2096 Hplc Jobs - Page 8

Designation: Associate Scientist(8-I) Job Location: Bangalore Department: DDS-SATT 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 around the world. 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 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation. Job Purpose (1-2 Lines): Purification Scientist to work as a team member in purification team. Key Responsibilities: (Maximum 5-8 Points) Proven ability to independently develop analytical methods for both reverse-phase (achiral) and polar organic (chiral) separations, with experience in scaling up methods to preparative scale. Hands-on experience with preparative HPLC systems, including MS-based Prep HPLC; familiarity with LC-MS and UPLC techniques is a strong advantage. Skilled in performing minor instrument troubleshooting, calibrations, and recovery analyses as required. Excellent written and verbal communication skills. Strong adherence to company health, safety, and compliance protocols. Flexibility to undertake additional responsibilities from the Line Manager in alignment with business needs. Educational Qualification: M. Sc. in Chemistry / analytical chemistry Technical/functional Skills: (Maximum 4-6 Points) Preparative HPLC, MS based Prep HPLC, LC-MS, UPLC and SFC is an advantage. Experience: 5 to 7 years of hands-on experience in reverse phase Prep. HPLC or relevant area. Behavioral Skills: Must have very good communication skills Equal Opportunity Employer:

NOTE: Only Male & Candidates from AP & Telangana Preferred. Kindly Understand the JD It's not for the Clinical Trails Department 2Years Bond & Need to Submit your 10th Original Mark list with us during the Bond Period. Qualifications required: Bachelors / Masters (0-4 yrs. experience) degree level in biological/ life science, pharmacy qualification. Role and responsibility: In process quality control of ongoing studies. Review of raw data, chromatograms and reports of the method validations and studies. Checking of all the instruments and equipments for the calibration status and appropriate labeling. Checking and monitoring of the day-to-day activities in the lab for compliance to SOPs and GLP principles. Checking of the concentration data of subject samples before releasing to PK department. Generation, control and distribution of method SOPs. Logbook handling and archival of the completed logbooks. Performing the routine glassware validations and monitoring of the temperature and humidity in the Bio-analytical lab. Calibration of pipettes and multipedes. Coordinating for training programs on SOPs. Ensure cleanliness of laboratory and disposal of non-bio-waste & Bio-waste.

Hi we are hiring Experience;- 1 to 3 years Post;- QC CTC;- 20 to 35 k Location;-Baddi Knowledge ;- HPLC Interested candidate Apply;- Mail ID ;-Tisha.singh@unitedgroupmail.com Contact number ;- 9041666549

Education Qualification : MSC Chemistry Monitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc.) Isolate product and Optimize reaction conditions for improved yields and output Required Candidate profile Please Share your Profile capitalplacement04@gmail.com 9315507817

Job Description Summary Join GE Digital as a Technical Delivery Manager, where youll provide your expertise in sustained customer success and growth in the post-sales customer lifecycle. Youll lead a team of GE Project Software Engineers, Partners and Contracted Technical SMEs from Partners and Contractors assigned to the Project Team, developing project delivery strategy and delivering solutions against the scoped requirements to a high level of quality as per the Contract and Schedule. As a knowledge leader on our EMS/DMS/MMS or Asset Management systems, youll have the unique opportunity to contribute and shape the future of our global team. Job Description Role Summary Responsibilities will include Lead a PSA team to deliver the ADMS/AEMS/WAMS projects Youll own the End-to-End responsibility on the Software PSA Delivery technical element of projects to meet the contracted requirements, timeline and quality commitments Own the Solution, ensuing that any non-Product requirements are reviewed Collaborate with the Delivery Manager in relation to the Project Scope, ensuring that the deliverables are in accordance with the Scope of Work Engineering and code development for the EMS, DMS systems that meets the high standards. Parameterization, optimization, testing of EMS, DMS systems. Good technical background is required. The development of professional skills is achieved, in time, by involvement in the team activities and by trainings. Knowledge of the power systems phenomena and processes and related mathematical models(power flow, state estimator, short-circuit analysis, contingency analyst, voltage control, load-frequency control, power systems optimal regimes, load forecast, stability analysis, transient analysis, modeling of equipment and of automation and protection systems in power plants and power grids, DTS, models for the energy market); C / C ++ programmer skills or similar; Responsible for the documentation of requirements, schedule and WBS for any Change Requests within the Project Confirm the completion of deliverables against milestones and stage reviews Leadership: Has the ability to lead a team of 6-8 people with motivation and high energy level Ability to take ownership of projects and deliver while mentoring and helping team. Excellent stakeholder management and ability to deal with multiple functions/ projects in parallel. Prepare work breakdown structure, work instructions, estimation tools by working with subject matter experts and prepare a solution package. Acts as a go-to person for subordinates both in terms of solution expertise but also in terms of performance management and professional development. Proactively engages with cross-functional teams to resolve issues and design solutions. Qualifications / Requirements: Engineering Post Graduate from an accredited university (M.E./M. Tech/ Eng. Power System Engineering Degree) 8+ years of experience in T&D Domain and implementation services Strong analytical skills. Strong written, and interpersonal communication skills. Ability to make formal and informal presentation. Prior experience of Product management for software solution offerings would be highly desirable. Desired Characteristics: Committed to maintaining the highest standards of service quality in all aspects of project delivery Demonstrated ability to manage multiple projects simultaneously Strong organizational, analytical, and problem-solving abilities Familiar with contract terms Experience working with global teams / partners Strong oral and written communications skills Strong interpersonal and leadership skills Additional Information Relocation Assistance Provided: Yes

