590 Gc Jobs - Page 3

Walk In Drive For Quality Control Department In Formulation Division @ Burgula Department :- Quality Control Qualification :- BSC | B Pharmacy | MSC | M Pharmacy Experience :- 5 to 6 Years Interview Date:- 30-07-2025 Interview Time:- 9AM TO 2.00PM Work Location: - MSNF-VI,Burgula Venue Address:- X59Q+P95, Mothighanapur, Burgula, Telangana 509202 Note:- Candidate should bring Update Resume , Offer Letter, Increment Letter,CTC,Payslips ,Bank Statement, Certificates,Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Its involve developing, validating, and implementing analytical methods for pharmaceutical products, ensuring compliance with quality and regulatory standards and require expertise in various analytical techniques like HPLC, GC, and spectrophotometry

Approving all Specifications, Test Methods, and Batch Process and Control Records (BMRs). approving validation protocols and reports, and conducting the General Good Manufacturing Practices (GMP) training.

We are looking for a highly skilled and experienced Analyst-QC to join our team at eClerx Services Ltd. The ideal candidate will have a strong background in IT Services & Consulting, with excellent analytical and quality control skills. Roles and Responsibility Collaborate with cross-functional teams to identify and prioritize testing requirements. Develop and implement comprehensive test plans and cases to ensure high-quality deliverables. Conduct thorough analysis of test results and identify areas for improvement. Work closely with the development team to resolve defects and enhance overall product quality. Participate in continuous improvement initiatives to optimize testing processes. Maintain accurate records of test cases, results, and defect reports. Job Requirements Strong understanding of software testing principles, methodologies, and tools. Excellent analytical, problem-solving, and communication skills. Ability to work effectively in a fast-paced environment and meet deadlines. Experience with quality control processes and procedures. Familiarity with industry standards and best practices for software testing. Strong attention to detail and ability to identify defects and errors.

Qualification :- M.Sc Chemistry Experience :- 0 to 3 year in Pharma or Chemical Company Location :- Jarod ( Vadodara ) Related Experience in HPLC , GC , Wet Analysis

HIRING FOR OSD - PRODUCTION & QC PRODUCTION(OSD) Experience: (01-07Years) Compression, Granulation, Coating, Capsule filling, Inspection QC Experience: (02-09Years) HPLC, GC, RM,PM, Stability, IP/FP, Method Development, Method Transfer QUALIFICATION : ITI/DIPLOMA/BSC/MSC/B PHARM/M PHARM With relevant Experience ITI/DIPLOMA/BSC/MSC/B PHARM Freshers can Apply DESIGNATIONS: Operator/Sr Operator/Jr Officer/Officer/Jr Executive/Executive INTERVIEW VENUE: SK Consultancy Services, H.No-1-77, 3rd Floor, Bachupally X Road, Opposite Sri Swastik Multi Specialty Hospital, Towards Nizampet Road DATE &TIME: 26th July 2025 ( Saturday); From 09.00 A.M. to 03.00 P.M NEED TO CARRY: Resume 3 Month Pay slips Increment letter Previous company relieving letters Education Documents and ID Proofs Help Us Spread the Word (Refer): Circulate it in your Social Networking sites and groups for better reach and Refer your friends and colleagues, it could be a great opportunity for someone in need! WORK LOCATION: Hetero Labs Limited, UNIT V Polleypally, Jadcherla, Mahabubnagar CONTACT INFO: E-mail: Ashok.ch@hetero.com & Contact:8555912639 for further info.

About Apotex Inc. Apotex Inc. is a Canadian-based global health company dedicated to producing high-quality, affordable medicines for patients worldwide. With a workforce of almost 7,200 employees engaged in manufacturing, research and development, and commercial operations, Apotex medicines are available to patients in over 75 countries. The company's focus on generic, biosimilar, and specialty products is supported by vertical integration. Job Summary As a member of the ARD-Test Centre team, you will work under the guidance of a Supervisor or senior chemist. Your responsibilities will include conducting method validation for new products, performing full testing of API, in-process and finished dosages, and preparing regulatory submission documentation. You will also play a key role in project working teams. Job Responsibilities - Conduct validation of analytical testing procedures for drug substances and drug products. - Perform initial testing, stability sample testing, in-process testing, and raw material testing according to specifications. - Carry out additional tests required for dosage submissions. - Document and report results following established Standard Operating Procedures (SOPs). - Provide technical support to other departments in responding to deficiency letters from regulatory agencies. - Work collaboratively and safely as part of a team to achieve desired outcomes. - Exhibit behaviors aligned with organizational Values: Collaboration, Courage, Perseverance, and Passion. - Adhere to all compliance programs, including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety, Health and Environment policies, and HR policies. - Collaborate with peers in R&D solid dosage to enhance expertise and address their needs. - Refer complex issues, along with recommendations, to the Supervisor. - Ensure all work is carried out in compliance with regulatory, compliance, and safety requirements. - Provide compliant advice to internal contacts and make complex decisions in alignment with regulations. - Perform any other relevant duties as assigned. Job Requirements Education: A graduate/postgraduate degree in Chemistry/Pharmacy from a recognized school/university. Knowledge, Skills, and Abilities: - Proficiency in wet chemistry, analytical bench techniques, and Window-based software. - Familiarity with automated data acquisition systems is advantageous. - Experience with Auto/Manual dissolution tests and GC is beneficial. - Strong written and verbal communication skills in English. Experience: BSc with 5 years or MSc with 3-4 years of experience in a pharmaceutical lab within an R&D environment. Apotex is dedicated to creating an inclusive and accessible work environment where all employees are valued, respected, and supported. Accommodations are available for applicants with disabilities during the recruitment process. If you require accommodation for an interview or testing, please inform us.,

