Job Tag: Pharma Jobs in Visakhapatnam

  • Pfizer Quality Assurance Associate Vacancy | Vizag

    Pfizer Quality Assurance Associate Vacancy | Vizag

    Pfizer Quality Assurance Associate Recruitment

    Apply for Pfizer’s Associate – Quality Assurance role in Vizag. Openings for graduates in pharma, science. Start your QA career today.


    At Pfizer, quality isn’t just a standard — it’s a promise to patients worldwide. As an Associate – Quality Assurance in Vizag, you will play a vital role in ensuring every product meets the highest global standards of safety and effectiveness. This is your opportunity to join a global leader in pharmaceuticals where your work directly impacts patient health outcomes.


    Company Overview

    Pfizer is one of the world’s largest biopharmaceutical companies, trusted for its commitment to advancing science and delivering medicines that improve lives. With a strong culture of compliance, innovation, and collaboration, Pfizer consistently upholds its mission of bringing breakthroughs that change patients’ lives. The Vizag site plays a pivotal role in manufacturing and quality operations for regional and global supply.


    Job Role & Responsibilities

    As an Associate – Quality Assurance, you will:

    • Evaluate and review clinical and commercial drug batches for quality compliance.
    • Conduct product and process document verification using statistical process controls.
    • Identify deviations in manufacturing and packaging and initiate corrective measures.
    • Approve investigations and monitor change control activities in line with compliance policies.
    • Support manufacturing and packaging teams in real-time error detection and resolution.
    • Maintain inspection readiness for regulatory and customer audits.
    • Assist with quality risk management assessments and continuous improvement initiatives.

    This role is central to Pfizer’s dedication to Good Manufacturing Practices (cGMP) and risk-based quality assurance.


    Eligibility / Qualifications

    Minimum Requirements:

    • Bachelor’s degree in Pharmacy, Life Sciences, Biotechnology, Microbiology, Chemistry, or related fields
    • OR Associate’s degree with 4 years of experience
    • OR High school diploma with 6 years of relevant experience
    • Knowledge of pharmaceutical manufacturing and quality systems
    • Familiarity with current Good Manufacturing Practices (GMP/GxP)
    • Strong teamwork and communication skills

    Preferred Qualifications:

    • Hands-on experience at a manufacturing site
    • Expertise in deviation management, batch record review, ERP systems, and root cause analysis
    • Experience with change control management
    • Strong problem-solving and time management skills

    Relevant courses: B.Pharm, M.Pharm, B.Sc (Chemistry, Biotechnology, Microbiology, Life Sciences), M.Sc (Chemistry, Microbiology, Biotechnology).


    Location & Salary

    • Location: Vizag, India
    • Work Type: Full-time, On-site
    • Salary: Competitive package aligned with Pfizer’s global standards (details discussed during hiring process)
    Pfizer Quality Assurance Associate Vacancy | Vizag
    Pfizer Quality Assurance Associate Vacancy | Vizag

    Application Process

    Interested candidates can apply directly through Pfizer’s official careers portal:
    👉 Apply Here

    Apply before the closing date to secure your chance of joining Pfizer’s QA team.


    FAQs

    Q1: Who can apply for Pfizer’s Quality Assurance Associate role in Vizag?
    Candidates with a degree in Pharmacy, Life Sciences, Biotechnology, or Chemistry (freshers and experienced) can apply.

    Q2: What skills are required?
    Knowledge of GMP, pharmaceutical quality systems, problem-solving, and teamwork are essential.

    Q3: Is prior pharma experience mandatory?
    Not mandatory, but prior exposure to manufacturing sites, deviation management, or batch record review is preferred.

    Q4: How can I apply?
    You can apply online through Pfizer’s official careers site using the provided application link.

    Q5: What is the work type?
    This is a full-time, on-site role based in Vizag.


    Why Join Pfizer?

    • Global leader in pharmaceuticals with strong career growth opportunities.
    • Commitment to patient safety and regulatory excellence.
    • Exposure to world-class manufacturing and QA practices.
    • Work with a diverse team of professionals making a real-world impact.

    Call to Action

    Don’t miss this opportunity to build a rewarding career in Quality Assurance with Pfizer.
    👉 Apply today and be part of a team that ensures safe, effective, and life-saving medicines reach patients worldwide.


