PHARMA STUFF

Job Tag: Pharma Jobs in Vadodara

  • Regulatory Affairs Officer Vacancy – Elysium Pharma

    Regulatory Affairs Officer Vacancy – Elysium Pharma Vadodara

    Apply for Regulatory Affairs Officer at Elysium Pharma Vadodara. Openings for M.Pharm/B.Pharm with 1–3 years RA experience. Apply today!

    Elysium Pharmaceutical Ltd, a rapidly growing pharmaceutical company, is hiring a Regulatory Affairs (RA) Officer at its Vadodara location. This is a valuable opportunity for pharmacy professionals with expertise in global regulatory submissions, dossier preparation, and compliance. If you are passionate about ensuring products meet international standards and want to build your career in regulatory affairs, Elysium Pharma welcomes your application.

    Company Overview

    Elysium Pharmaceutical Ltd is a trusted name in the pharmaceutical sector, dedicated to delivering high-quality, safe, and effective medicines. With a strong presence across multiple therapeutic categories, the company focuses on formulations, APIs, and innovative drug delivery systems. Elysium is committed to upholding regulatory excellence, quality compliance, and patient safety, making it a strong platform for professionals aiming to advance their careers in global regulatory affairs.

    Job Role & Responsibilities

    As a Regulatory Affairs Officer, you will be responsible for ensuring compliance with international guidelines and supporting global submissions:

    • Preparation and submission of regulatory dossiers (CTD/ACTD formats).
    • Handling queries from regulatory authorities and ensuring timely responses.
    • Coordinating with internal teams including QA, QC, R&D, and Production.
    • Supporting product registrations across multiple markets.
    • Staying up-to-date with evolving global regulatory guidelines.
    • Ensuring strong documentation and compliance practices for submissions.

    Eligibility / Qualifications

    Educational Background:

    Experience Required:

    • 1–3 years of professional experience in Regulatory Affairs.
    • Hands-on exposure in OSD (Oral Solid Dosage), Injectables, or API regulatory submissions preferred.

    Skills Required:

    • Strong knowledge of global regulatory guidelines (ICH, USFDA, EMA, WHO).
    • Excellent documentation, data handling, and communication skills.
    • Team-oriented approach with ability to coordinate across departments.

    Location & Salary

    Location: Vadodara, Gujarat, India
    Industry: Pharmaceuticals – Regulatory Affairs
    Salary: Competitive as per industry standards.

    Regulatory Affairs Officer Vacancy – Elysium Pharma
    Regulatory Affairs Officer Vacancy – Elysium Pharma

    Application Process

    If you meet the above criteria and are ready to take the next step in your Regulatory Affairs career, apply now:

    📩 Send your CV to:

    Subject line: Application for RA Officer – Elysium Pharmaceutical Ltd

    👉 Apply before the opportunity closes to secure your position with Elysium Pharma.

    FAQs

    1. Who can apply for the RA Officer position at Elysium Pharma?
    Candidates with M.Pharm/B.Pharm degrees and 1–3 years of experience in Regulatory Affairs can apply.

    2. Is prior RA experience mandatory?
    Yes, a minimum of 1 year of Regulatory Affairs experience in OSD, Injectables, or API is required.

    3. Where is this job based?
    The position is based at Elysium Pharmaceutical Ltd in Vadodara, Gujarat.

    4. What is the mode of application?
    Candidates can apply via email by sending their CV to hr@elysiumpharma.com or aman.kumar@elysiumpharma.com.

    5. What are the growth opportunities?
    Employees gain exposure to global regulatory submissions, international compliance practices, and career advancement within the pharma sector.

     Elysium Pharmaceutical Ltd Job Summary Table

    Company Elysium Pharmaceutical Ltd
    Vacancies Regulatory Affairs Officer
    Required Education M.Pharm, B.Pharm (Regulatory Affairs/Pharmaceutics)
    Experience 1–3 years in Regulatory Affairs (OSD/Injectables/API)
    Location Vadodara, Gujarat
  • Executive Regulatory Affairs Vacancy | Sun Pharma

    Executive Regulatory Affairs Vacancy | Sun Pharma

    Executive Regulatory Affairs Vacancy | Sun Pharma Tandalja

    Apply for Executive Regulatory Affairs role at Sun Pharma Tandalja. Open for Life Science graduates in regulatory submissions and labeling.

