Category: Featured

Quality and Compliance Assistant | Labcorp

Labcorp is hiring a Quality and Compliance Assistant for its Corporate Affairs team in India. The role focuses on supporting quality and compliance operations, administrative activities, metric collation, Veeva Quality Systems, and customer health check discussions. Candidates with a Master’s degree in Life Sciences and 1 year of experience can apply. The position is remote-based, with a Monday to Friday schedule from 2:00 PM to 11:00 PM.

Job Details

Position

Quality and Compliance Assistant

Company

Labcorp

Job ID

2633009

Department

Corporate Affairs

Location

Bengaluru, India

Work Mode

Remote

Employment Type

Full Time

Experience

1 Year

Work Schedule

Monday to Friday
2:00 PM – 11:00 PM

Work Arrangement

Remote Based

Quality & Compliance Responsibilities

• Perform administrative tasks as required by the Quality and Compliance group.
• Support metric collation activities as required.
• Learn to use Veeva Quality Systems.
• Assist in Customer Hallmark Health Check discussions.
• Adapt techniques to new procedures or specific requirements as directed.
• Recommend modifications to processes where appropriate.
• Learn to schedule and manage multiple assignments.
• Maintain a clean and safe work environment.
• Learn to organize the work environment effectively.
• Work under regular supervision.
• Perform other related duties as assigned.

Veeva Quality Systems

The selected candidate will receive exposure to Veeva Quality Systems and support quality-related activities under the guidance of the Quality and Compliance group.

The role also involves learning established procedures and adapting to new processes according to business requirements.

Eligibility & Qualifications

Minimum Qualification

• Master’s degree in Life Sciences
• 1 year of experience in the job discipline

Preferred Qualification

An associate-level qualification in any of the following areas or equivalent is preferred:

• Laboratory Technology
• Animal Technology
• Biological Sciences
• Pharmacy
• Medical Nursing

Eligible Qualification Courses

M.Sc. Life Sciences | M.Sc. Biotechnology | M.Sc. Microbiology | M.Sc. Biochemistry | M.Pharm | Pharm.D | B.Pharm | B.Sc. Life Sciences | B.Sc. Biological Sciences | Nursing

The official posting specifically requires a Master’s degree in Life Sciences as the minimum qualification.

Key Skills

• Good English speaking, writing, and reading skills.
• Strong time-management skills.
• Good communication skills.
• User knowledge of Microsoft Office and software applications.
• Good verbal, numerical, and visual skills.
• Strong attention to detail.
• Ability to manage multiple assignments.
• Ability to adapt to new procedures and processes.
• Ability to work under regular supervision.
• Quality and compliance orientation.

Additional Requirements

• Mandatory immunizations and screening may be required.
• Limited travel may be required for business-related purposes, including site visits.
• Overtime, weekend, and holiday work may be required depending on business needs.

How to Apply

Interested and eligible candidates can apply for the Quality and Compliance Assistant position through the official Labcorp careers portal.

Apply for Quality and Compliance Assistant – Labcorp

Job ID: 2633009

Work Mode: Remote Based

Job Summary

Scientist I – Protein Biology | Thermo Fisher Scientific

Thermo Fisher Scientific is hiring a Scientist I – Protein Biology in Bangalore, Karnataka for its Research & Development team. The role focuses on antibody validation and characterization, protein biology, cell and molecular biology, and immunoassay development. Candidates with a Master’s degree and 2–5 years of experience or a PhD in Immunology, Biochemistry, Biotechnology, or Molecular Biology can apply. The position is fully onsite and involves laboratory-based research activities.

Job Details

Position

Scientist I – Protein Biology

Company

Thermo Fisher Scientific

Job ID

R-01344458

Category

Research & Development

Team

Protein Biology

Location

Bangalore, Karnataka, India

Work Arrangement

Fully Onsite

Employment Type

Full Time

Work Schedule

Monday to Friday

Work Environment

Laboratory Setting

About the Protein Biology Team

The Protein Biology team works on large-scale functional validation of antibodies, with a focus on reagent quality and specificity.

