Category: Featured

Windlas Biotech Limited is hiring freshers for Apprentice positions across multiple business functions.
The openings are available in Supply Chain, Business Development, Warehouse, and Customer Relationship Management departments.
Candidates with Any Graduate or Post Graduate qualification and no prior experience can apply.
The position is based in Dehradun, and interested candidates can share their updated CV with the recruitment team.

Windlas Biotech – Apprentice Recruitment

Windlas Biotech – Apprentice

Position: Apprentice
Qualification: Any Graduate / Post Graduate
Experience: Freshers
Location: Dehradun

Windlas Biotech – Departments

Windlas Biotech – Supply Chain Department

Apprentice opportunities are available in the Supply Chain function.

Windlas Biotech – Business Development Department

Apprentice opportunities are available in the Business Development function.

Windlas Biotech – Warehouse Department

Apprentice opportunities are available in the Warehouse function.

Windlas Biotech – Customer Relationship Management Department

Apprentice opportunities are available in the Customer Relationship Management function.

Eligibility & Qualifications

Windlas Biotech – Educational Qualification

Any Graduate | Post Graduate

Windlas Biotech – Experience

Freshers

The recruitment poster specifically lists Freshers as the required experience level.

Windlas Biotech – Job Location

Windlas Biotech Limited

Dehradun, Uttarakhand

How to Apply

Interested candidates can share their updated CV at:

Email: hr@windlasbiotech.com

After sharing the resume, candidates can contact:

Ms. Aarti
Phone: +91 9149082350

Job Summary

Morepen Proprietary Drug Research is hiring for the position of Jr. Medicinal Chemist in its research team.
The role requires an M.Sc. in Medicinal or Organic Chemistry with 2–4 years of pharmaceutical experience.
The position involves designing and optimizing synthesis routes, chemical synthesis, purification, and compound analysis.
Candidates will work on drug development projects involving analytical techniques such as NMR, HPLC, and MS.

Morepen Proprietary Drug Research – Medicinal Chemistry Department

Morepen PDR – Jr. Medicinal Chemist

Position: Jr. Medicinal Chemist
Qualification: M.Sc. in Medicinal / Organic Chemistry
Experience: 2–4 Years of Pharma Experience
Location: Medchal-Malkajgiri, Telangana

Morepen PDR – Job Responsibilities

Morepen PDR – Chemical Synthesis & Drug Research

• Design and optimize synthesis routes (RoS).
• Perform chemical synthesis and purification.
• Analyze compounds using NMR, HPLC, and MS.
• Support drug development projects.

Morepen PDR – Eligibility & Qualifications

Morepen PDR – Educational Qualification

M.Sc. in Medicinal Chemistry | M.Sc. in Organic Chemistry

Morepen PDR – Experience

2–4 Years of pharmaceutical experience

Candidates should have relevant experience in pharmaceutical research and medicinal chemistry activities.

Morepen PDR – Key Skills

Medicinal Chemistry & Analytical Skills

Relevant experience or knowledge in the following areas is applicable to the role:

• Chemical synthesis
• Synthesis route design and optimization
• Purification
• Compound analysis
• NMR
• HPLC
• Mass Spectrometry
• Drug development support

Morepen PDR – Job Location

Morepen Proprietary Drug Research

Gagillapur X Junction, Gaddapotharam Road,
Medchal-Malkajgiri District, Telangana – 500043

How to Apply

Interested candidates can share their updated resume with:

Email: jobs@morepenpdr.com
Contact: +91 6302 451 459

Candidates can also visit the company’s website mentioned in the recruitment poster:

www.morepenpdr.com

Job Summary

Ipca Laboratories Limited is hiring experienced professionals for Drug Substance Manufacturing at its Bio-Manufacturing, Sec 3 facility in Pithampur, Dhar.
The openings are for Executive / Senior Executive roles in Upstream Processing and Downstream Processing.
Candidates should have 5–9 years of relevant experience in biotech, biosimilar, or injectable manufacturing.
The role requires exposure to QMS activities, process operations, and regulatory requirements such as USFDA/EU.

