1437 Gc Jobs - Page 19

Responsibilities: * Source top talent through US staffing networks. * Manage bench sales pipeline from opt-in candidates. * Collaborate with recruiters on W2/C2C placements. * Meet monthly hiring targets for US IT roles. Health insurance Food allowance

Analytical chemist Shift - 9 am to 6 pm Package - 25 k to 40 k(3 year experience) location- patiala Skills- pharma Wtsapp me resume at 8295842337- Mr. Bansal

Review overall QC documents, Prepare training modules as required and provide training to QC staff, Approve COAs for water analysis from the microbiology dpt, Required Candidate profile Propose new Standard Operating Procedures (SOPs) and analytical instruments, HPLC/UHPLC/GC/UV/FTIR, and stability data, Approve new equipment qualification (DQ/IQ/OQ/PQ).

Conduct final inspection and testing of finished products to ensure compliance with quality standards and customer specifications. Hands-on experience in testing of Finished products Instruments must be handled like HPLC, GC, KF, IR, DT, and Dissolution. Hands-on experience like software like Empower and LIMS. Qualification M.SC/B.Pharma 3 to 6 years Additional Information

Role & responsibilities To be responsible for review of samples on HPLC, UV etc. as per specified in method of analysis. 1 To be responsible for all the investigations related to any incident, OOS, OOT and deviation related to raw material and packing material. 2 To ensure and implementation of pharmaceutical quality system, cGMP, GLP and good documentation practice in accordance with guidelines in QC. 3 Responsible for any other work allotted by the HOD/ Designee.

Developing and validating analytical methods for the development of new and existing products. Designing and executing experiments to develop and validate analytical methods. Analyzing and interpreting data from experiments. Documenting and interpreting the analytical data in a timely manner as per GLP / GMP requirements to maintain records and compliance of regulatory norms Perform maintenance and calibration of lab instruments / equipment to get accurate and reproducible analytical result for proper interpretation Ensuring compliance with safety regulations. Working with other departments to ensure successful product development. Knowledge of analytical techniques such as HPLC, GC, and UV-...

Company: Strides Pharma Science Ltd Department: Quality Control (QC) Position: Senior Executive Job Location: Alathur, Chennai Qualification: M.Sc. (Chemistry), B-Pharm, M-Pharm Experience: 4.5 to 8 Years Skills required: Experience on Raw material, In-process, Finished product, Stability and Microbiological testing. Work experience on FDA regulatory plants Flexible to work in shifts Job responsibility: Handling of Sophisticated instruments such as HPLC, GC, UPLC, UV, AAS & Dissolution Tester Analysis in LIMS e-RDS Experience on Microbiological testing Instrument Qualification knowledge on IQ, OQ, PQ. Regards, Srinidhi S HR Talent Acquisition

Job Summary We are seeking a highly skilled Analytical Scientist in to join our Research and Development team for Injectable Division for developing and validating analytical methods for injectable products, ensuring compliance with the regulatory requirements, conducting literature reviews, scaling up for manufacturing of batches, coordinating manufacturing readiness, overseeing plant execution, and facilitating seamless technology transfer. This role demands a strong understanding of analytical principles, excellent documentation skills, and the ability to work effectively in a collaborative team environment. scaling up for manufacturing of batches, coordinating manufacturing readiness, ov...

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

Role & responsibilities handling of HPLC system with chromeleon software and integration in HPLC. Up-keep of all Instrument Usage Log, Inward Register, Training Records etc. Usage of SOPs, Specifications and STP for Inprocess, Intermediate, Finish Product, Recovered Solvents, and Cleaning Sample. Preferred candidate profile Msc Chemistry Preferred Experience of GC / HPLC

Method development : HPLC/GC Stability study Wet chemistry analysis (UV, IR, SOR, Titration...etc) Reaction monitor Routine support GLP awareness Role: Research & Development - Other Industry Type: Pharmaceutical & Life Sciences Department: Research & Development Employment Type: Full Time, Permanent Role Category: Research & Development - Other Education PG: MS/M.Sc(Science) in Organic Chemistry

Roles and Responsibilities Conduct stability analysis, method validation, and OOS investigations to ensure product quality. Ensure compliance with regulatory requirements by maintaining accurate records and documentation. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Perform HPLC, GC, FP, and OSD testing as per SOPs.