The team’s activities include:

• Data mining and processing
• Western blotting
• Immunofluorescence imaging
• Immunohistochemistry
• Chromatin Immunoprecipitation (ChIP)
• Gene silencing
• Antibody validation and characterization

The program focuses on high-quality product validation and creating product information to support research applications.

Role & Responsibilities

The selected candidate will contribute to the antibody validation workflow and support target biology validation using innovative experimental methods.

Antibody Validation & Protein Biology

• Contribute to antibody validation and characterization activities.
• Apply knowledge of key aspects of protein biology to deliver antibody validation results.
• Understand target biology validation requirements.
• Validate antibodies for reproducibility.
• Develop and generate datasets that support product differentiation.
• Demonstrate scientific proficiency in experimental planning and execution.

Experimental Design & Laboratory Research

• Design experiments carefully to meet program goals.
• Work with cell and molecular biology experimental workflows.
• Support the design and development of protein assays.
• Maintain accurate records of experimental results in data sheets and laboratory notebooks.
• Follow defined schedules and maintain strong attention to detail.

Immunoassays & Analytical Techniques

The role involves experience with immunoassay techniques such as:

• Western Blotting
• Immunofluorescence
• Immunohistochemistry
• Flow Cytometry
• ELISA
• Co-immunoprecipitation for protein-protein interaction studies

Research Data & Literature

• Regularly review scientific literature.
• Stay updated with developments in antibody validation.
• Compile and present research data in written and oral formats.
• Participate actively in team meetings.
• Communicate research findings effectively.
• Provide technical troubleshooting to resolve scientific problems.

Eligibility & Qualifications

Educational Qualification

Candidates should have either:

• Master’s degree with 2–5 years of relevant experience, or
• PhD

in one of the following fields:

• Immunology
• Biochemistry
• Biotechnology
• Molecular Biology

Eligible Qualification Courses

M.Sc. Biotechnology | M.Sc. Biochemistry | M.Sc. Molecular Biology | M.Sc. Immunology | M.Pharm | M.Tech Biotechnology | PhD in Biotechnology | PhD in Biochemistry | PhD in Molecular Biology | PhD in Immunology

Experience

Candidates should have:

• 2–5 years of experience with a relevant Master’s degree, or
• A PhD in a relevant scientific discipline.

Experience working within a research team and a proven ability to set goals, manage work-related customer concerns, and deliver work according to program objectives will be beneficial.

Technical Skills

• Strong understanding of protein biology.
• Cell and molecular biology experimental workflows.
• Protein assay design and development.
• Protein-protein interaction studies.
• Co-immunoprecipitation.
• Immunoassay development.
• Western blotting.
• Immunofluorescence.
• Immunohistochemistry.
• Flow cytometry.
• ELISA.
• Experimental planning and execution.
• Scientific data analysis and presentation.
• Technical troubleshooting.
• Literature review and scientific research.
• Basic understanding of computational biology tools.
• Basic knowledge of databases and programming languages.

Key Competencies

• Scientific proficiency and research-oriented thinking.
• Strong experimental design skills.
• Attention to detail.
• Excellent laboratory record keeping.
• Ability to work according to schedules and timelines.
• Good verbal and written communication skills.
• Ability to present scientific data clearly.
• Technical problem-solving and troubleshooting.
• Ability to work collaboratively within a research team.
• Commitment to maintaining high-quality research standards.

How to Apply

Interested and eligible candidates can apply for the Scientist I – Protein Biology position through the official Thermo Fisher Scientific careers portal.

