Author: Sudheer vanguri

  • NATCO Pharma Walk-In Interview | Production & QC

    NATCO Pharma is conducting a Walk-In Interview for experienced candidates across Production, Quality Control and Microbiology departments.
    The openings are available for Operators, Supervisors, Quality Control and Microbiology roles at the Formulation Division.
    Candidates with qualifications including ITI, Diploma, B.Sc, B.Pharm, M.Sc and M.Sc Microbiology can apply for relevant positions.
    The walk-in interview will be held on 04 October 2026 in Hyderabad for candidates interested in working at the Kothur location.

    NATCO Pharma Production Recruitment

    Operators & Supervisors – Production

    Department: Production
    Area: OSD | Oncology & Non-Oncology
    Experience: 2–6 Years

    Operator

    Qualification: ITI / Diploma / B.Sc / B.Pharm

    Key Responsibilities:

    • Operation and handling of granulation equipment such as GEA, Tapasya and ACG.
    • Experience in handling HME and Roll Compactor.
    • Experience in operating compression machines such as GEA, IMA and Sejong.
    • Experience in operating coating equipment such as Neocota and ACG Coater.
    • Experience in operating capsule filling machines such as BOSCH, AF90T, ZRO 90T and IMA Imatic.
    • Experience in handling Track & Trace systems (Optel) and labeling operations.
    • Operation of blister packing and cartoners such as IMA PG & CAM.
    • Experience in bottle packing (CVC).
    • Experience in spray dryer operations.

    Supervisor

    Qualification: ITI / Diploma / B.Sc / B.Pharm

    Key Responsibilities:

    • Supervision and coordination of manufacturing operations in Oncology production areas.
    • Handling manufacturing activities including Granulation, Compression, Coating and Packing.

    NATCO Pharma Quality Control Recruitment

    Quality Control

    Qualification: M.Sc / B.Pharm
    Experience: 1–3 Years

    Key Responsibilities:

    • Experience in the analysis of raw materials, packing materials, in-process samples and finished products.
    • Experience using HPLC, GC and other laboratory instruments.

    Candidates with relevant pharmaceutical quality control experience can apply for the Quality Control position.

    NATCO Pharma Microbiology Recruitment

    Microbiology

    Qualification: M.Sc Microbiology
    Experience: 0–5 Years

    Key Responsibilities:

    • Experience in Environmental Monitoring.
    • Candidates with relevant microbiology experience can apply.
    • Male candidates are preferred.

    Eligibility & Qualifications

    The eligible qualifications mentioned for the different positions include:

    ITI | Diploma | B.Sc | B.Pharm | M.Sc | M.Sc Microbiology

    Candidates should meet the relevant educational and experience requirements for the position applied for.

    NATCO Pharma Experience Requirements

    • Production Operators & Supervisors: 2–6 Years
    • Quality Control: 1–3 Years
    • Microbiology: 0–5 Years

    NATCO Pharma Walk-In Interview Details

    Interview Date & Time

    Date: 04 October 2026 (Sunday)
    Time: 9:00 AM to 2:00 PM

    Interview Venue

    Natco House
    Road No. 2, Banjara Hills,
    Hyderabad – 34
    Opp. AP Productivity Council, Hyderabad.

    Work Location

    NATCO Pharma, Kothur Formulation Division, Hyderabad

    Candidates interested in working at the Kothur location are requested to attend the interview.

    How to Apply

    Interested candidates should attend the walk-in interview at the above-mentioned venue with their updated resume and relevant educational and experience documents.

    Candidates should be willing to work in rotational shifts.

    Important Note:

    • Only candidates interested in working at the Kothur location are requested to attend the interview.
    • Candidates should be willing to work in rotational shifts.

    Job Summary

    Company NATCO Pharma
    Vacancies Production Operator, Production Supervisor, Quality Control, Microbiology
    Required Education ITI / Diploma / B.Sc / B.Pharm / M.Sc / M.Sc Microbiology
    Experience 0–6 Years, depending on the position

  • Gufic Biosciences Walk-In Interview | Pharma Jobs

    Gufic Biosciences Ltd. is conducting a Walk-In Interview for experienced pharmaceutical professionals at its injectable facility in Navsari, Gujarat.
    The company has openings across Quality Assurance, Quality Control, QC Microbiology and EHS departments.
    Candidates with M.Pharm, B.Pharm, M.Sc, B.Sc, B.E. and M.E. qualifications can apply for the relevant positions.
    The walk-in interview is scheduled for 03 October 2026, from 10:00 AM to 04:00 PM, at the Gufic Biosciences facility in Navsari.