    Sun Pharmaceutical Industries Ltd, a global leader in innovative pharmaceuticals, is seeking an Executive – Regulatory Affairs at its Tandalja R&D facility. This role is ideal for professionals with expertise in regulatory submissions, labeling compliance, and USFDA guidelines, contributing to the safe and timely launch of pharmaceutical products.

    Company Overview

    Sun Pharma is one of the largest and most trusted pharmaceutical companies in the world, renowned for its commitment to innovation, quality, and regulatory excellence. With a diverse portfolio of generic and specialty medicines, Sun Pharma focuses on improving patient lives globally. The company fosters a collaborative environment where regulatory professionals can advance their careers while ensuring the highest standards of compliance.

    Job Role & Responsibilities

    As an Executive in Regulatory Affairs, your key responsibilities will include:

    New Submissions: Work with Product Development (For Drug products) & other CFT (within and outside

    R&D) to ensure that sufficient and timely regulatory information and controls are included

    during design and development of drug products as per country specific regulatory requirements

    a. Provide feedback in terms of document requirements & regulatory filing strategy during development

    of new DF (Drug Formulation). Review and approve documents on behalf of regulatory.

    b. Preparation/review and submission of good quality dossiers thereby enabling faster approvals and

    timely launch

    c. Preparation and submission of meeting packages/scientific discussion with Agency related to product

    development

    d. Anticipate expected deficiencies and prepare mitigation plans

    2. Approval: Prepare and submit timely response to deficiencies enabling approval of products.

    3. Lifecycle Management for approved drug products

    a. Timely preparation and submission of annual reports/renewals

    b. Evaluation, preparation and submission of changes through variations, supplements etc that impact

    product supplies

    c. Regulatory Compliance – Ensure timely implementation of regulatory decisions for change

    management and other activities in DF plants

    d. Ensure reposition of comprehensive product information into central repository

    4. Self Development

    a. Awareness of regulatory guidelines, participating and delivering presentations

    Eligibility / Qualifications

    • Education: M. Pharm
    • Experience: 2-5 years Relevant experience in regulatory affairs, 
    • Technical Skills:
      • Knowledge of USFDA labeling requirements and ANDA/NDA processes.
      • Proficiency in SPL creation and regulatory submission software.
      • Strong coordination, communication, and documentation skills.
    • Desirable: Experience coordinating with cross-functional teams and managing REMS requirements.

    Relevant courses include: BPharm, MPharm, MSc Biotechnology, MSc Life Sciences, Regulatory Affairs Certification.

    Location & Salary

    • Location: Tandalja, Vadodara, Gujarat, India.
    • Work Type: Full-time, on-site.
    • Salary: Competitive, aligned with industry standards, including benefits and career growth opportunities.
    Executive Regulatory Affairs Vacancy | Sun Pharma
    Executive Regulatory Affairs Vacancy | Sun Pharma

    Application Process

    Interested candidates are encouraged to apply early to secure their spot. Sun Pharma maintains a transparent and inclusive recruitment process.

    👉 Apply directly here

    FAQs

    1. Who can apply for this role?
    Candidates with a degree in Pharmacy, Life Sciences, or Biotechnology, with experience in regulatory affairs, labeling, or USFDA submissions.

    2. What are the key responsibilities?
    Preparation, review, and submission of drug labeling, coordination with cross-functional teams, and managing REMS requirements.

