PHARMA STUFF

Job Tag: Pharma Jobs in Ahmedabad

  • QC Microbiology Apprentice/Officer Vacancy – Swiss Parenteral

    QC Microbiology Apprentice/Officer Vacancy – Swiss Parenteral, Ahmedabad

    Apply for QC Microbiology Apprentice/Officer at Swiss Parenteral Ltd, Bavla Ahmedabad. 0–1 year experience, M.Sc/B.Sc Pharma/Microbiology eligible. Swiss Parenteral Limited, a WHO-GMP certified and ISO 9001:2008 accredited pharmaceutical company, is inviting fresh graduates and early professionals to join its sophie rain nude leakedQC Microbiology Department in Bavla, Ahmedabad. This role is ideal for candidates eager to build a strong foundation in microbiology, pharmaceuticals, and regulatory compliance.

    Company Overview

    Swiss Parenteral Limited is a trusted pharmaceutical manufacturer with cutting-edge facilities in Ahmedabad. The company complies with stringent global standards, including USFDA, EU GMP, TGA, and MCC guidelines. With a focus on sterile formulations, injectable medicines, and parenteral products, Swiss Parenteral is committed to improving healthcare through quality-driven and innovative solutions.

    Job Role & Responsibilities

    As a QC Microbiology Apprentice/Officer, you will play a key role in ensuring pharmaceutical products meet the highest safety and compliance standards. Responsibilities include:

    • Conducting environmental monitoring of cleanrooms.
    • Performing water sampling and water analysis.
    • Sampling and analyzing raw materials.
    • Carrying out Microbial Limit Testing (MLT).
    • Executing sterility testing for parenteral formulations.
    • Conducting bioburden analysis and Bacterial Endotoxin Testing (BET).
    • Preparing media and performing growth promotion tests.
    • Ensuring compliance with microbiology lab documentation.

    This position provides exposure to advanced regulatory systems, WHO-GMP standards, and internationally accepted QC practices.

    Eligibility / Qualifications

    • Education: B.Sc / M.Sc in Microbiology, Biotechnology, Life Sciences, Pharmacy, Industrial Microbiology
    • Experience: 0–1 year (freshers encouraged to apply)
    • Gender: Male candidates only (as per company requirement)
    • Skills Required:
      • Strong microbiology fundamentals
      • Attention to detail in compliance and documentation
      • Ability to work in sterile and regulated environments
      • Good communication and team collaboration

    Location & Salary

    • Location: Bavla, Ahmedabad (Pharmaceutical Manufacturing Facility)
    • Salary: As per industry standards, with opportunities for professional growth and training.
    • Work Environment: Exposure to state-of-the-art microbiology labs, cleanrooms, and regulatory-compliant systems.
    QC Microbiology Apprentice/Officer Vacancy – Swiss Parenteral,
    QC Microbiology Apprentice/Officer Vacancy – Swiss Parenteral,

    Application Process

    Interested candidates can apply directly by sending their updated CV to:

    📌 Ensure to mention “Application for QC Microbiology – Apprentice/Officer” in the subject line of your email.

    Apply before the vacancies are filled to secure your place in Swiss Parenteral’s growing QC team!

    Why Join Swiss Parenteral?

    • Opportunity to work in a globally recognized WHO-GMP pharmaceutical company
    • Hands-on training in advanced QC Microbiology techniques
    • Career growth opportunities in sterile manufacturing and regulatory compliance
    • Supportive work culture with emphasis on innovation and continuous learning

    FAQs

    1. Who can apply for this QC Microbiology role?
    Fresh graduates with B.Sc/M.Sc in Microbiology, Biotechnology, Life Sciences, or Pharmacy with 0–1 year of experience can apply. Only male candidates are eligible.

    2. Is prior experience mandatory?
    No, freshers are encouraged to apply. Training will be provided.

    3. What is the work shift and location?
    The job is based at Bavla, Ahmedabad. Work shifts align with pharma manufacturing QC schedules.

    4. What kind of growth opportunities are available?
    Candidates gain exposure to international regulatory guidelines, WHO-GMP practices, and can grow into senior QC or Regulatory positions.

    5. How do I apply?
    Send your CV to hr1@swiss.in or contact 6352978952 for more details.

    Summary Table

    Company Swiss Parenteral Limited
    Vacancies QC Microbiology – Apprentice/Officer
    Required Education B.Sc / M.Sc in Microbiology, Biotechnology, Life Sciences, Pharmacy
    Experience 0–1 Year (Freshers Eligible)

  • DSP Apprentice at Intas Pharmaceuticals | Fresher Opportunity

    DSP Apprentice at Intas Pharmaceuticals | Fresher Opportunity

    Apply for DSP Apprentice at Intas Plasma Fractionation Centre. M.Sc/B.Tech Biotechnology fresher opportunity with hands-on experience in downstream process.

    Intas Pharmaceuticals is inviting enthusiastic freshers to join their Downstream Process (DSP) team at the Intas Plasma Fractionation Centre. This is an excellent opportunity for Biotechnology graduates to gain hands-on experience in biopharmaceutical production, working with state-of-the-art equipment and contributing to life-saving plasma-based therapeutics.

    Company Overview

    Intas Pharmaceuticals is a globally recognized biopharmaceutical company specializing in the development, manufacturing, and marketing of high-quality therapeutics. With a strong presence in India and international markets, Intas is committed to innovation, patient safety, and operational excellence. The company offers robust career growth, continuous learning opportunities, and exposure to advanced technologies in plasma fractionation and biotechnology.

