1426 Gc Jobs - Page 4

Date: 17 Oct 2025 Location: Bangalore, KA, IN, 560099 Division: Discovery Services Job Description Job Title: Senior Research Associate (Level 9-II) Job Location: Bangalore Department: Discovery Chemistry - Analytical 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. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spiri...

Date: 17 Oct 2025 Location: Bangalore, KA, IN, 560099 Division: Discovery Services Job Description Job Title: Senior Research Associate (Level 9-II) Job Location: Bangalore Department: Discovery Chemistry - Analytical 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. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spiri...

Conduct routine analysis of raw materials, in-process (batch) samples & finished products using various analytical techniques HPLC, GC, UV-Vis. Operate, calibrate, & maintain analytical instruments & equipment used in Analytical laboratory. Required Candidate profile Male Candidates required from Bio Technology Industry only.

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Friday 31-10-2025. 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 i...

Sr. Executive / Executive based in Kadi, Mehsana District, Gujarat. The ideal candidate brings 5-8 Years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/...

QC Head 1 Pos based in Kathua, Jammu & Kashmir. The ideal candidate brings 12 - 15 yrs exp. and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Mana...

R&D Officer Formulation & Dossier Filing (02 Positions) based in Vapi, Gujarat. The ideal candidate brings 5 to 7 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improv...

The ideal candidate brings 1-6 Years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen) Lead microbiology practices including EM, MLT, sterility assur...

JOB DESCRIPTION OF CHEMIST/Sr.CHEMIST An edible oil industry chemist's job description involves performing chemical analyses on raw materials and finished products, troubleshooting quality issues, and ensuring compliance with food safety standards. Key duties include using instruments like GC and HPLC, monitoring quality parameters such as free fatty acids and peroxide value, performing water and effluent testing, and maintaining quality control throughout the production process. Key responsibilities Chemical analysis: Perform a range of analyses on edible oils, refinery by-products, and other materials like water and coal. Quality control: Monitor the quality of raw materials, in-process pr...

Hiring for below multiple roles in Analytical R&D LCMS, NMR, Solid state characterization, Preparative purification, GC, HPLC, Wet lab, Peptide purification job role: Technical expertise in analytical method development for APIs/ NCE’s, handling of projects with end-to-end responsibility in support of PR&D activities. Develop analytical methods and validated methods by HPLC, GC, LC-MS for various drug substances, their Intermediates, and Raw materials under various Instrumental and Classical techniques. Comply to the GMP / GLP standards.

Key Responsibilities Method Development and Validation : Conduct analytical method development, verification, validation, and transfers. This includes methods for related substances, assay, residual solvents, and cleaning procedures. Analytical Support : Provide analytical support to process development teams. This involves analyzing samples using instruments such as HPLC (High-Performance Liquid Chromatography) , GC (Gas Chromatography) , IR (Infrared Spectroscopy) , KF Titrator (Karl Fischer Titrator) , SOR (Specific Optical Rotation) , ROI (Residue on Ignition) , and LOD (Loss on Drying) . Documentation and Compliance : Ensure the timely completion of all analysis, documentation, data rev...

About The Role - Grade Specific Must Have 1) Strong Informix database Skills (IDS. XPS, 4GL, ESQLC) 2) DB Upgrade and Design for Informix Skills. 3) Design/ Migrations to Informix from old version and XPS to IDS 4) Automation/Scripting skills - python, AI 5) Experience with rewriting SQL queries, stored procedures, triggers, and views. 6) Work on performance tuning and query optimization 7) Well versed with CDC concepts. 8) Experience with Performance tuning and Health Checks 9) Product installation, including Informix 4GL Tools, Informix Server, and Informix Client SDK 10)Informix HDR, ER, CM, RSS, SDS 11)Informix Backup using ontape and onbar

WORK LOCATION: Baddi, Himachal Pradesh DEPARTMENTS AND EXPERIENCE: Quality Control: Stability/ FP / HPLC/ GC / Microbiology o Qualification & Experience: (02 - 06Years) •B.Sc, B.Pharma & M.Sc with relevant experience Designations: •Jr. Officer, Officer & Jr.Executive ARD: Stability/ FP /AMV/ HPLC Qualification & Experience: (02 - 05Years) •B.Sc, B.Pharma , M.Sc & M.Pharma with relevant experience Designations: •Jr. Research Associate & Research Associate-I PACKING: Blister& Bottle Packing(ELMACH-3522), Bulk Packing (IMA-PG) Qualification & Experience: (01 - 06Years) •ITI, Diploma & B.Sc with relevant experience Designations: •Jr. Operator, Operators & Sr. Operator INTERVIEW VENUE: oHetero La...

Company: Strides Pharma Science Ltd Department: Quality Control (QC) Position: Trainee Job Location: Alathur Qualification: B-Pharm, M-Pharm Experience: 0 to 1 Year Key responsibilities: Analysis of Material / Product by referring current version of specification STP with relevant material code. Responsible for initial set up of Instrument/Equipment before starting the analysis with relevant online entries in usage Log / LIMS. Perform the Assay and RS by LC/UV/Dissolution, content uniformity by LC analysis with simple and complex products Tests as per SOP/STP. Proper handling of chromatographic column used for analysis. Maintain data integrity and appropriate traceability Regards, Srinidhi S...

