1426 Gc Jobs - Page 9

Responsibilities: Ensure timely and Accurately material testing (RAW/ In Process/Finish/ R&D). Accurate and On-time Reporting and documentation at all stages. Proper Calibration. Understanding of analytical chemistry. Hands-on experience in HPLC /GC Required Skills: Candidate must have good communication skill. Good leadership quality and time management. Ability to work independently and as part of a team. Required Qualification: - B.Sc/M.Sc - Chemistry

Responsibilities: Lead formulation development for OSD, external preparations, oral liquids, and injectables. Oversee pre-formulation studies, prototype development, and scale - up activities. Ensure compliance with regulatory guidelines (ICH, WHO, USFDA, etc.). Collaborate with cross-functional teams (QA, QC, RA, Production) for tech transfer. Mentor junior scientists and manage project timelines and documentation. Required skills: Strong knowledge of formulation science and process optimization. Experience in QbD, DoE, and stability studies. Excellent leadership and communication skills. Required Qualification: - B.Pharm/M.Pharm

Responsibilities: Effectively perform chemical analysis techniques specifically using HPLC, GC, Karl Fischer, Melting Point, IR, and UV-Vis instrumentation. Completes documentation relating to material analysis and enters data into database/software systems. Assist with production activities as required. Laboratory environment requiring the ability to carry out laboratory operating procedures in a safe manner, while maintaining a clean and orderly workspace. Carried out instructions from senior staff. Work effectively with computer software and hardware, including analytical instruments, spreadsheets, and word-processing applications. Maintain and perform regular Calibration and verification...

About The Role Project Role : VIS & BI Strategy Practitioner Project Role Description : Develop a VIS/BI vision, business case, and modernization strategy; discover and assess VIS/BI opportunities; identify industry- and function-centered VIS/BI use cases; guide clients on industry and function relevant measures and metrics; develop a VIS/BI roadmap and operating model; help drive adoption, decision making and behavior change; measure VIS/BI value. Must have skills : Kinaxis Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a VIS & BI Strategy Practitioner, you will engage in the development of a comprehe...

Roles and Responsibilities Conduct quality control tests on raw materials, in-process samples, and finished products using HPLC, GC, and other analytical techniques. Ensure compliance with cGMP guidelines during manufacturing processes by monitoring equipment maintenance schedules and conducting regular inspections. Collaborate with cross-functional teams to resolve issues related to product quality, stability testing, and documentation. Develop and implement effective warehousing procedures for storing biologics products under controlled conditions. Provide technical support to production staff on fermentation processes and troubleshoot problems as needed.

Walk-In Interview QC Department (1 to 9 Years Experience) Hyderabad 11th & 12th October On 11th October 2025 (Saturday) Time : 9:00 AM to 3:00 PM Location: 7-2-A2, Hetero Corporate , Industrial Estates, Sanathnagar,Hyderabad-500018 Location: Annora Pharma Private Limited, Sy No.261, Plot No13, Annaram (Village), Ginnaram (mandal), Hyderabad On 12th October 2025 (Sunday ) Time : 9:00 AM to 3:00 PM 3. Location: Hotel Krithunga Restaurant, 01st Floor, Above Reliance Smart, Opposite New Bus Stand, Jadcherla Hiring For: Quality Control (QC) API / Formulations / Injectables Experience Required : 1 to 9 Years Qualification : B.Sc / M.Sc / B.Pharm / M.Pharm Department : Quality Control HPLC, GC, Wet...

Role Overview: As a Research Associate / Executive in the API Research & Development (R&D) team, your main responsibilities will include chemical synthesis, process optimization, and scale-up of Active Pharmaceutical Ingredients (APIs). You will be tasked with designing and executing synthetic routes, improving process efficiency, and ensuring cost-effectiveness. Your role will also involve analyzing and characterizing products using advanced analytical techniques such as HPLC, GC, while maintaining regulatory and quality compliance throughout the development process. Collaborating with cross-functional teams to facilitate smooth technology transfer and troubleshooting will be a key aspect o...

As a Scientist I at the U.S. Pharmacopeial Convention (USP), you will play a crucial role in supporting the development of Reference materials. Your responsibilities will include: - Supporting reaction monitoring, scale up, and final analysis of samples as per monograph/in-house procedures, including method development if required. - Preparing development reports for Synthetic Support projects and being involved in project acceptance. Executing projects per approved test protocols when assigned. - Preparing, executing, and completing IQ/OQ/PQ of new instruments. Indenting the required glassware, chemicals, and columns for the ARD projects. Maintaining GLP and implementing safety procedures w...

About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions. For more information visit: www.apotex.com. Job Summary Under the guidance of Manager-Instrumentation/R&D, responsible for installation...

Key Accountabilities And Responsibilities Analytical Method Development of various pharmaceutical dosage forms like oral solid, oral liquid, Injectables, Nasal Spray. Analytical Method Validation of various pharmaceutical dosage forms like oral solid, oral liquid, Injectables, Nasal Spray. Analytical Method Transfer of various pharmaceutical dosage forms like oral solid, oral liquid, Injectables, Nasal Spray. JOB SPECIFICATION Analytical method development and validation for pharmaceutical dosage forms. Literature search related to the drug substance, create analytical profiles. Execution of analytical method transfer for pharmaceutical dosage forms. Analysis of routine samples (product deve...