    Job Role & Responsibilities

    As a DSP Apprentice in the Downstream Process Department, you will actively participate in the production and quality assurance of plasma-derived products. Key responsibilities include:

    • Executing production batches during shift operations.
    • Performing chromatography and buffer preparation.
    • Maintaining proper documentation and records, including logbooks, BPCRs, and reports in accordance with Good Documentation Practices (GDP).
    • Supporting Performance Verification (PV), Performance Qualification (PQ), and commissioning of new equipment.
    • Ensuring compliance with current Good Manufacturing Practices (cGMP).
    • Coordinating with Engineering, QA, QC, and R&D teams to ensure smooth execution of production batches.

    Eligibility / Qualifications

    • Educational Qualification: M.Sc or B.Tech in Biotechnology.
    • Experience: Fresher candidates are encouraged to apply.
    • Strong commitment to learning and adherence to cGMP and safety protocols.
    • Excellent documentation, coordination, and interpersonal skills.

    Location & Salary

    • Job Location: Intas Plasma Fractionation Centre, India.
    • Salary: As per company norms and industry standards for apprentices.
    DSP Apprentice at Intas Pharmaceuticals | Fresher Opportunity
    DSP Apprentice at Intas Pharmaceuticals | Fresher Opportunity

    Application Process

    Interested candidates are encouraged to apply by sending their CV to careers_pfu@intaspharma.com. Joining the Intas Talent Network ensures you stay informed about future opportunities in the company.

    Vertical Summary Table

    Category Details
    Company Intas Pharmaceuticals Pvt Ltd
    Vacancies DSP Apprentice, Fresher
    Required Education M.Sc/B.Tech in Biotechnology
    Experience Fresher

    FAQs

    Q1: Can freshers apply for the DSP Apprentice role?
    A1: Yes, the position is open for freshers with M.Sc/B.Tech in Biotechnology.

    Q2: What are the primary responsibilities of this role?
    A2: Executing production batches, chromatography, buffer preparation, documentation, performance verification, and ensuring cGMP compliance.

    Q3: How to apply for the DSP Apprentice position?
    A3: Send your CV to careers_pfu@intaspharma.com to join the Intas Talent Network.

    CTA: Apply now to start your career in biopharmaceutical downstream processing and gain practical exposure at Intas Pharmaceuticals. Spots are limited – submit your CV today!

  • Intas Diploma Freshers Walk-in Drive 2025

    Intas Diploma Freshers Walk-in Drive 2025

    Intas Diploma Freshers Walk-in Drive 2025 | Ahmedabad Vacancies

    Intas Pharmaceuticals hiring Diploma freshers 2024/2025 batch in Ahmedabad. Walk-in drive on 27 Sept 2025. Apply today!

    Intas Pharmaceuticals, one of the global leaders in the pharmaceutical industry, is conducting a walk-in recruitment drive for fresh Diploma graduates. This is an excellent opportunity for candidates from Polytechnic or Pharmacy backgrounds (2024 & 2025 pass-outs) to launch their careers with one of India’s fastest-growing pharma companies. Intas is known for its commitment to innovation, affordability, and healthcare advancements, making this an ideal platform for young professionals.

    Company Overview

    Intas Pharmaceuticals Ltd. is a leading multinational pharmaceutical company with a strong presence in over 85 countries. Headquartered in India, Intas focuses on research, manufacturing, and marketing of affordable medicines that meet global quality standards. With a strong emphasis on biotechnology, oncology, and critical care, Intas continues to drive innovation and deliver sustainable healthcare solutions worldwide.

    Job Role & Responsibilities

    Selected candidates will be part of Intas’s production and operations teams, contributing to manufacturing, quality, and compliance processes. Responsibilities include:

    • Supporting day-to-day manufacturing activities in compliance with GMP standards.
    • Assisting in quality checks, documentation, and reporting.
    • Ensuring adherence to safety and regulatory guidelines.
    • Learning and applying pharma industry best practices for continuous improvement.

    Eligibility / Qualifications

    Location & Salary

    • Job Location: Intas Pharmaceuticals Ltd., Matoda Village, Sanand Taluka, Ahmedabad, Gujarat – 382210.
    • Compensation: Salary will be as per company standards, with attractive growth opportunities and career development support.
    Intas Diploma Freshers Walk-in Drive 2025
    Intas Diploma Freshers Walk-in Drive 2025

    Application Process

    • Walk-in Date: Saturday, 27th September 2025
    • Time: 09:30 AM to 03:00 PM
    • Venue: Intas Pharmaceuticals Ltd., Plot No. 457, 458, Sarkhej Bavla Highway, Matoda Village, Sanand Taluka, Ahmedabad, Gujarat – 382210.

    What to Carry:

    • Updated resume
    • Passport-size photographs
    • Government-issued ID proof

    👉 Apply in person at the above venue. Don’t miss this opportunity to start your pharma career with Intas!

    Why Join Intas Pharmaceuticals?

    • Global exposure with one of the world’s top pharmaceutical companies.
    • Hands-on learning in state-of-the-art manufacturing facilities.
    • Career growth opportunities in production, quality, and R&D.
    • Be part of a company focused on healthcare innovation and global expansion.

    FAQs

    1. Who can apply for this Intas walk-in drive?
    Diploma holders in Polytechnic or Pharmacy (2024 and 2025 batches only).