Job Title: Senior Bench Sales Recruiter Location: Hyderabad (Onsite) Hyderabad (Madhapur) Experience: 4 to 7 Years Job Type: Full-Time Share Resumes at srikar@ipolarityllc.com Job Summary We are looking for a proactive and driven Bench Sales Recruiter with 48 years of experience in US IT staffing. The ideal candidate will be responsible for marketing our bench consultants (H1B, GC, CPT, OPT, EAD, and USC) to implementation partners and direct clients. This position requires excellent communication, relationship-building skills, and a strong understanding of the US IT recruitment ecosystem. Key Responsibilities Effectively market bench consultants to new and existing clients/vendors. Maintain and expand relationships with implementation partners and direct clients. Identify suitable requirements through job boards, social media, and vendor networks. Negotiate rate and contract terms with vendors and clients. Prepare and submit consultants for relevant requirements, ensuring quick turnarounds. Coordinate interviews, follow-ups, and ensure successful closures. Regularly update and maintain the consultant database and activity trackers. Assist consultants with resume formatting, interview preparation, and documentation. Stay current with market trends and technologies. Required Skills 4--to -7 years of experience in Bench Sales in US IT Staffing. Strong knowledge of employment types (C2C, W2, 1099) and work authorizations. Hands-on experience with job portals like Dice, Monster, CareerBuilder, Indeed, and LinkedIn. Excellent written and verbal communication skills. Ability to work in a fast-paced, target-driven environment. Strong negotiation and interpersonal skills. Experience in working with OPT/CPT, H1B, and GC consultants. Preferred Qualifications Bachelors degree in any field. Prior experience with applicant tracking systems (Ceipal, Bullhorn, etc.). Strong vendor/client database is a plus. like prime vendors, Desi vendors,End client, implementation part Etc.... Role & responsibilities Preferred candidate profile

Instrumentation HPLC & GC, LCMS, GMP Knowledge. Perform method transfers, verifications, and troubleshooting in support of process development and scale-up.

Perform analysis using GC, HPLC, UV, KF & wet methods. Ensure GLP, timely reporting, data review, instrument calibration & method validation. Handle OOS, guide juniors & coordinate with QA/production for batch release. Ensure SOP/ISO compliance.

Perform analysis of raw, in-process & finished goods. Operate GC, HPLC, UV, KF, IR. Maintain records, follow GLP & SOPs. Support method validation. Ensure ISO/regulatory compliance & coordinate with QA/production for batch release.

Must Abide by the rules & regulations of the laboratory. Responsible for Performing tests as per authorization and ensuring the TAT Compliance. Ensure Safe Handling of Equipment’s. Filling all logbooks for the equipment’s as per usage Ensure to wear all the PPE’s and lap aprons before performing the tests without fail. Ensure to follow safety rules & Maintain 5S. Pesticides & Mycotoxins analysis in food & agriculture as per authorization. Follow ISO 17025 requirements in lab with respect to Quality compliance and other regulatory requirements. Internal calibration of equipment’s Maintenance. Handling, Operating & Calibration, Maintenance of LC MSMS. Handling, Operating & Calibration, Maintenance of GC MSMS. CRM Management, Preparation, Storage, Disposal and Record maintenance. Roles and Responsibilities • Must Abide by the rules & regulations of the laboratory. • Responsible for Performing tests as per authorization and ensuring the TAT Compliance. • Ensure Safe Handling of Equipment’s. • Filling all logbooks for the equipment’s as per usage • Ensure to wear all the PPE’s and lap aprons before performing the tests without fail. • Ensure to follow safety rules & Maintain 5S. • Pesticides & Mycotoxins analysis in food & agriculture as per authorization. • Follow ISO 17025 requirements in lab with respect to Quality compliance and other regulatory requirements. • Internal calibration of equipment’s Maintenance. • Handling, Operating & Calibration, Maintenance of LC MSMS. • Handling, Operating & Calibration, Maintenance of GC MSMS. • CRM Management, Preparation, Storage, Disposal and Record maintenance.

