PHARMA STUFF

Job Tag: pharma jobs in hyderabad

  • Pfizer Walk-In Drive – Manufacturing Roles in Hyderabad

    Pfizer Walk-In Drive – Manufacturing Roles in Hyderabad

    Pfizer Walk-In Drive – Manufacturing Roles in Hyderabad (Sep 21, 2025)

    Attend Pfizer Walk-In Drive in Hyderabad on Sep 21, 2025, for Manufacturing roles. Openings for Operators, Supervisors, and Equipment Specialists.

    Pfizer Healthcare India Pvt Ltd, a global leader in pharmaceuticals, is conducting a Walk-In Drive for experienced professionals in manufacturing injectables. The event will be held on Sunday, 21st September 2025, from 8:30 AM onwards, at Hotel Aditya Park Sarovar Portico, Ameerpet, Hyderabad.

    This drive presents an exciting opportunity for diploma holders, science graduates, pharmacy, and engineering professionals to join Pfizer’s world-class manufacturing team.

    Company Overview

    Pfizer is one of the world’s most respected pharmaceutical companies, known for its commitment to breakthroughs that change patients’ lives. With operations spanning across multiple therapeutic areas, Pfizer is at the forefront of manufacturing excellence, compliance, and innovation. Employees benefit from working in a regulated global environment (USFDA-approved facilities) that emphasizes safety, quality, and professional growth.

    Job Role & Responsibilities

    1. Manufacturing – Experience Operators

    • Qualification: Diploma / B.Sc
    • Experience: 2 to 12 years in injectable manufacturing
    • Key Skills:
      • Operating equipment such as vial filling, washing, capping, sealing, compounding, terminal sterilization, and stopper processes.
      • Ensuring compliance with cGMP standards.

    2. Manufacturing – Supervisors

    • Qualification: M.Pharmacy / M.Sc (6–10 years) or B.Pharmacy (8–12 years)
    • Key Skills:
      • Supervising manufacturing operations (Upstream/Downstream injectables).
      • Strong people management experience in regulated manufacturing.
      • Sound knowledge of cGMP.
      • Strong leadership, communication, and decision-making skills.

    3. Manufacturing – Senior Equipment Specialists (SES)

    • Qualification: Diploma / BE / B.Tech / ME / M.Tech in Mechanical Engineering
    • Experience: 6 to 10 years in Pharma/Chemicals/FMCG/Food & Beverages/Cosmetics.
    • Key Skills:
      • Preventive and corrective equipment maintenance.
      • Equipment reliability planning and documentation.
      • Root cause analysis of equipment losses and execution of corrective actions.

    Eligibility / Qualifications

    • Operators: Diploma, B.Sc with 2–12 years in injectable manufacturing.
    • Supervisors: M.Pharm/M.Sc (6–10 years) or B.Pharm (8–12 years).
    • Senior Equipment Specialists: Diploma/BE/B.Tech/ME/M.Tech (Mechanical Engineering) with 6–10 years of relevant industry experience.

    Relevant courses: B.Sc Chemistry, M.Sc Chemistry, B.Pharmacy, M.Pharmacy, BE/B.Tech Mechanical Engineering, M.Tech Mechanical Engineering, Diploma in Mechanical/Industrial Engineering.

    Location & Salary

    • Work Location: Pfizer Healthcare India Pvt Ltd – Visakhapatnam manufacturing site.
    • Interview Venue: Hotel Aditya Park Sarovar Portico, Aditya Trade Center, Satyam Theatre Road, Opp. Aster Prime Hospital, Kumar Basti, Ameerpet, Hyderabad – 500038.
    • Date & Time: Sunday, 21st September 2025, from 8:30 AM onwards.
    • Compensation: Competitive salary as per Pfizer standards and experience.

    Application Process

    Eligible candidates should attend the walk-in drive with:

    • Updated Resume
    • Last 3 Months’ Pay Slips
    • Recent Increment Letter

    Visit the official Pfizer careers website for more details: www.pfizer.co.in

    Why Join Pfizer?

    • Be part of a company known for global regulatory compliance (USFDA, EMA-approved plants).
    • Contribute to manufacturing life-saving injectable therapies.
    • Work with advanced technologies in a high-quality, safety-driven environment.
    • Competitive compensation and growth-oriented career pathways.
    • Exposure to a global pharmaceutical manufacturing network.

    FAQs

    Q1: What is the eligibility for Operators?
    Diploma/B.Sc with 2–12 years’ experience in injectable manufacturing.

    Q2: What is the eligibility for Supervisors?
    M.Pharm/M.Sc with 6–10 years, or B.Pharm with 8–12 years in manufacturing injectables.

    Q3: What is the eligibility for Senior Equipment Specialists?
    Diploma/BE/B.Tech/ME/M.Tech (Mechanical Engineering) with 6–10 years in pharma/related industries.

    Q4: Where is the interview venue?
    Hotel Aditya Park Sarovar Portico, Ameerpet, Hyderabad.

    Q5: What documents should I carry?
    Updated resume, 3 months’ pay slips, and latest increment letter.

    Summary Table

    Category Details
    Company Pfizer Healthcare India Pvt Ltd
    Vacancies Multiple (Operators, Supervisors, Senior Equipment Specialists)
    Required Education Diploma, B.Sc, B.Pharm, M.Pharm, M.Sc, BE/B.Tech, ME/M.Tech
    Experience 2–12 years depending on the role
  • Clarivate Hiring Associate STEM Content Analyst – Hyderabad (Freshers Eligible)

    Clarivate Hiring Associate STEM Content Analyst – Hyderabad (Freshers Eligible)

    Clarivate Hiring Associate STEM Content Analyst – Hyderabad (Freshers Eligible)

    Apply at Clarivate Hyderabad for Associate STEM Content Analyst role. Life sciences graduates with 0–1 year experience in clinical research can apply. melania trump nude Macarena

    Clarivate, a global leader in healthcare analytics, clinical research intelligence, and pharmaceutical data solutions, is looking for an Associate STEM Content Analyst to join its Clinical Studies team in Hyderabad, Telangana. This hybrid opportunity is ideal for freshers and early-career professionals in Life Sciences and Pharmacy who want to contribute to global clinical trial intelligence and drug development insights.