    Gufic Biosciences Ltd. Quality Assurance Recruitment

    Quality Assurance (Injectable) | Officer / Sr. Officer

    Experience: 2 to 6 Years
    Qualification: M.Pharm / B.Pharm / M.Sc

    Key Skills & Experience:

    • Knowledge of injectable plant operations.
    • Experience in IPQA.
    • Knowledge of GLP and QMS.
    • Experience in validation.
    • Vendor qualification.
    • Audit compliance.

    Gufic Biosciences Ltd. Quality Control Recruitment

    Quality Control | Officer / Sr. Officer / Executive

    Experience: 3 to 10 Years
    Qualification: M.Pharm / B.Pharm / M.Sc

    Key Skills & Experience:

    • Knowledge of analytical instruments such as HPLC and UPLC.
    • Experience in the AMV section.

    Gufic Biosciences Ltd. Quality Control Microbiology Recruitment

    Quality Control (Micro) | Apprentice / Officer / Sr. Officer

    Candidate Preference: Male Candidate Only
    Experience: Fresher to 7 Years
    Qualification: M.Sc. (Micro/Biotechnology) / B.Sc. (Micro/Biotechnology)

    Key Skills & Experience:

    • Knowledge of BET.
    • Environment monitoring.
    • Sterility.
    • MLT.
    • Culture.
    • Media preparation.

    Gufic Biosciences Ltd. EHS Recruitment

    EHS | Officer / Sr. Officer / Executive

    Candidate Preference: Male Candidate Only
    Experience: 3 to 10 Years
    Qualification: B.E. / M.E. Environmental Engineering / ADIS or PDIS (Mandatory)

    Key Skills & Experience:

    • Work Permit.
    • MSDS.
    • GPCB.
    • Fire Hydrant System.
    • Mock Drill.
    • HIRA.
    • HAZOP Study.

    Eligibility & Qualifications

    M.Pharm | B.Pharm | M.Sc | B.Sc | M.Sc Microbiology | M.Sc Biotechnology | B.Sc Microbiology | B.Sc Biotechnology | B.E. Environmental Engineering | M.E. Environmental Engineering | ADIS | PDIS

    Candidates should meet the relevant educational and experience requirements specified for each department.

    Gufic Biosciences Walk-In Interview Details

    Walk-In Date & Time

    Date: 03 October 2026, Saturday
    Time: 10:00 AM to 04:00 PM

    Interview Venue

    Gufic Biosciences Ltd.
    N.H. 48, Near GEB Grid,
    Kabilpore, Navsari – 396424, Gujarat.

    How to Apply

    Interested candidates should bring their updated CV and one photograph to the walk-in interview.

    Candidates who are unable to attend can send their updated CV to:

    Email: binal.kapadia@guficbio.com
    Mobile: +91 63599 21281

    Job Summary

    Company Gufic Biosciences Ltd.
    Vacancies Officer / Sr. Officer – Quality Assurance (Injectable); Officer / Sr. Officer / Executive – Quality Control; Apprentice / Officer / Sr. Officer – Quality Control (Micro); Officer / Sr. Officer / Executive – EHS
    Required Education M.Pharm / B.Pharm / M.Sc / B.Sc / M.Sc Microbiology / Biotechnology / B.Sc Microbiology / Biotechnology / B.E. / M.E. Environmental Engineering / ADIS / PDIS
    Experience 2–6 Years – QA; 3–10 Years – QC; Fresher to 7 Years – QC Micro; 3–10 Years – EHS

  • Sun Pharma Walk-In Interview | Production & QA Jobs

    Sun Pharmaceutical Industries Ltd. is conducting a walk-in interview for its Greenfield Project at Pithampur, Indore.
    The company is hiring Senior Officer, Executive and Senior Executive professionals with 3–9 years of experience across multiple pharmaceutical functions.
    Opportunities are available in Production, Engineering, Quality Assurance, QC Microbiology, QC Chemistry, Validation and MSTG/Technology Transfer.
    Eligible candidates can attend the walk-in interview on 11 October 2026 with their updated CV and required documents.

    Sun Pharma Production Recruitment

    Production | Senior Officer / Executive / Senior Executive

    Qualification: B.Pharm / M.Sc.
    Experience: 3–9 Years

    Key Areas:

    • Fill Vial
    • Autoclave
    • Sterile Packing
    • Vial Filling
    • Visual Inspection

    Sun Pharma Engineering Recruitment

    Engineering | Senior Officer / Executive / Senior Executive

    Qualification: B.Tech / M.Tech
    Experience: 3–9 Years

    Key Areas:

    • Plant Maintenance
    • HVAC
    • Process Engineering
    • Electrical & Utilities