    2. Is prior experience required?
    No, this drive is exclusively for freshers.

    3. What documents should I carry for the walk-in?
    Latest resume, passport-size photographs, and a valid government ID.

    4. Will there be an interview process?
    Yes, shortlisted candidates will undergo interviews and assessments as per Intas’s selection procedure.

    5. What is the job location?
    The openings are based in Intas’s Ahmedabad facility (Matoda, Sanand Taluka).

    ⚡ Apply before 27th September 2025 to secure your spot in this exclusive walk-in drive!
    🚀 Start your career with Intas Pharmaceuticals today!

    Summary Table

    Company Intas Pharmaceuticals Ltd.
    Vacancies Diploma Freshers (2024 & 2025 batches)
    Required Education Diploma in Pharmacy, Diploma in Polytechnic streams (Mechanical, Electrical, Chemical, Biotechnology)
    Experience Freshers only (2024/2025 pass-outs)
    Location Ahmedabad, Gujarat
  • Ribosome Research Centre (RRC) hiring for In Vitro Scientists, QA Auditors, and HR Executives. Openings for M.Sc, M.Pharm

    Ribosome Research Centre (RRC) hiring for In Vitro Scientists, QA Auditors, and HR Executives. Openings for M.Sc, M.Pharm

    Ribosome Research Centre Hiring Scientists, QA & HR – Apply Now

    Ribosome Research Centre (RRC) hiring for In Vitro Scientists, QA Auditors, and HR Executives. Openings for M.Sc, M.Pharm, MBA graduates. Apply today.

    Ribosome Research Centre Pvt. Ltd. (RRC), a leading global contract research organization (CRO), is inviting applications for multiple positions across Research, Quality Assurance, and Human Resources. This is an excellent opportunity for professionals in biotechnology, microbiology, pharmacology, zoology, and management to build their careers with a globally recognized CRO.

    Company Overview

    Ribosome Research Centre (RRC) is a reputed contract research organization specializing in cutting-edge biomedical research, pre-clinical testing, and regulatory-compliant services. With expertise in OECD GLP-certified studies, ISO/IEC 17025:2017 standards, and advanced in vitro models, RRC partners with global pharma, biotech, and healthcare companies to accelerate innovation. The company is committed to fostering scientific excellence and career growth for its employees.

    Job Role & Responsibilities

    1. In Vitro Scientist – Jr. Research Scientist / Research Scientist

    • Qualification: M.Sc Biotechnology / Microbiology
    • Experience: 0 to 5 years
    • Preferred Skills:
      • Experience in genotoxicity, cytotoxicity, and cell line-based studies.
      • Familiarity with OECD GLP standards.
    • Responsibilities:
      • Conduct in vitro assays and cellular experiments.
      • Support R&D projects with accurate documentation and data analysis.
      • Ensure compliance with international laboratory standards.

    2. Quality Assurance Auditor – Jr. QA Officer to Manager

    • Qualification: M.Sc Zoology / M.Pharm Pharmacology
    • Experience: 0 to 8 years
    • Preferred Skills:
      • Knowledge of OECD GLP & ISO/IEC 17025:2017 standards.
      • Experience in QA auditing and compliance documentation.
    • Responsibilities:
      • Conduct internal audits, identify gaps, and ensure regulatory compliance.
      • Collaborate with teams to develop and implement corrective actions.
      • Prepare quality reports for regulatory bodies and clients.

    3. Human Resources – Executive to Manager

    • Qualification: MBA (Human Resources)
    • Experience: 0 to 8 years
    • Preferred Skills:
      • Experience in payroll, HR policies, recruitment, and employee engagement.
    • Responsibilities:
      • Oversee recruitment, training, and HR operations.
      • Support organizational development initiatives.
      • Ensure compliance with labor laws and HR best practices.

    Eligibility / Qualifications

    • In Vitro Scientist: M.Sc Biotechnology, M.Sc Microbiology (0–5 yrs).
    • QA Auditor: M.Sc Zoology, M.Pharm Pharmacology (0–8 yrs).
    • HR Roles: MBA in HR (0–8 yrs).

    Relevant courses: Biotechnology, Microbiology, Zoology, Pharmacology, MBA-HR, Life Sciences.

    Location & Salary

    • Work Location: Ribosome Research Centre Pvt. Ltd. (RRC), India.
    • Salary: Attractive salary based on qualifications and experience.
    • Designation: Junior to Managerial levels depending on experience.
    Ribosome Research Centre (RRC) hiring for In Vitro Scientists, <a class=
    QA Auditors, and HR Executives. Openings for M.Sc, M.Pharm,” width=”1200″ height=”675″ /> Ribosome Research Centre (RRC) hiring for In Vitro Scientists, QA Auditors, and HR Executives. Openings for M.Sc, M.Pharm,

    Application Process

    Interested candidates can apply by sharing their CVs to the respective department emails:

    For business-related queries: bd2@ribosomeresearch.com
    WhatsApp/Contact: +91 7434936625 / +91 9904155567

    Why Join RRC?

    • Work with a globally recognized CRO on cutting-edge biomedical research projects.
    • Exposure to GLP, ISO/IEC 17025:2017, and regulatory-driven environments.
    • Opportunities across Research, QA, and HR – from entry-level to managerial roles.
    • Learn and grow under industry experts while contributing to life sciences innovation.