    Company Overview

    Clarivate is a trusted multinational analytics company providing data-driven insights to accelerate innovation in pharmaceuticals, biotechnology, healthcare, and life sciences. The company powers its clients’ decision-making with platforms like Cortellis Clinical Trial Intelligence and Cortellis Drug Discovery Intelligence. With a focus on delivering reliable clinical and drug pipeline data, Clarivate enables pharma companies, researchers, and regulatory authorities to make evidence-based decisions for better patient outcomes.

    Job Role & Responsibilities

    As an Associate STEM Content Analyst (Clinical Studies team), you will:

    • Actively collect and analyze clinical trial data from multiple reliable sources (scientific meetings, trial registries, press releases, and conferences).
    • Maintain and update Clarivate’s proprietary Cortellis Clinical Trial Intelligence database with accurate, real-time information.
    • Cross-reference and validate clinical records for consistency and quality.
    • Deliver weekly targets and meet content accuracy and compliance standards.
    • Interpret complex data related to clinical trials, drug pipelines, and development phases.
    • Conduct secondary research to extract and synthesize valuable insights for global stakeholders.
    • Collaborate with a team of 20 content experts to ensure streamlined workflows and timely outputs.

    Eligibility / Qualifications

    • Education: B.Pharmacy, M.Pharmacy, M.Sc Biotechnology, M.Sc Microbiology, or equivalent Life Sciences qualification.
    • Experience: 0–1 year in analyzing, updating, or researching clinical trial and drug development information.
    • Technical Skills:
      • Knowledge of clinical research, pharmaceutical pipelines, and drug development phases.
      • Proficiency in secondary research and data analysis.
    • Soft Skills:
      • Strong English communication (written and verbal).
      • Analytical mindset with problem-solving abilities.
      • Attention to detail and commitment to data quality.

    Relevant courses under eligibility: B.Pharm, M.Pharm (Pharmaceutics, Clinical Research, Pharmaceutical Analysis), M.Sc Biotechnology, M.Sc Life Sciences, M.Sc Microbiology, M.Sc Biochemistry.

    Location & Salary

    • Location: Hyderabad, Telangana, India
    • Work Model: Hybrid (Monday to Friday, 9 AM – 6 PM IST)
    • Employment Type: Full-time
    • Compensation: Competitive salary based on company standards
    <img class="size-full wp-image-123177" src="https://bpharmacyjobs.com/wp-content/uploads/2025/09/Clarivate-Hiring-Associate-STEM-Content-Analyst-–-Hyderabad-Freshers-Eligible.webp" alt="Clarivate Hiring Associate STEM Content Analyst – Hyderabad (Freshers Eligible)” width=”1200″ height=”675″ /> Clarivate Hiring Associate STEM Content Analyst – Hyderabad (Freshers Eligible)

    Application Process

    Interested candidates can apply directly via Clarivate’s official career portal:
    Apply Here

    Why Join Clarivate?

    • Work on industry-leading platforms like Cortellis Clinical Trial Intelligence.
    • Build a career in clinical research content management and drug development analytics.
    • Gain exposure to global pharmaceutical pipelines and industry insights.
    • Structured learning environment with hybrid flexibility.
    • Opportunity to collaborate with international pharma clients and stakeholders.

    FAQs

    Q1: Is this role open for freshers?
    Yes, candidates with 0–1 year of relevant experience are eligible.

    Q2: What qualifications are required?
    B.Pharm, M.Pharm, or M.Sc in Biotechnology, Life Sciences, or Microbiology.

    Q3: What skills are most valuable?
    Knowledge of clinical trial processes, pharmaceutical drug pipelines, data analysis, and excellent communication.

    Q4: What is the work model?
    Hybrid – Monday to Friday, 9 AM to 6 PM IST.

    Q5: How do I apply?
    Apply directly via Clarivate’s official careers portal (link above).

    Summary Table

    Category Details
    Company Clarivate
    Vacancies Multiple (Associate STEM Content Analyst)
    Required Education B.Pharm, M.Pharm, M.Sc Biotechnology, M.Sc Microbiology, M.Sc Life Sciences, M.Sc Biochemistry
    Experience 0–1 year (Freshers eligible)
  • Aurobindo Pharma hiring Experienced Formulation IPR Professionals

    Aurobindo Pharma hiring Experienced Formulation IPR Professionals

    Aurobindo Pharma Hiring IPR Professionals – 5–9 Years, Hyderabad

    Aurobindo Pharma is hiring IPR professionals with 5–9 years of experience in Formulation IPR at Bachupally, Hyderabad. Apply now.

    Aurobindo Pharma, a global leader committed to healthier lives, is inviting applications for experienced Intellectual Property Rights (IPR) professionals specializing in Formulation IPR. This is an excellent opportunity for pharmacy graduates with IPR expertise to join the company’s APLRC1 campus in Bachupally, Hyderabad.

    Company Overview

    Aurobindo Pharma is one of India’s largest pharmaceutical companies with a strong global presence in over 150 countries. Known for its high-quality formulations, APIs, and specialty generics, the company has a rich legacy of research-driven innovation and compliance with international regulatory standards. Aurobindo values intellectual property management as a core function, ensuring the protection of innovation, competitive advantage, and regulatory success across global markets.

