PHARMA STUFF

Job Tag: Pharma Jobs in Bangalore

  • Syngene Biopharmaceutical Operations Walk-In | Upstream, Downstream, Documentation

    Syngene Biopharmaceutical Operations Walk-In | M.Sc/M.Tech Openings | Bengaluru

    Apply for Syngene Biopharmaceutical Operations walk-in drive in Bengaluru. Openings for M.Sc/M.Tech graduates with 2–10 years experience.

    Syngene International, a global leader in contract research and manufacturing, is inviting skilled life sciences professionals to join its Biopharmaceutical Operations team. This exclusive walk-in drive is scheduled in Hyderabad for multiple openings in upstream and downstream manufacturing and documentation roles. Candidates with expertise in monoclonal antibodies (mAbs), USP, DSP, mammalian cell culture, and regulatory documentation are encouraged to apply. This is a unique opportunity to be part of one of India’s most trusted biopharma organizations and contribute to cutting-edge healthcare solutions.

    Company Overview

    Syngene International Ltd. is one of India’s most respected integrated research, development, and manufacturing service providers. With a state-of-the-art facility and over 30 years of experience, Syngene partners with top global pharmaceutical, biotechnology, and healthcare companies to accelerate innovation. The company is known for its robust compliance framework, commitment to quality, and advanced infrastructure in biologics manufacturing.

    Job Role & Responsibilities

    Syngene is hiring for multiple positions in Biopharmaceutical Operations across upstream and downstream processes, as well as manufacturing documentation. Selected candidates will be responsible for:

    • Executing upstream and downstream biologics manufacturing activities.
    • Managing biopharmaceutical documentation in compliance with cGMP standards.
    • Supporting monoclonal antibody production processes (mAbs).
    • Handling USP (Upstream Processing) and DSP (Downstream Processing).
    • Ensuring adherence to regulatory guidelines and internal SOPs.
    • Collaborating with cross-functional teams to ensure smooth manufacturing and documentation workflows.

    Available Positions:

    1. Upstream Manufacturing – Req ID: 61301
      Apply Here
    2. Downstream Manufacturing – Req ID: 61307
      Apply Here
    3. Upstream Manufacturing Documentation – Req ID: 60956
      Apply Here
    4. Downstream Manufacturing Documentation – Req ID: 60959
      Apply Here

    Eligibility / Qualifications

    • Education: M.Sc. or M.Tech in Life Sciences, Biotechnology, Biochemistry, Microbiology, or related fields.
    • Experience: 2–10 years in upstream/downstream biologics manufacturing; 5–10 years in documentation roles.
    • Skills: mAbs, USP, DSP, mammalian cell culture, GMP documentation.
    • Soft Skills: Strong communication, documentation accuracy, and compliance mindset.

    Location & Salary

    • Job Location: Bengaluru, Karnataka
    • Walk-in Venue: Syngene Scientific Solution Ltd., Knowledge Square Park – 9000, Plot No.7, Survey No.542, MN Park, Synergy Square 2, Genome Valley, Kolthur Shamirpet, Medchal, Hyderabad, Telangana – 500078.
    • Date & Time: 11th October 2025, 09:00 AM – 12:00 PM
    • Salary: Competitive, commensurate with experience and industry standards.
    Syngene Biopharmaceutical Operations Walk-In | Upstream, Downstream, Documentation
    Syngene Biopharmaceutical Operations Walk-In | Upstream, Downstream, Documentation

    Application Process

    • Walk-in with your updated CV, academic and experience certificates.
    • Alternatively, apply online using the links provided under each role.
    • For queries, write to Sulake.Divyasree@syngeneintl.com with the subject line “Syngene Biopharmaceutical Operations Walk-in Drive on 11th Oct 2025”.

    Why Join Syngene?

    • Work with cutting-edge biopharma technologies.
    • Be part of a global leader in biologics manufacturing.
    • Opportunity to grow in upstream, downstream, and regulatory documentation domains.
    • Exposure to international quality standards and regulatory compliance.