Ipca Laboratories – Drug Substance Manufacturing

Ipca Laboratories – Executive / Senior Executive

Department: Drug Substance Manufacturing
Position: Executive / Senior Executive
Experience: 5–9 Years
Qualification: M.Sc. / M.Tech. / B.Tech. in Biotechnology & Biochemistry

Ipca Laboratories – Downstream Processing

Ipca Laboratories – Executive / Senior Executive – Downstream Processing

Experience: 5–9 Years
Qualification: M.Sc. / M.Tech. / B.Tech. in Biotechnology & Biochemistry

Ipca Laboratories – Downstream Processing Requirements

• Downstream processing
• TFF system
• Buffer preparation
• Handling QMS elements such as:

  • Change Control
  • Deviation
  • CAPA
  • OOS
  • OOT for downstream processes

Ipca Laboratories – Executive / Senior Executive – Downstream Processing

Experience: 5–9 Years
Qualification: M.Sc. / M.Tech. / B.Tech. in Biotechnology & Biochemistry

Ipca Laboratories – Downstream Processing Skills

• Downstream processing
• Resolute Column packing
• Chromatography systems (ILC)
• TFF system
• Buffer preparation
• Mammalian cell culture

Ipca Laboratories – Upstream Processing

Ipca Laboratories – Executive / Senior Executive – Upstream Processing

Experience: 5–9 Years
Qualification: M.Sc. / M.Tech. / B.Tech. in Biotechnology & Biochemistry

Ipca Laboratories – Upstream Processing Requirements

• Upstream processing
• Vial revival
• Seed propagation
• Media & Seed preparation
• Bioreactors operation
• Handling QMS elements such as:

  • Change Control
  • Deviation
  • CAPA
  • OOS
  • OOT for upstream processes

Ipca Laboratories – Executive / Senior Executive – Upstream Processing

Experience: 5–9 Years
Qualification: M.Sc. / M.Tech. / B.Tech. in Biotechnology & Biochemistry

Ipca Laboratories – Upstream Processing Skills

• Upstream processing
• Vial revival
• Seed propagation
• Media & Feed preparation
• Bioreactors operation
• Clarification process

Eligibility & Qualifications

Ipca Laboratories – Drug Substance Manufacturing

M.Sc. | M.Tech. | B.Tech. in Biotechnology & Biochemistry

Candidates should have relevant experience in Biotech / Biosimilar / Injectable manufacturing plants.

Experience Requirements

Ipca Laboratories – Drug Substance Manufacturing

5–9 Years

The recruitment specifically seeks experienced professionals with exposure to Biotech, Biosimilar or Injectable manufacturing.

Ipca Laboratories – Regulatory Exposure

Drug Substance Manufacturing

Candidates should have experience in manufacturing environments with regulatory exposure such as:

USFDA | EU

Ipca Laboratories – Important Requirement

Relevant Manufacturing Experience

Only candidates with Biotech / Biosimilar manufacturing experience will be considered.

Job Location

Ipca Laboratories – Bio-Manufacturing Unit

Ipca Laboratories Limited
Bio-Manufacturing, Sec 3
Pithampur, Dhar, Madhya Pradesh

How to Apply

Interested candidates can share their updated resume at:

Email: geetanjali.sahu@ipca.com
Email: sneha.ankolnerkar@ipca.com

Candidates should mention the relevant Drug Substance Manufacturing / Upstream / Downstream position while applying.

Recruitment Notice

Ipca Laboratories – Recruitment Process

The recruitment notice states that Ipca does not request any payment for employment and has not authorized any agency or individual to collect fees or charges for recruitment.

Job Summary

BioMatrix Healthcare is conducting a Virtual Interview for Quality Control (QC) professionals.
The opening is for Sr. Officer to Executive positions with 4–6 years of experience in Quality Control.
Candidates with B.Sc. or M.Sc. qualifications can apply for the role.
The virtual interviews are scheduled for 25th and 26th September 2026, from 01:00 PM to 04:00 PM.