    Sun Pharma Quality Assurance Recruitment

    Quality Assurance | Senior Officer / Executive / Senior Executive

    Qualification: B.Pharm / M.Sc.
    Experience: 3–9 Years

    Key Areas:

    • Process & Cleaning Validation
    • IPQA
    • Compliance
    • Stability
    • Documentation

    Sun Pharma QC Microbiology Recruitment

    QC – Microbiology | Senior Officer / Executive / Senior Executive

    Qualification: M.Sc. in Microbiology
    Experience: 3–9 Years

    Key Areas:

    • Environmental Monitoring
    • Sterility
    • MLT
    • BET

    Sun Pharma QC Chemistry Recruitment

    QC – Chemist | Senior Officer / Executive / Senior Executive

    Qualification: B.Pharm / M.Sc.
    Experience: 3–9 Years

    Key Areas:

    • HPLC
    • Stability
    • Raw Material Analysis
    • Finished Product Analysis

    Sun Pharma Validation Recruitment

    Validation | Senior Officer / Executive / Senior Executive

    Qualification: B.Pharm / M.Sc.
    Experience: 3–9 Years

    Key Areas:

    • OOS
    • PAT & SAP
    • Documentation
    • Equipment and Process Validation

    Sun Pharma MSTG / Technology Transfer Recruitment

    MSTG / Technology Transfer | Senior Officer / Executive / Senior Executive

    Qualification: B.Pharm / M.Sc.
    Experience: 3–9 Years

    Key Areas:

    • Exhibit Batches
    • Scale-up Batches
    • Technology Transfer
    • Process Equipment
    • Qualification

    Eligibility & Qualifications

    B.Pharm | M.Sc. | B.Tech | M.Tech | M.Sc. Microbiology

    Relevant qualifications depend on the department and position. Candidates should have 3–9 years of relevant pharmaceutical industry experience.

    Sun Pharma Walk-In Interview Details

    Walk-In Date & Time

    Date: 11 October 2026
    Time: 10:00 AM to 3:00 PM

    Job Location

    Sun Pharmaceutical Industries Ltd.
    Pithampur, Indore

    Interview Venue

    Red Maple Mashal Hotel
    Rau, Indore

    How to Apply

    Eligible candidates interested in the Sun Pharma Greenfield Project recruitment can attend the walk-in interview with the required documents.

    Documents to Carry

    • Updated CV
    • Passport-size photograph
    • ID copies
    • Educational documents
    • Experience documents
    • Latest 3 salary slips

    Important: Sun Pharma does not charge any fee for recruitment. Candidates should be cautious of fraudulent requests for payment.

    Job Summary

    Company Sun Pharmaceutical Industries Ltd.
    Vacancies Senior Officer / Executive / Senior Executive – Production; Engineering; Quality Assurance; QC – Microbiology; QC – Chemist; Validation; MSTG / Technology Transfer
    Required Education B.Pharm / M.Sc. / B.Tech / M.Tech / M.Sc. Microbiology
    Experience 3–9 Years

  • Kamla Lifesciences Ointment Officer Recruitment

    Kamla Lifesciences Ltd. is hiring an experienced Ointment Officer for its Ointment Manufacturing Unit.
    The position is suitable for B.Pharm and M.Pharm candidates with 2–6 years of experience in pharmaceutical manufacturing.
    Candidates should have relevant experience in ointment manufacturing, GMP, SOPs and batch documentation.
    The job location is Boisar, Tarapur, and male candidates are preferred for this position.

    Kamla Lifesciences Ointment Manufacturing Recruitment

    Ointment Officer

    Department: Ointment Manufacturing
    Designation: Ointment Officer
    Experience: 2–6 Years
    Location: Boisar, Tarapur
    Gender Preference: Male candidates preferred

    Job Responsibilities & Skills

    Candidates with relevant pharmaceutical manufacturing experience, strong knowledge of GMP, SOPs, batch documentation, and ointment manufacturing processes are encouraged to apply.

    The role involves working in the Ointment Manufacturing Unit and handling activities related to pharmaceutical ointment manufacturing in accordance with applicable manufacturing procedures and quality requirements.

    Eligibility & Qualifications

    B.Pharm | M.Pharm

    Candidates should have 2–6 years of relevant pharmaceutical manufacturing experience. Experience in ointment manufacturing, GMP, SOPs and batch documentation will be relevant to the position.

    How to Apply

    Interested candidates can send their updated CV to:

    Email: anjali.yadav@kamlagroup.co.in
    Contact: 8956480712

    Candidates with relevant experience and qualifications are encouraged to apply for the Ointment Officer position at Kamla Lifesciences Ltd.