Experience Range: 4 to 6 Years Roles & Responsibilities: Tolerance simulations of heavy commercial vehicle components using 3DCS software. The candidate would need to interact and align with the global group companies and external partners for development areas. Additional Skills: Strong knowledge of Tolerance management, advanced GD & T methods in the automotive industry Good to Have: Knowledge of VW methods and documents in tolerance management Knowledge of working experience in Wind-chill, Enovia , VIS VSA German language (Read, Write, Speak) Sound knowledge of Automotive systems and Aggregates Good Hands-on experience in 3DCS, CATIA V5 Can able to Define reference points system (RPS), Create and execute 3D simulation models and Kinematic analysis Can able to do acquisition of tolerance chains, evaluation of the simulation results, suggestions for improvement, and corrective measures according to Contributors. Can able to do Iterative testing by integrating measurement data from Master data, Generate data for measurement plans Good experience in Checking the stability of planned assembly processes (Cp, Cpk, ...) Understanding of build sequence at the assembly level Good understanding of 1D and 2D stack-up Know-how of types of fixtures Can able to prepare final analysis reports Can work in CFT to support to Project team Strong knowledge of automotive Chassis, cabin, and components design. Basic knowledge of Machine Design and Material theory. Good interpersonal skills, Communication skills, presentation skills and Team player Should be able to handle assigned tasks independently Should work offline at MTB-I Pune office location Flexibility for international travel (if needed)

We are actively looking for credible team members who would be primarily responsible for: Encompassing literature survey. Identifying techno commercially attractive and non infringing route for fluoro-specialty molecules identified for commercialization in time bound manner. Develop standardize industrially feasible processes and also meet long term cost targets. Identify develop new products. Prepare feasibility report, cost analysis report, monthly progress report and TDR Demonstrate/validate the lab scale process up to commercial scale Essential Lead a team of scientist and chemists for new products / process development and improvement of the existing products. Knowledge and understanding of synthetic methods, analytical methods and relevant products. Excellent skills in interpretation of analytical data from UV, IR, NMR, GC, GCMS HPLC, LCMS, MS and so on. Well versed with GLP, GMP and IMS guidelines. Understanding of literature/ patents. Understanding and accomplishment of Customer requirements. Knowledge of SAP IMS

We are actively looking for credible team members who would be primarily responsible for: Encompassing literature survey. Identifying techno commercially attractive and non infringing route for fluoro-specialty molecules identified for commercialization in time bound manner. Develop standardize industrially feasible processes and also meet long term cost targets. Identify develop new products. Prepare feasibility report, cost analysis report, monthly progress report and TDR Demonstrate/validate the lab scale process up to commercial scale Essential Lead a team of scientist and chemists for new products / process development and improvement of the existing products. Knowledge and understanding of synthetic methods, analytical methods and relevant products. Excellent skills in interpretation of analytical data from UV, IR, NMR, GC, GCMS HPLC, LCMS, MS and so on. Well versed with GLP, GMP and IMS guidelines. Understanding of literature/ patents. Understanding and accomplishment of Customer requirements. Knowledge of SAP IMS

We are actively looking for credible team members who would be primarily responsible for: Encompassing literature survey. Identifying techno commercially attractive and non infringing route for fluoro-specialty molecules identified for commercialization in time bound manner. Develop standardize industrially feasible processes and also meet long term cost targets. Identify develop new products. Prepare feasibility report, cost analysis report, monthly progress report and TDR Demonstrate/validate the lab scale process up to commercial scale Essential Lead a team of scientist and chemists for new products / process development and improvement of the existing products. Knowledge and understanding of synthetic methods, analytical methods and relevant products. Excellent skills in interpretation of analytical data from UV, IR, NMR, GC, GCMS HPLC, LCMS, MS and so on. Well versed with GLP, GMP and IMS guidelines. Understanding of literature/ patents. Understanding and accomplishment of Customer requirements. Knowledge of SAP IMS