BioMatrix Healthcare – Quality Control Department

BioMatrix Healthcare – Sr. Officer to Executive

Department: Quality Control
Designation: Sr. Officer to Executive
Experience: 4–6 Years
Qualification: B.Sc. / M.Sc.

BioMatrix Healthcare – QC Job Description

BioMatrix Healthcare – Analytical Testing

The role includes:

• Performing analytical testing of raw materials, in-process samples, finished products, and stability samples.
• Operating analytical instruments such as HPLC and GC.
• Working on Drug Substance and Drug Product AMV activities.
• Ensuring compliance with GMP, GLP, and regulatory requirements.

Eligibility & Qualifications

BioMatrix Healthcare – Quality Control

B.Sc. | M.Sc.

The recruitment poster specifically lists B.Sc. and M.Sc. as the required qualifications.

Experience Requirements

BioMatrix Healthcare – QC

4–6 Years

The opening is intended for candidates with relevant Quality Control experience.

BioMatrix Healthcare – Company Profile

BioMatrix Healthcare

The recruitment material describes BioMatrix as a manufacturer and exporter of Oral Solids, Liquids, and Dry Syrup, supported by EU-GMP, Health Canada and WHO-GMP standards and R&D capabilities.

BioMatrix Healthcare – Virtual Interview Process

Interview Stages

The recruitment poster lists the following process:

1. Share Your CV
2. HR Screening
3. Virtual Interview
4. Technical Discussion
5. HR Discussion & Next Steps

Virtual Interview Requirements

BioMatrix Healthcare – Candidate Requirements

Candidates should arrange:

• Laptop, desktop, or smartphone with camera and microphone
• Stable internet connection
• Quiet and well-lit place
• Updated CV ready
• Relevant documents, if required
• Professional dress
• Join 5–10 minutes early
• Keep phone on silent mode

Walk-In / Virtual Interview Details

BioMatrix Healthcare – Virtual Interview

Dates: 25th & 26th September 2026
Time: 01:00 PM – 04:00 PM

Job Location

BioMatrix Healthcare

Survey No. 624, Sarkhej-Bavla Highway,
Vill. Rajoda, Ahmedabad, Gujarat

How to Apply

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

career@biomatrixhealthcare.com
hr@biomatrixhealthcare.com

Contact: 6357410551 / 6358970525
WhatsApp: 9725901031 / 9228893058

Website: www.biomatrixhealthcare.com

Job Summary

Arne Lifesciences Limited is hiring immediate joiners for multiple functions across its API bulk drug operations.
The openings cover Production, Engineering/Maintenance, Quality Control, Quality Assurance, PD Lab, and Corporate Quality Assurance roles.
Experience requirements range from 1 to 14 years, depending on the department and level.
The recruitment drive is being conducted from 19th to 27th September 2026, with work locations listed across the company’s Telangana facilities.

Arne Lifesciences – Production Department

Arne Lifesciences – Chemists & Senior Chemists

Experience: 2–5 Years
Area: API Bulk Drug

Arne Lifesciences – Production Requirements

• Pressure Reactor Handling
• Clean Rooms
• Documentation
• Packing

Arne Lifesciences – Engineering / Maintenance Department

Arne Lifesciences – Engineering & Maintenance

Experience: 2–5 Years

Arne Lifesciences – Engineering Requirements

• Documentation
• AHU
• RO Water System

Arne Lifesciences – Quality Control Department

Arne Lifesciences – Quality Control

Experience: 2–5 Years

Arne Lifesciences – QC Areas

• Microbiology
• Instrumentation

Arne Lifesciences – Quality Assurance Department

Arne Lifesciences – Quality Assurance

Experience: 2–5 Years

Arne Lifesciences – QA Area

• IPQA

Arne Lifesciences – PD Lab Department

Arne Lifesciences – PD Lab

Experience: 1–2 Years

The recruitment poster lists PD Lab as an opening area but does not provide a detailed role description.