    3. Where is the position based?
    The role is located at Tandalja, Vadodara, Gujarat, India.

    4. Is prior USFDA experience necessary?
    Yes, familiarity with ANDA/NDA labeling requirements is essential.

    5. How can I apply?
    Submit your application through the official Sun Pharma careers portal link provided above.

    Job Summary Table

    Category Details
    Company Sun Pharmaceutical Industries Ltd
    Vacancies Executive – Regulatory Affairs
    Required Education BPharm, MPharm, MSc Biotechnology, MSc Life Sciences, Regulatory Affairs Certification
    Experience Relevant experience in regulatory affairs, labeling, or USFDA submissions
    Location Tandalja, Vadodara, Gujarat, India
  • Alembic Pharma Walk-in QC & Manufacturing Trainee roles

    Alembic Pharma Walk-in QC & Manufacturing Trainee roles

    Alembic Pharma Walk-in for Freshers | QC & Manufacturing Trainees | Vadodara

    Alembic Pharma hiring freshers for QC & Manufacturing Trainee roles at Vadodara. M.Sc Chemistry & Diploma 2025 pass-outs eligible. Walk-in on 28th Aug 2025.

    Alembic Pharmaceuticals Ltd., a Great Place to Work-certified pharma company, is conducting a walk-in interview on 28th August 2025 in Vadodara, Gujarat for freshers interested in starting their careers in Quality Control (QC) and Manufacturing. With a legacy of over 100 years in touching lives through innovation and trust, Alembic invites 2025 pass-out graduates to begin their professional journey with one of India’s most reputed pharmaceutical companies.

    Company Overview

    Alembic Pharmaceuticals Ltd. is a pioneer in the Indian pharmaceutical industry, with a strong presence in formulations, APIs, and specialty chemicals. With approvals from global regulatory agencies such as USFDA, MHRA, and TGA, Alembic is known for its world-class infrastructure, R&D strength, and employee-friendly culture. Being certified as a Great Place to Work, Alembic offers an ideal environment for freshers to gain exposure, develop technical expertise, and grow in their careers.

    Job Role & Responsibilities

    Trainee – Quality Control (QC)

    • Eligibility: M.Sc (Organic Chemistry, Analytical Chemistry, Applied Chemistry, Industrial Chemistry) – 2025 pass-outs only.
    • Responsibilities:
      • Perform routine QC analysis of raw materials, intermediates, and finished formulations.
      • Support method development and validation under senior chemists’ guidance.
      • Maintain GLP compliance and laboratory documentation.
      • Ensure adherence to SOPs, GMP, and regulatory requirements.

    Trainee – Manufacturing

    • Eligibility: Diploma (Mechanical/Electrical) – 2025 pass-outs only.
    • Responsibilities:
      • Support production operations in formulation and API facilities.
      • Operate and maintain production equipment under supervision.
      • Ensure compliance with GMP, safety, and quality protocols.
      • Assist in batch documentation and process monitoring.

    Eligibility / Qualifications

    • Education:
      • M.Sc in Organic Chemistry, Analytical Chemistry, Applied Chemistry, Industrial Chemistry (QC Trainee).
      • Diploma in Mechanical or Electrical Engineering (Manufacturing Trainee).
    • Year of Passing: 2025 pass-outs only.
    • Other Requirements: No backlogs or ATKT at the time of application; good English communication skills; willingness to work in rotational shifts.

    Location & Salary

    • Walk-in Venue: Alembic Pharmaceuticals Limited, “Sanskruti Hall,” Alembic Colony, Opp. Bhailal Amin General Hospital, Alembic Road, Vadodara, Gujarat.
    • Date & Time: 28th August 2025 | Thursday | 9:00 AM – 1:00 PM
    • Salary: Competitive stipend and benefits as per industry standards.

    Application Process

    • Candidates should attend the walk-in with updated resume, educational certificates, and valid ID proof.
    • Those unable to attend may email their resume to: trainee@alembic.co.in (mention the job title in subject line).

    Important:

    • Candidates who attended interviews at Alembic in the last 3 months should not re-apply.
    • Alembic Pharma does not engage consultants or agents charging money for job offers. Beware of fraudulent calls.

    FAQs

    1. Who is eligible for Alembic’s walk-in drive?
    Only 2025 pass-out batch M.Sc Chemistry and Diploma (Mechanical/Electrical) candidates are eligible.

    2. Are backlogs allowed?
    No, candidates must not have any active backlogs or ATKT at the time of application.

    3. What roles are available?
    Trainee – Quality Control (QC) and Trainee – Manufacturing.

    4. What is the selection process?
    A written test (technical + aptitude), followed by an interview for shortlisted candidates.

