Author: Sudheer vanguri

  • Milan Laboratories Quality Assurance Laboratory Jobs

    Milan Laboratories India Private Limited is looking for a detail-oriented and quality-focused professional to join its Quality Assurance – Laboratory team.
    The role focuses on laboratory quality systems, analytical review, documentation, data integrity, investigations, and GMP compliance.
    Candidates with B.Pharm, M.Pharm, M.Sc., or an equivalent qualification and 2–5 years of QA/QC experience in pharmaceutical formulation manufacturing can apply.
    Experience in Laboratory QA / QC QA will be preferred.

    Milan Laboratories – Quality Assurance Department

    Milan Laboratories – Quality Assurance Laboratory

    Department: Quality Assurance – Laboratory
    Experience: 2–5 Years
    Qualification: B.Pharm. / M.Pharm. / M.Sc. / Equivalent

    Milan Laboratories – Key Responsibilities

    Laboratory Quality Assurance

    • Review laboratory activities for compliance with GMP, GLP, and approved SOPs.
    • Review analytical test results, worksheets, specifications, and laboratory records.
    • Ensure appropriate laboratory documentation and data integrity practices.
    • Review and support investigations related to OOS, OOT, deviations, and laboratory incidents.
    • Review analytical method validation and verification documentation.
    • Ensure proper handling, calibration, and maintenance of laboratory instruments.
    • Participate in internal audits, regulatory inspections, and compliance activities.
    • Review laboratory SOPs, protocols, reports, and other quality documents.
    • Monitor adherence to cGMP, GDP, and ALCOA+ principles.
    • Coordinate with QC and other cross-functional departments for timely closure of quality-related activities.

    Milan Laboratories – Eligibility & Qualifications

    Milan Laboratories – Educational Qualification

    B.Pharm. | M.Pharm. | M.Sc. | Equivalent Qualification

    Milan Laboratories – Experience

    2–5 Years

    Candidates should have experience in QA/QC within a pharmaceutical formulation manufacturing environment.

    Milan Laboratories – Candidate Profile

    Required Knowledge & Skills

    • Good knowledge of GMP and GLP.
    • Understanding of Data Integrity requirements.
    • Knowledge of OOS, OOT, Deviations, and CAPA.
    • Strong documentation and analytical review skills.
    • Good communication skills.
    • Experience in Laboratory QA / QC QA will be preferred.

    Milan Laboratories – Job Location

    Location

    The supplied recruitment content does not specify the job location. The hashtags mention Panvel Jobs and Maharashtra Jobs, but these have not been treated as a confirmed location.

    How to Apply

    Interested candidates can share their updated CV at:

    Email: talentpool@milanlabs.com

    HR Contact

    Miss Ranna Bhatt: 8828829932

    Job Summary

    Company Milan Laboratories India Private Limited
    Vacancies Quality Assurance – Laboratory
    Required Education B.Pharm. / M.Pharm. / M.Sc. / Equivalent
    Experience 2–5 Years in QA/QC within a pharmaceutical formulation manufacturing environment

  • Kwality Pharmaceuticals Quality Control Jobs

    Kwality Pharmaceuticals Ltd. is hiring for its Quality Control Department at its EU-GMP certified sites.
    The opening covers AMV, HPLC and FG activities for candidates with relevant pharmaceutical experience.
    Candidates with B.Pharm, B.Sc. or M.Sc. qualifications and 1–6 years of experience can apply.
    Interested candidates can forward their CV through the email or WhatsApp contact provided by the company.

    Kwality Pharmaceuticals – Quality Control Department

    Kwality Pharmaceuticals – Quality Control Role

    Department: Quality Control
    Role: AMV / HPLC / FG
    Experience: 01–06 Years
    Qualification: B.Pharm. / B.Sc. / M.Sc.

    Kwality Pharmaceuticals – AMV / HPLC / FG

    Quality Control – AMV / HPLC / FG

    The recruitment advertisement lists the Quality Control opening under the following areas:

    • AMV
    • HPLC
    • FG

    The advertisement does not provide a detailed job description or individual responsibilities for these areas.

    Eligibility & Qualifications

    Kwality Pharmaceuticals – Quality Control

    B.Pharm. | B.Sc. | M.Sc.

    Candidates with the above qualifications and relevant Quality Control experience can apply.