We are actively looking for credible team members who would be primarily responsible for: Encompassing literature survey. Identifying techno commercially attractive and non infringing route for fluoro-specialty molecules identified for commercialization in time bound manner. Develop standardize industrially feasible processes and also meet long term cost targets. Identify develop new products. Prepare feasibility report, cost analysis report, monthly progress report and TDR Demonstrate/validate the lab scale process up to commercial scale Essential Lead a team of scientist and chemists for new products / process development and improvement of the existing products. Knowledge and understanding of synthetic methods, analytical methods and relevant products. Excellent skills in interpretation of analytical data from UV, IR, NMR, GC, GCMS HPLC, LCMS, MS and so on. Well versed with GLP, GMP and IMS guidelines. Understanding of literature/ patents. Understanding and accomplishment of Customer requirements. Knowledge of SAP IMS

Vacancy for Instrument Technician / Officer in Analytical Development Lab Job Location : Kandivali (w), Mumbai Educational qualifications : Diploma in instrumentation Experience: 3- 5 years Job description: 1) Manage and maintain analytical instruments which includes HPLC, Dissolution, UV Spectrophotometer , GC, Particle size, Milli Q water purification system, Analytical/Precision balance etc. 2) Co-ordination with service engineer for breakdown and preventive maintenance 3) Oversee repair and calibration of instruments/equipments 4) Ensuring adherence to quality standards and best practices to ensure zero downtime 5) Co-ordination with CFT team for PO and spares

As a Senior Chemist-QC at Ravindra Heraeus Pvt. Ltd., you will be responsible for overseeing the daily operations of the chemistry lab in Vizag. Your main focus will be to ensure compliance with regulatory standards and accurate metal content analysis using Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES). Your role will require technical expertise in ICP-OES method development, validation, and troubleshooting across various industries such as pharmaceuticals, environmental testing, or food safety. In this role, your key responsibilities will include managing lab operations, scheduling, workflow, and resource allocation. You will also be involved in training, mentoring, and evaluating laboratory staff while ensuring adherence to SOPs, safety protocols, and regulatory guidelines. Additionally, your technical duties will involve performing and supervising routine/non-routine metal analysis using ICP-OES, developing, validating, and optimizing ICP-OES methods, and troubleshooting instrument issues. Furthermore, you will be expected to review data for accuracy, compliance, and integrity, maintain detailed documentation, calibrate and maintain ICP-OES equipment, and coordinate external servicing. Your role will also require you to prepare for audits/inspections, collaborate with QA, R&D, and production teams, and update SOPs to ensure alignment with industry standards. To qualify for this position, you should have a Master's degree in Chemistry or related field, with at least 5 years of experience in a QC lab, including 2+ years in a supervisory role. Hands-on experience with ICP-OES, method development, validation, and analysis is essential. Proficiency in ICP-OES operation, maintenance, and data software, along with strong knowledge of regulatory requirements, leadership, communication, and problem-solving abilities are also required. Preferred skills include experience with ICP-MS, HPLC, or GC. If you meet these qualifications and are interested in this opportunity, please email your resume to Hr@choksiheraeus.com. This is a full-time position with benefits such as food provision, health insurance, leave encashment, life insurance, paid sick time, and Provident Fund. The work schedule is fixed, and additional bonuses may be provided based on performance. The job requires a minimum of 5 years of experience in analytical chemistry. Please note that the work location is remote.,

The Assistant Manager - QC position at Bharuch SEZ requires a candidate with complete experience in API/Bulk/Intermediates industries as per global regulatory requirements. The individual will be responsible for the implementation and compliances of 21CFR-Part11, ICH-Q7A, cGMP, WHO-GMP, ISO9001, FSSC, HACCP, and other global QMS requirements at the SEZ site. Key responsibilities include regularizing QC activities as per cGMP requirements, ensuring regulatory and pharmacopeia compliance in the lab, reviewing hybrid and electronic data for IPQC and FG analysis, conducting analytical method validation, OOS, and OOT. The candidate should have knowledge about IMS system, analytical skills for QC instruments like GLC, HPLC, UV-Visible, FTIR, ICP, K/F, Melting point, and should be able to coordinate with QC staff, R&D, Commercial, and Production for quality and dispatch related activities. The Assistant Manager - QC will also be responsible for troubleshooting related to QC activities, training subordinates on 21 CFR Part 211, 111 with data integrity (Part-11) compliance in the lab, and maintaining awareness about responsible care (Environment, Health, Safety, and Security). The ideal candidate should have an M.Sc. in Chemistry with 8-12 years of experience. Competencies required include being responsible for implementation and compliances of various regulatory standards, hands-on experience as a reviewer of electronic data and hybrid systems in regulatory environments like US-FDA, WHO, and knowledge about 21 CFR Part 211, 111 with data integrity (Part-11). This role reports to the QC Head and will have 2-3 reportees. The Assistant Manager - QC will work closely with the Site Quality Head, CQA & RA Head, and Unit HR Head.,