    5. Where is the walk-in venue?
    Alembic Pharmaceuticals Ltd., “Sanskruti Hall,” Alembic Colony, Vadodara.

    Apply now or attend the walk-in on 28th August 2025 to start your pharma career with Alembic – one of India’s most trusted pharmaceutical companies!

    Summary Table

    Company Alembic Pharmaceuticals Ltd.
    Vacancies Trainee – Quality Control, Trainee – Manufacturing
    Required Education M.Sc Chemistry (Organic/Analytical/Applied/Industrial), Diploma (Mechanical/Electrical)
    Experience Freshers (2025 pass-outs only)
    Alembic Pharma Walk-in QC & Manufacturing Trainee roles
    Alembic Pharma Walk-in QC & Manufacturing Trainee roles
  • Zytex Biotech hiring Production, QA, and QC Officers

    Zytex Biotech hiring Production, QA, and QC Officers

    Biotechnology & Microbiology Openings at Zytex Biotech, Vadodara

    Zytex Biotech is hiring Production, QA, and QC Officers in Vadodara. Apply now for exciting biotech career opportunities. Multiple vacancies open!

    Zytex Biotech Pvt. Ltd., a leading name in industrial biotechnology, is inviting applications for multiple positions at its state-of-the-art Fermentation Manufacturing Unit located in Manjusar GIDC, Vadodara, Gujarat. This is an excellent opportunity for professionals in biotechnology, microbiology, and quality assurance to build a rewarding career in one of India’s fastest-growing biotech organizations.

    Company Overview

    Zytex Biotech has established itself as a pioneer in the biotechnology sector with a strong presence in enzyme production, probiotics, fermentation technology, and microbial solutions. The company is well recognized for innovation, regulatory compliance, and delivering quality-driven products to industries across the globe. Joining Zytex means working in a USFDA-compliant environment with world-class facilities and opportunities for career advancement.

    Job Role & Responsibilities

    1. Production Officer – Fermentation Plant (Male Only)

    • Oversee fermentation plant operations.
    • Operate fermenters and related equipment as per SOPs.
    • Monitor and control process parameters to ensure optimal yield and quality.
    • Support in process validation and scale-up activities.

    2. QA Officer – Fermentation Plant (Male Only)

    • Conduct in-process quality assurance for fermentation products.
    • Ensure strict compliance with GMP, GLP, and regulatory guidelines.
    • Review and approve documents, SOPs, and production batch records.
    • Support regulatory audits and customer inspections.

    3. Jr. Officer / Trainee – QC Microbiologist (Male Only)

    • Perform microbial testing, sterility checks, and contamination control.
    • Analyze fermentation samples using microbiological techniques.
    • Prepare and maintain laboratory records in compliance with GLP.
    • Assist in environmental monitoring and quality documentation.

    Eligibility / Qualifications

    • Production Officer: M.Sc. Biotechnology/Microbiology, B.Tech/BE Biotechnology with 2–8 years of relevant experience.
    • QA Officer: M.Sc. Biotechnology/Microbiology, B.Tech/BE Biotechnology/Food Technology with 5–8 years of experience (CTC up to ₹6.5 LPA).
    • QC Microbiologist (Jr. Officer/Trainee): M.Sc. Microbiology with 6 months–2 years of experience (CTC up to ₹3.3 LPA).

    Location & Salary

    • Work Location: Zytex Biotech Pvt. Ltd., Fermentation Manufacturing Unit, Manjusar GIDC, Vadodara, Gujarat.
    • Salary: Competitive; role-specific CTC mentioned above.

    Application Process

    Interested candidates can apply by sharing their updated CV at hr2.baroda@zytex.com or send via WhatsApp at +91 77779 20621.

    Apply early to secure your chance as interviews are ongoing!

    FAQs

    1. Who can apply for these positions?
    Candidates with degrees in Biotechnology, Microbiology, or Food Technology and relevant experience in production, QA, or QC can apply.

    2. What is the salary range for these roles?

    • QA Officer: up to ₹6.5 LPA
    • QC Jr. Officer/Trainee: up to ₹3.3 LPA
    • Production Officer: salary as per industry standards.