    Job Role & Responsibilities

    As a Formulations IPR Professional, you will play a vital role in supporting the company’s research and legal teams with intellectual property-related activities. Your responsibilities include:

    • Conducting Freedom-to-Operate (FTO) analysis and non-infringement evaluations.
    • Reviewing Intellectual Property (IP) landscape reports to identify risks and opportunities.
    • Filing and prosecuting patent applications related to pharmaceutical formulations.
    • Providing IPR support for ANDA litigations and compliance.
    • Monitoring, reviewing, and supporting intellectual property strategies for new and existing formulations.
    • Collaborating with cross-functional teams to ensure IP compliance and competitive positioning in global markets.

    Eligibility / Qualifications

    • Education: M.Pharmacy (Pharmaceutics, Pharmaceutical Chemistry, or related fields).
    • Experience: 5–9 years of relevant industry experience in Formulation IPR.
    • Skills Required:
      • Strong expertise in Formulation IPR within the pharma industry.
      • Proficiency in patent filing, FTO analysis, and non-infringement evaluation.
      • Hands-on experience in ANDA litigations and patent prosecution.
      • Analytical skills for reviewing IP landscapes and identifying business risks.

    Relevant courses under eligibility: M.Pharm in Pharmaceutics, Pharmaceutical Chemistry, Drug Regulatory Affairs, or Intellectual Property Management.

    Location & Salary

    • Location: APLRC1, Bachupally, Hyderabad
    • Work Model: On-site (Full-time)
    • Compensation: Competitive salary and benefits, aligned with candidate experience and company standards
    <img class="size-full wp-image-123172" src="https://bpharmacyjobs.com/wp-content/uploads/2025/09/aurobindo-IPR-JOBS.webp" alt="Aurobindo Pharma is hiring IPR professionals with 5–9 years of experience in Formulation IPR at Bachupally, Hyderabad. Apply now.” width=”800″ height=”800″ /> Aurobindo Pharma is hiring IPR professionals with 5–9 years of experience in Formulation IPR at Bachupally, Hyderabad. Apply now.

    Application Process

    Interested candidates can share their profiles directly via email:
    📩 sreeja.yangam@aurobindo.com

    Apply early to maximize your chances of selection.

    Why Join Aurobindo Pharma?

    • Work with one of India’s top pharmaceutical companies with a strong international presence.
    • Opportunity to build a career in Intellectual Property Rights (IPR) within pharma formulations.
    • Exposure to global ANDA filings, patent prosecution, and litigation support.
    • Collaborative and innovation-driven workplace environment.
    • Competitive salary with strong growth opportunities.

    FAQs

    Q1: What is the required experience for this role?
    Candidates must have 5–9 years of experience in Formulation IPR.

    Q2: What qualifications are needed?
    M.Pharmacy in Pharmaceutics, Pharmaceutical Chemistry, or related fields.

    Q3: What skills are most important?
    Patent filing, FTO analysis, non-infringement evaluation, and ANDA litigation support.

    Q4: Where is the job located?
    At APLRC1, Bachupally, Hyderabad.

    Q5: How do I apply?
    By sending your resume to sreeja.yangam@aurobindo.com.

    Summary Table

    Category Details
    Company Aurobindo Pharma
    Vacancies Multiple (Formulation IPR Professionals)
    Required Education M.Pharm (Pharmaceutics, Pharmaceutical Chemistry, related fields)
    Experience 5–9 years in Formulation IPR
  • Walk-in Drive – Gland Pharma Quality & Production Roles – Hyderabad

    Walk-in Drive – Gland Pharma Quality & Production Roles – Hyderabad

    Walk-in Drive – Gland Pharma Quality & Production Roles – Hyderabad

    Gland Pharma walk-in interviews on Sept 16, 2025, for Quality & Production roles at Dundigal Plant, Hyderabad. Apply with B.Pharm/M.Pharm/M.Sc.

    Gland Pharma Ltd., a leading name in sterile injectables and pharmaceutical manufacturing, is conducting a walk-in interview drive for experienced professionals in Production and Quality roles at its Dundigal Plant, Hyderabad. This hiring drive is scheduled for Tuesday, 16th September 2025, from 9:30 AM to 11:30 AM.

    Company Overview

    Gland Pharma is among India’s largest and most respected pharmaceutical companies specializing in injectables, complex generics, and biosimilars. With a strong global presence across regulated markets, the company is known for its robust compliance, innovation, and world-class manufacturing facilities. Gland Pharma provides its employees a dynamic environment with opportunities for continuous learning, leadership, and career advancement.

    Job Role & Responsibilities

    Production – Incharge (10+ Years Experience)

    • Efficiently plan and manage production schedules to optimize manpower utilization.
    • Handle Quality Management System (QMS) events with detailed investigations.
    • Propose effective Corrective and Preventive Actions (CAPAs).
    • Collaborate with cross-functional teams to ensure timely project deliverables.
    • Minimize downtimes and rejection rates through strategic planning.
    • Lead teams through regulatory and customer audits, ensuring continuous compliance.

    Production – Chemist to Executive (2–6 Years Experience)

    • Hands-on experience in compounding, aseptic operations, and aseptic behavior protocols.
    • Troubleshooting equipment issues with solution-oriented approaches.
    • Ensure online documentation and compliance during operations.
    • Collaborate with cross-functional teams for smooth production activities.

    Eligibility / Qualifications

    • Incharge Roles (10+ years): B.Pharm, M.Pharm, M.Sc.
    • Chemist/Executive Roles (2–6 years): M.Pharm, M.Sc.

    Relevant courses under eligibility: B.Pharmacy, M.Pharmacy (Pharmaceutics/Pharmaceutical Analysis/Pharmaceutical Technology), M.Sc (Microbiology, Biotechnology, Chemistry).