    Vertical Summary Table

    Company Pfizer
    Vacancies Associate – Quality Assurance
    Required Education B.Pharm, M.Pharm, B.Sc (Chemistry, Biotechnology, Microbiology, Life Sciences), M.Sc (Chemistry, Biotechnology, Microbiology)
    Experience Freshers and experienced candidates (0–6+ years)
  • Pfizer Walk-in QC & Microbiology

    Pfizer Walk-in QC & Microbiology

    Pfizer QC & Microbiology Openings | 1-10 Yrs Exp | Vizag

    Walk-in at Pfizer Visakhapatnam for QC & Microbiology roles. Hiring M.Sc/B.Pharm/M.Pharm with 1–10 yrs exp. Apply on 27th July 2025.


    Pfizer Healthcare India is conducting a walk-in drive in Visakhapatnam for experienced professionals in Quality Control (QC) and Microbiology. This is a golden opportunity to work with a global pharmaceutical leader known for innovation, regulatory compliance, and patient-centric solutions. If you are passionate about ensuring product quality and safety, Pfizer offers the right platform to advance your career.


    Company Overview

    Pfizer Healthcare India Pvt. Ltd. is part of the globally renowned Pfizer Inc., one of the largest biopharmaceutical companies in the world. With a strong focus on research, innovation, and high-quality manufacturing, Pfizer has consistently contributed to life-saving therapies. The Visakhapatnam facility is a state-of-the-art plant, meeting stringent USFDA, EMA, and WHO compliance standards, producing formulations that serve patients across the globe.


    Job Role & Responsibilities

    1. Quality Control (Chemistry)

    • Conduct routine chemical testing of raw materials, intermediates, and finished products.
    • Hands-on experience in analytical instruments such as HPLC, LIMS, GC, AAS, ICP-MS, UV, IR.
    • Prepare, analyze, and interpret test reports.
    • Ensure compliance with GMP, GLP, and regulatory guidelines.
    • Maintain documentation accuracy and data integrity.

    2. Quality Control – Microbiology (1–5 Years Exp)

    • Perform microbiological tests including water analysis, MLT, BET, and handling Bio ball cultures.
    • Conduct microbial analysis of finished products, raw materials, and packaging components.
    • Support environmental monitoring and aseptic testing practices.
    • Maintain laboratory equipment and follow strict quality compliance protocols.

    3. Quality Control – Microbiology (6–10 Years Exp)

    • Lead method validation and transfer activities, prepare protocols and reports.
    • Review and approve test method validation, media preparation, and equipment qualification records.
    • Conduct microbiology-related investigations and corrective action recommendations.
    • Manage LIMS entries and laboratory data reviews.
    • Act as a senior team member in cross-functional investigations.

    Eligibility / Qualifications

    • Education: M.Sc. (Chemistry/Microbiology), B.Pharm, M.Pharm.
    • Experience: 1–10 years (depending on role).
    • Strong knowledge of analytical/microbiological techniques.
    • Proficiency in GMP documentation and compliance systems.
    • Good communication and collaboration skills.

    Location & Walk-In Details

    • Company: Pfizer Healthcare India Pvt. Ltd.
    • Venue: Ginger Hotel, Gajuwaka, #27-8-308/1/1, Srinagar, Rear Vadlapudi Railway Gate, Visakhapatnam – 530044.
    • Date & Time: Sunday, 27th July 2025 | 09:00 AM – 04:00 PM.

    Application Process

    Interested candidates should attend the walk-in interview with:

    • Updated Resume
    • Educational Certificates
    • Latest Payslips & CTC Breakup
    • Government ID Proof (Aadhar/PAN)

    If you are unable to attend, you can also share your resume via Pfizer’s official career portal.


    FAQs

    1. Who can apply for Pfizer QC roles?
    Candidates with M.Sc. Chemistry/Microbiology, B.Pharm, or M.Pharm with relevant experience in QC or microbiology.

    2. Is prior pharma experience mandatory?
    Yes, 1–10 years of QC/microbiology experience in the pharmaceutical industry is required.

    3. What skills are essential for selection?
    Expertise in analytical techniques (HPLC, GC, LIMS, etc.), microbiological testing, GMP compliance, and data integrity practices.