Job Type: Permanent Shift: Night shift Job Summary: We are seeking a dynamic and experienced HR Manager with a strong background in USA immigration , HR operations (from onboarding to offboarding), compliance management as per software Industry standards. The ideal candidate will be well-versed in U.S. immigration processes, including H-1B,H4 EAG, L-1, OPT, GC, and PERM processes. Key Responsibilities: Immigration & Compliance: Manage and oversee the full lifecycle of USA immigration processes, including H-1B, H4 EAD, OPT, Green Card (PERM & I-140) filings. Ensure timely filing and renewal of work authorizations and visas. Maintain immigration records and ensure full legal compliance with US...

As a Senior Analyst in Bioanalytical Research at Veeda Lifesciences, your role involves conducting bioanalytical research activities including method development, validation, and sample analysis using techniques like HPLC, GC, mass spectrometry, chromatography, spectrophotometry, and polarimeter. You will be responsible for developing and validating methods for bioanalysis of biologics and biosimilars in compliance with regulatory requirements such as USFDA. Collaboration with cross-functional teams is key to ensuring the timely delivery of high-quality results. Additionally, you will perform stability testing of biological products under various conditions and troubleshoot issues related to...

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...

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 5 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...

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...

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...

Role & responsibilities 4-8 years of experience in ADL/QC Having Exposure to perform the Analytical Method Validation/Verification by HPLC/GC

Interview for MSc Chemistry on 18th Male / Female for Dahej Location in Chemical Company Contact Urvi Madam on 9712914207 & Visit Our Office Share with yr friends Golden opportunity to Start career with SDP HR Solution

Job Alert Sr. GM / Associate Vice President – Quality Control Location: North India Industry: API / Chemicals Manufacturing Salary: Open (Attractive hike on current package) Experience: 16+ Years | Age: 50 Years We are seeking a dynamic Quality Control leader for a reputed API Manufacturing organization . The candidate must have strong exposure to regulatory-driven companies with proven expertise in leading global regulatory audits (USFDA, EMA, MHRA, etc.) and managing large QC operations. Key Responsibilities: Head the Quality Control department ensuring compliance with cGMP & international regulatory guidelines. Lead a QC team of 150–200 employees , driving efficiency, compliance, and tech...

Role & responsibilities Perform chemical analysis using ICP-MS and AAS for a diversity of applications. Familiarity with GLP and ISO 17025 quality system standards. Expert in sample Preparation for metal analysis.. Having Good Experience in metal analysis in food and water. Develop and validate ICP-MS methods in support of API and/or drug product manufacture as well as stand-alone analytical projects. Write protocols, methods and reports; as well as be involved in client project meetings; whilst being a point of contact for technical issues relating to ICP-MS analysis. Responsible for equipment maintenance and qualification, and interaction with vendor services and application support.

Key Responsibilities: 1. Stability Study Design & Planning Define study protocols, including time points, conditions (temperature, humidity, light exposure), and container types. Collaborate with formulation scientists and regulatory affairs teams to ensure studies align with regulatory guidelines (e.g., ICH, FDA). Plan long-term and accelerated stability testing for new and existing products 2. Compliance & Documentation Document study protocols, deviations, results, and reports. Maintain comprehensive stability study records for internal reference and regulatory submissions. Prepare stability data for inclusion in regulatory filings, ensuring compliance with ICH, FDA, or other relevant gui...

As a Quality Control (QC) Officer in the pharmaceutical (Formulation) industry located at Waghodia GIDC, Vadodara, your main responsibilities will include: - Performing quality checks on raw materials, in-process materials, and finished products. - Carrying out lab testing using instruments like HPLC, GC, UV, FTIR, etc. - Ensuring all work complies with GMP (Good Manufacturing Practices), GLP (Good Laboratory Practices), and other regulatory requirements. - Identifying and reporting any issues like defects, deviations, or non-conformities. - Maintaining accurate records, including test reports and documentation. - Working closely with production and QA teams to address and resolve quality-re...

As a Chemical Research Scientist C in the R&D Department in Bangalore, your role involves conducting literature search and review using basic software knowledge like Sci-Finder, Chem-draw, and other databases. You will also need to have a basic understanding of AI & Chat GPT. Your responsibilities include: - Executing synthesis and scale up of small organic molecules/intermediates, active ingredient/polymers/dispersions to multi-kilogram quantities under the supervision of the department head, adapting to evolving project requirements. - Employing techniques such as column chromatography, recrystallization, fractional, column & vacuum distillation, and different techniques. - Utilizing HPLC,...