    Location & Salary

    • Work Location: Gland Pharma Limited, Dundigal Plant, Near Gandimaisamma X Road, Medchal – Malkajgiri District, Hyderabad, Telangana.
    • Interview Venue: Gland Pharma Limited, SY. No: 143 To 148, 150 & 151, D.P. Pally, Dundigal – Gandimaisamma, Hyderabad 500043.
    • Date & Time: Tuesday, 16th September 2025, 9:30 AM – 11:30 AM.
    • Compensation: Competitive salary as per industry standards and candidate experience.
    <img class="size-full wp-image-123169" src="https://bpharmacyjobs.com/wp-content/uploads/2025/09/gland-pharma-jobs-sep2025.webp" alt="Walk-in Drive – Gland Pharma Quality & Production Roles – Hyderabad” width=”800″ height=”450″ /> Walk-in Drive – Gland Pharma Quality & Production Roles – Hyderabad

    Application Process

    This is a walk-in interview drive. Eligible candidates are required to attend with the following documents:

    • Updated Resume
    • Educational Certificates
    • Relieving Letters
    • Latest Increment Letter
    • Last 3 Months Payslips
    • Aadhaar & PAN Card
    • Passport Size Photographs

    Important Note: Gland Pharma does not charge any fees or involve third-party agencies for recruitment.

    Why Join Gland Pharma?

    • Work with one of India’s top injectable manufacturing companies.
    • Gain experience in a global regulatory environment.
    • Opportunities for leadership and professional growth.
    • Exposure to advanced production and aseptic techniques.
    • Competitive salary with a stable and supportive work environment.

    FAQs

    Q1: Who can apply for this walk-in drive?
    Candidates with 2–6 years or 10+ years of pharma production experience in injectables and QMS.

    Q2: What are the required qualifications?
    B.Pharm, M.Pharm, or M.Sc in pharmaceutical or life sciences streams.

    Q3: What type of experience is preferred?
    Experience in aseptic operations, compounding, QMS handling, regulatory audits, and injectable production.

    Q4: Where is the interview being held?
    At Gland Pharma Dundigal Plant, near Gandimaisamma X Road, Hyderabad.

    Q5: What documents should I carry?
    Resume, certificates, payslips, increment letter, Aadhaar, PAN, and photographs.

    Summary Table

    Category Details
    Company Gland Pharma Ltd.
    Vacancies Multiple (Production – Incharge, Chemist to Executive)
    Required Education B.Pharm, M.Pharm, M.Sc
    Experience 2–6 years (Chemist/Executive), 10+ years (Incharge)
  • MSN Labs Hiring Freshers & Experienced Pharma Graduates

    MSN Labs Hiring Freshers & Experienced Pharma Graduates

    Walk-in Interviews – MSN Labs Hiring Freshers & Experienced Pharma Graduates – Telangana

    MSN Laboratories walk-in drive for Production & Formulation roles in Telangana. Openings for Diploma, B.Sc, M.Sc, B.Pharm, M.Pharm, B.Tech, M.Tech. Apply now.

    MSN Laboratories, a trusted and certified Great Place To Work (2024–2025), is conducting a mega walk-in drive for multiple roles in Production (Injectables) and Formulation departments. The recruitment drive is scheduled at RK Puram, Telangana on Saturday, 13th September 2025, from 9:00 AM to 4:00 PM.

    This hiring opportunity is open for both freshers and experienced candidates (2–8 years), making it a great chance for pharmacy and life sciences graduates to join one of India’s leading pharmaceutical companies.

    Company Overview

    MSN Laboratories is one of India’s fastest-growing pharmaceutical companies with a strong global presence. Known for its innovation and commitment to research, MSN specializes in API (Active Pharmaceutical Ingredients), Formulations, and Contract Manufacturing. With multiple state-of-the-art facilities, the company provides a collaborative environment that encourages career growth, learning, and innovation.

    Certified as a Great Place To Work (2024–2025), MSN fosters a professional culture that values employee development, patient-centric innovation, and sustainable healthcare solutions.

    Job Role & Responsibilities

    MSN is hiring across multiple functions in Production and Formulation (Injectables). Depending on the role, responsibilities may include:

    • Injectables Production: Manufacturing sterile injectables under GMP guidelines.
    • Formulation: Preparation, development, and scale-up of pharmaceutical formulations.
    • Filling & Packing: Handling blister, lyophilization (Lyo), and PFS (Pre-Filled Syringes) operations.
    • Machine Operation: Operating vial filling, stoppering, sealing, autoclave, and other pharma production machinery.
    • Quality Management Systems (QMS): Ensuring compliance with SOPs and regulatory standards.

    Eligibility / Qualifications

    Freshers (2024 & 2025 Passed Outs):

    • Diploma, B.Tech, B.Sc, M.Sc, B.Pharmacy, M.Pharmacy, M.Tech.
    • Only male candidates are preferred for fresher roles.

    Experienced Candidates (2–8 years):

    Relevant courses under eligibility: Diploma in Pharmacy, B.Pharmacy, M.Pharmacy, B.Sc Life Sciences, M.Sc Biotechnology, M.Sc Chemistry, B.Tech/M.Tech Chemical Engineering, ITI Technical Trades.

    Location & Salary

    • Work Locations:
      • MSN Formulation Unit-II, Kothur
      • MSN Formulation Unit-5, RK Puram
    • Interview Venue: MSN Labs, Unit-5, RK Puram, Solipur, Telangana – 509216 (Google Plus Code: 25GX+XHX)
    • Date & Time: 13th September 2025, 9:00 AM – 4:00 PM
    • Compensation: Competitive salary based on qualifications and experience

    Application Process

    This is a walk-in recruitment drive. Eligible candidates should attend the interview at the venue with the following documents:

    • Updated Resume
    • Photocopies of Educational Certificates
    • Latest Increment Letter
    • Last 3 Months Pay Slips
    • Last 6 Months Bank Statements
    • Passport Size Photographs
    • Aadhar Card Copy

    Note: Candidates must scan the QR code (provided in the official notification) to find the exact location.