    Job Summary

    Company Kamla Lifesciences Ltd.
    Vacancies Ointment Officer
    Required Education B.Pharm / M.Pharm
    Experience 2–6 Years

  • Concord Biotech Walk-In Interview | Production & QC

    Concord Biotech Limited, Unit-II, Valthera, is conducting a Walk-In Interview for experienced professionals in Production and Quality Control (QC).
    The recruitment drive includes positions ranging from Executive and Supervisor to Assistant Manager/Sr. Executive, along with QC analytical roles.
    Candidates with qualifications including M.Sc, B.Pharm, M.Pharm, B.Sc and ITI/Diploma can apply for the relevant positions.
    The interview is scheduled for 02 October 2026 at the Concord Biotech facility in Valthera, Ahmedabad.

    Concord Biotech Production & Quality Control Recruitment

    Concord Biotech Production Department

    Assistant Manager / Sr. Executive / Executive

    Experience: 5 to 10 Years
    Qualification: M.Sc / B.Pharm / M.Pharm

    Job Responsibilities:

    • Experienced shift in-charge to manage daily manufacturing operations.
    • Ensure strict cGMP, safety and regulatory compliance.
    • Key duties include production planning and ensuring execution as per plan, preparing batch records and qualification documents (IQ/OQ/PQ), and coordinating with QC/Warehouse for uninterrupted workflow.
    • Responsible for equipment maintenance, calibration tracking and leading team training to ensure minimal downtime and high-quality output.

    Supervisor / Officer

    Experience: 3 to 5 Years
    Qualification: B.Pharm / M.Pharm

    Job Responsibilities:

    • Experience in the manufacturing process.
    • Experience in granulation, coating and capsule filling machines.

    Granulation / Coating / Capsule Operator

    Experience: 3 to 7 Years
    Qualification: ITI / Diploma

    Job Responsibilities:

    • Experience in granulation with FBP (Top Spray Granulation) machine.
    • Experience operating coating machines.
    • Experience operating capsule machines.

    Concord Biotech Quality Control Department

    HPLC Analyst

    Experience: 6 to 8 Years
    Qualification: B.Sc / M.Sc / B.Pharm

    Job Responsibilities:

    • Experience in performing analysis using HPLC instruments for raw materials, finished products and in-process samples.

    Dissolution and Chemical Analyst

    Experience: 2 to 5 Years
    Qualification: B.Sc / M.Sc / B.Pharm

    Job Responsibilities:

    • Experience in handling dissolution test apparatus.
    • Experience with Karl Fischer apparatus, auto titrator, UV instrument, ICP-OES/MS and other chemical analysis instruments.

    QC Reviewer

    Experience: 8 to 10 Years
    Qualification: B.Sc / M.Sc / B.Pharm

    Job Responsibilities:

    • Review of GMP documents.
    • Data review of raw materials and finished product analysis.
    • Troubleshooting of analytical instruments.

    Concord Biotech Eligibility & Qualifications

    Candidates with the following qualifications can apply for the relevant Production and Quality Control positions:

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

    Concord Biotech Experience Requirements

    • Assistant Manager / Sr. Executive / Executive: 5–10 Years
    • Supervisor / Officer: 3–5 Years
    • Granulation / Coating / Capsule Operator: 3–7 Years
    • HPLC Analyst: 6–8 Years
    • Dissolution and Chemical Analyst: 2–5 Years
    • QC Reviewer: 8–10 Years

    Concord Biotech Walk-In Interview Details

    Walk-In Date & Time

    Date: 02 October 2026
    Time: 10:00 AM to 02:00 PM

    Walk-In Venue

    Concord Biotech Limited, Unit-II
    297–298/2P, At Valthera,
    Taluka Dholka, Dist. Ahmedabad,
    Gujarat – 382225, India.

    How to Apply

    Interested candidates can appear for the walk-in interview with their updated CV, current salary proof and passport-size photograph.

    Candidates who are unable to attend the interview can apply by sending their updated CV to:

    Email: careerfdf@concordbiotech.com

    Candidates should clearly mention the position applied for in the subject line.

    Documents to Carry

    • Updated CV
    • Current salary proof
    • Passport-size photograph

    Job Summary

    Company Concord Biotech Limited
    Vacancies Assistant Manager / Sr. Executive / Executive – Production; Supervisor / Officer – Production; Granulation / Coating / Capsule Operator – Production; HPLC Analyst – QC; Dissolution and Chemical Analyst – QC; QC Reviewer – QC
    Required Education M.Sc / B.Pharm / M.Pharm / B.Sc / ITI / Diploma
    Experience 2 to 10 Years, depending on the position

  • Ajanta Pharma Walk-In Interview Recruitment

    Ajanta Pharma Ltd. is conducting a Walk-In Interview for experienced professionals at its US FDA-approved OSD formulation facility.
    The openings are available across Process Mechanical Maintenance, Process Electrical Maintenance, HVAC Electrical Maintenance, OSD Manufacturing, OSD Packing and PPIC.
    Candidates with Diploma, B.E./B.Tech, B.Pharm or M.Pharm qualifications and relevant pharmaceutical manufacturing experience can apply.
    Professionals with experience in regulated plants and documentation requirements such as cGMP/ICDP will be preferred.

