Category: Featured

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

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

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

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

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

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

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

Brooks Steriscience Ltd. is conducting a Walk-In Recruitment Drive for experienced professionals across Quality Assurance, Production, Quality Control and API operations.
The company is looking for candidates with relevant experience in API and pharmaceutical formulation manufacturing.
Openings are available across operator, officer, executive, senior executive and management-level positions, depending on the department.
The walk-in interview is scheduled for 27 September 2026, from 10:00 AM to 06:00 PM, at Vapi, Gujarat.

Brooks Steriscience – Quality Assurance Department

Brooks Steriscience – QMS Executive / Sr. Executive

Qualification: M.Pharm. / B.Pharm. / M.Sc.
Experience: 5–8 Years

Brooks Steriscience – QMS Responsibilities

• Risk assessment
• Deviation handling
• Change control
• Market complaints
• Audits

Brooks Steriscience – Validation Officer / Sr. Officer

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

Brooks Steriscience – Validation Responsibilities

• Equipment qualification
• DQ, IQ, OQ and PQ
• Protocol preparation
• Execution
• Compilation
• Report preparation

Brooks Steriscience – Lab QA Chemical Officer / Sr. Officer

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

Brooks Steriscience – Lab QA Chemical Responsibilities

• Knowledge of instruments and chemicals
• GLP activities

Brooks Steriscience – Lab QA Micro Officer / Sr. Officer

Qualification: B.Sc. Microbiology / M.Sc. Microbiology / M.Sc. Biotechnology
Experience: 2–5 Years

Brooks Steriscience – Lab QA Micro Responsibilities

• Knowledge of MLT
• BET
• Sterility-related activities

Brooks Steriscience – IPQA Officer / Executive / Sr. Executive

Qualification: M.Pharm. / B.Pharm. / M.Sc.
Experience: 2–8 Years

Brooks Steriscience – IPQA Responsibilities

• Line clearance activities
• Sampling activities
• Aseptic practices

Brooks Steriscience – Production Department

Brooks Steriscience – Aseptic Area Operator

Qualification: ITI / Diploma / B.Sc. / D.Pharm.
Experience: 3–6 Years

Brooks Steriscience – Aseptic Area Responsibilities

• Aseptic liquid filling
• Lyophilization filling machine operation
• Equipment troubleshooting

Brooks Steriscience – Lyophilizer Machine Operator

Qualification: ITI / Diploma / B.Sc. / D.Pharm.
Experience: 2–5 Years

Brooks Steriscience – Lyophilizer Responsibilities

• Lyophilizer machine operation
• Troubleshooting

Brooks Steriscience – Production Area Supervisor

Qualification: B.Pharm. / M.Sc.
Experience: 5–7 Years

Brooks Steriscience – Production Responsibilities

• Injectables manufacturing exposure
• Aseptic area operations
• Regulatory exposure

Brooks Steriscience – Visual Inspector

Qualification: ITI / Diploma
Experience: 1–3 Years

Brooks Steriscience – Visual Inspection Responsibilities

• Injectable product visual inspection
• Dry powder product visual inspection
• Lyophilized product visual inspection

Brooks Steriscience – Packing Supervisor

Qualification: D.Pharm. / B.Pharm. / B.Sc. / M.Sc.
Experience: 5–8 Years

Brooks Steriscience – Packing Responsibilities

• Packing supervision

Brooks Steriscience – QMS Supervisor / Officer / Sr. Officer / Executive

Qualification: B.Pharm. / M.Pharm. / B.Sc. / M.Sc.
Experience: 3–8 Years

Brooks Steriscience – QMS Responsibilities

• QMS exposure
• EDMS operations
• TrackWise operations

Brooks Steriscience – API Production Department

Brooks Steriscience – AGM / DGM – Sterile & Non-Sterile API

Qualification: B.Sc. / M.Sc.
Experience: 15–20 Years

Brooks Steriscience – API Manufacturing Responsibilities

• Lead and manage API manufacturing operations.
• Ensure production targets are achieved.
• Maintain product quality and regulatory compliance.
• Ensure safety standards.
• Support cost optimization and continuous improvement.
• Work in accordance with cGMP requirements.