    Why Join MSN Laboratories?

    • Certified Great Place To Work (2024–2025).
    • 200+ global product portfolio across therapeutic areas.
    • Opportunity to work in modern, GMP-compliant facilities.
    • Strong focus on employee training and professional development.
    • Be part of an organization dedicated to Research for Better Medicines.

    FAQs

    Q1: Who can attend the MSN Labs walk-in drive?
    Fresh graduates (2024 & 2025 pass-outs) and experienced professionals with 2–8 years in pharma production and formulation.

    Q2: What are the required qualifications?
    Diploma, ITI, B.Sc, M.Sc, B.Tech, M.Tech, B.Pharmacy, M.Pharmacy.

    Q3: What roles are available?
    Production (Injectables), Formulation, Packing, Blister, Lyo, PFS, Machine Operators, QMS, Vial Filling & Stoppering.

    Q4: Where is the interview conducted?
    At MSN Labs, Unit-5, RK Puram, Solipur, Telangana.

    Q5: What documents should I carry?
    Resume, educational certificates, payslips, bank statements, photographs, and ID proof.

    Summary Table

    Category Details
    Company MSN Laboratories
    Vacancies Multiple (Freshers & Experienced)
    Required Education Diploma, ITI, B.Sc, M.Sc, B.Tech, M.Tech, B.Pharmacy, M.Pharmacy
    Experience Freshers (2024 & 2025 pass-outs) & Experienced (2–8 years)
  • Associate QC Vacancy – Amgen Pharma, Hyderabad

    Associate QC Vacancy – Amgen Pharma, Hyderabad

    Apply for Associate QC role at Amgen Hyderabad. l_ynn family therapy Master’s degree with 1–3 years QC experience required. Full-time onsite role. Apply today.

    Amgen, a pioneer in biotechnology and one of the world’s leading pharmaceutical innovators, is inviting applications for the role of Associate QC – QC Systems Templating at its Hyderabad facility. This is an excellent opportunity for candidates with pharmaceutical quality control experience who are passionate about advancing healthcare and working in a global, innovation-driven environment.

    Company Overview

    Amgen has been at the forefront of biotechnology for over 40 years, developing innovative medicines that improve the lives of millions worldwide. Headquartered in the U.S., Amgen combines advanced science with cutting-edge technology to fight serious diseases. The company’s mission is to serve patients by pushing the boundaries of biology and genetics to discover solutions that make life easier, fuller, and longer.

    Amgen India (AIN) supports global operations across multiple time zones, making Hyderabad a hub for collaboration, innovation, and life sciences excellence.

    Job Role & Responsibilities

    As an Associate QC, you will support the Electronic Lab Notebook (ELN) and consumable inventory system infrastructure across Amgen’s Quality Control network. The position involves shift-based work schedules to ensure smooth operations and global collaboration.

    Key Responsibilities:

    • Create, revise, and qualify templates for analytical method executions in ELN.
    • Create and update consumable templates for QC activities.
    • Ensure adherence to SOPs, quality standards, and service-level agreements.
    • Collaborate with cross-functional teams within AIN and global Amgen sites.
    • Provide metrics and performance reporting to support QC efficiency.
    • Maintain up-to-date training and compliance records.
    • Utilize virtual communication tools effectively for global team coordination.
    • Assist in process improvement and standardization within QC.

    Eligibility / Qualifications

    • Education: Master’s degree in Pharmacy, Biotechnology, Life Sciences, or related fields.
    • Experience: 1–3 years in Quality Control within pharmaceutical or biotech commercial/clinical manufacturing.
    • Technical Skills:
      • QC lab testing exposure.
      • Hands-on experience with ELN applications.
      • Proficiency in Microsoft Office.
      • Understanding of GMP (Good Manufacturing Practices) and GDP (Good Documentation Practices).
    • Soft Skills:
      • Strong verbal and written English communication.
      • Quick learner with excellent attention to detail.
      • Ability to deliver accurate results in team-based environments.

    Relevant courses under eligibility: M.Pharm, M.Sc Biotechnology, M.Sc Life Sciences, M.Sc Microbiology, M.Sc Biochemistry, M.Tech Biotechnology.

    Location & Salary

    • Location: Hyderabad, India (Amgen India-AIN)
    • Work Model: On-site, shift-based schedule
    • Employment Type: Full-time
    • Compensation: Competitive (based on qualifications and company norms)
    <img class="size-full wp-image-123155" src="https://bpharmacyjobs.com/wp-content/uploads/2025/09/Associate-QC-Vacancy-–-Amgen-Pharma-Hyderabad.webp” alt=”Associate QC Vacancy – Amgen Pharma, Hyderabad,” width=”1200″ height=”675″ /> Associate QC Vacancy – Amgen Pharma, Hyderabad,

    Application Process

    Candidates can apply directly via Amgen’s official career portal:
    Apply Here

    Apply early to secure your opportunity with one of the world’s most respected biotech leaders.

    Why Join Amgen?

    • Work with a global biotech leader recognized for innovation and patient-focused research.
    • Be part of a mission-driven culture dedicated to advancing human health.
    • Collaborate with international teams across multiple time zones.
    • Access professional growth and career development opportunities.
    • Contribute directly to life-saving medicines and healthcare solutions.

    FAQs

    Q1: What qualifications are required for the Associate QC role?
    A Master’s degree with 1–3 years of QC experience in Pharma/Biotech.

    Q2: What skills are desirable?
    Experience with ELN, Microsoft Office, GMP/GDP knowledge, and QC lab testing exposure.

    Q3: Is this role on-site or hybrid?
    The position is fully on-site at Amgen’s Hyderabad facility.

    Q4: Does the role involve shifts?
    Yes, candidates must be flexible with shift-based schedules to support global operations.