Arne Lifesciences – Corporate Quality Assurance Department

Arne Lifesciences – Assistant Manager / Deputy Manager

Experience: 8–14 Years

Arne Lifesciences – Corporate QA Requirements

• Knowledge of Instrumentation
• Knowledge of LIMS

Arne Lifesciences – Quality Control Department

Arne Lifesciences – Quality Control Senior Roles

Experience: 5–8 Years

Arne Lifesciences – QC Requirements

• QMS
• Documentation
• LIMS
• Method Validations
• HPLC
• GC
• Raw Materials
• In-process Testing
• Wet Analysis
• Volumetric Analysis

Arne Lifesciences – Quality Assurance Department

Arne Lifesciences – Quality Assurance Senior Roles

Experience: 3–8 Years

Arne Lifesciences – QA Requirements

• QMS Activities
• IPQA
• AQA
• QMS and Maintenance Activities
• Batch Release

The poster also mentions Assistant Manager and Deputy Manager roles with experience in QMS, maintenance activities, and batch release.

Eligibility & Qualifications

Arne Lifesciences – Educational Qualification

The supplied recruitment poster does not mention specific educational qualifications for the listed positions.

Because the poster is focused on experience requirements and functional expertise, candidates should confirm the qualification criteria with the recruitment team before applying.

Experience Requirements

Arne Lifesciences – Department-wise Experience

Production: 2–5 Years
Engineering / Maintenance: 2–5 Years
Quality Control: 2–5 Years
Quality Assurance: 2–5 Years
PD Lab: 1–2 Years
Corporate Quality Assurance: 8–14 Years
Quality Control – Senior Roles: 5–8 Years
Quality Assurance – Senior Roles: 3–8 Years

Arne Lifesciences – Immediate Joiners

Immediate Joining Opportunity

The recruitment poster specifically highlights Immediate Joiners.

Arne Lifesciences – Walk-In Recruitment

Walk-In Dates

19th to 27th September 2026

Work Location for QC & QA Departments

Arne Lifesciences (Unit-2) Pvt. Ltd.
Sy. No. 412/A, Veliminedu Village,
Chityal (M), Nalgonda (D),
Telangana – 508114

Contact: 7674889921
Email: humanresources.u2@arenelife.com

Arne Lifesciences – Work Location & Venue

Arne Lifesciences Pvt. Ltd.

Sy. No. 48–50, 209–211, IDA II,
Pashamylaram Village, Patancheru (M),
Sangareddy (D), Telangana – 502307

Contact: +91 7674888964
Email: humanresources@arenelife.com

How to Apply

Interested candidates can share their updated CV with the Arne Lifesciences recruitment team.

Candidates should use the contact corresponding to the relevant work location or department mentioned in the recruitment advertisement.

Job Summary

Emcure Pharmaceuticals is hiring professionals for Quality Control – Microbiology roles at its Injectable Manufacturing Unit in Sanand, Ahmedabad.
The available designations include Officer, Executive and Assistant Manager positions.
Candidates with 2–10 years of experience are invited to apply, with relevant experience in an injectable plant specifically requested.
The recruitment artwork asks interested candidates to share their current organization, designation, CTC, experience details and updated CV.

Emcure Pharmaceuticals – Quality Control Microbiology Department

Emcure Pharmaceuticals – Officer / Executive / Assistant Manager

Department: Quality Control – Microbiology
Positions: Officer / Executive / Assistant Manager
Experience: 2–10 Years
Job Location: Sanand, Ahmedabad
Industry Area: Injectable Manufacturing

Emcure Pharmaceuticals – Experience Requirements

QC Microbiology – Injectable Manufacturing

2–10 Years

The recruitment artwork specifically asks candidates to provide their experience in an injectable plant, including the number of years.

Emcure Pharmaceuticals – Eligibility & Qualifications

Educational Qualification

The supplied recruitment artwork does not specify an educational qualification for the QC Microbiology positions.

Candidates should refer to the recruitment team for the applicable qualification requirements before applying.