    FAQs

    Q1: Who can apply for In Vitro Scientist roles?
    M.Sc Biotechnology/Microbiology graduates with 0–5 years’ experience.

    Q2: What is the eligibility for QA roles?
    M.Sc Zoology or M.Pharm Pharmacology with 0–8 years’ experience.

    Q3: Can freshers apply?
    Yes, freshers are welcome for all positions if they meet the educational criteria.

    Q4: What is the eligibility for HR positions?
    MBA in HR with 0–8 years’ experience in HR operations and payroll.

    Q5: How to apply?
    Send your resume to the respective department email provided above.

    Summary Table

    Category Details
    Company Ribosome Research Centre Pvt. Ltd.
    Vacancies In Vitro Scientist, QA Auditor, HR Executive/Manager
    Required Education M.Sc Biotechnology/Microbiology, M.Sc Zoology, M.Pharm Pharmacology, MBA (HR)
    Experience 0–8 years (Freshers & Experienced candidates eligible)
  • Global Pharma Hiring Business Development & Regulatory Affairs

    Global Pharma Hiring Business Development & Regulatory Affairs

    B.Pharm/MBA Pharma Openings – 3 Roles | Ahmedabad

    Apply for 3 pharma vacancies in Ahmedabad! Openings for Business Development & Regulatory Affairs at Innmedics Global Pharma. Apply today!

    Are you a pharma professional looking to advance your career with a global pharmaceutical company? Innmedics Global Pharma Pvt. Ltd., based in Ahmedabad, is hiring for multiple roles in Business Development and Regulatory Affairs. This is your opportunity to join a company that is committed to delivering trust and quality in pharmaceuticals worldwide.

    Company Overview

    Innmedics Global Pharma Pvt. Ltd. is a trusted pharmaceutical organization headquartered in Ahmedabad, Gujarat. With a strong presence in domestic and international markets, the company is known for its high-quality formulations, ethical business practices, and commitment to healthcare excellence. Innmedics aims to bridge the gap between innovation and accessibility by delivering affordable, safe, and effective medicines.

    Job Role & Responsibilities

    1. Business Development Manager

    • Build and maintain strong client relationships in domestic and international markets.
    • Identify new business opportunities and drive revenue growth.
    • Negotiate contracts, pricing, and product agreements.
    • Coordinate with cross-functional teams to ensure successful business execution.

    2. Business Development Executive

    • Assist in developing and implementing business strategies.
    • Conduct market research to identify potential leads and customers.
    • Support client communication, presentations, and follow-ups.
    • Work closely with the manager to achieve sales targets.

    3. Regulatory Affairs Manager

    • Handle regulatory submissions and compliance for global markets (ROW, US, EU).
    • Prepare, review, and submit dossiers in CTD/ACTD formats.
    • Manage MOH queries and regulatory correspondences.
    • Stay updated on global regulatory guidelines and ensure compliance.

    Eligibility / Qualifications

    Business Development Manager

    • Education: B.Pharm / MBA / Any Post Graduate
    • Experience: 3-5 years (mandatory pharma industry experience)

    Business Development Executive

    • Education: D.Pharm, B.Pharm, M.Pharm, B.Sc., M.Sc., MBA
    • Experience: 1-3 years (pharma experience preferred)

    Regulatory Affairs Manager

    Location & Salary

    • Location: Ahmedabad, Gujarat
    • Salary: As per industry standards; commensurate with experience.

    Application Process

    Interested candidates can apply by sending their updated resume to:
    hr@innmedics.in
    +91 9925071921
    www.innmedics.in

    FAQs

    Q1: Is pharma experience mandatory for all roles?
    Yes, pharma experience is mandatory for the Business Development Manager and Regulatory Affairs Manager positions. For the Business Development Executive, prior pharma experience is preferred but not compulsory.

    Q2: What kind of markets will I handle in Regulatory Affairs?
    You will be responsible for ROW, US, and EU regulatory submissions, including dossier preparation and MOH query handling.

    Q3: Are freshers eligible to apply?
    No, all current roles require prior experience in the pharmaceutical domain.

    Q4: Is the role office-based or remote?
    The roles are office-based in Ahmedabad.

    Q5: What documents should I carry if shortlisted?
    Updated resume, educational certificates, experience letters, and ID proofs.

    Summary Table

    Company Innmedics Global Pharma Pvt. Ltd.
    Vacancies 3 (BD Manager, BD Executive, RA Manager)
    Required Education B.Pharm, M.Pharm, D.Pharm, MBA, M.Sc, B.Sc
    Experience 1–5+ years depending on role
    Location Ahmedabad, Gujarat
    Global Pharma Hiring Business Development & Regulatory Affairs
    Global Pharma Hiring Business Development & Regulatory Affairs
  • JB Pharma hiring Officers/Executives in QA, QC, Production, R&D & Engineering

    JB Pharma hiring Officers/Executives in QA, QC, Production, R&D & Engineering

    JB Pharma Hiring Officers & Executives | Panoli | 1–5 Yrs Exp

    JB Pharma hiring Officers/Executives in QA, QC, Production, R&D & Engineering at Panoli. 1–5 years’ experience. Apply now at jbpharma.com

    JB Pharma, a leading name in the pharmaceutical industry, is hiring Officers and Executives across multiple departments at its Panoli facility. If you have 1–5 years of experience in QA, QC, Production, R&D, or Engineering, this is a golden opportunity to advance your pharma career.