    Q5: How can I apply?
    Applications are accepted via Amgen’s official careers portal (link provided above).

    Summary Table

    Category Details
    Company Amgen
    Vacancies Multiple (Associate QC)
    Required Education Master’s in Pharmacy, Biotechnology, Life Sciences, Microbiology, Biochemistry, M.Tech Biotechnology
    Experience 1–3 years in Quality Control (Pharma/Biotech)
  • Sri Krishna Pharma Walk-in for Production, QA, QC, and Warehouse

    Sri Krishna Pharma Walk-in for Production, QA, QC, and Warehouse

    B.Pharm, M.Pharm, M.Sc Openings – 50+ Vacancies | Sri Krishna Pharma Nacharam & Bollaram

    Sri Krishna Pharma hiring for corinna kopf boobsProduction, QA, QC, and Warehouse with 50+ vacancies in Nacharam & Bollaram. Walk-in interviews on 25-26 August 2025.

    Looking to grow your career in pharmaceutical manufacturing and quality management? Sri Krishna Pharmaceuticals, a trusted name in the pharma industry, is conducting a Walk-in Drive for multiple roles across Production, Quality Assurance, Quality Control, and Warehouse departments. This is an excellent opportunity for professionals with 2–10 years of experience to join one of India’s leading pharma organizations.

    Company Overview

    Sri Krishna Pharma is a reputed pharmaceutical manufacturer with a strong footprint in the OSD (Oral Solid Dosage) and API (Active Pharmaceutical Ingredient) segments. With a history of consistent growth and global compliance, the company has established itself as a trusted partner for quality medicines. Employees benefit from structured career development, regulatory exposure, and learning opportunities in a highly professional work environment.

    Job Role & Responsibilities

    Production Department (Nacharam)

    • Operate and manage Packing Machines (BQS, Blister, HI Cart).
    • Handle processes related to Granulation, Compression, and Coating.
    • Ensure compliance with GMP and production protocols.
    • Maintain batch records and follow safety practices.

    Warehouse Department (Nacharam)

    • Manage Dispatches, Finished Goods, and Raw Materials.
    • Maintain accurate SAP records.
    • Ensure timely availability of materials for production.
    • Comply with audit and documentation requirements.

    Quality Control (OSD) – Nacharam

    • Conduct testing using HPLC, GC, UV/IR Spectroscopy, KF, Dissolution, Wet Analysis, and Stability.
    • Maintain analytical documentation.
    • Ensure product quality compliance with regulatory standards.

    Quality Assurance (OSD & API) – Nacharam & Bollaram

    • Perform IPQA, Sampling, BMR Review, and Cleaning Validations.
    • Manage QMS activities like deviations, CAPA, and change control.
    • Ensure compliance with GMP and audit readiness.

    Eligibility / Qualifications

    Location & Interview Details

    • Production/Warehouse/QC (OSD): Nacharam Unit, Hyderabad.
    • QA (OSD & API): Nacharam & Bollaram Units.
    • Interview Date: 25th & 26th August 2025 (Monday & Tuesday).
    • Time: 10:00 AM to 03:00 PM.
    • Venue: Sri Krishna Pharmaceuticals Unit-II (Nacharam) & Unit-IV (Bollaram, Jinnaram Mandal).

    Application Process

    Interested candidates are requested to attend the walk-in interview with the following documents:

    • Updated Resume
    • Educational Certificates
    • ID Proof (Aadhar)
    • Experience Certificates
    • Latest CTC & Salary Slips

    For those unable to attend, resumes can be shared via HR contact at the venue.

    FAQs

    1. Who can apply for these openings?
    Candidates with 2–10 years of experience in Production, QC, QA, or Warehouse in the pharma sector, specifically OSD and API, are eligible.

    2. Are freshers eligible?
    No, only experienced professionals are invited for this drive.

    3. What type of shifts are expected?
    Candidates must be open to rotational shifts as per production and quality requirements.

    4. What is the interview process?
    It is a walk-in interview where candidates will be screened based on technical knowledge, experience, and role suitability.

    5. Is there any fee for applying?
    No, Sri Krishna Pharma does not charge any fee for recruitment.

    Summary Table

    Company Sri Krishna Pharmaceuticals Ltd.
    Vacancies 50+ across Production, QA, QC, Warehouse
    Required Education B.Pharm, M.Pharm, M.Sc, B.Sc, Diploma, B.Tech, Inter
    Experience 2 to 10 years (Audit exposure preferred)
    Location Nacharam & Bollaram, Hyderabad
    <img class="size-full wp-image-123110" src="https://bpharmacyjobs.com/wp-content/uploads/2025/08/Sri-Krishna-Pharma-Walk-in-for-Production-QA-QC-and-Warehouse-1.jpg” alt=”Sri Krishna Pharma Walk-in for Production, QA, QC, and Warehouse” width=”456″ height=”468″ /> Sri Krishna Pharma Walk-in for Production, QA, QC, and Warehouse <img class="size-full wp-image-123111" src="https://bpharmacyjobs.com/wp-content/uploads/2025/08/Sri-Krishna-Pharma-Walk-in-for-Production-QA-QC-and-Ware.webp” alt=”Sri Krishna Pharma Walk-in for Production, QA, QC, and Warehouse” width=”456″ height=”468″ /> Sri Krishna Pharma Walk-in for Production, QA, QC, and Warehouse
  • Cronus Pharma Walk-in Operators & Engineers (Injectables, OSD, Engineering)

    Cronus Pharma Walk-in Operators & Engineers (Injectables, OSD, Engineering)

    B.Sc/M.Sc Operators & Engineers Walk-In – Cronus Pharma Hyderabad

    Cronus Pharma hiring Operators & Engineers (Injectables, OSD, Camilla Camilla leakedEngineering). Walk-in on 31st Aug 2025 at Hyderabad. Apply now!