Brooks Steriscience – Executive / Sr. Executive – Sterile / Non-Sterile Shift Incharge

Qualification: B.Sc. / M.Sc. Chemistry / B.E. / B.Tech.
Experience: 8–12 Years

Brooks Steriscience – API Shift Incharge Responsibilities

• Handling of autoclave
• DHS machine
• ANFD
• Co-mill
• Sterile batch mixture
• Filter integrity machine
• NVPC machine
• Knowledge of sterile processes
• Media fill
• SAP

Brooks Steriscience – Officer / Sr. Officer – Sterile Filling & Crystallization

Qualification: B.Sc. / M.Sc. Chemistry / B.E. / B.Tech.
Experience: 2–5 Years

Brooks Steriscience – Sterile Filling Responsibilities

• Handling of autoclave
• DHS machine
• ANFD
• Co-mill
• Sterile batch mixture
• Filter integrity machine
• NVPC machine
• Knowledge of sterile processes
• Media fill
• SAP

Brooks Steriscience – Officer / Sr. Officer – Non-Sterile Crystallization

Qualification: B.Sc. / M.Sc. Chemistry / B.E. / B.Tech.
Experience: 2–5 Years

Brooks Steriscience – Non-Sterile Crystallization Responsibilities

• Validation and qualification activities
• Hydrogenation reaction
• Handling different equipment
• Sparkler filter
• Centrifuge
• VTD
• FBD

Brooks Steriscience – Officer / Sr. Officer – Documentation

Qualification: B.Sc. / M.Sc. Chemistry / B.E. / B.Tech.
Experience: 4–7 Years

Brooks Steriscience – Documentation Responsibilities

• QMS exposure
• Change control
• CAPA

Brooks Steriscience – API Quality Assurance

Brooks Steriscience – IPQA Officer / Sr. Officer / Executive

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

Brooks Steriscience – API IPQA Responsibilities

• Monitor compliance with approved BMR and BPR.
• Perform line clearance.
• Conduct area verification.

Eligibility & Qualifications

Brooks Steriscience – Quality Assurance

M.Pharm. | B.Pharm. | M.Sc. | B.Sc. Microbiology | M.Sc. Microbiology | M.Sc. Biotechnology

Brooks Steriscience – Production

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

Brooks Steriscience – API Production

B.Sc. | M.Sc. Chemistry | B.E. | B.Tech.

The recruitment poster also states that graduates and postgraduates in Pharmacy, Microbiology, Biotechnology, Chemistry and Analytical Chemistry can share their updated CV.

Brooks Steriscience – Experience Requirements

Department-wise Experience

Quality Assurance: 2–8 Years depending on the position
Formulation Production: 1–8 Years depending on the position
API Production: 2–20 Years depending on the position

Brooks Steriscience – Employee Benefits

Benefits Offered

• Free AC bus transportation from Vadodara
• Highly subsidized canteen facility
• Health insurance for employee family
• Accidental insurance
• Term life insurance

Job Location

Brooks Steriscience Ltd.

Block No. 61/62, Manglej Village,
Nareshwar Road, Karjan Taluka,
Vadodara, Gujarat – 391243, India

The recruitment material identifies the company facility at the above address and the walk-in venue separately.

Walk-In Interview Details

Brooks Steriscience – Walk-In Recruitment Drive

Date: 27th September 2026
Time: 10:00 AM – 06:00 PM

Interview Venue

Fortune Park Galaxy
NH 48, GIDC
Vapi – 396195, Gujarat

How to Apply

Interested candidates can share their updated CV with the recruitment team at:

Email: preeti.yadav@brookssteriscience.com

Contact: 8155009405

Candidates with relevant API and formulation experience are encouraged to apply.

Job Summary

Analyst – Biomonitoring PMOps | Merck

Merck is hiring an Analyst – Biomonitoring PMOps in Bangalore, Karnataka for its Biomonitoring business. The role supports Product Life Cycle Management (PLCM), New Product Introduction (NPDI), master data management, SAP operations, web data maintenance, and portfolio review activities. Candidates with a Postgraduate degree in Life Sciences, particularly Biochemistry, Biotechnology, or Microbiology, and 1–3 years of experience in the scientific industry can apply. The position involves working with cross-functional teams and maintaining quality, productivity, and stakeholder requirements.

Job Details

Position

Analyst – Biomonitoring PMOps

Company

Merck

Job ID

302960

Department / Business

Biomonitoring Business

Location

Bangalore, Karnataka, India

Employment Type

Full Time

Experience

1–3 Years

About the Role

The Analyst will support Product Managers, Marketing Managers, and Project Managers in executing activities related to Product Life Cycle Management and New Product Introduction for the Biomonitoring business.