As an Organic Chemist - Industrial Postdoc at altM, the candidate will be responsible for designing, synthesizing, and characterizing organic compounds for various applications. Primary functions will include conducting laboratory experiments, analyzing data, and interpreting results to drive innovation and advance research goals. Responsibilities Design and execute organic synthesis routes to target compounds. Perform purification and characterization of organic molecules using analytical techniques such as NMR, HPLC, GC-MS, and IR spectroscopy. Analyze and interpret experimental data to troubleshoot reactions and optimize synthetic routes. Collaborate with cross-functional teams to develop innovative solutions and address project challenges. Maintain accurate records of experimental procedures, results, and observations. Stay current with literature and technological advancements in organic chemistry to contribute to the development of novel methodologies and technologies. Adhere to safety protocols and best practices in the laboratory environment. Requirements PhD / Master&aposs degree in organic chemistry / related field(s), or evidence of exceptional ability. 1-2+ years of industrial experience preferred. Strong theoretical and practical knowledge of organic chemistry principles and techniques. Hands-on experience with organic synthesis, purification, and characterization methods. Proficiency in using laboratory equipment and analytical instruments. Ability to work effectively in a fast-paced research environment and manage multiple projects simultaneously. Excellent problem-solving skills and attention to detail. Strong communication and interpersonal skills, with the ability to collaborate effectively in a team setting. Commitment to safety, compliance, and ethical conduct in scientific research. This is an onsite role and requires physical presence. Compensation and Benefits Competitive cash compensation, negotiable for the right talent. altM is an equal opportunity employer, committed to diversity and inclusion in the workplace. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, age, national origin, disability, gender identity or any other protected characteristic outlined in any central, state, or local laws. Show more Show less

Date: 4 Sept 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Dedicated Centre Job Description Designation: Senior Research Associate (9-II) Job Location: Bangalore Department: DAS 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 around the world. 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 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation. Job Purpose Senior Research Associate (9-II) is to work as team member in preparatory HPLC purification team. Key Responsibilities High throughput purification of reaction mixture, utilizing mass-triggered reverse phase preparative HPLC. Able to utilize appropriate purification methods based on physical and chemical properties of target molecules. Expertise in analytical method development and problem solving. Able to perform LCMS and HPLC analysis. Minor trouble shooting of instrument and experimental issues. Able to communicate effectively within team and with Chemistry functions. Laboratory compliance to the QA and applicable regulatory guidelines. Corrective and preventive actions as and where applicable. EHSS adherence. Other activities as defined from time to time assigned by the head of the department. Educational Qualification: M.Sc. (Chemistry/Analytical Chemistry) Technical/functional Skills Practical knowledge of resolving simple instrument-related challenges. Thorough understanding of various analytical techniques and methods developments (LC-MS, HPLC and prepHPLC). Hands on experience using instrumental/commercial software for data processing Basic knowledge of wet analysis. Basic knowledge of chemistry is desirable. Must be a team player and be quick to adapt to the needs of end users Experience 2 to 5 years of experience for Senior Research Associate (9-II). Behavioral Skills Able to follow instructions and perform the tasks under the supervision of the project leader and section head Fair interpersonal skills Excellent attention to detail and record keeping Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status about public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities. Show more Show less