    Cronus Pharma is conducting a walk-in interview in Hyderabad for multiple positions across Production (Injectables & OSD) and Engineering departments. This is a great opportunity for skilled pharma professionals to advance their careers in a leading global pharmaceutical company.

    Company Overview

    Cronus Pharma is a trusted name in the pharmaceutical sector, specializing in the development and manufacturing of high-quality generic and specialty products. With state-of-the-art facilities and a focus on global regulatory compliance, Cronus Pharma provides an excellent platform for pharma professionals to build their careers.

    Job Role & Responsibilities

    Open Positions:

    • Operators – Production (Injectables)
      • Responsible for injectable production processes.
      • Operate and maintain equipment as per GMP standards.
    • Operators – Production (OSD)
      • Manage manufacturing activities for oral solid dosage forms.
      • Ensure compliance with SOPs and quality standards.
    • Engineering (Injectables) – HVAC/Instrumentation/Process Maintenance
      • Handle plant engineering operations.
      • Oversee HVAC systems, instrumentation, and maintenance of production utilities.

    Eligibility / Qualifications

    • Education: B.Sc, M.Sc, B.Pharm, Diploma, or relevant engineering qualification
    • Experience: Freshers & experienced candidates (1–6 years) in Production/Engineering.
    • Skills:
      • Knowledge of GMP, regulatory compliance, cleanroom practices.
      • Hands-on exposure to HVAC, instrumentation, and process equipment preferred for engineering roles.

    Location & Walk-In Details

    • Interview Date: 31st August 2025 (Sunday)
    • Time: 09:30 AM – 03:00 PM
    • Venue: Hotel VR Ashoka Grand, 1-112/7/102, Allwyn X Roads, Miyapur, Hyderabad, Telangana – 500049

    Application Process

    • Interested candidates should attend the walk-in interview with:
      • Updated Resume
      • Educational Certificates
      • ID Proofs
      • Recent Payslips (if applicable)

    For queries, contact:
    Mahesh: 7337445197
    Suchitra: 7337445157
    Email: mesari@cronuspharma.com, sguttula@cronuspharma.com

    Why Join Cronus Pharma?

    • Opportunity to work in injectables and OSD manufacturing units.
    • Exposure to international regulatory audits (USFDA, EU, WHO).
    • Career growth in a fast-growing pharma company.

    FAQs

    Q1: Who can apply for these positions?

    Candidates with B.Sc, M.Sc, B.Pharm, Diploma, or Engineering backgrounds with relevant pharma/engineering experience can apply.

    Q2: Is this opportunity open for freshers?
    Yes, freshers with good academic records may also apply for Production roles.

    Q3: What should I carry for the walk-in interview?
    Updated resume, ID proof, academic certificates, and payslips (if applicable).

    Q4: What is the job location after selection?
    Selected candidates will be placed at Cronus Pharma’s Hyderabad facility.

    Summary Table

    Company Cronus Pharma
    Vacancies Production Operators (Injectables & OSD), Engineering (HVAC, Instrumentation, Process Maintenance)
    Required Education B.Sc, M.Sc, B.Pharm, Diploma, B.Tech/Engineering
    Experience Freshers & Experienced (1–6 years)
    Location Hyderabad (Interview at Hotel VR Ashoka Grand, Miyapur)
    <img class=”size-full wp-image-123102″ src=”https://bpharmacyjobs.com/wp-content/uploads/2025/08/Cronus-Pharma-Walk-in-Operators-Engineers-Injectables-OSD-Engineering-1.webp” alt=”Cronus Pharma Walk-in Operators & Engineers (Injectables, OSD, Engineering)” width=”1080″ height=”1350″ /> Cronus Pharma Walk-in Operators & Engineers (Injectables, OSD, Engineering)
  • Eugia Pharma Hiring Officers, Executives & Assistants in Production, QC & Engineering

    Eugia Pharma Hiring Officers, Executives & Assistants in Production, QC & Engineering

    Eugia Pharma Walk-in Interview | Production, QC, Engg | Jedcherla

    Eugia Pharma hiring Officers, Executives & Assistants in Production, QC & Engineering at Jedcherla SEZ Plant. Walk-in on 30th Aug 2025.

    Eugia SEZ Private Limited, a unit of Venor Pharma Ltd., is inviting skilled professionals to join its team at the Jedcherla SEZ facility in Telangana. This walk-in interview offers an exciting chance to work with one of the leading names in injectables manufacturing and expand your pharma career.

    Company Overview

    Eugia SEZ Pvt. Ltd. is a renowned pharmaceutical company with a strong global presence, specializing in formulations, injectables, and APIs. With a reputation for compliance, innovation, and affordability, Eugia is committed to producing high-quality medicines that meet regulatory standards worldwide. The Jedcherla SEZ plant is a state-of-the-art facility supporting domestic and international markets.

    Job Role & Responsibilities

    Production – Injectables

    • Area: DPI Filling / LYO Filling, Injectable Production
    • Skills: Autoclave operations, Vial Washing & Sealing, Dry Powder and Liquid Filling
    • Designation: Technical Assistant / Executive
    • Qualification: ITI / Diploma / B.Sc / B.Pharmacy
    • Experience: 2–6 years
    • Responsibilities: Operating production machinery, ensuring GMP compliance, overseeing aseptic operations, handling injectable manufacturing processes, and maintaining accurate documentation.

    Eligibility / Qualifications

    • Education: ITI, Diploma, B.Sc, B.Pharm
    • Experience: 2–6 years in pharmaceutical injectables production
    • Skills: Strong technical expertise in aseptic production processes, familiarity with QMS and GMP compliance, ability to handle audits.