    Experience Requirements

    Kwality Pharmaceuticals – Quality Control

    01–06 Years

    Kwality Pharmaceuticals – Job Location

    Kwality Pharmaceuticals Ltd.

    Village Nag Kalan, Majitha Road,
    Amritsar – 143601, Punjab

    Kwality Pharmaceuticals – Recruitment

    EU-GMP Certified Sites

    The recruitment advertisement states that the openings are for EU-GMP certified sites of Kwality Pharmaceuticals Ltd.

    How to Apply

    Interested candidates can forward their updated CV through the following channels:

    Email: career@kwalitypharma.com
    WhatsApp: +91 9639893691

    Candidates should mention the relevant Quality Control position / area while applying.

    Job Summary

    Company Kwality Pharmaceuticals Ltd.
    Vacancies Quality Control – AMV / HPLC / FG
    Required Education B.Pharm. / B.Sc. / M.Sc.
    Experience 01–06 Years

  • Chiron Behring Jobs | Warehouse & Packing Vacancies

    Chiron Behring Vaccines Pvt. Ltd. is conducting a Walk-In Interview for experienced professionals in its Warehouse and Packing departments.
    The recruitment offers 5 openings in Warehouse and 5 openings in Packing, with experience requirements of 3–8 years and 5–10 years, respectively.
    Candidates with Any Graduate / Post Graduate, B.Sc, ITI, B.Pharm, or M.Sc qualifications can apply for the relevant positions.
    The walk-in interview is scheduled for 22 September 2026, from 10:00 AM to 03:00 PM, at the company’s Ankleshwar facility.

    Chiron Behring Vaccines – Warehouse Department

    Junior Executive / Executive – Warehouse

    Open Positions: 5
    Designation: Junior Executive / Executive
    Experience: 3–8 Years
    Qualification: Any Graduate / Post Graduate
    Preferred: B.Sc.

    Chiron Behring Vaccines – Warehouse Responsibilities

    • Material & Inventory Management: Receipt, storage and issuance of raw materials, packing materials and auxiliary supplies.
    • Material Planning & Procurement: Raise Purchase Requisitions (PR).
    • Dispensing & Issuance: Execute material dispensing and issuance procedures.
    • SAP Expertise: Material movements, SAP transactions and inventory management.
    • QMS: Change control, CAPA and deviations.
    • Documentation: SOPs, qualification reports and quality system documents.
    • Compliance: GMP, regulatory and audit compliance.
    • Knowledge of warehouse area and equipment qualification.

    Chiron Behring Vaccines – Packing Department

    Technician / Junior Executive / Executive – Packing

    Open Positions: 5
    Designation: Technician / Junior Executive / Executive
    Experience: 5–10 Years
    Qualification: ITI / B.Pharm. / B.Sc. / M.Sc.

    Chiron Behring Vaccines – Packing Responsibilities

    • Packing Line Operations: Independently handle packing line and shift operations.
    • SAP: SAP entries, material procurement and posting related to packing.
    • Packing Equipment: Handling of Track & Trace and labelling machines.
    • Cold Chain: Knowledge of cold chain product handling.
    • Production Planning: Maintain plan vs. actual output of the shift.
    • Compliance: Ensure compliance against online observations.
    • Maintain required packing documentation and GMP compliance / QMS.
    • Labelling machine operation.
    • Operation of cartoner and traceable GMP.
    • Documentation.
    • Troubleshooting.

    Eligibility & Qualifications

    Chiron Behring Vaccines – Warehouse

    Any Graduate | Post Graduate | B.Sc.

    Chiron Behring Vaccines – Packing

    ITI | B.Pharm. | B.Sc. | M.Sc.

    Experience Requirements

    Chiron Behring Vaccines – Warehouse

    3–8 Years

    Chiron Behring Vaccines – Packing

    5–10 Years

    Chiron Behring Vaccines – Employee Benefits

    Benefits

    • 5 Working Days
    • Canteen Facility
    • Transport Facility
    • Mediclaim
    • Other employee benefits

    Chiron Behring Vaccines – Walk-In Interview Details

    Chiron Behring Vaccines – Walk-In Interview

    Date: 22nd September 2026, Tuesday
    Time: 10:00 AM – 03:00 PM

    Interview Venue

    Chiron Behring Vaccines Pvt. Ltd.
    Plot No. 3502, GIDC Estate,
    Ankleshwar, Gujarat – 393002

    How to Apply

    Interested candidates are requested to attend the walk-in interview with their updated CV and relevant documents.

