1459 Gc Jobs - Page 26

Key Responsibilities: Ensure proper installation, calibration, and maintenance of analytical instruments and equipment. Handle and troubleshoot Chromatographic systems (HPLC, GC), Atomic Spectrophotometers, Analytical Balances, pH / Conductivity meters, and Autoclaves. Support validation and qualification of instruments as per regulatory guidelines (USFDA, EU, WHO). Coordinate preventive and corrective maintenance schedules with vendors. Maintain calibration records and ensure compliance with GMP and GLP requirements. Provide technical support to analytical teams for smooth lab operations. Key Skills: Strong technical knowledge of laboratory instrumentation. Familiarity with pharma quality a...

Department - Quality Control Experience - 2 to 5 years Qualification - M.Sc chemistry (Full time) Section - HPLC / GC / Wet lab To ensure that training is acquired for each activity/instrument prior to its execution/operation and that it is as per respective TNI. To perform Analysis (Chemical)of raw material/packaging material/in-process samples /intermediate /bulk & finished products/ process validation samples/ stability samples/ cleaning validation/method transfer sample, PD lab sample etc. To ensure that all tests carried out in the laboratory are documented contemporaneously in an appropriate authorized and controlled worksheet/ bound book. To make entries in the sample inward register ...

Responsibilities: * Conduct quality control tests using HPLC, GC, UV, Karl Fischer, Potentiometer methods * Hands on experience on QC instruments such as GC and HPLC and Titration and potentiometry is must Provident fund Annual bonus

Interested candidates are requested to share their resumes at dipika.parmar@milanlabs.com for interview scheduling on 7th September 2025 at Hotel Ginger, Bharuch. Please note that it is mandatory to pre-schedule the interview before reporting at the venue. Key Responsibilities: Perform routine and non-routine analysis of raw materials, intermediates, finished products, and stability samples related to SVP. Execute and document activities related to Analytical Method Validation (AMV) and Analytical Method Transfer (AMT) as per approved protocols. Conduct instrument handling, calibration, and troubleshooting for analytical techniques such as HPLC, GC, Dissolution, UV-Vis, FTIR, and other QC in...

Project Role : Application Developer Project Role Description : Design, build and configure applications to meet business process and application requirements. Must have skills : Java Full Stack Development Good to have skills : Spring BootMinimum 3 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Developer, you will design, build, and configure applications to meet business process and application requirements. Your typical day will involve collaborating with team members to develop innovative solutions and ensure seamless application functionality. Roles & Responsibilities:- Expected to perform independently and become an...

This is a full-time Reomte role located in Noida for a US Bench Sales Recruiter. The sales recruiter will be responsible for full-life cycle recruiting, hiring, account management, and effective communication with clients and candidates.

Hikal Ltd is looking for Officer to join our dynamic team and embark on a rewarding career journey The Senior Officer plays a crucial role in the organization, responsible for overseeing and executing various tasks and projects to ensure the smooth functioning of operations This role requires strong leadership, analytical skills, and the ability to collaborate effectively with team members and stakeholders Key Responsibilities: Leadership:Provide leadership and guidance to team members, fostering a positive work environment Lead by example, demonstrating professionalism, integrity, and dedication to the organization's goals and values Project Management:Manage and coordinate projects from in...

Greetings from MSN Laboratories...! We are conducting a walk-in interview for Experienced & Freshers candidates in Our APICHEM Unit Vangapalli (Near to Yadagirigutta) on 5th Sept 2025 (Friday). Department- Production Req Exp- 3 to 8 Yrs Qualification- B. Sc Chemistry/ Any Graduate Designations- Executive/ Jr. Executive/ Sr. Executive Department- QC Req Exp- Freshers Qualification- M. Sc Chemistry Designations- Trainee Eligibility- 2022/23/24/2025 Passed Outs only Venue Details- APICHEM Laboratories Pvt. Ltd, Vangapalli (V), Yadagirigutta (M), Yadadri Bhuvangiri (D), Telangana. Date- 05th Sept 2025 (Friday)

M.Sc/B.Sc Chemistry Experience - 3 + yrs from Aroma/Chemical/Pharma analytical chemistry, handle lab instruments independently, knowledge of analytical, Must GC,HPLC, karl Fisher,chemistry, handle lab instruments independently, good grasping,

The ideal candidate brings 1-7 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 improvement (5S/Lean/Kaizen) Lead microbiology practices including EM, MLT, sterility assur...

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...

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...

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/...

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Saturday 06-09-2025. 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...

Role & responsibilities R&D Synthesis: Experience in API synthesis, process development, and DMF filing. Develop cost-effective, high-quality, and eco-friendly processes as per ICH guidelines. Optimize lab processes, validate products, and transfer technology to pilot plant. Design and propose specifications for KSM, intermediates, and APIs. Proficient in NMR, Mass, IR characterization and troubleshooting synthesis/impurity issues. Prepare documentation for process development and technology transfer. ADL: Method Development by HPLC. Method Validation by HPLC. Preparation, Review, and Technical input for specification and method of analysis. Experience in GLP related activities i.e., calibra...