    3. Is prior experience mandatory?
    Yes, except for the QC Trainee role, where freshers with up to 6 months of experience are encouraged to apply.

    4. What is the mode of interview?
    Shortlisted candidates will be contacted by HR for the next steps, which may include technical interviews and HR discussions.

    5. Does Zytex Biotech offer career growth opportunities?
    Yes, Zytex provides a structured career path with training, regulatory exposure, and opportunities to work in global projects.

    Summary Table

    Company Zytex Biotech Pvt. Ltd.
    Vacancies Production Officer, QA Officer, QC Jr. Officer/Trainee
    Required Education M.Sc. Biotechnology, M.Sc. Microbiology, B.Tech Biotechnology, BE Biotechnology, Food Technology
    Experience 6 months – 8 years (role specific)
  • Exemed Pharma hiring QA, Engineering, EHS & Warehouse professionals

    Exemed Pharma hiring QA, Engineering, EHS & Warehouse professionals

    Exemed Pharma Hiring QA, Engineering, EHS, Warehouse | Vadodara

    Exemed Pharmaceuticals hiring QA, Engineering, EHS & Warehouse professionals in Vadodara. Apply with B.Sc/M.Sc/B.E/B.Com/ITI/Diploma, 2–9 years exp.

    Exemed Pharmaceuticals, a fast-growing pharmaceutical manufacturer, is inviting applications for multiple vacancies at its Vadodara facility. The company is seeking experienced professionals in Quality Assurance (QA), Engineering, Environment Health & Safety (EHS), and Warehouse Management. These openings provide excellent career opportunities for skilled candidates to join a reputed organization known for its commitment to quality, compliance, and innovation.

    Company Overview

    Exemed Pharmaceuticals is a trusted name in the pharmaceutical sector, specializing in the development and manufacturing of high-quality formulations for regulated markets. With a focus on innovation, compliance, and customer satisfaction, Exemed has earned approvals from global regulatory bodies and built a strong presence in domestic and international markets.

    Employees at Exemed benefit from working in a culture that emphasizes excellence, growth, and career advancement, making it a preferred employer for pharma professionals.

    Job Roles & Responsibilities

    Quality Assurance (QA) – Executive / Sr. Executive

    • Specialization: Analytical Quality Assurance (AQA), Quality Management Systems (QMS).
    • Monitor and maintain QMS documentation and regulatory compliance.
    • Support in audits, validations, and implementation of SOPs.

    Engineering – Executive

    • Qualification: B.E with 5–7 years’ experience.
    • Manage preventive and corrective maintenance of production equipment.
    • Troubleshoot instrumentation and electrical issues.
    • Ensure equipment calibration and compliance with safety standards.

    Environment, Health & Safety (EHS) – Fireman

    • Qualification: ITI/Diploma in Fire & Safety with 2–5 years’ experience.
    • Maintain fire safety systems and ensure compliance with EHS protocols.
    • Conduct safety drills, audits, and documentation.
    • Support QMS and regulatory EHS compliance.

    Warehouse – Officer / Sr. Officer

    • Qualification: B.Com with 3–5 years’ experience.
    • Manage warehouse operations including receiving, storage, and dispatch.
    • Ensure inventory accuracy, documentation, and compliance with GMP standards.
    • Coordinate with procurement and production teams.

    Eligibility / Qualifications

    • QA Executive/Sr. Executive: B.Sc / M.Sc with 7–9 years of relevant QA experience.
    • Engineering Executive: B.E with 5–7 years of experience in maintenance and troubleshooting.
    • EHS Fireman: ITI / Diploma in Fire & Safety with 2–5 years of experience.
    • Warehouse Officer/Sr. Officer: B.Com with 3–5 years of experience in warehouse management.

    Location & Salary

    • Work Location: Exemed Pharmaceuticals, Block No. 628 (A&B), ECP Canal Road, Village Luna, Taluka Padra, Vadodara – 391440.
    • Salary: Competitive and as per industry standards, based on qualifications and experience.