    Company Overview

    JB Pharma is one of India’s fastest-growing pharmaceutical companies with a strong global footprint. Renowned for its high-quality formulations and APIs, JB Pharma continues to expand its workforce with skilled professionals who can contribute to its mission of delivering affordable and reliable medicines worldwide.

    Job Role & Responsibilities

    Quality Assurance (QA – API & Formulation)

    • Position: Officer/Executive
    • Qualification: M.Sc / B.Pharm / M.Pharm
    • Experience: 2–5 years
    • Responsibilities:
      • Handle IPQA & QMS activities (market complaints, deviations, CAPA, change control).
      • Ensure compliance with regulatory requirements.

    Product Development Lab / R&D

    • Position: Officer/Executive
    • Qualification: M.Sc (Organic Chemistry)
    • Experience: 1–3 years
    • Responsibilities:
      • Conduct synthesis, trials, and development activities.
      • Support process optimization in API & Formulations.

    Production – Packing

    • Position: Officer/Executive
    • Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
    • Experience: 1–3 years
    • Responsibilities:
      • Manage and supervise formulation packing operations.
      • Ensure compliance with GMP standards.

    Quality Control (QC – API & Formulation)

    • Position: Officer/Executive
    • Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
    • Experience: 2–5 years
    • Responsibilities:
      • Hands-on experience in HPLC, GC, TOC instruments.
      • Conduct stability testing and analytical documentation.

    Engineering (API & Formulation)

    • Position: Officer/Executive
    • Qualification: BE (Mechanical)
    • Experience: 1–3 years
    • Responsibilities:
      • Perform plant maintenance and equipment troubleshooting.
      • Ensure smooth functioning of utilities.

    Eligibility / Qualifications

    • Education: M.Sc, B.Sc, B.Pharm, M.Pharm, BE (Mechanical).
    • Experience: 1–5 years in relevant pharma roles.
    • Skills Required:
      • Strong technical knowledge in QA, QC, Production, R&D, or Engineering.
      • Familiarity with GMP, QMS, and regulatory compliance.
      • Good analytical, documentation, and communication skills.

    Location & Salary

    • Job Location: Panoli, Gujarat
    • Job Type: Full-time
    • Salary: Competitive and based on experience.

    Application Process

    Interested candidates can send their updated CVs to:

    FAQs

    1. Who can apply for these openings at JB Pharma?
    Candidates with 1–5 years’ experience and relevant qualifications in QA, QC, Production, R&D, or Engineering.

    2. Is experience in formulations mandatory?
    Yes, experience in formulations and API manufacturing is required.

    3. What is the job location?
    Panoli, Gujarat.

    4. What technical skills are required for QC?
    Hands-on experience in HPLC, GC, and TOC instruments.

    5. How do I apply?
    Send your resume to Navneet.kaur@jbpharma.com.

    Advance your pharma career with JB Pharma at Panoli – Apply now and secure your future in one of India’s most reputed pharmaceutical companies.

    Summary Table

    Company JB Pharma
    Vacancies QA, QC, Production (Packing), R&D, Engineering
    Required Education B.Sc, M.Sc, B.Pharm, M.Pharm, BE (Mechanical)
    Experience 1–5 years
    <img class="size-full wp-image-123072" src="https://bpharmacyjobs.com/wp-content/uploads/2025/08/JB-Pharma-hiring.webp" alt="JB Pharma hiring Officers/Executives in QA, QC, Production, R&D & Engineering” width=”816″ height=”1056″ /> JB Pharma hiring Officers/Executives in QA, QC, Production, R&D & Engineering
  • Rednex Pharma walk-in QA Managers, Sr. Officers, Executives & Production Heads

    Rednex Pharma walk-in QA Managers, Sr. Officers, Executives & Production Heads

    QA & Production Openings | Rednex Pharma | Ahmedabad

    Rednex Pharma hiring QA Managers, Sr. Officers, Executives & Production Heads in Ahmedabad. Interview on 24th Aug 2025. Apply now!

    Rednex Pharmaceuticals Limited, a WHO-GMP certified company, is conducting a walk-in interview for multiple positions in Quality Assurance, Production, and Graphics Design at its Ahmedabad facility. This is an excellent opportunity for pharma professionals and fresh graduates to join a reputed pharmaceutical formulations manufacturer.

    Company Overview

    Rednex Pharmaceuticals is a trusted name in the formulations industry, producing high-quality tablets, capsules, oral liquids, and external preparations. With WHO-GMP certification and a focus on innovation, compliance, and patient safety, the company offers long-term career growth opportunities for pharma professionals.

    Job Role & Responsibilities

    1. Quality Assurance (QA)

    • Manager/Head (9–10 years exp.)
      • Develop, implement & maintain quality systems.
      • Conduct internal & external audits, oversee corrective actions.
      • Ensure compliance with regulatory requirements.
    • Sr. Officer (2–3 years exp.)
      • Documentation, QMS, Qualification, Validation, Calibration, IPQA.
    • Sr. Executive (3–4 years exp.)
      • Documentation, QMS, Validation, Calibration, IPQA, APQR, Audit & Compliance.

    2. Production Head

    • Qualification: B.Sc / M.Sc / B.Pharm
    • Experience: 8–10 years
    • Responsibilities: Oversee production of tablets, capsules, oral liquids, and external preparations ensuring compliance with GMP standards.