    Ajanta Pharma Walk-In Interview: Job Details

    Ajanta Pharma Process Maintenance: Officer / Sr. Officer

    Experience: 5 to 8 Years

    Process Mechanical Maintenance

    Qualification: Diploma / B.E. Mechanical

    Job Responsibilities:

    • OSD process equipment maintenance.
    • Mechanical breakdown maintenance of process equipment, including FBP, coating, compression and blister packing equipment.

    Process Electrical Maintenance

    Qualification: Diploma / B.E. Electrical

    Job Responsibilities:

    • OSD process equipment maintenance.
    • Electrical breakdown maintenance of process equipment.
    • Knowledge of PLC and SCADA and software breakdowns.

    HVAC Electrical Maintenance

    Qualification: Diploma / B.E. Electrical

    Job Responsibilities:

    • HVAC operation and maintenance.
    • Handle BMS systems.
    • Knowledge of humidifier and dehumidifier and electrical panels.

    Ajanta Pharma OSD Production: Executive / Sr. Executive

    Experience: 9 to 12 Years
    Qualification: B.Pharm / M.Pharm

    OSD Manufacturing Production

    Job Responsibilities:

    • Exposure to OSD manufacturing operations such as granulation, compression, coating, pellet coating and capsule filling.
    • Knowledge of PAS-X and SCADA.

    OSD Packing Production

    Job Responsibilities:

    • Experience in primary and secondary packing sections.
    • Knowledge of PAS-X, E-log, track and trace, and e-BMR.

    PPIC Production

    Job Responsibilities:

    • Working knowledge of production planning and inventory control.
    • Well-versed with Advanced Microsoft Excel and PowerPoint presentation.
    • Knowledge of Power BI and related AI tools.

    Ajanta Pharma: Eligibility & Qualifications

    Candidates with the following qualifications can apply for the relevant positions:

    Diploma Mechanical | B.E. Mechanical | Diploma Electrical | B.E. Electrical | B.Pharm | M.Pharm

    Ajanta Pharma Experience Requirements

    • Process Mechanical Maintenance: 5–8 Years
    • Process Electrical Maintenance: 5–8 Years
    • HVAC Electrical Maintenance: 5–8 Years
    • OSD Manufacturing Production: 9–12 Years
    • OSD Packing Production: 9–12 Years
    • PPIC Production: 9–12 Years

    Ajanta Pharma Walk-In Interview Details

    Ajanta Pharma Walk-In Date & Time

    Date: Friday, 2nd October 2026
    Time: 10:00 AM to 04:00 PM

    Ajanta Pharma Walk-In Venue

    Ajanta Pharma Ltd.
    Plot No. 3 & 4, Gangotri Apartment,
    Opp. Deogiri Bank, N-5, CIDCO,
    Chhatrapati Sambhajinagar – 431005.

    Work Location: Paithan, District Chhatrapati Sambhajinagar, Maharashtra.

    Ajanta Pharma: Preferred Experience

    Candidates having exposure to regulatory requirements, documentation, cGMP/ICDP and experience working in regulated plants will be preferred.

    Interested candidates who have worked in USFDA/MHRA-approved facilities may attend the interview with the required documents.

    Documents to Carry

    Candidates should carry:

    • Updated CV
    • Current CTC structure
    • 3 recent salary slips
    • Educational qualification documents
    • Previous employment documents

    How to Apply

    Interested candidates can attend the walk-in interview at the above-mentioned venue with their updated CV and relevant documents.

    Candidates who are unable to attend the interview can forward their updated CV to:

    Email: cv.ptn@ajantapharma.com

    Job Summary

    Company Ajanta Pharma Ltd.
    Vacancies Officer / Sr. Officer – Process Mechanical Maintenance, Process Electrical Maintenance & HVAC Electrical Maintenance; Executive / Sr. Executive – OSD Manufacturing, OSD Packing & PPIC
    Required Education Diploma / B.E. Mechanical / Diploma / B.E. Electrical / B.Pharm / M.Pharm
    Experience 5–8 Years for Maintenance roles; 9–12 Years for OSD Production and PPIC roles

  • Hetero Biopharma Production & Packing Recruitment

    Hetero Biopharma Limited is conducting a Walk-In Interview for Production FP and Packing positions.
    The openings are available for Jr. Operator, Operator, Sr. Operator, Officer, Executive and Jr. Executive roles.
    Candidates with ITI, Diploma, Any Graduation, B.Pharm, M.Pharm or M.Sc. qualifications can apply for the relevant positions.
    The recruitment drive covers opportunities in Production FP and Packing, with experience requirements ranging from 2 to 10 years.