As an AM Research and Development, you will be responsible for planning, setting up, monitoring, and working up chemical reactions independently. You will need to monitor the progress of reactions using standard methods and analytical techniques such as TLC, GC, HPLC, LCMS, etc. It will be your duty to isolate products, optimize reaction conditions for improved yields, and purify compounds using chromatography, distillation, and crystallization methods. Additionally, you will be required to characterize and identify compounds using UV, IR, NMR, LCMS, and GCMS techniques. Ensuring the parallel execution of multiple reactions conducted by both yourself and the team will be essential. You will ...

Job Title: Quality Control Analyst Formulation (OSD & Injectables) Experience: 2 to 8 Years Work Location: MSN Formulation Unit-II, Kothur , Hyderabad Department: Quality Control - Formulations Employment Type: Full-time Job Posting Purpose: We are looking for an experienced and motivated Formulation QC Analyst with 2 to 8 years of hands-on experience in testing Oral Solid Dosage (OSD) and Injectable formulations . This role involves executing and supporting analytical testing, method validation, and regulatory compliance for pharmaceutical products. The ideal candidate will have a strong understanding of GMP/GLP , be proficient with analytical instruments , and have exposure to regulatory a...

You will be responsible for planning, setting up, monitoring, and executing chemical reactions independently within the Agrochemical Industry located in Saykha, Gujarat. Your key tasks will include monitoring the progress of reactions using standard methods and analytical techniques such as TLC, GC, HPLC, and LCMS. You will be required to isolate products, optimize reaction conditions to enhance yields, and purify compounds using chromatography, distillation, and crystallization methods. Characterization and identification of compounds using UV, IR, NMR, LCMS, and GCMS will also be part of your responsibilities. In addition, you will need to oversee the parallel execution of multiple reactio...

You will be a Quality Assurance & Analytical Chemist at FMC, where your primary responsibility will be to provide daily analysis support by developing, validating, and applying various modern analytical technologies and approaches for the development and commercialization of agricultural products. You will ensure that FMC quality standards and good laboratory practices are implemented at the Toller site by conducting cross-checks and on-site audits as per business needs. Your role will involve knowing, understanding, and practicing all aspects of laboratory safety and industrial hygiene protocols, developing, validating, and implementing methods for qualitative and quantitative analysis, con...

You are seeking an Assistant General Manager- Research & Development position at an Indian Pharmaceutical MNC located in Thane, Maharashtra. As the Associate General Manager, you will lead the Analytical Method Validation team, overseeing validation activities for various dosage forms and managing a team of 15+ scientists. Your responsibilities include ensuring regulatory compliance, driving quality and efficiency, and fostering collaboration with R&D, Regulatory, and Plant QA/QC teams. Your key responsibilities will involve providing leadership for analytical method validation across different formulations, overseeing RM and PM characterization, managing method validation projects in alignm...

This is a full-time on-site role for a Quality Control Officer. As a Quality Control Officer, you will be responsible for ensuring the quality and safety of products through laboratory testing and data analysis. Your primary duties will include conducting analytical tests using instruments such as HPLC, GC, UV, IR, Water content by KF, Auto titrator, and Dissolution Apparatus. Additionally, you will be responsible for quality assurance activities and effectively communicating results with team members and clients. To excel in this role, you should possess strong analytical and laboratory skills, along with hands-on experience in operating various testing instruments. Your ability to follow S...

As a Quality Control & Quality Assurance Manager at our Tarapur plant, you will report to the Regional Senior QFS Manager with a dotted line to the Plant Manager. Your role involves overseeing QC & QA routine activities to achieve departmental targets. You will be responsible for various quality control activities including approving/rejecting pre-shipment samples, raw materials, in-process, and finished goods. Implementing quality control procedures, setting quality standards, and conducting vendor audits are key aspects of your role. Managing customer complaints, collaborating with different departments to resolve issues, and ensuring departmental performance aligns with targets and budget...

This is where your work makes a difference. At Baxter, we believe every person-regardless of who they are or where they are from-deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. ...

*Sound knowledge of GC, HPLC *Wet Lab Analysis *GDP & GMP. *Monitoring and analyzing processes to identify areas for improvement . *Maintaining accurate documentation and records of quality control activities, test results. Required Candidate profile "Male Candidates, 1 to 3 Years experience only"

Job Description Manager Quality (QA & QC) Position: Manager Quality (QA & QC) Location: Taloja Manufacturing Site Reports To: Senior Management / Plant Head / Director Quality Department: Quality Assurance & Quality Control About KCIL Specialty Chemicals KCIL Specialty Chemicals is one of Indias leading chemical manufacturing companies with a strong legacy of innovation, quality, and sustainability . With a robust turnover of 350 crores and ambitious plans to reach 500 crores in the next 4 years, KCIL is rapidly expanding its footprint in the specialty chemicals sector. We operate from 5 strategic manufacturing locations in Taloja , supported by state-of-the-art infrastructure that ensures h...