    Candidates can also contact the recruitment team:

    Email: pooja.n.shah@chironbehring.com
    Contact: 6358817057

    Job Summary

    Company Chiron Behring Vaccines Pvt. Ltd.
    Vacancies Junior Executive / Executive – Warehouse; Technician / Junior Executive / Executive – Packing
    Required Education Any Graduate / Post Graduate / B.Sc.; ITI / B.Pharm. / B.Sc. / M.Sc.
    Experience 3–8 Years for Warehouse; 5–10 Years for Packing

  • Hetero API Division QC & QA Jobs | HPLC, GC, IPQA

    Hetero is conducting a Walk-In Drive for its API Division for experienced professionals in Quality Control and Quality Assurance.
    The openings include HPLC / GC roles in Quality Control and QMS / IPQA / MQA roles in Quality Assurance.
    Candidates with M.Sc., B.Pharm., or M.Pharm. qualifications and relevant experience can attend the interview.
    The walk-in drive is scheduled for 26th and 27th September 2026, from 09:00 AM to 03:30 PM, in Hyderabad.

    Hetero – Quality Control Department

    Hetero – QC HPLC / GC

    Role: HPLC / GC
    Qualification: M.Sc. / B.Pharm. / M.Pharm.
    Experience: 2–6 Years

    Candidates with relevant experience in HPLC or GC can apply for the Quality Control opening.

    Hetero – Quality Assurance Department

    Hetero – QA QMS / IPQA / MQA

    Role: QMS / IPQA / MQA
    Qualification: M.Sc. / B.Pharm. / M.Pharm.
    Experience: 1–4 Years

    Candidates with relevant experience in QMS, IPQA, or MQA can apply for the Quality Assurance opening.

    Hetero – Eligibility & Qualifications

    Hetero – Quality Control

    M.Sc. | B.Pharm. | M.Pharm.

    Hetero – Quality Assurance

    M.Sc. | B.Pharm. | M.Pharm.

    Hetero – Experience Requirements

    Hetero – Quality Control

    2–6 Years

    Hetero – Quality Assurance

    1–4 Years

    Hetero – API Division Recruitment

    Hetero – Experienced Professionals

    The recruitment is for the API Division, with openings in Quality Control and Quality Assurance. The advertisement specifically highlights HPLC, GC, QMS, IPQA and MQA as the relevant areas.

    Hetero – Joining Bonus

    Hetero – Immediate Joiners

    The recruitment advertisement mentions a joining bonus for experienced immediate joiners.

    Walk-In Interview Details

    Hetero – API Division Walk-In Interview

    Dates: 26th & 27th September 2026
    Time: 09:00 AM – 03:30 PM

    Interview Venue

    Hetero Office 7-2 A2, Sanath Nagar IE,
    Sanath Nagar, Hyderabad, Telangana – 500018

    Contact: Abbas – HR – 9100189615

    Documents to Carry

    Hetero – Walk-In Interview Documents

    Candidates should bring:

    • Updated Resume
    • Educational Certificates
    • Latest Increment Letter
    • Last 3 Months’ Payslips
    • Last 6 Months’ Bank Statements
    • Passport-Size Photos
    • Aadhaar Copy

    How to Apply

    Interested and eligible candidates can attend the walk-in interview at the Hetero office on 26th or 27th September 2026 during the specified interview timings.

    Candidates should carry the required documents and mention the relevant QC or QA position during the recruitment process.

    Hetero – Recruitment Notice

    Direct Recruitment

    The advertisement states that Hetero conducts recruitment only through direct channels and does not authorize or engage agencies or third parties for its recruitment process.

    For recruitment-related queries or to report suspicious recruitment activity, the advertisement directs candidates to hrd@hetero.com.

    Job Summary

    Company Hetero
    Vacancies Quality Control – HPLC / GC; Quality Assurance – QMS / IPQA / MQA
    Required Education M.Sc. / B.Pharm. / M.Pharm.
    Experience 1–6 Years depending on the position

  • Vee Healthtek Medical Coding Walk-In Drive – 100+ Vacancies

    Vee Healthtek Walk-In Drive for Medical Coders – 100+ Vacancies

    Vee Healthtek is conducting a Massive Walk-In Drive for Experienced Medical Coding Professionals across Bangalore and Chennai. The company is hiring 100+ professionals for positions including Medical Coder, Senior Coder, and QA. Candidates with 1–6 years of medical coding experience and certifications such as CPC, CCS, CIC, or COC can attend the walk-in drive. The openings cover specialties including IP DRG, E/M IP, Surgery, ED Facility, and CDI.