Date: 1 Sept 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Development Services Job Description Designation: Analyst Special Instrumentation and Method validation Job Location: Bangalore About Syngene 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 spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to companys integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements always in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngenes quality standards always Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Job Description: Performing analytical method validations and related documentation, as well as analysis of RM, PM, Intermediates, API, and Finished products. Key Responsibilities Following Good Laboratory Practices while working in the QC Laboratory. To maintain and clean responsibility allotted for individual instruments. Use of required safety apparel while sampling, analyzing, and working in the laboratory. Carry out the analysis of validation samples as per the protocol. Initiation of laboratory incidents and deviation. Preparation of calculation sheets and making draft reports. Disposal of sample for analysis after use. Taking any other job allocated by HOD or Section Head. Analysis of Intermediate, finished product, and working standard qualification as per the specification. Ensure that the instrument usage log is verified and reviewed periodically, and check the labels accordingly as per SOP. Preparation of protocols and Observation data sheets. Should be well versed with the latest analytical techniques like HPLC/GC, KF/KFC, IR/UV, LC-MS, GC-MS, IC, and ICP-OES/ICP-MS, etc... Being well-versed in the Chromeleon data management application and LIMS will be advantageous. To ensure safety compliance as per Syngene policy and EHSS requirements. Educational Qualification: M Sc / M Pharma (Analytical/General chemistry Technical/Functional Skills Should be well versed with the latest analytical techniques like HPLC/GC, KF/KFC, IR/UV, LC-MS, GC-MS, IC, ICP-OES/ICP-MS, DSC, TGA, etc... Being well-versed in the Chromeleon data management application and LIMS will be advantageous. Experience: 1- 4 years Behavioral Skills Should be an adaptive learner. Should demonstrate effective Communication skills. Organization and ability to balance work and Life. Should possess good Time Management abilities. Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status about public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. Show more Show less

Responsible for accurate verification and timely closure of entries in the E/IDPMS system. Coordinates communication with customers regarding pending entries and works closely with internal teams and external stakeholders to resolve discrepancies. Manages data operations across CBS, TRRACS, and E/IDPMS platforms, and collaborates with the TRRACS vendor to troubleshoot upload/download issues Roles and Responsibilities Ensure accurate verification, matching, and timely closure of entries in the Export/Import Data Processing and Monitoring System (E/IDPMS). Coordinate the dispatch of RPAD (Registered Post Acknowledgement Due) or emails to customers regarding pending entries. Liaise with Branches, BBU (Banking Business Units), CBU (Corporate Banking Units), and customers to resolve outstanding entries. Perform upload and download operations in CBS (Core Banking System), TRRACS application, and E/IDPMS portal. Collaborate with the TRRACS application vendor to troubleshoot and resolve errors encountered during data upload/download processes.

Role & responsibilities 1. To review batch release documents for raw material/packing material /in process/intermediate /finished product/stability like test protocol / report, electronic data, chromatograms, audit trail, spectra, etc. 2. To execute audit trails and review the activity to verify the integrity of data. 3. To review electronic data back up and verification of restoration study, computer system validation, etc. 4. To review calibration/qualification/PM schedule/installation documents for instruments in Quality Control department. 5. To review analyst qualification and training related documents of quality control department. 6. To review documents related to working standard / reference standard / impurity standard / reference material / GC standard. 7. To review stability schedule and related analytical data. 8. To review holding time stability study data & related analytical data. 9. To review quality management system related activity for Quality Control (Change Control, Deviation, Quality Complaints, QRM). 10. To review investigation and ensure closure of laboratory incidents. 11. To review investigation and ensure closure of OOS/OOT/OOC in Quality Control department. 12. To review all the trends related to quality control activity 13. To review of documents related to microbiological activity like, environmental monitoring, water testing, finished product testing, validation-based testing, instrument calibration and validation activities, etc. 14. To take QC rounds and support in maintaining GLP, logbooks review, etc. 15. To review SOPs, specification and method of analysis, test reports / protocols / documents related to QC. 16. Review of analytical method transfer and analytical method validation documents.

As a skilled Formulation & Development Scientist for the Nutraceutical Division, your primary responsibility will be to lead the development of innovative dietary supplements, functional foods, and health products. This role involves conducting research, formulating new products, and optimizing existing formulations while ensuring adherence to regulatory guidelines. Your key responsibilities will include designing and developing new formulations for a variety of dietary supplements such as tablets, capsules, powders, gummies, and liquids. You will also be tasked with optimizing existing formulations to enhance stability, bioavailability, and efficacy. Evaluating new ingredients, excipients, and delivery systems for nutraceutical products will be an essential part of your role. You will conduct various tests and analyses, including stability studies, compatibility tests, and dissolution studies. Collaboration with analytical teams will be necessary to maintain quality and consistency in the formulations. Ensuring compliance with regulatory bodies such as FSSAI, FDA, EFSA, and other international regulations will be a critical aspect of the role. Additionally, you will be responsible for preparing technical documents like COAs, MSDS, and formulation dossiers. To stay abreast of the latest trends in nutraceutical science, herbal extracts, probiotics, and functional foods, you will need to engage in continuous research and innovation. Developing and implementing novel delivery technologies to enhance bioavailability will be key to your success. Collaboration with cross-functional teams including procurement, manufacturing, quality, and marketing will be essential for scale-up and commercialization of products. As a Formulation & Development Scientist, you will troubleshoot formulation challenges related to solubility, stability, and taste masking. Process optimization to improve manufacturing efficiency and product performance will be part of your responsibilities. Your expertise in nutraceutical formulation techniques, knowledge of herbal extracts, vitamins, minerals, amino acids, and probiotics, and familiarity with Good Manufacturing Practices (GMP) and Quality Control (QC) protocols will be invaluable. Strong analytical skills, experience with testing techniques such as HPLC, FTIR, and a problem-solving mindset with attention to detail are essential for this role. Good documentation and regulatory knowledge will also be required. Preferred experience includes working with tablets, capsules, soft gels, gummies, and effervescent formulations, ideally in an R&D, F&D, or Nutraceutical/Pharma company. This is a full-time, permanent position with benefits such as Provident Fund. The work schedule is during the day, and the location is in person.,