Apply for Scientist I – Protein Biology – Thermo Fisher Scientific

Job ID: R-01344458

Location: Bangalore, Karnataka, India

Job Summary

Associate STEM Content Analyst – Chemistry Patent Abstraction | Clarivate

Clarivate is hiring an Associate STEM Content Analyst – CPI for its Abstraction Team in IP Operations. The role focuses on chemistry patent abstraction, patent analysis, technical content creation, and editorial enhancement for Derwent products. Candidates with an M.Sc. in Chemistry or Polymer Science can apply, and freshers are preferred. The position offers a full-time hybrid work arrangement with working hours of 9:00 AM to 6:00 PM IST.

Job Details

Position

Associate STEM Content Analyst – CPI

Company

Clarivate

Department

Intellectual Property – IP Operations

Team

Abstraction Team

Job ID

JREQ136092

Location

Chennai, Tamil Nadu, India

Work Arrangement

Hybrid

Employment Type

Full Time, Permanent

Working Hours

9:00 AM – 6:00 PM IST

About the Role

The Associate STEM Content Analyst will work with Clarivate’s Abstraction Team in IP Operations, which is responsible for enriching and curating high-quality patent content for Patent Intelligence products.

The role involves analyzing patents and creating value-added technical summaries while following established abstraction policies, production targets, and quality standards.

Chemistry Patent Abstraction Responsibilities

• Prepare abstracts for patents according to the DWPI Abstracting Policy.
• Perform detailed analysis of patents to provide accurate and editorially enhanced technical information.
• Create technical summaries containing:

  • Descriptive titles
  • Uses
  • Novel features
  • Advantages
  • Other important information related to the invention

• Capture useful insights from patent data.
• Generate editorially enhanced technical summaries of patent records.
• Use Clarivate-specific tools for content editing, abstraction, and curation.
• Maintain defined quality standards and production targets.
• Contribute to the enrichment and curation of patent content for Patent Intelligence products.

Eligibility & Qualifications

Educational Qualification

Candidates should be graduates with an M.Sc. in one of the following areas:

• General Chemistry
• Organic Chemistry
• Inorganic Chemistry
• Physical Chemistry
• Analytical Chemistry
• Polymer Science

Eligible Qualification Courses

M.Sc. Chemistry | M.Sc. Organic Chemistry | M.Sc. Inorganic Chemistry | M.Sc. Physical Chemistry | M.Sc. Analytical Chemistry | M.Sc. Polymer Science

Experience

• Freshers are preferred.
• Candidates with up to 1 year of experience in content abstraction or editing can also apply.
• Strong domain knowledge in Chemistry and related technology fields is required.

Patent & Technical Skills

Candidates should have:

• Good understanding of patents.
• Strong knowledge of Chemistry and related technology domains.
• Understanding of patent drafting is beneficial.
• Ability to analyze technical patent information.
• Strong English comprehension skills.
• Ability to create clear and accurate technical summaries.

Preferred Skills

The following skills will be an added advantage:

• Typing certification.
• Extensive knowledge of patents.
• Knowledge of patent drafting.
• Strong English comprehension.
• Content abstraction experience.
• Content editing experience.

About the IP Operations Team

Clarivate’s Abstraction Team in IP Operations focuses on the enrichment and curation of high-quality content sets. The team analyzes patents and creates value-added content that enhances the research value of Patent Intelligence products for customers.

How to Apply

Interested and eligible candidates can apply for the Associate STEM Content Analyst – Chemistry Patent Abstraction position through the official Clarivate careers portal.

Apply for Associate STEM Content Analyst – Chemistry Patent Abstraction

Job ID: JREQ136092

Posted: August 7, 2026

Job Summary

Associate – External Applications | Labcorp

Labcorp is hiring an Associate – External Applications for its Yashwantpur office in Bengaluru. The role is part of the Customer Support/Call Centers function and involves supporting user access requests, application-related queries, troubleshooting, and issue resolution. Candidates with a Master’s degree in Life Sciences can apply for this opportunity. The position is office-based with rotational shifts, including night shifts.