    Walk-In Drive Details

    Company

    Vee Healthtek

    Positions

    Medical Coder | Senior Coder | QA

    Vacancies

    100+

    Experience

    1–6 Years

    Work Mode

    Work From Office

    Specialties

    • IP DRG
    • E/M IP
    • Surgery
    • ED Facility
    • CDI

    Required Certifications

    • CPC
    • CCS
    • CIC
    • COC

    Medical Coding Opportunities

    Vee Healthtek is looking for experienced medical coding professionals for its Medical Coder, Senior Coder, and QA positions.

    Candidates should have relevant experience in medical coding and knowledge of the applicable coding specialties. The recruitment drive covers opportunities for professionals with 1 to 6 years of experience.

    Eligibility & Qualifications

    Educational Qualification

    Candidates with relevant qualifications in Medical Coding, Life Sciences, Healthcare, Pharmacy, Nursing, or other healthcare-related fields can apply, subject to the company’s role requirements.

    Eligible Qualification Courses

    B.Pharm | M.Pharm | Pharm.D | B.Sc. Life Sciences | B.Sc. Nursing | Allied Health Sciences | Healthcare-Related Courses

    Certification

    Candidates must have one of the following medical coding certifications:

    CPC | CCS | CIC | COC

    Experience

    • 1–6 years of relevant experience in Medical Coding.
    • Experience in IP DRG, E/M IP, Surgery, ED Facility, or CDI is relevant to the available positions.

    Walk-In Interview – Chennai

    Date & Time

    19th & 20th September 2026
    10:00 AM to 2:00 PM

    Venue

    Vee Healthtek Chennai
    Tower-3, Special Module
    Chennai One IT Park SEZ
    Pallavaram to 200 Feet Radial Road
    Thoraipakkam, Chennai – 600097

    Walk-In Interview – Bangalore

    Date & Time

    19th & 20th September 2026
    10:00 AM to 2:00 PM

    Venue

    Vee Healthtek Bangalore
    1st Floor, No. 15, IndiQube Platina
    Commissioner Road, Ashok Nagar
    Near Garuda Mall, Off MG Road
    Bengaluru – 560025

    Important Details

    • Experience: 1–6 Years
    • Certifications: CPC, CCS, CIC, or COC
    • Work Mode: Work From Office
    • Candidates can attend the walk-in interview at the relevant location.
    • Carry an updated resume and relevant professional documents.

    How to Apply

    Interested and eligible Medical Coders, Senior Coders, and QA professionals can attend the Vee Healthtek walk-in drive on 19th or 20th September 2026, between 10:00 AM and 2:00 PM.

    Contact for Queries

    Ramesh: 9443238706
    Rajiv Stephens: 9563546666
    Kalaiyarasi: 9566406546

    Candidates should attend the walk-in interview at either the Chennai or Bangalore venue mentioned above.

    Job Summary

    Category Details
    Company Vee Healthtek
    Vacancies 100+ Medical Coder, Senior Coder, QA
    Required Education Healthcare, Life Sciences, Pharmacy, Nursing, Allied Health Sciences, or related field
    Experience 1–6 Years

  • Cliantha Research Hiring | Medical Writer & CDM Roles

    Cliantha Research is hiring professionals across Medical Writing, Proposal Development, Clinical Data Management and Business Development functions.
    The openings are based in Ahmedabad and cover both mid-level and senior positions.
    Candidates with relevant experience in scientific writing, proposal development, CDM or business development can apply for the respective roles.
    The required qualifications include M.Pharm, B.Pharm and Pharm.D, depending on the position.