As a Pharma Subject Matter Expert (SME) Trainer, you will be responsible for training candidates in various aspects of Quality Control (QC), Cell Culture Techniques, and Laboratory Procedures. Your role involves providing hands-on experience in analytical testing, microbiological testing, and pharmaceutical laboratory operations. It is essential to educate candidates on method validation, stability testing, and data integrity while ensuring compliance with FDA, USP, and cGMP regulations. Additionally, you will train individuals in utilizing HPLC, GC, UV-Vis, FTIR, PCR, ELISA, and Spectroscopy techniques. Your responsibilities include conducting mock interviews, assisting with resume preparation, and providing real-world project training to enhance the skills of the candidates. You will be required to ensure that trainees understand deviation handling, OOS/OOT investigations, CAPA processes, and regulatory audit procedures. Collaboration with the sales team is crucial to ensure that the trainees meet the expectations of their future employers. The ideal candidate should possess hands-on experience in cell culture, microbiology, and analytical laboratory techniques. Proficiency in HPLC, GC, FTIR, UV-Vis, and PCR is essential for this role. A strong understanding of data integrity, compliance documentation, and industry regulations such as cGMP, ICH, USP, and FDA guidelines is also required. Previous experience in stability testing, method validation, and impurity profiling will be beneficial. Your excellent mentoring and training skills, coupled with a passion for upskilling candidates, will be key to your success in this position. In addition to the specific responsibilities mentioned above, you will be expected to conduct one-on-one in-person training sessions, coordinate with internal teams for seamless training execution, and provide support to candidates in resume building, interview preparation, and exposure to real-time projects. Keeping abreast of industry trends and continuously updating training content accordingly is an integral part of this role. Please note that candidates who successfully complete two years with us will be eligible for visa sponsorship. If you are enthusiastic about mentoring and developing future pharmaceutical professionals, we look forward to receiving your application.,

The ADL Research Associate role at our organization in Vadodara requires 1-3 years of experience and a qualification of BSc/MSc Chemistry. As an ADL Research Associate, you will be responsible for developing, validating, and implementing analytical methods to support pharmaceutical product development. Your expertise in analytical instrumentation and regulatory guidelines will ensure compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Collaborating closely with R&D, Quality Assurance (QA), and Regulatory Affairs teams, you will contribute to formulation development, stability studies, and technology transfers. Your key responsibilities will include developing and validating analytical methods for various substances, conducting routine and non-routine analysis using analytical instruments like HPLC, GC, UV-Vis Spectroscopy, FTIR, Dissolution Apparatus, and LC-MS, and ensuring accurate and reproducible results compliant with regulatory standards. You will also be involved in stability studies as per ICH guidelines, providing analytical data for regulatory submissions, and supporting method transfer activities to Quality Control (QC) laboratories and contract research organizations (CROs). Maintaining accurate laboratory records, adhering to GMP, GLP, and ALCOA+ principles, and improving analytical techniques for enhanced lab efficiency and compliance are integral aspects of this role. Troubleshooting analytical challenges, investigating deviations, and implementing CAPA in a timely manner will be part of your routine tasks. Your dedication to continuous process improvement and adherence to regulatory requirements such as FDA, ICH, USP, EP, BP, and WHO will contribute to the success of our organization. This is a full-time position with a day shift schedule. The ideal candidate will have a Bachelor's degree and at least 1 year of experience in HPLC. If you are passionate about analytical method development, regulatory compliance, and process improvement, we welcome you to apply for this challenging and rewarding opportunity.,