    Hetero Biopharma Production & Packing: Walk-In Interview

    Hetero Biopharma Production FP: Job Openings

    Jr. Operator / Operator / Sr. Operator

    Experience: 2 to 10 Years
    Qualification: ITI / Diploma / Any Graduation

    Key Skills:

    • Vial washing
    • Depyrogenation
    • HPHV
    • Steam Sterilizer
    • Production

    Officer / Executive / Sr. Executive

    Experience: 2 to 10 Years
    Qualification: B.Pharm / M.Pharm / M.Sc.

    Key Skills:

    • Production planning
    • Filling activities
    • cGMP
    • SOP
    • DQ
    • IQ
    • PQ
    • OQ
    • Preventive maintenance
    • Lyophilizer
    • Aseptic media fills
    • HPHV
    • Handling filter integrities
    • QMS

    Hetero Biopharma Packing: Job Openings

    Operator

    Experience: 2 to 5 Years
    Qualification: ITI / Diploma / Any Graduation

    Key Skills:

    • Labelling machine operation for bottles and syringes

    Jr. Executive / Executive

    Experience: 3 to 5 Years
    Qualification: B.Pharm / M.Pharm / M.Sc.

    Key Skills:

    • Labelling machine operation
    • Printer operation
    • Supervision of packing lines
    • QMS

    Hetero Biopharma: Eligibility & Qualifications

    Candidates with the following qualifications can apply for the relevant positions:

    ITI | Diploma | Any Graduation | B.Pharm | M.Pharm | M.Sc.

    Hetero Biopharma: Experience Requirements

    • Production FP – Jr. Operator / Operator / Sr. Operator: 2–10 years
    • Production FP – Officer / Executive / Sr. Executive: 2–10 years
    • Packing – Operator: 2–5 years
    • Packing – Jr. Executive / Executive: 3–5 years

    Hetero Biopharma: Key Responsibilities

    Production FP Responsibilities

    • Handle vial washing and depyrogenation activities.
    • Operate HPHV and steam sterilizer equipment.
    • Support production activities and filling operations.
    • Follow cGMP and SOP requirements.
    • Handle DQ, IQ, PQ and OQ activities.
    • Support preventive maintenance activities.
    • Handle lyophilizer and aseptic media filling activities.
    • Perform filter integrity-related activities.
    • Maintain QMS requirements.

    Packing Responsibilities

    • Operate labelling machines for bottles and syringes.
    • Handle printer operations.
    • Supervise packing lines.
    • Follow applicable QMS requirements.

    Hetero Biopharma: Walk-In Interview Details

    Hetero Biopharma Walk-In Date & Time

    Date: 4th October 2026
    Time: 10:00 AM to 03:00 PM

    Hetero Biopharma Work Location

    Hyderabad, Jadcherla

    Hetero Biopharma Interview Location

    Hotel Neha Vilas Bhavan
    Near HP Bunk, NH5 Road, Kummarapalem,
    Visakhapatnam, Andhra Pradesh – 530046.

    How to Apply

    Interested candidates can attend the walk-in interview at the above-mentioned interview venue.

    Candidates who are interested or know someone who may be a good fit can also share the profile with:

    Email: A.Sagar@hetero.com

    Candidates should carry their updated resume and relevant documents for the interview.

    Job Summary

    Company Hetero Biopharma Limited
    Vacancies Jr. Operator / Operator / Sr. Operator; Officer / Executive / Sr. Executive; Packing Operator; Jr. Executive / Executive
    Required Education ITI / Diploma / Any Graduation / B.Pharm / M.Pharm / M.Sc.
    Experience 2–10 Years for Production FP; 2–5 Years for Packing Operator; 3–5 Years for Packing Jr. Executive / Executive

  • Torrent Pharmaceuticals Executive Bioanalytical Recruitment

    Torrent Pharmaceuticals Ltd. is conducting a walk-in interview for the position of Executive – Bioanalytical at its R&D Centre.
    The opportunity is for professionals with 3 to 8 years of experience in bioanalytical laboratory activities.
    Candidates with M.Pharm or M.Sc. qualifications and relevant experience in bioanalytical method development and validation can apply.
    The role involves bioanalytical methods, sample analysis, laboratory instruments, GDP/GLP compliance and regulatory requirements.