    Application Process

    Interested candidates can apply by sharing their updated CVs at recruitment@exemedpharma.com. Applicants should clearly mention the department and position they are applying for in the subject line of their email.

    Why Join Exemed Pharmaceuticals?

    • Opportunity to work with a trusted pharmaceutical company with a strong domestic and global presence.
    • Exposure to regulatory compliance and QMS-driven environments.
    • Career advancement opportunities across QA, Engineering, EHS, and Warehouse.
    • Competitive salary packages and employee development programs.

    FAQs

    1. What qualifications are required for these roles?
    B.Sc/M.Sc for QA, B.E for Engineering, ITI/Diploma in Fire & Safety for EHS, and B.Com for Warehouse roles.

    2. What is the experience requirement?
    2–9 years of relevant industry experience depending on the role.

    3. Where is the work location?
    Exemed Pharmaceuticals, Vadodara (Luna, Padra, Gujarat).

    4. How should applicants apply?
    By sending their CVs to recruitment@exemedpharma.com with the position mentioned in the subject line.

    5. Are these vacancies open to freshers?
    No, these openings are for experienced professionals only.

    Summary Table

    Company Exemed Pharmaceuticals
    Vacancies QA Executive/Sr. Executive, Engineering Executive, EHS Fireman, Warehouse Officer/Sr. Officer
    Required Education B.Sc, M.Sc, B.E, ITI, Diploma in Fire & Safety, B.Com
    Experience 2–9 years depending on role
    <img class="size-full wp-image-122852" src="https://bpharmacyjobs.com/wp-content/uploads/2025/08/Exemed-Pharma-hiring-QA-Engineering-EHS-Warehouse-professionals-1.webp" alt="Exemed Pharma hiring QA, Engineering, EHS & Warehouse professionals” width=”1280″ height=”1810″ /> Exemed Pharma hiring QA, Engineering, EHS & Warehouse professionals
  • Innoxel Lifesciences Walk-in QC, Production, Engineering

    Innoxel Lifesciences Walk-in QC, Production, Engineering

    Innoxel Lifesciences Walk-in – QC, Production, Engineering, Vadodara

    Innoxel Lifesciences walk-in on 24th Aug 2025 at Vadodara. Hiring for QC, Production, Microbiology, Warehouse, Engineering & Packaging roles.

    Innoxel Lifesciences Pvt. Ltd., a trusted pharmaceutical manufacturer with a strong presence in sterile and injectable formulations, is conducting a walk-in interview drive for multiple positions across Quality Control, Production, Microbiology, Warehouse, Engineering, Packaging, and Project Management. This drive is scheduled for 24th August 2025 (Sunday) at the Vadodara facility.

    Company Overview

    Innoxel Lifesciences Pvt. Ltd. is a leading pharmaceutical organization specializing in sterile injectables with facilities compliant with USFDA, EU-GMP, and other international regulatory standards. The company is committed to quality, innovation, and operational excellence, making it a sought-after workplace for pharma professionals. By joining Innoxel, candidates get exposure to global regulatory environments and opportunities for long-term career growth.

    Job Role & Responsibilities

    Innoxel is hiring for the following departments:

    Quality Control (QC)

    • Role: Analysts (AMV, Report Preparation)
    • Experience: 1–10 years
    • Education: B.Sc./M.Sc. Chemistry (Sterile USFDA experience preferred)
    • Responsibilities: Analytical method validation, report preparation, compliance with sterile product testing protocols.

    Sterile Manufacturing

    • Role: Machine Operators & Production Officers
    • Experience: 1–8 years
    • Education: ITI/Diploma (Operators), B.Pharm/M.Pharm (Officers)
    • Responsibilities: Operate and manage sterile manufacturing equipment, ensure compliance with GMP standards, manage injectable production processes.

    Quality Control Microbiology (QC Micro)

    • Role: Microbiologists & EM (Environmental Monitoring)
    • Experience: 1–8 years
    • Education: B.Sc./M.Sc. Microbiology
    • Responsibilities: Conduct microbiological testing, sterility assurance, and environmental monitoring in sterile facilities.