You are invited to attend a walk-in interview for the position of Quality Control Analyst at Zydus Lifesciences Limited in Ahmedabad. The interview is scheduled to take place on the 2nd of March, 2025 in Indore. The position is based in our Moriaya unit in Ahmedabad. As a Quality Control Analyst, your responsibilities will include operating various QC equipment such as HPLC, GC, IR, UV, and Dissolution apparatus. Additionally, you will be involved in QC Method Validation and Transfer processes. To be eligible for this position, you should have a minimum educational qualification of B.Sc, M.Sc, B.Pharma, or M.Pharma. Furthermore, candidates with 2 to 8 years of relevant experience in Quality Control are encouraged to apply. If you possess the required qualifications and experience, we look forward to meeting you at the interview on the specified date and location. Please come prepared to discuss your expertise in HPLC, GC, IR, UV, Dissolution, and other relevant areas of Quality Control.,

About Us HCP Wellness Private Limited is a leading manufacturer of Skin Care, Cosmetics, and Oral Care products, committed to delivering innovative, high-quality solutions that combine science, safety, and customer trust. At HCP Wellness, we believe in teamwork, ownership, discipline, cleanliness, and safety values that guide every process from lab to shelf. Position Overview The Quality Control Chemist Job Vacancy will be responsible for ensuring that all raw materials, in-process materials, and finished products meet the highest standards of quality, safety, and compliance. This role requires strong technical knowledge, keen attention to detail, and adherence to GMP, GLP, and regulatory guidelines to maintain product integrity. Key Responsibilities Conduct quality control testing of raw materials, bulk, and finished goods as per SOPs. Perform physicochemical, instrumental, and microbiological analysis using methods such as HPLC, GC, UV, FTIR, pH meter, viscometer, and titrations. Ensure compliance with cGMP, GLP, and regulatory requirements (FDA, ISO, WHO-GMP). Prepare and review analytical reports, COAs, stability study data, and batch release documents. Monitor in-process quality at various manufacturing stages to prevent deviations. Collaborate with QA, R&D, and Production teams to resolve quality issues. Participate in internal audits, CAPA, and continuous improvement initiatives. Maintain proper documentation and ensure calibration, safety, and cleanliness of instruments and lab areas. Qualifications & Skills Education / Certifications B.Sc. / M.Sc. in Chemistry, Pharmaceutical Chemistry, Cosmetics, or related field. Additional certification in Quality Control / GMP / GLP preferred. Hard Skills Proficiency in analytical techniques (HPLC, GC, UV, FTIR, Titrations, etc.). Knowledge of stability studies, specifications, and pharmacopeia (IP, USP, BP, EP). Strong understanding of cosmetics, oral care, and skincare formulations. Hands-on experience with documentation, SOPs, and COA preparation. Familiarity with regulatory guidelines (FDA/ISO/WHO-GMP). Soft Skills Strong attention to detail and accuracy. Good communication and teamwork skills. Ability to troubleshoot and solve problems effectively. Discipline, ownership, and commitment to safety and cleanliness. Experience 2 3 years of experience in Quality Control within the Cosmetics, Skincare, Oral Care, or Pharmaceutical industry. Why Join HCP Wellness? Opportunity to work with a fast-growing, innovation-driven personal care manufacturer. Exposure to state-of-the-art laboratories and advanced testing techniques. Work culture built on teamwork, ownership, discipline, cleanliness, and safety. Growth opportunities within R&D, QA, and global compliance roles. Apply Now WhatsApp Apply Now WhatsApp Job Location : Bavla On Call Assistance: Email career@hcpwellness.in Job Type: Full-time Perks: Team Outings Cafeteria Soft Skill Training Job Training Health Insurance Office cab/shuttle