    Torrent Pharmaceuticals Executive – Bioanalytical: Job Details

    Torrent Pharmaceuticals Executive – Bioanalytical: Recruitment Details

    Company: Torrent Pharmaceuticals Ltd.
    Position: Executive – Bioanalytical
    Department: Bioanalytical
    Experience: 3 to 8 Years
    Qualification: M.Pharm / M.Sc.
    Job Location: R&D Centre, Gandhinagar, Gujarat

    Torrent Pharmaceuticals Executive – Bioanalytical: Eligibility & Qualifications

    Candidates with the following qualifications are eligible to apply:

    M.Pharm | M.Sc.

    Torrent Pharmaceuticals Executive – Bioanalytical: Experience

    • 3 to 8 years of relevant experience in bioanalytical laboratory activities.
    • Experience in developing and validating sensitive and rugged bioanalytical methods is required.
    • Experience in conducting sample analysis of Bioavailability/Bioequivalence studies independently with required accuracy is preferred.

    Torrent Pharmaceuticals Executive – Bioanalytical: Key Responsibilities

    Bioanalytical Method Development & Validation

    • Experience in developing and validating sensitive and rugged bioanalytical methods using different extraction techniques such as SPE and LLE.
    • Experience in quantitation using LCMS and HPLC techniques for analysis of drug substances.
    • Experience in conducting sample analysis of Bioavailability/Bioequivalence Studies independently with required accuracy.

    Laboratory Operations & Compliance

    • Experience in the operation, maintenance and calibration of laboratory instruments in accordance with written instrument operation procedures.
    • Ability to maintain GDP and GLP compliance in the laboratory.
    • Knowledge of current applicable regulatory requirements.

    Torrent Pharmaceuticals Executive – Bioanalytical: Walk-In Interview Details

    Torrent Pharmaceuticals Walk-In Date & Time

    Date: 4th October 2026, Sunday
    Time: 10:00 AM to 03:00 PM

    Important: Candidates interviewed during the last 6 months need not apply.

    Torrent Pharmaceuticals Walk-In Interview Venue

    Torrent Pharmaceuticals Ltd. R&D Centre
    Ahmedabad Airport Gandhinagar Highway,
    Besides Amul Mother Dairy & Kanoria Hospitals,
    Near Indira Bridge, Village: Bhat,
    Gandhinagar – 382428.

    How to Apply

    Interested candidates can attend the walk-in interview at the above-mentioned venue and share their updated resume through email.

    Email:
    meghamaheshwari@torrentpharma.com
    vilshashah@torrentpharma.com

    Candidates should carry their updated resume and relevant documents when attending the interview.

    Job Summary

    Company Torrent Pharmaceuticals Ltd.
    Vacancies Executive – Bioanalytical
    Required Education M.Pharm / M.Sc.
    Experience 3 to 8 Years

  • Clinical Research Associate Jobs – Biological E

    Biological E Hiring – Clinical Research Associate | Hyderabad

    Biological E is hiring a Clinical Research Associate (CRA) for its Clinical Development team in Hyderabad.
    The position is open to professionals with 4+ years of total experience, including experience as both a Clinical Research Coordinator and Clinical Research Associate/Monitor.
    Candidates with B.Pharm, M.Pharm or a Master’s degree in Life Sciences can apply.
    The role involves clinical trial site management, monitoring, regulatory compliance, investigator training and 50–60% travel.

    Clinical Research Associate – Clinical Development

    Job Details

    • Company: Biological E
    • Position: Clinical Research Associate
    • Department: Clinical Development
    • Location: Hyderabad, Jubilee Hills
    • Openings: 1
    • Experience: 4+ years total
    • Employment Type: Full-time, Permanent
    • Industry: Pharmaceutical & Life Sciences
    • Role Category: Pharmaceutical & Biotechnology

    Eligibility & Qualifications

    Educational Qualification

    • B.Pharm
    • M.Pharm
    • Master’s in Life Sciences

    Experience

    The source specifically requires:

    • 4+ years of total experience
    • Minimum 2+ years of experience as a full-time Clinical Research Coordinator
    • Minimum 2+ years of experience as a Clinical Research Associate / Monitor

    Clinical Research Associate – Key Responsibilities

    Clinical Trial Site Management

    • Act as a communication link between the Sponsor and the site.
    • Support the design of study tools, essential clinical documents and processes.
    • Perform Site Identification and conduct feasibility studies.
    • Conduct Site Selection Visits and Site Initiation Visits according to the protocol and applicable regulatory guidelines.
    • Conduct Site Monitoring Visits and Site Close-Out Visits according to the protocol and applicable regulatory guidelines.
    • Send follow-up letters to sites and submit visit reports to the Clinical Team Leader / Project Manager as required.