    Cliantha Research – Medical Writing Department

    Cliantha Research – Medical Writer

    Experience: 3–4 Years in Scientific Writing
    Qualification: M.Pharm. Pharmacology / Pharm.D
    Location: Ahmedabad

    Cliantha Research – Proposal Development Department

    Cliantha Research – Proposal Developer

    Experience: 2–3 Years as Proposal Developer
    Qualification: B.Pharm. / M.Pharm.
    Location: Ahmedabad

    Cliantha Research – Clinical Data Management Department

    Cliantha Research – Clinical Data Analyst

    Experience: 3–5 Years in CDM
    Qualification: B.Pharm. / M.Pharm. / Pharm.D
    Location: Ahmedabad

    Cliantha Research – Senior Clinical Data Analyst

    Experience: 5–6 Years in CDM
    Qualification: B.Pharm. / M.Pharm. / Pharm.D
    Location: Ahmedabad

    Cliantha Research – Business Development Department

    Cliantha Research – Business Development – Late Phase

    Experience: 8–12 Years in Business Development
    Qualification: B.Pharm. / M.Pharm. / Pharm.D
    Location: Ahmedabad

    Eligibility & Qualifications

    Cliantha Research – Medical Writer

    M.Pharm. Pharmacology | Pharm.D

    Cliantha Research – Proposal Developer

    B.Pharm. | M.Pharm.

    Cliantha Research – Clinical Data Analyst

    B.Pharm. | M.Pharm. | Pharm.D

    Cliantha Research – Senior Clinical Data Analyst

    B.Pharm. | M.Pharm. | Pharm.D

    Cliantha Research – Business Development – Late Phase

    B.Pharm. | M.Pharm. | Pharm.D

    Experience Requirements

    Cliantha Research – Medical Writer

    3–4 Years in Scientific Writing

    Cliantha Research – Proposal Developer

    2–3 Years as Proposal Developer

    Cliantha Research – Clinical Data Analyst

    3–5 Years in CDM

    Cliantha Research – Senior Clinical Data Analyst

    5–6 Years in CDM

    Cliantha Research – Business Development – Late Phase

    8–12 Years in Business Development

    Job Location

    Cliantha Research – Ahmedabad

    Ahmedabad, Gujarat

    How to Apply

    Interested candidates can share their updated resume with the Cliantha Research recruitment team.

    Email: jobs@cliantha.com

    Candidates should mention the relevant position while applying.

    Job Summary

    Company Cliantha Research
    Vacancies Medical Writer; Proposal Developer; Clinical Data Analyst; Senior Clinical Data Analyst; Business Development – Late Phase
    Required Education M.Pharm. Pharmacology / Pharm.D; B.Pharm. / M.Pharm.; B.Pharm. / M.Pharm. / Pharm.D
    Experience 2–12 Years depending on the position

  • Gufic Biosciences Production Jobs | B.Pharm, ITI

    Gufic Biosciences Limited is conducting a Walk-In Interview for Junior Technicians and Officers in its Production Department.
    The openings are specifically for professionals with experience in liquid sterile injectable manufacturing.
    Candidates with B.Pharm, Diploma, or ITI qualifications and 2–6 years of experience can apply.
    The interview is scheduled for 26th September 2026, from 10:00 AM to 3:00 PM, at the Gufic Biosciences facility in Pithampur.

    Gufic Biosciences – Production Department

    Gufic Biosciences – Junior Technicians & Officers

    Department: Production
    Positions: Junior Technicians & Officers
    Qualification: B.Pharm | Diploma | ITI
    Experience: 2–6 Years
    Industry Background: Liquid Sterile Injectable

    Gufic Biosciences – Special Requirement

    Candidates must strictly have a liquid sterile injectable background.

    Eligibility & Qualifications

    Gufic Biosciences – Production

    B.Pharm | Diploma | ITI

    Candidates with the above qualifications and relevant experience in liquid sterile injectable manufacturing are eligible to apply.

    Experience Requirements

    Gufic Biosciences – Junior Technicians & Officers

    2–6 Years

    The recruitment notice specifies 2 to 6 years of experience for the available Production positions.

    Gufic Biosciences – Job Location

    Gufic Biosciences Limited

    Smart Industrial Park, Natrip, Pithampur, Dhar – 454775, Madhya Pradesh

    Walk-In Interview Details

    Gufic Biosciences – Production Walk-In

    Date: 26th September 2026, Saturday
    Time: 10:00 AM – 3:00 PM

    Interview Venue

    Gufic Biosciences Limited
    Smart Industrial Park Natrip,
    Pithampur, Dhar – 454775

    How to Apply

    Interested candidates can share their updated resume at:

    Email: recruitment.indore@guficbio.com

    Candidates should ensure that their profile includes relevant liquid sterile injectable manufacturing experience.