Emcure Pharmaceuticals – Candidate Details Required

Information to Share

Interested candidates are asked to provide:

• Current Organization
• Current Designation
• Current CTC
• Expected CTC
• Total Experience
• Experience in Injectable Plant, including number of years
• Preferred Date & Time for Interview, within the next three working days
• Updated CV attached with the response

Emcure Pharmaceuticals – Candidate Preference

Recruitment Note

The recruitment artwork states: “Only Male Candidates Preferred.”

Job Location

Emcure Pharmaceuticals – Injectable Manufacturing Unit

Sanand, Ahmedabad, Gujarat

How to Apply

Interested candidates can share the requested details and updated CV through:

Email: dhruvi.rana@emcure.com
WhatsApp: 7383556373

Candidates should include their current organization, designation, current CTC, expected CTC, total experience, injectable plant experience and preferred interview date/time while applying.

Job Summary

Associate Analyst – CPC Certified Fresher | R1 RCM

R1 RCM is conducting a Walk-In Drive for Associate Analyst – CPC Certified Fresher in Chennai. The opportunity is aimed at graduates from Health Science and Paramedical backgrounds with knowledge of CPT coding and fundamental clinical concepts. Candidates who graduated from 2024 onwards with CPC or CCS certification can apply. The role is an entry-level opportunity for candidates interested in healthcare revenue cycle management and medical coding.

Walk-In Interview Details

Company

R1 RCM

Position

Associate Analyst – CPC Certified Fresher

Location

Chennai, Tamil Nadu

Experience

Entry-Level / Freshers

Graduation

2024 onwards

Walk-In Date

19 September 2026

Interview Time

10:00 AM to 12:00 PM

Work Location

Chennai

Employment Type

Full Time

Eligibility & Qualifications

Educational Qualification

Candidates should be from a Health Science or Paramedical background, including:

• BAMS
• BHMS
• BPT
• B.Pharm
• M.Pharm
• Nursing
• Life Sciences
• Other relevant healthcare or paramedical disciplines

Candidates who graduated from 2024 onwards with strong academic credentials are eligible.

Eligible Qualification Courses

BAMS | BHMS | BPT | B.Pharm | M.Pharm | Nursing | Life Sciences | Other Healthcare-Related Courses

Mandatory Certification

Candidates should hold a valid:

• CPC – Certified Professional Coder
• CCS – Certified Coding Specialist

CPC / CCS certification is mandatory.

Candidates should carry their CPC/CCS Membership ID to the walk-in interview.

Medical Coding Knowledge

Candidates should have sound knowledge of:

• CPT Coding
• ICD
• CPT
• HCPCS
• Fundamental clinical concepts
• Medical terminology
• Healthcare coding principles

Strong clinical knowledge in the following areas will be preferred:

• Pathophysiology
• Pharmacology
• Surgical Anatomy

Key Skills

• Medical Coding
• CPT Coding
• ICD Coding
• HCPCS Coding
• Clinical Knowledge
• Medical Terminology
• Analytical Skills
• Communication Skills
• Healthcare Revenue Cycle Management
• Attention to Detail

Walk-In Interview

Date & Time

19 September 2026
10:00 AM to 12:00 PM

Walk-In Venue

R1 RCM
B801, 8th Floor, Commerzone IT Park
Mount Poonamallee Road
Porur, Chennai – 600116

Documents Required

Candidates attending the walk-in interview should carry:

• CPC/CCS Membership ID
• Physical copy of Resume
• Aadhaar Card

Important Note

The HR contact numbers are reserved for WhatsApp inquiries only.

HR Contacts

Thushara
Phone: 9840681675
Email: traju4@r1rcm.com

Sudharsan
Phone: 8248546973
Email: slnu349@r1rcm.com

How to Apply

Eligible CPC/CCS certified freshers can attend the R1 RCM walk-in interview on 19 September 2026, between 10:00 AM and 12:00 PM, at the Chennai venue.

Candidates should carry their CPC/CCS Membership ID, physical resume, and Aadhaar Card.

Job Summary

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

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

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