    3. Graphics Designer

    • Qualification: Any Graduate
    • Experience: Fresher (0–1 year)
    • Responsibilities:
      • Design pharma packaging materials, brochures, and social media creatives.
      • Work with software tools like CorelDraw & Photoshop.

    Eligibility / Qualifications

    • QA Roles: B.Pharm / M.Pharm with 2–10 years of QA experience.
    • Production Head: B.Sc / M.Sc / B.Pharm with 8–10 years’ experience in formulations.
    • Graphics Designer: Any Graduate with design knowledge (CorelDraw/Photoshop).
    • Note: Only candidates with pharma formulation backgrounds will be considered.

    Location & Salary

    • Work Location: Bavla, Ahmedabad, Gujarat.
    • Job Type: Full-time
    • Salary: Competitive, as per experience & role.
    • Employee Benefits: Transportation facility & attractive HR policies.

    Application Process

    • Interview Date: 24th August 2025
    • Time: 9:00 AM – 3:30 PM
    • Venue: Rednex Pharma, Survey No: 586 & 231, Nr. SKF Bearing, Bavla Bagodara N.H.-8A, Kerala, Ta. Bavla, Ahmedabad – 382220.
    • Email: hr.rednex@gmail.com
    • Contact: +91 9313508271 / 8799692591 (Call between 9:00 AM to 4:20 PM)
    • Documents Required: Updated CV, Increment letter, last 3 months’ payslips, relieving/service certificates, educational certificates, Aadhaar card.

    FAQs

    1. What roles are available at Rednex Pharmaceuticals?
    QA Manager/Head, Sr. Officer, Sr. Executive, Production Head, and Graphics Designer.

    2. Who can apply for QA roles?
    B.Pharm or M.Pharm candidates with 2–10 years of QA experience.

    3. Is prior experience required for Graphics Designer?
    No, freshers with design knowledge can apply.

    4. What is the interview date and venue?
    24th August 2025 at Rednex Pharma, Bavla, Ahmedabad.

    5. Are there benefits apart from salary?
    Yes, transport facility and attractive HR policies.

    Gujarat-based candidates are encouraged to apply. Attend the walk-in interview at Rednex Pharma on 24th August 2025 and secure your career in a WHO-GMP certified company.

    Summary Table

    Company Rednex Pharmaceuticals Limited
    Vacancies QA (Manager, Sr. Officer, Sr. Executive), Production Head, Graphics Designer
    Required Education B.Pharm, M.Pharm, B.Sc, M.Sc, Any Graduate
    Experience 0–10 years (Freshers accepted for design role)
    <img class="size-full wp-image-123069" src="https://bpharmacyjobs.com/wp-content/uploads/2025/08/Rednex-Pharma-walk-in-QA-Managers-Sr.-Officers-Executives-Production-Heads-1.webp" alt="Rednex Pharma walk-in QA Managers, Sr. Officers, Executives & Production Heads” width=”800″ height=”1252″ /> Rednex Pharma walk-in QA Managers, Sr. Officers, Executives & Production Heads
  • Eris Therapeutics Hiring QA (IPQA), QC (HPLC), Production, Engineering (Maintenance & Utility)

    Eris Therapeutics Hiring QA (IPQA), QC (HPLC), Production, Engineering (Maintenance & Utility)

    Eris Therapeutics Hiring | QA, QC, Engineering | Apply Now

    Eris Therapeutics is hiring in QA, QC & Engineering. Openings for Sr. Officer, Asst. Manager & Operators.

    Eris Therapeutics, a fast-growing name in the pharmaceutical sector, is inviting applications for multiple openings across Quality Assurance, Quality Control, and Engineering departments. This recruitment drive is ideal for pharma professionals with 2–12 years of experience seeking long-term career growth in a reputable organization.

    Company Overview

    Eris Therapeutics is recognized for its commitment to innovation, quality, and compliance in the pharmaceutical industry. With a strong presence in formulations and drug development, the company offers excellent opportunities for professionals to contribute to the production of high-quality medicines while advancing their careers in a collaborative environment.

    Job Role & Responsibilities

    Quality Assurance (IPQA)

    • Positions: Assistant Manager (9–12 years), Sr. Executive/Sr. Officer (5–7 years)
    • Qualification: M.Pharm / B.Pharm
    • Responsibilities: In-process quality checks, compliance monitoring, process validation, and documentation.

    Production – OSD & Injection/Process

    • Position: Senior Officer (4–6 years)
    • Qualification: B.Tech (Electrical)
    • Responsibilities: Oversee production processes, ensure operational efficiency, and support regulatory compliance.

    Engineering – Maintenance

    • Position: Fitter (2–4 years)
    • Qualification: ITI / HSC / B.Com / Diploma
    • Responsibilities: Maintenance of equipment, troubleshooting, and plant upkeep.

    Engineering – Utility

    • Position: Electrician / Operator (3–5 years)
    • Qualification: ITI / Diploma
    • Responsibilities: Operation and maintenance of utility systems, electrical compliance, and support.

    Quality Control (HPLC)

    • Positions: Senior Officer / Officer (2–4 years)
    • Qualification: B.Pharm / M.Pharm / B.Sc Chemistry
    • Responsibilities: Analytical testing using HPLC, documentation of results, and support in stability studies.

    Eligibility / Qualifications

    • Education: B.Pharm, M.Pharm, B.Tech (Electrical), B.Sc Chemistry, ITI, Diploma, HSC, or equivalent.
    • Experience: 2–12 years depending on the role.
    • Skills Required:
      • Strong knowledge of QA, QC, or Engineering processes.
      • Familiarity with GMP guidelines and regulatory requirements.
      • Hands-on expertise with equipment such as HPLC and production machinery.