1. Supervise end to end operations of food Chemical lab maintain the TAT for all the samples. 2. Implementation of Quality System as per all applicable accreditations like ISO 17025, FSSAI, EIC, APEDA etc. 3. Maintain all relevant documentation and presents as needed for quality audits and Regulatory audits 4. Implementation and Complying to the other TUV SUD Process and Policies 5. Implementation of good laboratory practices 6. Ensure on time method development / verification and validation 7. Implementation of any new process as decided by the management 8. Monitoring the turnaround time of the sections / reports as per the given schedule 9. Testing capability confirmation to sales and co-ordination with sales team for smooth lab operation. 10. Immediate response to internal or external enquiries. 11. Implementation of the safety guidelines for the respective areas 12. Minimize wastages inside the laboratory 13. Support in data inputs for new investment planning 14. Regular employee engagement 15. Driving continual improvements projects 16. Monitoring Expenses and take the required actions as on required 17. Coordinate and ensure Calibration / Preventive Maintenance / repair schedule with adequate documentation. 18. Equipment /method troubleshooting / repairs 19. Shift management and leave Management of the lab team 20. Supporting technical manager for RCA and CAPA 21. Ensure on-time training of respective team as per training planner Roles and Responsibilities 1. Supervise end to end operations of food Chemical lab maintain the TAT for all the samples. 2. Implementation of Quality System as per all applicable accreditations like ISO 17025, FSSAI, EIC, APEDA etc. 3. Maintain all relevant documentation and presents as needed for quality audits and Regulatory audits 4. Implementation and Complying to the other TUV SUD Process and Policies 5. Implementation of good laboratory practices 6. Ensure on time method development / verification and validation 7. Implementation of any new process as decided by the management 8. Monitoring the turnaround time of the sections / reports as per the given schedule 9. Testing capability confirmation to sales and co-ordination with sales team for smooth lab operation. 10. Immediate response to internal or external enquiries. 11. Implementation of the safety guidelines for the respective areas 12. Minimize wastages inside the laboratory 13. Support in data inputs for new investment planning 14. Regular employee engagement 15. Driving continual improvements projects 16. Monitoring Expenses and take the required actions as on required 17. Coordinate and ensure Calibration / Preventive Maintenance / repair schedule with adequate documentation. 18. Equipment /method troubleshooting / repairs 19. Shift management and leave Management of the lab team 20. Supporting technical manager for RCA and CAPA 21. Ensure on-time training of respective team as per training planner

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Friday 25-07-2025. 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 interact with cross - functional and cross - cultural teams. Previous experience of running analytical techniques such as HPLC, Dissolution, KF, IC with the ability to extract and prep various samples in a variety of forms. As this role involves liaising with other departments on a regular basis, you will need good communication skills and the ability to work effectively as part of a team. Note : Formulation Quality Control Candidates also eligible. Interview Date : 25-07-2025 Department : Formulation Analytical Research & Development(FAR&D) Experience : 1 to 6 Years Qualification : M. Pharmacy / M.Sc. / B Pharm Position: Executive Work Location : MSN R&D Center, Pashamylaram, Hyderabad Interview Venue Details MSN Laboratories, R&D Center,Pashamylaram, Hyderabad

Hiring For Electrical Manager in Jhagadia BE Electrical 15 to 20 Years Up to 18.0 LPA Budget Experience in Power Turbine must Send CV on sdpbharuch@gmail.com with Subject: Electrical Manager Jhagadia No Charges Share with your Friends Required Candidate profile Share Job with Your Friends Interview Venue: SDP HR Solution, Sixth Floor, 610, Golden Square, Beside Dmart, Near ABC Circle, Bholav, Bharuch Best Job Placement Consultancy in Gujarat

Market bench consultants Build vendor relationships Submit consultant profiles Negotiate rates with vendors Coordinate interviews Close placement deals Update CRM regularly Ensure quick placements Meet daily/weekly targets

Conduct quality control tests on API samples using various analytical techniques such as HPLC, GC, UV, etc. Method Verification, Calibration

Should be capable of handling instrument like HPLC, GC , UV, IR and potentiometry Should have the GMP knowledge and compliance requirement of QC Should have the knowledge on Good laboratory practices .