    4. Will freshers be considered?
    No, these openings are for experienced professionals only.

    5. How do I prepare for the walk-in?
    Review your technical knowledge in QC/microbiology, carry all required documents, and be prepared to discuss regulatory compliance and problem-solving scenarios.


    Summary Table

    Company Pfizer Healthcare India Pvt. Ltd.
    Vacancies Multiple (QC Chemistry & Microbiology)
    Required Education M.Sc. Chemistry/Microbiology, B.Pharm, M.Pharm
    Experience 1–10 Years
    Location Visakhapatnam, Andhra Pradesh

    Pfizer Walk-in QC & Microbiology
    Pfizer Walk-in QC & Microbiology
  • Neuland Walk-in Production, QC & Engineering

    Neuland Walk-in Production, QC & Engineering

    Neuland Walk-in Interviews – B.Sc/M.Sc/B.Pharm Vacancies in Hyderabad

    Neuland Labs hiring B.Sc, M.Sc, B.Pharm candidates for Production, QC & Engineering roles. Walk-in interviews on 30th & 31st Aug 2025 at Visakhapatnam.


    If you are a pharma professional looking for a career boost, Neuland Laboratories invites you to its walk-in interview drive for multiple departments including Production, Quality Control, and Engineering. With opportunities across chemist, officer, and executive levels, this is your chance to join a reputed pharmaceutical company with strong global presence.


    Company Overview

    Neuland Laboratories is a trusted pharmaceutical company known for manufacturing high-quality APIs and intermediates for global markets. With a commitment to compliance, innovation, and growth, Neuland offers excellent career development opportunities for pharma professionals. The company continues to expand its operations with state-of-the-art facilities and a focus on delivering value-driven healthcare solutions.


    Job Role & Responsibilities

    Neuland is hiring across multiple roles:

    Production

    • Intermediate / Clean Room
      • Positions: Chemist / Officer
      • Responsibilities: Operate and monitor production processes, ensure compliance with GMP guidelines, and maintain cleanroom standards.
    • Production DCS (Automation)
      • Positions: Executives
      • Responsibilities: Handle automated production systems, oversee process controls, and support troubleshooting.

    Quality Control (QC)

    • HPLC, GC, LC-MS & ICP-MS
      • Positions: Chemist / Officer
      • Responsibilities: Conduct analytical testing, method validation, and documentation as per regulatory standards.

    Plant Engineering

    • Mechanical Maintenance, Electrical, Instrumentation & Utility
      • Positions: Shift In-charge, Officer, Executives
      • Responsibilities: Perform maintenance of plant machinery, oversee utility operations, and ensure smooth functioning of production units.

    Eligibility / Qualifications

    Experience Required:

    • Production: 3–9 years
    • QC: 4–6 years
    • Engineering: 6–8 years

    Location & Interview Details

    • Work Location: Hyderabad (Pharma Manufacturing Units)
    • Interview Venue: Quality Inn Ramachandra, #31-41/10/1, Revenue Ward No.58, Duvvada Railway Station Road, Near Flyover, Duvvada, Visakhapatnam – 530046 (AP)
    • Interview Dates: 30th & 31st August 2025 (Saturday & Sunday)
    • Timings: 09:00 AM – 05:00 PM

    Application Process

    Interested candidates should attend the walk-in with the following documents:

    • Updated CV
    • Last 2 months’ pay slips
    • Increment letter / salary proof

    Alternatively, you may share your profile at:


    Why Join Neuland Labs?

    • Exposure to world-class pharma facilities
    • Opportunity to work with global regulatory standards
    • Career progression with skill development programs
    • Strong focus on employee welfare and benefits

    FAQs

    1. Who can attend the Neuland walk-in interview?
    Candidates with B.Sc, M.Sc, B.Pharm, or B.Tech qualifications and 3–9 years of relevant experience in Production, QC, or Engineering.

    2. What documents should I bring?
    Updated CV, last 2 months’ pay slips, increment letter, and relevant educational certificates.