    Location & Salary

    • Work Location: Eris Therapeutics facility (details shared upon shortlisting).
    • Job Type: Full-time
    • Salary: Competitive, aligned with experience and qualifications.

    Application Process

    Interested candidates can apply by sending their CV to:

    FAQs

    1. Who can apply for these openings at Eris Therapeutics?
    Candidates with qualifications in Pharmacy, Engineering, Chemistry, or related fields and 2–12 years of experience.

    2. What departments are open for recruitment?
    Quality Assurance (IPQA), Quality Control (HPLC), Production (OSD/Injection), and Engineering (Maintenance & Utility).

    3. Is HPLC experience mandatory for QC roles?
    Yes, hands-on HPLC experience is required for QC openings.

    4. What is the career growth at Eris Therapeutics?
    Employees gain exposure to global quality standards, regulatory audits, and cross-functional training, enabling long-term career growth.

    5. How to apply?
    Send your CV to recruitment@eristherapeutics.com or contact via the given phone numbers.

    Apply today and build your career with Eris Therapeutics in QA, QC, or Engineering departments!

    Summary Table

    Company Eris Therapeutics
    Vacancies QA (IPQA), QC (HPLC), Production, Engineering (Maintenance & Utility)
    Required Education B.Pharm, M.Pharm, B.Tech, B.Sc Chemistry, ITI, Diploma
    Experience 2–12 years
    <img class="size-full wp-image-123058" src="https://bpharmacyjobs.com/wp-content/uploads/2025/08/Eris-Therapeutics-Hiring-QA-IPQA-QC-HPLC-Production-Engineering-Maintenance-Utility-1.webp” alt=”Eris Therapeutics Hiring QA (IPQA), QC (HPLC), Production, Engineering (Maintenance & Utility)” width=”1200″ height=”1200″ /> Eris Therapeutics Hiring QA (IPQA), QC (HPLC), Production, Engineering (Maintenance & Utility)
  • Steril-Gene Life Sciences Hiring QA, EHS, Production Chemists & Tech Transfer

    Steril-Gene Life Sciences Hiring QA, EHS, Production Chemists & Tech Transfer

    Steril-Gene Life Sciences Hiring | QA, EHS, Production, Tech Transfer | Puducherry

    Steril-Gene Life Sciences Puducherry hiring for QA, EHS, Production Chemists & Tech Transfer. Apply today for multiple pharma vacancies.

    Steril-Gene Life Sciences Pvt. Ltd., a USFDA and MHRA-approved pharmaceutical facility located in Puducherry, is hiring professionals across multiple departments. With openings in Quality Assurance, Environment Health & Safety (EHS), Production (Sterile), and Technology Transfer, this recruitment drive offers excellent career opportunities in a global-standard manufacturing facility.

    Company Overview

    Steril-Gene Life Sciences Pvt. Ltd. is a joint venture between The Madras Pharmaceuticals (India) and Lloyd Laboratories (Philippines). With its world-class greenfield facility in Puducherry, the company has established itself as a trusted contract manufacturing partner, meeting stringent international quality and regulatory standards. Its approvals from USFDA, MHRA, and other global agencies highlight its strong commitment to compliance, innovation, and patient safety.

    Job Role & Responsibilities

    1. Quality Assurance (2–5 Years)

    • Roles: IPQA, Validation, Process Validation, Training, QMS, DQA, CSV
    • Responsibilities: Ensuring in-process quality assurance, conducting process validations, managing QMS, and ensuring compliance with regulatory guidelines.

    2. Environment Health & Safety (EHS)

    • Qualification: ME / M.Tech in Industrial Safety
    • Experience: 5–8 years (with mandatory process safety experience)
    • Responsibilities: Implementing EHS policies, conducting risk assessments, process safety management, and ensuring regulatory compliance.

    3. Production Chemist – Sterile (1–5 Years)

    • Qualification: B.Pharm / M.Pharm / M.Sc (Chemistry / Pharmaceutical Sciences)
    • Responsibilities: Sterile manufacturing operations, compliance with GMP, documentation, and coordination with QA teams.

    4. Technology Transfer (Freshers)

    • Qualification: M.Pharm (Pharmaceutics / Pharmaceutical Technology)
    • Experience: Freshers welcome
    • Responsibilities: Support technology transfer activities, documentation, and product development transition from R&D to production.

    Eligibility / Qualifications

    • QA: B.Pharm / M.Pharm / M.Sc with 2–5 years’ experience in QA functions.
    • EHS: ME / M.Tech in Industrial Safety with 5–8 years’ process safety experience.
    • Production Chemist: B.Pharm / M.Pharm / M.Sc with 1–5 years’ experience in sterile manufacturing.
    • Tech Transfer: M.Pharm freshers specializing in pharmaceutics/pharma technology.

    Location & Salary

    • Work Location: Puducherry, India
    • Job Type: Full-time
    • Salary: Competitive; based on qualifications and relevant experience.

    Application Process

    Interested candidates can apply by sharing their updated resume to:

    Applicants are encouraged to apply early to secure their chance in this hiring drive.

    FAQs

    1. Who can apply for Steril-Gene Life Sciences vacancies?
    Qualified candidates with relevant education and experience in QA, EHS, or Production, and M.Pharm freshers for Tech Transfer can apply.