Role & responsibilities Required for Quality Control(Formulations) Quality Control(QC)- Need 1 to 5 years of experience. *Analysis of Finished Product & Stability *GLP and LIMS, Documentation Preferred candidate profile Perks and benefits

Good technical knowledge of analytical techniques and instrumentation: Chromatography technique like High-Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC), Spectroscopy technique like UV-Vis and Infrared (IR), KF titration, zettaliter, Osmometer and Dissolution etc Skills in developing, optimizing, and validating analytical methods to ensure accuracy, precision, and reliability. Understanding of Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), Data integrity and relevant regulatory guidelines (e.g., ICH, FDA, EP) to ensure compliance. Should have strong strong understanding & experience in injectables is mandatory Immediate joiners preferred Email : monisha.lahiri@randstad.in

Oversees QC activities, staff training, SOPs, calibrations, GLP compliance, audits, records, and lab investigations (OOS/OOT) and aligns QC goals with production and ensures lab standards (candidates having approval from Raj. FDA will be preferred).

Role & responsibilities Quality Control: Qualification: B. Pharm/ M. Pharm / M. Sc chemistry Experience: 1 to 6 years of experience in Pharmaceutical Quality Control experience. Job Description: Perform HPLC analysis. Familiarity with analytical laboratory equipment's like HPLC, GC, AAS,ICP-MS, UV, IR and etc., Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments. Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions. Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies. Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current. Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports. Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction. Demonstrated technical skills in method validation and testing Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations Knowledge of Good Manufacturing Practices and its application standards, processes, and policies. Excellent organizational skills and strong ability to multi-task Strong written and verbal communication skills Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation Experience with laboratory work, particularly using analytical HPLC (High Pressure Liquid Chromatography) techniques Create, review, and approve test method transfer and validation protocols, reports, and equipment qualification records. Maintain compliance with Current Good Manufacturing Practices in Quality Control and Stability laboratories. Perform testing on various samples, manage Laboratory Information Management System builds. Detail-oriented with robust knowledge of quality control process Effective written and verbal communication, as well as interpersonal skills Experience with Laboratory Information Management Systems (LIMS) Quality Control - Microbiology Qualification: M. Sc(Microbiology) Experience: 1 to 6 years of experience in Pharmaceutical Quality Control - Microbiology. Demonstrated technical skills in microbiology testing Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures Assist in the preparation and maintenance of media stocks, including sterilization of accessories by autoclave cycles. Manage receipt, storage, and handling of Bio ball cultures, and assist in the maintenance of Master cultures and preparation of Cryo vials. Perform various microbiological tests such as water analysis, Microbial Limit Test, , Bacterial Endotoxin Test, Ensure training records are updated and correctly filed to reflect current testing capabilities. Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments. Conduct analyses on finished products, raw materials, and components, including data entry, review, Effective written and verbal communication, as well as interpersonal skills

Exp: 2- 6 yrs • Knowledge in Method Development on Assay, RS, dissolution for formulation complex molecules. • understanding of Q1/Q2 evaluation • PEQ processes and characterization • Instruments: HPLC, GC, KF, UV, IR, etc. pranathi.p@orbicular.co.in

Plan and conduct multi-step organic syntheses to develop novel molecules.Work closely with cross-functional teams, including medicinal chemists,biologists, and analytical scientists to advance drug discovery projects. Required Candidate profile - Experience in medicinal chemistry or CRO environment, preferably in drug discovery, or custom synthesis. - Proficiency in synthetic organic chemistry.

We invite Postgraduates and Ph.D. holders to participate in our Walk-in Drive and become a valued part of the Althera family. Please carry a copy of the following documents with you: Updated Resume Recent Payslips/Increment letter and appointment letter Relieving Letter (if applicable) Educational Qualification Certificates We look forward to meeting talented professionals like you. Join us and take the next step in your career with Althera! Roles and Responsibilities Candidate should be very strong in Method development on HPLC for assay, Relates substances & dissolution for Regulated and Semi-regulated markets for tablets & capsules. Should have knowledge on Analytical Method Validation Analytical Method Transfer. Well versed with Regulatory guidelines (ICH and EU). The candidate should be ready to work full time in the lab. Desired Candidate Profile Masters degree or Phd in Pharmacy or Chemistry 1 to 6 years of experience in Solid dosage forms or experience in Peptides (Injectable and solid dosage form). Handling of instruments like HPLC, Dissolution apparatus, UV-VIS spectrophotometers etc. Understand the ICH and other guidelines Preparation and review of Department SOPs. Good knowledge on analytical method development, validations, transfer, stability analysis etc. Candidates from Testing labs can also apply.