    FAQs

    Q1: Who can apply for Syngene’s Biopharmaceutical Operations openings?
    A: Candidates with M.Sc./M.Tech in Life Sciences, Biotechnology, Biochemistry, Microbiology, or related fields, with 2–10 years of experience.

    Q2: Is this a walk-in drive or online application?
    A: Both. Candidates can attend the walk-in drive or apply online via the provided job links.

    Q3: Where will the job location be?
    A: All selected candidates will be based at Bengaluru, Karnataka, though the walk-in is being conducted in Hyderabad.

    Q4: What skills are preferred?
    A: Experience in monoclonal antibodies, mammalian cell culture, USP, DSP, and GMP documentation.

    Q5: What should I bring to the walk-in?
    A: Updated resume, ID proof, academic certificates, and relevant experience documents.

    Call to Action

    🚨 Don’t miss this opportunity to join Syngene International! Attend the walk-in on 11th October 2025 (Saturday) between 9:00 AM – 12:00 PM in Hyderabad. Apply online today to secure your spot before positions close!

    Summary Table

    Company Syngene International Ltd.
    Vacancies Multiple (Upstream, Downstream, Documentation)
    Required Education M.Sc., M.Tech (Life Sciences, Biotechnology, Biochemistry, Microbiology)
    Experience 2–10 years (manufacturing), 5–10 years (documentation)

  • Junior Manager – Regulatory Affairs | Syngene International Limited

    Junior Manager – Regulatory Affairs | Syngene International Limited

    Job Title: Junior Manager – Regulatory Affairs
    Location: Syngene International Limited, Biocon SEZ, Biocon Park, Bommasandra Industrial Area, Jigani Link Road, Bengaluru, Karnataka 560099, India

    About Syngene

    Syngene International (www.syngeneintl.com) is an innovation-driven contract research, development, and manufacturing organization offering fully integrated scientific services – from early discovery to commercial supply. We work with leading global pharmaceutical, biotechnology, and healthcare companies, enabling them to advance new therapies that address unmet medical needs.

    At Syngene, safety and quality are at the heart of everything we do. Our culture emphasizes accountability, compliance, and the highest ethical standards while maintaining a healthy, collaborative workplace.

    Role Overview

    We are seeking a Junior Manager – Regulatory Affairs with expertise in CMC regulatory affairs, eCTD filing, and lifecycle management. The role requires close collaboration with internal teams and clients to ensure successful filings, product registrations, and post-approval maintenance across developed and emerging markets.

    Key Responsibilities

    • Provide CMC regulatory support throughout the drug development cycle for small molecules, biologics, and generics.
    • Lead and manage eCTD filings, regulatory document management systems (RDMS/EDMS), and QMS activities.
    • Research regulatory requirements for new molecules/categories and deliver feasibility and technical inputs.
    • Review plant and R&D documentation (BMR, BPR, method validation, process validation, specifications, development reports, etc.) for compliance.
    • Identify regulatory requirements for IND, NDA, MAA, ANDA, ANADA, and other dossiers; prepare checklists and ensure submission compliance.
    • Author, compile, and publish regulatory dossiers in a timely manner, including responses to agency queries.
    • Contribute to regulatory strategy development and provide guidance to stakeholders and clients.
    • Manage renewals and lifecycle updates of product dossiers/DMFs.
    • Oversee regulatory project management activities.
    • Review and maintain quality agreements and compliance trackers.
    • Mentor and train staff on regulatory policies and SOPs.

    Required Skills & Experience

    • Experience: 6–13 years in CMC Regulatory Affairs for APIs and formulations (preferably injectables) targeting the US, EU, and developed markets.
    • Hands-on experience with eCTD submissions and familiarity with RDMS, EDMS, and QMS systems.
    • Strong understanding of CMC (API & Drug Product) regulatory requirements.
    • Prior exposure to investigational medicinal products and marketing authorizations.
    • Additional experience with biologicals, ADCs, or veterinary drugs is a plus.