Job Details

Position

Associate – External Applications

Company

Labcorp

Job ID

2633208

Department

Customer Support / Call Centers

Location

Bengaluru, Karnataka, India

Work Location

Yashwantpur Office

Employment Type

Full Time

Work Mode

Office Based

Remote

No

Work Schedule

The position requires working in rotational shifts:

• 9:00 AM – 6:00 PM
• 2:00 PM – 11:00 PM
• 9:00 PM – 6:00 AM

All timings are in IST.

External Applications Responsibilities

• Review User Access Request Forms received from clients and internal teams for accuracy.
• Submit User Access Requests through IT Central.
• Follow applicable departmental Standard Operating Procedures (SOPs) and Work Instructions.
• Manage day-to-day tasks while maintaining quality and productivity.
• Complete required training within specified timelines.
• Ensure timely escalation and resolution of issues.
• Act as the first point of contact for internal and external clients.
• Perform troubleshooting to resolve issues within required timelines.
• Gather, investigate, and research background materials to understand subject matters and systems.
• Ensure regulatory requirements and corporate policies are followed.
• Build and maintain relationships with internal and external user communities.
• Liaise with internal collaborators for routing and escalation when required.
• Communicate through email, phone, or virtual meetings to answer queries, provide support, and escalate issues as needed.

Eligibility & Qualifications

Minimum Qualification

• Master’s degree in Life Sciences

Eligible Qualification Courses

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

The official job posting specifically requires a Master’s degree in Life Sciences.

Preferred Qualifications

Candidates with the following knowledge or experience will be preferred:

• Applications Support
• Project Management
• Customer Service
• Local language skills in addition to English

Technical Skills

Candidates should have experience and expertise in Microsoft Office tools, including:

• Microsoft Outlook
• Microsoft Excel
• Microsoft Teams
• Microsoft PowerPoint
• Microsoft Edge
• Microsoft OneNote

Key Competencies

• Problem-solving skills.
• Ability to use available knowledge bases and understand applications, user access management, and internal processes.
• Ability to work independently.
• Strong planning and prioritization skills.
• Good organizational and communication skills.
• Strong attention to detail.
• Excellent interpersonal skills.
• Ability to work effectively with internal and external teams.
• Ability to consistently deliver high-quality work.
• Ability to manage multiple tasks under demanding conditions.
• Professional approach to customer and user support.

How to Apply

Interested and eligible candidates can apply for the Associate – External Applications position through the official Labcorp careers portal.

Apply for Associate – External Applications – Labcorp

Job ID: 2633208

Location: Bengaluru, India

Job Summary

Rubicon is looking for professionals for Officer / Senior Officer positions in the Quality Control department at its manufacturing site in Ambernath, Mumbai.
The requirement is focused on candidates with strong hands-on experience in HPLC analysis.
Experience in the Finished Products and Stability section is specifically required for the role.
Interested candidates can share their CV directly with the recruitment team for consideration.

Rubicon – Quality Control Department

Rubicon – Officer / Senior Officer

Department: Quality Control
Position: Officer / Senior Officer
Location: Ambernath, Mumbai
Work Environment: Manufacturing Site

Rubicon – HPLC Analysis Requirements

Rubicon – QC HPLC Role

Candidates should have good hands-on experience in:

• HPLC analysis
• Finished Products section
• Stability section
• Quality Control laboratory activities related to pharmaceutical manufacturing

Eligibility & Qualifications

Rubicon – Quality Control

The original hiring requirement does not specify an educational qualification.

For a pharma QC/HPLC position, the commonly relevant qualifications include:

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

Rubicon – Experience Requirements

QC – HPLC Analysis

The hiring announcement does not specify a minimum number of years of experience.

Relevant hands-on experience in HPLC analysis, particularly in the Finished Products and Stability section, is required.

Rubicon – Job Location

Manufacturing Site

Ambernath, Mumbai, Maharashtra

How to Apply

Interested candidates can share their updated CV at:

Email: divya.maru@rubicon.co.in

Candidates should highlight their HPLC, Finished Products and Stability experience in the application.

Job Summary

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