Job Purpose and Impact The Assistant Manager - QC will provide expertise with all daily operations in quality control laboratories. In this role, you will support the buildup and maintenance of the rapid technology platform by providing reliable accurate analytical figures as well as perform validation and troubleshooting of new analytical methods to ensure they meet the requirements and deadlines. Key Accountabilities Provide analytical support to Rapid Technology Application platform by releasing precise and accurate results and ensure scope of testing parameter is sufficient to build MPA module. Provide ongoing technical support to stakeholders, investigate quality problems and deliver im...

Job Description Provides technical & application services & support to Agilent customers. This includes timely and cost-effective problem resolution with the objective to enhance our customer experience and meet Agilent contractual agreements. Leverage post sales interactions with customers to probe and qualify further revenue opportunities and provides highly qualified leads to sales. Performs a set of required admin tasks to ensure flawless customer service for contract and trade customers. Responsibilities of this position include but are not limited to; Responsible for providing remote post-sales hardware, software technical support and Application support services to external customers ...

Job Title: Executive – R&D Biotechnology 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 The candidate is expected to develop HP...

Role: QA/QC Chemist Loc: Choutuppal,Valigonda Exp: 5+ yrs in Quality Control within the API/API Intermediate Manufacturing Sal: 6 - 8 LPA Qual: BSc/MSc (Chemistry) Skills: instrumental analysis (HPLC, GC, UV, IR, KF, etc. HPLC, GC SRUTHI 8125254983

Candidate should be from API industry having knowledge of handling & troubleshooting of sophisticated Analytical Instruments. Like HPLC, GC, IR, UV, KF ETC He should be able to work, adopt and guide subordinates and juniors in following Good Laboratory Practices. He should be well versed with various regulatory & Statutory requirements should be able to face regulatory and customer audits independently. Candidate Profile : - Should have minimum 10 years experience including minimum 3 years as Deputy Manager. He should be able to guide the team for completing the task assigned. Also should be able to complete task timely assigned by the management Qualification : - B Sc / B Pharm M Sc./M Phar...

Candidate should have knowledge of handling and troubleshooting the sophisticated Analytical Instruments like HPLC, GC, IR, UV, KF ETC . Also He should be able to work, adopt and guide subordinates in following Good Laboratory Practices. He should be well versed with various regulatory & Statutory requirements. Candidate Profile : - Should have minimum Four years experience. He should be able to work with the team and be willing to take initiative & challenge for completing the task assigned. Qualification : - B Pharm/B Sc M Sc./M Pharm

Your Role: As part of our QC team, you'll focus on testing raw materials, in-process samples, and finished products to ensure they meet established specifications. Your job is to detect and prevent defects before products reach the market. Key Responsibilities: Conduct physical and chemical testing of raw materials and final products (pH, viscosity, stability, active ingredient analysis). Perform stability studies to ensure product consistency over its shelf life. Test emulsions, creams, lotions, gels, ointments, and serums for quality parameters like texture, fragrance, absorption, and spreadability. Verify the quality of packaging materials (bottles, tubes, jars, labels) to prevent contami...

Experienced with Agilent 8860 GC autosampler or equivalent,including method development and software. Required Candidate profile Candidates from Vasai-Virar or Palghar are preferred. Immediate joiners are welcome.

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 Title: Executive / Sr. Executive - Quality Management System (Analytical Assurance) Department: Quality Management System Reports to: Manager Location: Ankleshwar Position Type: Full-time Qualifications And Experience Education: B.Pharm / M.Pharm / M.Sc in Chemistry, Biotechnology, or related field. Experience: Minimum 68 years of experience in Analytical Assurance within the pharmaceutical industry Job Responsibilities & Accountabilities We are looking for an experienced Analytical Assurance professional to join our team and lead the Out of specification investigation, along with core QMS activities pertaining to QC. Key Responsibilities Trigger out of specification investigations upon ...

About Us Scimplify is a specialty chemicals manufacturing company offering a full-stack solutionfrom R&D and custom synthesis to large-scale manufacturing and doorstep delivery. Headquartered in Bengaluru, India, we serve multiple industries ranging from pharmaceuticals to agrochemicals and industrial chemicals to personal care and fragrances. We enable 500+ businesses across 20+ countries to develop and scale innovative chemicals from lab to commercial production. We have raised over $54 million from top tier investors such as Accel and Bertelsmann, We are a team of 250+ professionals with entities in India, Japan, USA, UAE, and Indonesia. Learn more about why Forbes thinks we are the top 1...

As a Scientist B in the Ayush/Pharma Department at Farelabs Pvt. Ltd., your role will involve conducting analytical procedures in alignment with Ayurveda, Yoga, Siddha, Unani, and Homeopathic pharmacopeia of medicine for the Ayush section. For the Pharma section, you will be responsible for having complete knowledge of different pharmacopeia such as IP, USP, BP, and utilizing analytical procedures accordingly. Additionally, you will need to be knowledgeable about regulatory authorities like NABL, USFDA, TGA, MHRA, WHO, and DCA (drugs and cosmetic act 1940). Key Responsibilities: - Well-versed with analytical procedures for Ayurveda, Yoga, Siddha, Unani, and Homeopathic pharmacopeia - Knowled...