    Education

    • B.Pharm / M.Pharm / Life Sciences degree.
    • Minimum of 5+ years of pharmaceutical or life sciences industry experience.

    Leadership & Values

    All Syngene employees are expected to uphold our values of:

    • Excellence
    • Integrity
    • Professionalism

    Equal Opportunity Employer

    Syngene is committed to providing equal employment opportunities regardless of age, gender, ethnicity, disability, or background. We also provide reasonable accommodations for qualified individuals with disabilities.

    Why Join Syngene?

    • Opportunity to contribute to life-changing therapies impacting global healthcare.
    • Work in a world-class research and manufacturing environment.
    • Career growth through continuous learning and development.
    • Culture that prioritizes safety, quality, and integrity.
    <img class="size-full wp-image-123618" src="https://bpharmacyjobs.com/wp-content/uploads/2025/10/Junior-Manager-–-Regulatory-Affairs-Syngene-International.webp" alt="Junior Manager – Regulatory Affairs | Syngene International” width=”1200″ height=”675″ /> Junior Manager – Regulatory Affairs | Syngene International

    How to Apply

    Apply directly through the official Syngene careers portal: Apply Here

    Quick Job Summary Table

    Position Junior Manager – Regulatory Affairs
    Company Syngene International Limited
    Location Bengaluru, Karnataka, India
    Experience 6–13 years (CMC Regulatory Affairs)
    Education B.Pharm / M.Pharm / Life Sciences
    Key Skills CMC, eCTD, Regulatory Strategy, QMS
    Apply Link Click Here

    FAQs

    Q1: What type of products will I work on?
    Small molecules, biologics, generics, and investigational medicinal products for developed and emerging markets.

    Q2: Is prior experience in eCTD filing mandatory?
    Yes, hands-on eCTD experience is essential for this role.

    Q3: What markets does this role primarily cover?
    US, EU, and other developed markets, with some support for emerging countries.

    Q4: Does the role involve people management?
    Yes, mentoring and training junior staff is part of the responsibilities.

    Q5: Are biologicals and ADC regulatory experience necessary?
    Not mandatory but highly desirable.

  • CIGNA Hiring international insurance claims Representative

    CIGNA Healthcare Hiring Alert!
    Claims Representative | Bengaluru, Karnataka

    Company Overview

    CIGNA Healthcare, a division of The Cigna Group, is committed to making financial lives better and promoting better health for people at every stage of life. With a strong focus on Responsible Growth, CIGNA offers a diverse and inclusive workplace where employees can learn, grow, and make a meaningful impact. CIGNA invests in its teammates with competitive benefits and flexible work arrangements to support physical, emotional, and financial well-being.

    Job Role & Responsibilities

    CIGNA is seeking a Claims Representative to handle international insurance claims for members, providing accurate, timely, and customer-focused support.

    Key responsibilities include:

    • Adjudicate international pharmacy claims following policy terms to meet team productivity and quality goals.
    • Monitor high-cost claims and alert relevant parties.
    • Ensure claims are settled within required turnaround times, escalating delays to supervisors.
    • Respond to enquiries regarding plan design, eligibility, and claims status, aiming for first-call resolution.
    • Interface effectively with internal and external customers to resolve issues.
    • Identify potential process improvements and recommend to senior team members.
    • Support team members and contribute to achieving team goals.
    • Work across international business lines according to service needs.
    • Perform other ad hoc tasks as required.
    • Adhere to company policies, training, and certification requirements.

    Eligibility / Qualifications

    • Education: Graduate (Any discipline) – Medical, Paramedical, Pharmacy, or Nursing preferred.
    • Experience: Minimum 1 year in healthcare services or healthcare insurance claims processing.
    • Strong understanding of insurance industry and federal/state regulations.
    • Excellent English communication skills, both verbal and written.
    • Proficient in MS Office and computer literate.
    • Critical thinking and decision-making skills.
    • Attention to detail with high accuracy.
    • Customer-focused with strong interpersonal skills.
    • Ability to work proactively and implement process improvements.
    • Experience in medical administration, claims environment, or contact center is advantageous.