    Job Summary

    Company Gufic Biosciences Limited
    Vacancies Junior Technicians & Officers – Production
    Required Education B.Pharm
    Experience 2–6 Years

  • Ipca Laboratories Jobs | QC, Microbiology & EHS

    Ipca Laboratories Ltd. is hiring for multiple positions at its Dewas Unit II across EHS & Safety, Quality Control, and Microbiology departments.
    The available roles include Executive, Officer, and Trainee positions depending on the department.
    Pass-out Apprentices are also eligible to apply for the Quality Control and Microbiology positions.
    Interested candidates can share their updated resume with the recruitment team for consideration.

    Ipca Laboratories – EHS & Safety Department

    Ipca Laboratories – Executive / Officer

    Designation: Executive and Officer

    The recruitment poster does not specify the educational qualification or experience requirement for these EHS & Safety positions.

    Ipca Laboratories – Quality Control Department

    Ipca Laboratories – Executive / Officer / Trainee

    Designation: Executive, Officer and Trainee

    Ipca Laboratories – QC Eligibility

    The recruitment poster specifically states that pass-out Apprentices are eligible to apply for Quality Control positions.

    The poster does not mention a specific educational qualification or experience requirement for these roles.

    Ipca Laboratories – Microbiology Department

    Ipca Laboratories – Executive / Officer / Trainee

    Designation: Executive, Officer and Trainee

    Ipca Laboratories – Microbiology Eligibility

    Pass-out Apprentices are also eligible to apply for the Microbiology positions.

    The recruitment poster does not specify the required educational qualification or experience.

    Eligibility & Qualifications

    Ipca Laboratories – EHS & Safety

    Qualification: Not specified in the recruitment poster.

    Ipca Laboratories – Quality Control

    Qualification: Not specified in the recruitment poster.
    Additional Eligibility: Pass-out Apprentices are eligible.

    Ipca Laboratories – Microbiology

    Qualification: Not specified in the recruitment poster.
    Additional Eligibility: Pass-out Apprentices are eligible.

    Experience Requirements

    Ipca Laboratories – EHS & Safety

    Experience: Not specified.

    Ipca Laboratories – Quality Control

    Experience: Not specified.

    Ipca Laboratories – Microbiology

    Experience: Not specified.

    Ipca Laboratories – Job Location

    Ipca Laboratories – Dewas Unit II

    Location: Dewas Unit II, Madhya Pradesh, India

    How to Apply

    Interested candidates can share their updated resume with:

    Email: preeti.upadhyay@ipca.com

    Candidates should mention the relevant department or position while applying.

    Job Summary

    Company Ipca Laboratories Ltd.
    Vacancies EHS & Safety – Executive / Officer; Quality Control – Executive / Officer / Trainee; Microbiology – Executive / Officer / Trainee
    Required Education Not specified in the recruitment poster
    Experience Not specified in the recruitment poster

  • MSN Laboratories Quality Control & AR&D Jobs

    MSN Laboratories is conducting a Walk-In Interview for experienced professionals in Quality Control and AR&D for its API manufacturing operations.
    The openings are suitable for candidates with 2–10 years of relevant experience in API manufacturing or the pharmaceutical industry.
    Candidates with hands-on experience in XRD, ICP-MS, Analytical Method Validation, AR&D, or Quality Control laboratory operations are encouraged to attend.
    The walk-in interview will be conducted on 24th and 25th September 2026 at Hotel Kinara Residency, Chanda Nagar, Hyderabad.

    MSN Laboratories – Quality Control & AR&D Department

    MSN Laboratories – Quality Control / AR&D

    Industry: API Manufacturing / Pharmaceutical
    Experience: 2–10 Years

    MSN Laboratories – Required Skills

    MSN Laboratories – XRD

    X-Ray Diffraction (XRD) experience is listed among the required technical skills.

    MSN Laboratories – ICP-MS

    Experience with Inductively Coupled Plasma Mass Spectrometry (ICP-MS) is required for relevant Quality Control and analytical operations.

    MSN Laboratories – Analytical Method Validation

    Candidates with experience in Analytical Method Validation can apply for the available positions.

    MSN Laboratories – AR&D

    Experience in Analytical Research & Development (AR&D) is listed as a required skill area.

