sales Recruiter Location: Onsite (Hyderabad) Working Days: Monday to Friday Gender Preference: None Type: Full-Time Urgent Requirement Company Overview: MBIT Associates LLC is a US-based staffing and recruiting firm, supported offshore by MBSIT Software Private Limited, Hyderabadour sister concern, incorporated on October 24, 2017. In addition to staffing, MBSIT specializes in software development, mobile applications, and website solutions. Position Summary: We are actively seeking a Senior Bench Sales Recruiter with 46 years of hands-on experience in US IT Bench Sales. This role involves working with candidates holding various work authorisations (OPT, CPT, H1B, GC, USC, EAD, and TN) and includes end-to-end bench marketing and client/vendor coordination. Requirements: 4+ years of proven experience in US IT Bench Sales (Mandatory). Expertise in marketing candidates across various work authorizations (OPT, CPT, H1B, GC, USC, EAD, TN). Skilled in H1B profile transfers and working with third-party vendors. Proficient in resume formatting and tailoring according to client/job requirements. Strong knowledge of major job portals (Dice, Monster, Indeed, LinkedIn, etc.). Ability to identify and target relevant job opportunities and submit consultants accordingly. Experience in broadcasting consultant profiles and hotlists periodically. Key Responsibilities: Market and place bench consultants across various technologies. Coordinate closely with consultants to understand their skillset and preferences. Submit candidates to suitable job openings and follow up on submissions regularly. Maintain transparency across the team to prevent duplicate submissions. Schedule vendor and client interviews and prepare consultants accordingly. Negotiate rates with clients and vendors to ensure optimal placement deals. Monitor consultant performance post-placement and address concerns. Maintain strong, professional relationships with clients, vendors, and consultants. Continuously identify new vendor partnerships and nurture existing ones.authorisations

Role & responsibilities Responsible for sampling of Raw material, Packaging material and Finished product. Responsible for analysis of Raw material, Packaging material, Utility Raw material, In-process, Half finished product and Finished product. Preparation of reagents, solutions and standardization. Calibration and testing of instrument/equipment as per schedule. Handling of wet chemical analysis instruments Responsible to identify Out of specification results, Out of trend result and to inform the respective person then carry out investigation according to Head QC instruction. Responsible for analysis of tests in Stability study. Work as per the work instructions and follow all the safety standards. Responsible for sampling and analysis of Demineralized water, condensate water, reverse osmosis, raw water and ETP water. Establish and maintain effective working relationships with co-workers and with colleagues of other departments. Responsible for line Clearance of the critical process equipment during product change over cleaning in the production Orient, impart training to trainees and instruct them to carry out their duties efficiently and ensure that they follow all the safety instructions on their duties. Duties & responsibilities would include the above but not limited to and would be responsible to carry out any other duties & responsibilities assigned by the HODs / reporting head. Preferred candidate profile Good Knowledge in cGMP and Analytical chemistry Immediate joiner preferred

Role & responsibilities Responsible for sampling of Raw material, Packaging material and Finished product. Responsible for analysis of Raw material, Packaging material, Utility Raw material, In-process, Half finished product and Finished product. Preparation of reagents, solutions and standardization. Calibration and testing of instrument/equipment as per schedule. Handling of wet chemical analysis instruments Responsible to identify Out of specification results, Out of trend result and to inform the respective person then carry out investigation according to Head QC instruction. Responsible for analysis of tests in Stability study. Work as per the work instructions and follow all the safety standards. Responsible for sampling and analysis of Demineralized water, condensate water, reverse osmosis, raw water and ETP water. Establish and maintain effective working relationships with co-workers and with colleagues of other departments. Responsible for line Clearance of the critical process equipment during product change over cleaning in the production Orient, impart training to trainees and instruct them to carry out their duties efficiently and ensure that they follow all the safety instructions on their duties. Duties & responsibilities would include the above but not limited to and would be responsible to carry out any other duties & responsibilities assigned by the HODs / reporting head. Preferred candidate profile Good Knowledge in cGMP and Analytical chemistry Immediate joiner preferred

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Saturday 19-07-2025. 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 : 19-07-2025 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