    Warehouse

    • Role: Officers – Dispensing & Warehousing Management
    • Experience: 3–7 years
    • Education: B.Sc./M.Sc./B.Com with injectable USFDA experience
    • Responsibilities: Manage raw material dispensing, inventory, warehousing, and compliance for sterile operations.

    Project Management

    • Role: Project Management Executives
    • Experience: 0–8 years
    • Education: M.Pharm (Freshers eligible)
    • Responsibilities: Support project planning, execution, and coordination with multiple pharma functions.

    Engineering

    • Role: Process Maintenance (Autoclave Troubleshooting)
    • Experience: 3–5 years
    • Education: B.E./M.E. – Mechanical/Industrial Maintenance (Sterile USFDA experience required)
    • Responsibilities: Troubleshoot autoclave operations, maintain sterile engineering systems.

    Packaging

    • Role: Packaging Executives (Visual Inspection, Track & Trace)
    • Experience: 1–5 years
    • Education: B.Sc./M.Sc./B.Pharm with injectable USFDA experience
    • Responsibilities: Handle visual inspection, track & trace systems, and ensure packaging compliance.

    Eligibility / Qualifications

    • Education: B.Sc, M.Sc (Chemistry, Microbiology, Life Sciences), B.Pharm, M.Pharm, B.E./M.E. (Mechanical/Industrial Maintenance), ITI, Diploma, B.Com.
    • Experience: Freshers (Project Management) to experienced professionals (1–10 years).
    • Special Requirement: Preference given to candidates with sterile manufacturing and USFDA compliance experience.

    Location & Salary

    • Work Location: Innoxel Lifesciences Pvt. Ltd., Survey No. 534/1, Village Kotambi, Nr. VCA Stadium, Taluka Waghodia, Vadodara.
    • Walk-in Time: 10:00 AM – 4:00 PM
    • Salary: Competitive pay based on qualifications and experience.

    Application Process

    Interested candidates can attend the walk-in interview with their updated resumes and necessary documents.

    • Date: Sunday, 24th August 2025
    • Time: 10:00 AM – 4:00 PM
    • Venue: Innoxel Lifesciences Pvt. Ltd., Vadodara (near VCA Stadium).
    • Email (For those unable to attend): hr1@innoxells.com

    Documents Required: Resume, educational certificates, experience letters, ID proofs.

    Apply early and attend the walk-in to secure your spot in one of India’s fastest-growing sterile pharma companies.

    Why Join Innoxel Lifesciences?

    • Opportunity to work in a sterile injectable USFDA-compliant facility.
    • Exposure to international quality and regulatory practices.
    • Career growth prospects in QC, Production, Microbiology, Engineering, and Packaging.
    • Supportive work environment with training and development programs.

    FAQs

    1. Who can apply for the walk-in drive?
    Candidates with qualifications in B.Sc, M.Sc, B.Pharm, M.Pharm, B.E./M.E., ITI, Diploma, B.Com with 0–10 years of pharma experience.

    2. Are freshers eligible?
    Yes, freshers with M.Pharm qualifications can apply for Project Management roles.

    3. What departments have openings?
    QC, Sterile Manufacturing, QC Micro, Warehouse, Project Management, Engineering, and Packaging.

    4. Where is the walk-in venue?
    Innoxel Lifesciences Pvt. Ltd., Survey No. 534/1, Village Kotambi, Nr. VCA Stadium, Vadodara.

    5. How can I apply if I cannot attend the walk-in?
    Send your resume to hr1@innoxells.com.

    Quick Summary Table

    Company Innoxel Lifesciences Pvt. Ltd.
    Vacancies QC, Sterile Manufacturing, QC Micro, Warehouse, Project Management, Engineering, Packaging
    Required Education B.Sc, M.Sc, B.Pharm, M.Pharm, B.E./M.E., ITI, Diploma, B.Com
    Experience 0–10 years (Freshers to Experienced)
    Location Vadodara, Gujarat
    Interview Date 24th August 2025 (10:00 AM – 4:00 PM)
    Application Email hr1@innoxells.com
    Innoxel Lifesciences Walk-in QC, Production, Engineering
    Innoxel Lifesciences Walk-in QC, Production, Engineering