    MSN Laboratories – Quality Control Operations

    Hands-on experience in Quality Control laboratory operations is preferred.

    Eligibility & Qualifications

    MSN Laboratories – Quality Control & AR&D

    The recruitment poster does not specify a particular educational qualification for the available positions.

    Candidates with relevant technical and analytical experience in API manufacturing / pharmaceutical operations are encouraged to attend.

    Experience Requirements

    MSN Laboratories – Quality Control & AR&D

    2–10 Years

    The recruitment specifically states that only candidates with 2–10 years of relevant experience are eligible. Freshers are not eligible.

    MSN Laboratories – Relevant Experience

    API Manufacturing / Pharmaceutical Industry

    Candidates with hands-on experience in the following areas are encouraged to attend:

    XRD | ICP-MS | AR&D | Quality Control Laboratory Operations | Analytical Method Validation

    Walk-In Interview Details

    MSN Laboratories – Walk-In Interview

    Dates: 24th & 25th September 2026

    Interview Venue

    Hotel Kinara Residency
    Chanda Nagar, Hyderabad, Telangana

    Candidates can scan the QR code provided in the recruitment poster for the exact location.

    Documents to Carry

    MSN Laboratories – Interview Documents

    Interested candidates should carry their:

    • Updated CV
    • Relevant documents

    How to Apply

    Interested candidates can attend the MSN Laboratories Walk-In Interview on the scheduled dates with their updated CV and relevant documents.

    The recruitment poster also provides a QR code for location details.

    Job Summary

    Company MSN Laboratories
    Vacancies Quality Control & AR&D positions
    Required Education Not specified in the recruitment poster
    Experience 2–10 Years of relevant experience

  • Jubilant Biosys Research Associate NMR Jobs

    Jubilant Biosys is hiring Research Associate / Senior Research Associate professionals for its Analytical Department with expertise in NMR.
    The role is based in Greater Noida and requires 2–6 years of experience, preferably in a CRO environment.
    Candidates with a postgraduate qualification in Chemical or Life Sciences, including M.Pharm. or M.Sc., can apply.
    The position focuses on NMR analysis, structure characterization, instrument maintenance, calibration, documentation, and qNMR activities.

    Jubilant Biosys – Analytical Department

    Jubilant Biosys – Research Associate / Senior Research Associate

    Department: Analytical – Expertise in NMR
    Designation: Research Associate / Senior Research Associate
    Experience: 2–6 Years, preferably in CRO
    Location: Greater Noida

    Jubilant Biosys – NMR Responsibilities

    Jubilant Biosys – NMR Analysis & Characterization

    • Perform acquisition and processing of routine final compounds using NMR.
    • Participate in the planning and execution of higher experiments for structure characterization.
    • Prepare reports related to structure characterization studies.
    • Maintain the turnaround time of NMR reports according to defined targets.
    • Perform periodic maintenance of NMR instruments.
    • Support calibration of NMR instruments.
    • Complete instrument-related documentation on time.
    • Perform quantitative analysis using qNMR whenever required.

    Jubilant Biosys – Candidate Requirements

    Jubilant Biosys – Educational Qualification

    Postgraduate Degree in Chemical / Life Sciences

    M.Pharm. | M.Sc.

    Jubilant Biosys – Technical Knowledge

    Candidates should have relevant technical knowledge for NMR-based analytical activities, structure characterization, and associated laboratory operations.

    Jubilant Biosys – Experience Requirements

    Jubilant Biosys – Analytical NMR

    2–6 Years

    Preferred: Experience in a CRO environment.

    Jubilant Biosys – Job Location

    Greater Noida

    Location: Greater Noida, Uttar Pradesh

    Jubilant Biosys – Role Focus

    Analytical Research & NMR

    The position is focused on analytical research activities involving:

    NMR Acquisition | NMR Processing | Structure Characterization | NMR Reporting | Instrument Maintenance | Instrument Calibration | qNMR

    How to Apply

    Jubilant Biosys – Application

    Candidates can apply through the Apply Now option provided in the recruitment advertisement.

    The supplied recruitment poster does not display a specific email address or phone number for applications.

    Job Summary

    Company Jubilant Biosys
    Vacancies Research Associate / Senior Research Associate – Analytical (NMR)
    Required Education Postgraduate Degree in Chemical / Life Sciences; M.Pharm. / M.Sc.
    Experience 2–6 Years, preferably in CRO