    Location & Salary

    • Work Location: Eugia SEZ Pvt. Ltd., Pollepally Village, Jedcherla, Mahabubnagar District, Telangana, India
    • Interview Date & Time: Saturday, 30th August 2025, 10:00 AM – 03:00 PM
    • Salary: Competitive; aligned with candidate experience and industry standards.

    Application Process

    FAQs

    1. Who can attend the Eugia walk-in interview?
    Candidates with ITI, Diploma, B.Sc, or B.Pharm degrees and 2–6 years of experience in injectables manufacturing.

    2. What is the interview date and venue?
    30th August 2025 at Eugia SEZ Pvt. Ltd., Pollepally Village, Jedcherla, Telangana.

    3. What roles are open?
    Technical Assistants and Executives in Production – DPI/LYO/Injectables.

    4. What documents should I bring?
    Updated resume, ID proofs, payslips, increment letter, CTC breakup, educational certificates.

    5. Is there an option to apply online?
    Yes, candidates who cannot attend the walk-in may email their resumes to the provided HR contacts.

    Don’t miss the opportunity to join Eugia Pharma’s growing team at Jedcherla. Walk in on 30th August 2025 and take the next step in your pharmaceutical career!

    Summary Table

    Company Eugia SEZ Pvt. Ltd.
    Vacancies Technical Assistant / Executive – Production (Injectables)
    Required Education ITI, Diploma, B.Sc, B.Pharm
    Experience 2–6 years
    <img class="size-full wp-image-123085" src="https://bpharmacyjobs.com/wp-content/uploads/2025/08/Eugia-Pharma-Hiring-Officers-Executives-Assistants-in-Production-QC-Engineering-1.webp" alt="Eugia Pharma Hiring Officers, Executives & Assistants in Production, QC & Engineering” width=”1080″ height=”1529″ /> Eugia Pharma Hiring Officers, Executives & Assistants in Production, QC & Engineering
  • Provis Biolabs hiring in Production, Quality Control & Quality Assurance

    Provis Biolabs hiring in Production, Quality Control & Quality Assurance

    Provis Biolabs Hiring | Production, QC & QA | Hyderabad

    Provis Biolabs hiring in Production, Quality Control & Quality Assurance at Hyderabad. 5–15 yrs experience required. Apply now!

    Provis Biolabs, a trusted name in the biopharmaceutical sector, is hiring for multiple positions across Production (Upstream & Downstream), Quality Control (Analytical, QMS), and Quality Assurance (IPQA) at its Hyderabad facility. Professionals with 5–15 years of experience are invited to apply.

    Company Overview

    Provis Biolabs is a growing biopharmaceutical organization dedicated to innovation, compliance, and high-quality biologics manufacturing. With advanced facilities and a strong focus on regulatory compliance, the company has built credibility in delivering biopharma solutions across therapeutic areas. Provis offers its employees opportunities for career growth in a collaborative and research-driven environment.

    Job Role & Responsibilities

    Production (Upstream & Downstream)

    • Experience: 5–15 years
    • Qualification: Graduate / Postgraduate in Life Sciences, Biotechnology, or Pharmacy
    • Responsibilities:
      • Operate and monitor upstream and downstream processes.
      • Ensure compliance with cGMP guidelines.
      • Collaborate with cross-functional teams for efficient production.

    Quality Control (Analytical, QMS)

    • Experience: 5–15 years
    • Qualification: Graduate / Postgraduate in Life Sciences, Biotechnology, or Pharmacy
    • Responsibilities:
      • Perform analytical testing and stability studies.
      • Ensure compliance with QMS standards.
      • Prepare and review analytical documentation.

    Quality Assurance (IPQA)

    • Experience: 5–15 years
    • Qualification: Graduate / Postgraduate in Life Sciences, Biotechnology, or Pharmacy
    • Responsibilities:
      • Conduct in-process quality checks and compliance audits.
      • Support process validation and documentation.
      • Ensure adherence to regulatory and internal quality standards.

    Eligibility / Qualifications

    • Education: Graduate or Postgraduate in Pharmacy, Life Sciences, Biotechnology, or related fields.
    • Experience: 5–15 years depending on role.
    • Skills Required:
      • Hands-on experience in production or quality functions.
      • Strong knowledge of GMP, QMS, and regulatory requirements.
      • Excellent communication and documentation skills.

    Location & Salary

    • Work Location: Hyderabad, Telangana
    • Job Type: Full-time
    • Salary: Competitive, aligned with industry standards and candidate experience.

    Application Process

    Interested candidates can apply by sending their updated CV to:

    FAQs

    1. Who can apply for Provis Biolabs’ openings?
    Graduates and postgraduates in Pharmacy, Biotechnology, or Life Sciences with 5–15 years of relevant experience.

    2. What roles are available?
    Openings in Production (Upstream/Downstream), Quality Control (Analytical/QMS), and Quality Assurance (IPQA).

    3. Is prior industry experience mandatory?
    Yes, a minimum of 5 years’ experience in the respective domain is required.

    4. Where is the work location?
    Hyderabad, Telangana.

    5. How do I apply?
    Send your CV to careers@provisbiolabs.com with the job title mentioned in the subject line.

    Take the next step in your pharma career by applying to Provis Biolabs’ Hyderabad openings today!

    Summary Table

    Company Provis Biolabs
    Vacancies Production (Upstream/Downstream), Quality Control (Analytical/QMS), Quality Assurance (IPQA)
    Required Education Graduate / Postgraduate in Life Sciences, Biotechnology, Pharmacy
    Experience 5–15 years
    <img class="size-full wp-image-123061" src="https://bpharmacyjobs.com/wp-content/uploads/2025/08/Provis-Biolabs-hiring-in-Production-Quality-Control-Quality-Assurance-1.webp" alt="Provis Biolabs hiring in Production, Quality Control & Quality Assurance” width=”1131″ height=”1600″ /> Provis Biolabs hiring in Production, Quality Control & Quality Assurance