    2. What experience is required for QA roles?
    2–5 years of experience in IPQA, QMS, Validation, DQA, or CSV functions is required.

    3. Can freshers apply?
    Yes, M.Pharm freshers can apply for Technology Transfer roles.

    4. What is the qualification for the EHS role?
    ME/M.Tech in Industrial Safety with 5–8 years’ process safety experience is mandatory.

    5. Where is the job located?
    All positions are based at Steril-Gene’s Puducherry facility.

    Apply now and be part of Steril-Gene Life Sciences’ world-class pharma team in Puducherry!

    Summary Table

    Company Steril-Gene Life Sciences Pvt. Ltd.
    Vacancies QA, EHS, Production Chemist, Technology Transfer
    Required Education B.Pharm, M.Pharm, M.Sc, ME/M.Tech (Industrial Safety)
    Experience Freshers (Tech Transfer) / 1–8 years (QA, EHS, Production)
    <img class="size-full wp-image-123011" src="https://bpharmacyjobs.com/wp-content/uploads/2025/08/Steril-Gene-Life-Sciences-Hiring-QA-EHS-Production-Chemists-Tech-Transfer-1.webp" alt="Steril-Gene Life Sciences Hiring QA, EHS, Production Chemists & Tech Transfer” width=”569″ height=”556″ /> Steril-Gene Life Sciences Hiring QA, EHS, Production Chemists & Tech Transfer
  • Macleods Pharma Hiring 11 (Bioanalytical Scientist – IVPT)

    Macleods Pharma Hiring 11 (Bioanalytical Scientist – IVPT)

    Bioanalytical Scientist Vacancies | M.Pharm/M.Sc/B.Pharm | Macleods Pharma

    Macleods Pharma hiring 11 Bioanalytical Scientists (IVPT). M.Pharm/M.Sc/B.Pharm with 2–5 years’ experience required. Apply today!

    Macleods Pharmaceuticals, a global leader in pharmaceutical research and development, is inviting applications for 11 openings in its Bioanalytical Section (IVPT). This opportunity is open to experienced professionals with a background in M.Pharm, M.Sc (Analytical Chemistry/Chemistry), or B.Pharm. If you are passionate about advancing your career in bioanalytical research and method development, this role provides an excellent platform within a globally reputed pharmaceutical company.

    Company Overview

    Macleods Pharmaceuticals is one of India’s top-ranked pharmaceutical companies with a strong global presence. With a focus on research, formulation development, and bioequivalence studies, Macleods has built a reputation for quality, compliance, and innovation. Its Bioanalytical division plays a critical role in drug development, ensuring accurate measurement of drug and metabolite concentrations to support preclinical and clinical studies.

    Job Role & Responsibilities

    Position: Bioanalytical Scientist (IVPT)
    Vacancies: 11
    Experience: 2–5 years

    Key Responsibilities:

    • Assist project leaders in conducting in vitro and bioanalytical studies.
    • Develop and validate bioanalytical and in vitro methods for drug/metabolite analysis.
    • Perform analysis of biological and in vitro samples for drug concentrations.
    • Write, review, and revise SOPs as required.
    • Maintain equipment and instruments, ensuring compliance with GLP guidelines.
    • Compile raw data in lab notebooks, data sheets, and maintain equipment logbooks.
    • Calibrate laboratory instruments such as pipettes, handysteps, and dispensers.
    • Ensure lab safety, housekeeping, and regulatory compliance in the bioanalytical section.
    • Support the project leader in report compilation and documentation.

    Eligibility / Qualifications

    • Education: M.Pharm, M.Sc (Analytical Chemistry, Chemistry), B.Pharm.
    • Experience: 2–5 years in a bioanalytical laboratory.
    • Skills Required: Strong knowledge of bioanalytical method validation, GLP compliance, SOP writing, and drug/metabolite quantification.
    • Note: Freshers are not eligible for this position.

    Location & Salary

    • Work Location: Macleods Pharma Bioanalytical Section (IVPT).
    • Job Type: Full-time
    • Salary: Competitive; based on experience and qualifications.

    Application Process

    Interested candidates should send their resumes to:

    Applicants should apply at the earliest as shortlisting will be on a rolling basis.

    FAQs

    1. Who can apply for the Bioanalytical Scientist role at Macleods Pharma?
    Candidates with M.Pharm, M.Sc (Analytical Chemistry/Chemistry), or B.Pharm and 2–5 years’ experience in bioanalytical research can apply.

    2. Are freshers eligible?
    No, only experienced candidates with 2–5 years’ background in bioanalytical methods are considered.

    3. What are the main responsibilities of this role?
    Developing and validating bioanalytical methods, analyzing drug/metabolite concentrations, maintaining GLP compliance, and assisting in reporting.

    4. How many vacancies are available?
    There are 11 vacancies in the Bioanalytical Section (IVPT).

    5. Where is the job located?
    The position is based at Macleods Pharma’s Bioanalytical Section (IVPT).

    Apply today to secure one of the 11 openings at Macleods Pharma’s Bioanalytical Section and advance your career in analytical research!

    Summary Table

    Company Macleods Pharmaceuticals Ltd.
    Vacancies 11 (Bioanalytical Scientist – IVPT)
    Required Education M.Pharm, M.Sc (Analytical Chemistry/Chemistry), B.Pharm
    Experience 2–5 years