The role involves collaboration with cross-functional teams and operational organizations using SAP, web data maintenance tools, and other business systems.

Product Life Cycle Management & NPDI

• Support Product Managers, Marketing Managers, and Project Managers with PLCM and NPDI activities.
• Act as a primary interface with operational organizations including Manufacturing, Purchasing, Technical Service, QA, and other relevant teams.
• Support Product Life Cycle Management and New Product Introduction activities through SAP and web data maintenance.
• Review NPDI completeness.
• Review master data for completeness and correctness.
• Support relevant steps of product life cycle management and portfolio review activities.
• Meet SLA and TAT requirements according to agreed guidelines with stakeholders.

Master Data Management

• Support master data management activities.
• Perform data reviews.
• Support data cleansing and data enrichment.
• Conduct data consistency checks.
• Review web data compilation and perform data cleansing.
• Troubleshoot Web PDP data issues.
• Extract data reports using ERP/SAP systems.

Product Documentation & Web Data

• Upload product documents on the web whenever required.
• Review and maintain:

  • Technical bulletins
  • Product information sheets
  • Certificate of Analysis
  • Certificate of Origin

• Create product listings on the website.
• Ensure internal and external customer requirements are met within agreed timelines.

Business Operations & Quality

• Demonstrate good process knowledge across assigned activities.
• Maintain defined standards for quality and productivity.
• Assist the Team Lead with ISO and other additional activities.
• Support stakeholder requirements and operational activities.
• Initiate process improvement projects and ideas.

Eligibility & Qualifications

Educational Qualification

Candidates should have a Postgraduate degree in Life Sciences from a reputed university, particularly in:

• Biochemistry
• Biotechnology
• Microbiology

Eligible Qualification Courses

M.Sc. Biochemistry | M.Sc. Biotechnology | M.Sc. Microbiology | M.Sc. Life Sciences | M.Pharm | Other Relevant Life Science Postgraduate Courses

Experience

• 1–3 Years of experience in the Scientific Industry.

Technical Skills

• In-depth scientific knowledge and functional proficiency in Life Sciences.
• Understanding of Business Operations roles and responsibilities.
• Proficiency with internet and email.
• Strong knowledge of Office 365, including:

  • Excel
  • Teams
  • Outlook
  • SharePoint

• Ability to set up complex database queries.
• Ability to navigate different SAP T-codes in PRD, PRE, and MDGM.
• ERP/SAP user knowledge for data extraction and reporting.
• Ability to initiate change records and support Controlled Document Management using TrackWise/Mango.
• Basic knowledge of Palantir.

Key Competencies

• Strong attention to detail.
• Good process and scientific understanding.
• Ability to manage multiple tasks and meet deadlines.
• Effective communication with internal and external stakeholders.
• Ability to work collaboratively with cross-functional teams.
• Customer-focused approach.
• Quality and productivity orientation.
• Problem-solving and process improvement mindset.
• Ability to work with business systems and data-management tools.

How to Apply

Interested and eligible candidates can apply for the Analyst – Biomonitoring PMOps position through the official Merck careers portal.

Apply for Analyst – Biomonitoring PMOps

Job ID: 302960

Location: Bangalore, Karnataka, India

Job Summary

Biodeal Pharmaceuticals Limited is hiring B.Pharm freshers for its PMT – Store Management Department.
The openings are for Officer / Junior Officer positions for candidates with no prior experience.
Immediate joiners are preferred, making this an entry-level opportunity for B.Pharm graduates.
Interested candidates can share their resume directly with the recruitment team for consideration.

Biodeal Pharmaceuticals – PMT Store Management Department

Officer / Junior Officer

Department: PMT – Store Management
Qualification: B.Pharm
Experience: Fresher
Joining: Immediate

Biodeal Pharmaceuticals – Eligibility & Qualifications

B.Pharm Freshers

B.Pharm

The source specifically states that B.Pharm freshers are eligible for the position.

Experience Requirements

Biodeal Pharmaceuticals – Officer / Junior Officer

Fresher

No prior work experience is mentioned for this opening.

Biodeal Pharmaceuticals – Joining Requirement

Immediate Joining

Candidates who can join at the earliest are encouraged to apply.

How to Apply

Interested candidates can share their updated resume at:

Email: hr4@biodealpharma.com

Candidates should mention the relevant position while sending their resume.

Job Summary