    3. Is this opportunity open for freshers?
    No, only experienced candidates (minimum 3 years) are eligible.

    4. Where is the work location?
    Selected candidates will work at Neuland’s pharma units in Hyderabad.


    Quick Summary Table

    Category Details
    Company Neuland Laboratories Ltd.
    Vacancies Production, QC, Engineering
    Required Education B.Sc, M.Sc, B.Pharm, B.Tech
    Experience 3–9 Years
    Work Location Hyderabad
    Interview Venue Quality Inn Ramachandra, Duvvada, Visakhapatnam
    Dates 30th & 31st August 2025
    Contact grabhilash@neulandlabs.com / +91 91820 63878 / 99083 55567
    <img class="size-full wp-image-123090" src="https://bpharmacyjobs.com/wp-content/uploads/2025/08/Neuland-Walk-in-Production-QC-Engineering-1.webp" alt="Neuland Walk-in Production, QC & Engineering” width=”1600″ height=”835″ /> Neuland Walk-in Production, QC & Engineering
  • Dr. Reddy’s Laboratories Hiring Production QMS

    Dr. Reddy’s Laboratories Hiring Production QMS

    Dr. Reddy’s Hiring Production QMS | 4-8 Yrs | Visakhapatnam

    Apply for Production QMS role at Dr. Reddy’s Injectable Site in Visakhapatnam. Pharma graduates with 4–8 years’ experience can apply today.


    Dr. Reddy’s Laboratories, one of India’s leading multinational pharmaceutical companies, is inviting applications for the position of Production QMS at its Injectable Site in Visakhapatnam. This opportunity is designed for pharma professionals with strong expertise in Quality Management Systems (QMS), investigations, and regulatory compliance. Candidates with prior experience in injectables production and QMS activities are highly encouraged to apply.


    Company Overview

    Dr. Reddy’s Laboratories is a globally recognized pharmaceutical giant committed to delivering affordable and innovative medicines to patients worldwide. With a strong presence across APIs, formulations, biosimilars, and injectables, the company operates with a mission to provide good health can’t wait. Employees at Dr. Reddy’s gain exposure to international regulatory standards, advanced technologies, and a culture of continuous learning and professional growth.


    Job Role & Responsibilities

    Production QMS – Injectable Division

    • Experience: 4–8 Years
    • Location: Visakhapatnam
    • Key Responsibilities:
      • Conduct root cause analysis (RCA) and manage Corrective and Preventive Actions (CAPA).
      • Investigate valid Out of Specification (OOS) and deviation cases.
      • Maintain and review deviations log, classify data, and ensure compliance.
      • Provide support during regulatory inspections and audits.
      • Ensure compliance with QMS for injectable production.
      • Align with global regulatory requirements for incident investigations.

    Eligibility / Qualifications

    • Education: B.Pharm, M.Pharm
    • Experience: 4–8 Years in Production QMS
    • Special Preference: Candidates with injectable QMS experience.

    Relevant courses: B.Pharm (Pharmaceutical Sciences, Pharmaceutical Technology), M.Pharm (Pharmaceutical Analysis, Pharmaceutical Chemistry, Industrial Pharmacy).


    Location & Salary

    • Work Location: Dr. Reddy’s Laboratories, Injectable Site, Visakhapatnam, Andhra Pradesh.
    • Salary: Attractive compensation package aligned with industry standards, along with benefits and growth opportunities.

    Application Process

    Interested professionals should apply by sending their updated resume to the below email address.

    Email: dhineshtejaummadisetti01@drreddys.com
    Subject Line: “QMS”

    Apply before 23rd August 2025 to secure your spot at one of India’s most prestigious pharmaceutical companies.


    FAQs

    1. Who can apply for the Production QMS role?
    Pharma graduates with 4–8 years’ experience in QMS, preferably in injectables.

    2. Is injectable experience mandatory?
    It is highly preferred since the role is based at an injectable site.

    3. What skills are important for this role?
    Root cause analysis, CAPA handling, deviation management, and knowledge of regulatory requirements.

    4. What is the selection process?
    Application screening followed by technical and HR interviews.

    5. Where is the job located?
    Visakhapatnam, Andhra Pradesh at Dr. Reddy’s Injectable Site.


    Summary Table

    Category Details
    Company Dr. Reddy’s Laboratories
    Vacancies Production QMS (Injectables)
    Required Education B.Pharm, M.Pharm
    Experience 4–8 Years