About Us HCP Wellness Private Limited is a leading manufacturer of Skin Care, Cosmetics, and Oral Care products, committed to delivering innovative, high-quality solutions that combine science, safety, and customer trust. At HCP Wellness, we believe in teamwork, ownership, discipline, cleanliness, and safety values that guide every process from lab to shelf. Position Overview The QC Chemist Jobs will be responsible for ensuring that all raw materials, in-process materials, and finished products meet the highest standards of quality, safety, and compliance. This role requires strong technical knowledge, keen attention to detail, and adherence to GMP, GLP, and regulatory guidelines to maintain product integrity. Key Responsibilities Conduct quality control testing of raw materials, bulk, and finished goods as per SOPs. Perform physicochemical, instrumental, and microbiological analysis using methods such as HPLC, GC, UV, FTIR, pH meter, viscometer, and titrations. Ensure compliance with cGMP, GLP, and regulatory requirements (FDA, ISO, WHO-GMP). Prepare and review analytical reports, COAs, stability study data, and batch release documents. Monitor in-process quality at various manufacturing stages to prevent deviations. Collaborate with QA, R&D, and Production teams to resolve quality issues. Participate in internal audits, CAPA, and continuous improvement initiatives. Maintain proper documentation and ensure calibration, safety, and cleanliness of instruments and lab areas. Qualifications & Skills Education / Certifications B.Sc. / M.Sc. in Chemistry, Pharmaceutical Chemistry, Cosmetics, or related field. Additional certification in Quality Control / GMP / GLP preferred. Hard Skills Proficiency in analytical techniques (HPLC, GC, UV, FTIR, Titrations, etc.). Knowledge of stability studies, specifications, and pharmacopeia (IP, USP, BP, EP). Strong understanding of cosmetics, oral care, and skincare formulations. Hands-on experience with documentation, SOPs, and COA preparation. Familiarity with regulatory guidelines (FDA/ISO/WHO-GMP). Soft Skills Strong attention to detail and accuracy. Good communication and teamwork skills. Ability to troubleshoot and solve problems effectively. Discipline, ownership, and commitment to safety and cleanliness. Experience 2 3 years of experience in Quality Control within the Cosmetics, Skincare, Oral Care, or Pharmaceutical industry. Why Join HCP Wellness? Opportunity to work with a fast-growing, innovation-driven personal care manufacturer. Exposure to state-of-the-art laboratories and advanced testing techniques. Work culture built on teamwork, ownership, discipline, cleanliness, and safety. Growth opportunities within R&D, QA, and global compliance roles. Apply Now WhatsApp Apply Now WhatsApp Job Location : Bavla On Call Assistance: Email career@hcpwellness.in Job Type: Full-time Perks: Team Outings Cafeteria Soft Skill Training Job Training Health Insurance Office cab/shuttle

About Us HCP Wellness Private Limited is a leading manufacturer of Skin Care, Cosmetics, and Oral Care products, committed to delivering innovative, high-quality solutions that combine science, safety, and customer trust. At HCP Wellness, we believe in teamwork, ownership, discipline, cleanliness, and safety values that guide every process from lab to shelf. Position Overview The QC Lab Chemist will be responsible for ensuring that all raw materials, in-process materials, and finished products meet the highest standards of quality, safety, and compliance. This role requires strong technical knowledge, keen attention to detail, and adherence to GMP, GLP, and regulatory guidelines to maintain product integrity. Key Responsibilities Conduct quality control testing of raw materials, bulk, and finished goods as per SOPs. Perform physicochemical, instrumental, and microbiological analysis using methods such as HPLC, GC, UV, FTIR, pH meter, viscometer, and titrations. Ensure compliance with cGMP, GLP, and regulatory requirements (FDA, ISO, WHO-GMP). Prepare and review analytical reports, COAs, stability study data, and batch release documents. Monitor in-process quality at various manufacturing stages to prevent deviations. Collaborate with QA, R&D, and Production teams to resolve quality issues. Participate in internal audits, CAPA, and continuous improvement initiatives. Maintain proper documentation and ensure calibration, safety, and cleanliness of instruments and lab areas. Qualifications & Skills Education / Certifications B.Sc. / M.Sc. in Chemistry, Pharmaceutical Chemistry, Cosmetics, or related field. Additional certification in Quality Control / GMP / GLP preferred. Hard Skills Proficiency in analytical techniques (HPLC, GC, UV, FTIR, Titrations, etc.). Knowledge of stability studies, specifications, and pharmacopeia (IP, USP, BP, EP). Strong understanding of cosmetics, oral care, and skincare formulations. Hands-on experience with documentation, SOPs, and COA preparation. Familiarity with regulatory guidelines (FDA/ISO/WHO-GMP). Soft Skills Strong attention to detail and accuracy. Good communication and teamwork skills. Ability to troubleshoot and solve problems effectively. Discipline, ownership, and commitment to safety and cleanliness. Experience 2 3 years of experience in Quality Control within the Cosmetics, Skincare, Oral Care, or Pharmaceutical industry. Why Join HCP Wellness? Opportunity to work with a fast-growing, innovation-driven personal care manufacturer. Exposure to state-of-the-art laboratories and advanced testing techniques. Work culture built on teamwork, ownership, discipline, cleanliness, and safety. Growth opportunities within R&D, QA, and global compliance roles. Apply Now WhatsApp Apply Now WhatsApp Job Location : Bavla On Call Assistance: Email career@hcpwellness.in Job Type: Full-time Perks: Team Outings Cafeteria Soft Skill Training Job Training Health Insurance Office cab/shuttle