    Subject Recruitment & Site Coordination

    • Maintain close association with clinical trial sites for:

      • Subject recruitment
      • Subject follow-up
      • Protocol-related activities

    • Maintain accurate and timely sponsor/site correspondence and communication.
    • Update the reporting authority regarding study status.

    Investigator Training & Study Meetings

    • Prepare training materials.
    • Coordinate with study sites for the successful conduct of Investigator Meetings.
    • Train investigators on the protocol and applicable regulatory guidelines.

    Regulatory & Ethics Committee Activities

    • Provide facilitation and documentation support for Ethics Committee submissions.
    • Assist the clinical team in preparing the Regulatory Binder.
    • Ensure compliance with applicable clinical research regulatory requirements, including ICH-GCP and CDSCO guidelines.

    Clinical Documentation & Trial Master File

    • Maintain updated Site Files.
    • Collect essential documents and project-related documents during site visits.
    • Support maintenance of the Trial Master File (TMF).
    • Perform eCRF verification according to project instructions.
    • Coordinate and distribute Clinical Study Material to study sites.
    • Archive study documents appropriately.

    Required Skills

    • Strong knowledge of applicable clinical research regulatory requirements.
    • Knowledge of ICH-GCP and CDSCO guidelines.
    • Strong clinical research and site monitoring skills.
    • Proficiency in:

      • Microsoft Word
      • Microsoft Excel
      • Microsoft PowerPoint

    • Strong written and verbal communication skills.
    • Good command of the English language.
    • Strong organizational and problem-solving skills.
    • Effective time management skills.
    • Willingness to travel extensively.

    Travel Requirement

    The position involves approximately 50–60% travel.

    Eligible Qualification Courses

    B.Pharm | M.Pharm | Master’s in Life Sciences

    Location & Work Details

    Location: Jubilee Hills, Hyderabad
    Department: Clinical Development
    Employment: Full-time, Permanent
    Openings: 1
    Experience: 4+ Years
    Travel: 50–60%

    How to Apply

    Interested and eligible candidates can apply through the job posting.

    Apply for Clinical Research Associate – Biological E

    Job Summary

    Category Details
    Company Biological E
    Vacancies Clinical Research Associate – 1
    Required Education B.Pharm, M.Pharm, Master’s in Life Sciences
    Experience 4+ years total, including 2+ years as Clinical Research Coordinator and 2+ years as Clinical Research Associate/Monitor

  • iCliniq Hiring – Squad Lead | Non-Clinical Role

    iCliniq Hiring – Squad Lead | Non-Clinical Role | Remote

    iCliniq is hiring a Squad Lead for a non-clinical role with the opportunity to lead a team of doctors and manage non-clinical operations remotely. The role is suitable for healthcare professionals looking to build a career beyond clinical practice through team leadership, execution management, workflow coordination and healthcare technology.

    Squad Lead – Non-Clinical Operations

    Job Responsibilities

    • Lead and manage a team of doctors.
    • Own end-to-end execution and outcomes.
    • Coordinate with cross-functional teams.
    • Ensure smooth workflows and effective team performance.
    • Drive problem-solving and decision-making.
    • Manage non-clinical operations and support the team in achieving assigned outcomes.

    Eligibility & Qualifications

    Educational Qualification

    Candidates with the following qualifications can apply:

    • MBBS
    • BDS
    • BPT
    • BHMS
    • BAMS
    • BUMS
    • B.Sc. Nursing
    • Pharm.D
    • B.Pharm

    Experience

    • 2–3 years of non-clinical experience

    Required Skills

    • Strong communication skills
    • People-management skills
    • Ownership and accountability
    • Problem-solving mindset
    • Good computer skills
    • Basic AI awareness
    • Ability to lead teams and coordinate with cross-functional stakeholders

    Good to Have

    • Medical certifications
    • Management certifications
    • Technology certifications
    • Exposure to digital or technical tools

    Location & Work Mode

    Role: Squad Lead – Non-Clinical Operations
    Work Mode: Remote
    Experience: 2–3 Years of non-clinical experience

    How to Apply

    Interested candidates can share their updated resume at:

    Email: hr@icliniq.com

    For More Details: +91 9677711482

    Eligible Qualification Courses

    MBBS | BDS | BPT | BHMS | BAMS | BUMS | B.Sc. Nursing | Pharm.D | B.Pharm

    Job Summary

    Category Details
    Company iCliniq
    Vacancies Squad Lead – Non-Clinical Operations
    Required Education MBBS, BDS, BPT, BHMS, BAMS, BUMS, B.Sc. Nursing, Pharm.D, B.Pharm
    Experience 2–3 years of non-clinical experience