1. Operate and maintain HPLC, weighing balances, pH meters, densitometers, tube heating blocks, and other QC equipment. 2. Perform CRM-197 protein testing using HPLC and SDS-PAGE. 3. Conduct free carrier protein testing on HiBTT, HiBTi conjugate, and Pneumo conjugate using HPLC. 4. Perform molecular size testing by HPLC on HiBTT, HiBTi conjugate, and Pneumo conjugate. 5. Ensure online documentation as per Good Documentation Practices (GDP). 6. Execute method validation for various products. Demonstrate proficiency in analytical procedures and method validation. 7. Evaluate LOD/LOQ for rinse samples. 8. Verify packing materials and consumables for the Production Department. Test and release r...

1. Analysis of finished product, stability samples,raw material, in process, packing material and validation samples as perrespective STP. 2. To maintain cGLP in Quality Control Laboratory. 3. To maintain compliance as per Standard OperatingProcedures. 4. Calibration of instruments as per schedule. 5. To prepare documents submission of reporttimely to section in charge. 6. To qualify the working standards volumetric solutions preparation and standardization. 7. Temperature monitoring in laboratory. 8. To execute any other work assigned byHOD/Section Manager.

Role Overview: You are sought after to join the Research and Development team at Dr. Reddys Laboratories Ltd. as an Analytical Scientist for the Injectable Division. Your role will involve developing and validating analytical methods for injectable products, ensuring compliance with regulatory requirements, conducting literature reviews, scaling up for manufacturing batches, coordinating manufacturing readiness, overseeing plant execution, and facilitating seamless technology transfer. It is essential to have a strong understanding of analytical principles, excellent documentation skills, and the ability to work effectively in a collaborative team environment. Key Responsibilities: - Develop...

Walk In Drive For Quality Control In Formulation Division @ Corporate Office Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharma Experience:- 2 to 8 Years Division :- Formulation Interview Date:-25-10-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location :- MSN Corporate, H. No. 2-91/10 & 11 /MSN, Whitefields, Kondapur, 500084 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make healt...

Role Overview: You will be responsible for conducting quality control tests on raw materials, packaging, intermediates, and finished products using instrumental methods such as HPLC, GC, UV, FTIR, and KF titrator, as well as wet chemistry techniques like titrations. Additionally, you will be involved in monitoring the stability of products to ensure shelf life and product integrity. Key Responsibilities: - Prepare and review analytical reports, Certificates of Analysis (CoA), and other necessary documents to record test results and maintain product quality. - Implement and maintain Quality Management Systems (QMS) to ensure compliance with cGMP, GLP, and FDA regulations. - Ensure proper main...

As a QC Technician at TAPI, your role is crucial in ensuring the integrity, compliance, and reliability of stability testing and analytical operations at our cutting-edge manufacturing facility. Key Responsibilities: - Analyze stability samples, Finish Product samples, and conduct working standard qualification activities as per defined procedures and monographs. - Demonstrate deep knowledge of HPLC, GC, KF, Auto titrator, and Vacuum open operation procedures, including troubleshooting following GLP practices. - Maintain a system of methods and specifications for all materials and products. - Fill and maintain data in logbooks, certificates, stability reports, and archive stability data. - I...

As a Bench Sales Recruiter at our company, your role will involve: - Having 3-15 years of experience in bench sales recruitment, including handling H1 Transfers, OPT, H1B, GC, and US Citizen visa consultants on Bench. - Being familiar with US Tax Terms and visa statuses. - Possessing good negotiation skills. - Demonstrating advanced knowledge of effective hiring platforms to attract suitable applicants. - Developing relationships with Prime Vendors and Direct Clients. - Exhibiting excellent interpersonal and communication skills. - Creating awareness of the company brand. - Proficiency in documenting processes and staying updated with industry trends. In terms of qualifications, we are looki...

As a Senior Chemist at Scimplify, you will be responsible for leading research and development projects in the Agro R&D team. Your role will involve taking ownership of synthesis, process development, and formulation projects, mentoring junior chemists, and ensuring the successful delivery of high-quality agrochemical products from lab to pilot scale. **Key Responsibilities:** - Lead synthesis, purification, and characterization of agrochemical intermediates and actives. - Optimize reactions, processes, and formulations for efficiency, yield, and cost-effectiveness. - Support scale-up from lab to pilot plant and transfer processes to manufacturing. - Mentor and guide junior chemists, review ...

As a Research Associate in the Analytical R&D team within the Peptide Synthesis division, your role will involve supporting the development and execution of analytical methods for peptide characterization. You will collaborate closely with cross-functional teams in R&D and Quality to ensure the quality assessment of peptides. Key Responsibilities: - Assist in developing and performing analytical methods (e.g., HPLC, UPLC, UV, FTIR, KF, LC-MS) for the characterization and quality assessment of peptides - Conduct routine testing of raw materials, intermediates, and final peptide products - Support method validation, transfer, and troubleshooting under the guidance of senior scientists - Docume...

Date: 14 Oct 2025 Location: Bangalore, KA, IN, 560099 Division: Development Services Job Description Designation: Junior Manager QMS EGMP Job Location: Bangalore Department: QC About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development, and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries worldwide. Syngene's clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its more than 4000- strong team of sc...

As a QA/QC Manager at our company, you will be responsible for liaising between various departments such as Planning, Production, Technical Services, Marketing, and Exports. Your role will involve the following key responsibilities: - Preparation, review, and implementation of SOPs and STPs. - Checking of all QC related records like analytical reports and logbooks. - Planning and distribution of samples for analysis of Raw Materials, Intermediates, and finished products. - Designing and conducting Stability studies as per ICH Guidelines. - Developing and validating analytical testing methodology used to control raw materials, production intermediates, and final products. - Preparation and ma...