    Work Timings & Location

    • Work Timings: 7:30 am – 16:30 pm IST
    • Location: Bengaluru (Bangalore), Karnataka
    CIGNA Hiring international insurance claims Representative
    CIGNA Hiring international insurance claims Representative

    Application Process

    Ready to launch your career in healthcare claims with a global leader?
    Apply here: CIGNA Careers – Claims Representative

    Tip: Apply early to secure your opportunity! Limited positions available.

    FAQs

    Q1. What is the eligibility for this role?
    A1. Graduates in Medical, Paramedical, Pharmacy, or Nursing with at least 1 year of relevant experience.

    Q2. Are prior claims or healthcare experience mandatory?
    A2. Experience is advantageous but not essential; foundational skills in international insurance claims are key.

    Q3. What skills are essential?
    A3. English communication, attention to detail, computer proficiency, critical thinking, and customer focus.

    Q4. How do I apply?
    A4. Click here to submit your application directly to CIGNA.

    Q5. What are the work hours?
    A5. 7:30 am – 16:30 pm IST.

    Vertical Summary Table

    Category Details
    Company CIGNA Healthcare
    Vacancies Claims Representative
    Required Education Graduate (Medical, Paramedical, Pharmacy, Nursing preferred)
    Experience Minimum 1 year in healthcare services or insurance claims processing
  • Pharmacovigilance Safety Specialist I Vacancy at Precision Medicine

    Pharmacovigilance Safety Specialist I Vacancy at Precision Medicine

    Safety Specialist I Vacancy for Pharmacy & Life Science Graduates | Bengaluru

    Apply for Safety Specialist I role at Precision Medicine Group in Bengaluru. Openings for Pharmacy/Life Sciences graduates with 3+ years’ experience.

    If you are passionate about pharmacovigilance and want to contribute to advancing patient safety, Precision Medicine Group has an excellent opportunity for you. We are hiring a Safety Specialist I in Bengaluru to strengthen our global safety team. This role is ideal for professionals with a background in pharmacy, nursing, or life sciences, and experience in clinical trial drug safety.

    Company Overview

    Precision Medicine Group is a leading global organization specializing in clinical research, pharmacovigilance, and advanced therapies. We work with pharmaceutical, biotechnology, and healthcare companies to deliver safe and effective treatments to patients worldwide. With a strong foundation in science and regulatory compliance, our team plays a vital role in improving healthcare outcomes.

    Our culture fosters collaboration, innovation, and continuous growth. As part of our safety department, you will work alongside industry experts while gaining exposure to diverse therapeutic areas, including immuno-oncology and advanced therapy medicinal products (ATMPs).

    Job Role & Responsibilities

    As a Safety Specialist I, you will:

    • Process Individual Case Safety Reports (ICSRs) in compliance with SOPs and regulatory guidelines.
    • Evaluate safety data for accuracy, completeness, and regulatory reportability.
    • Enter case details into the Argus Safety Database.
    • Code adverse events, medical history, medications, and tests using MedDRA and WHODrug.
    • Draft and review safety case narratives.
    • Manage follow-ups and resolve safety queries.
    • Generate timely expedited and periodic safety reports.
    • Collaborate with data management teams for reconciliation of safety data.
    • Support audits, inspections, and regulatory submissions.
    • Ensure compliance with ICH, GCP, GVP, and global drug safety regulations.
    • Contribute to trial master file documentation and project-specific safety deliverables.

    Eligibility / Qualifications

    To qualify for this role, you should have:

    • Education: Bachelor’s degree in Pharmacy, Nursing, Life Sciences, Biotechnology, Pharmacology, or equivalent. (Preferred: Pharmacy/Nursing graduates).
    • Experience: Minimum 3 years in clinical trial drug safety within the Pharma or CRO industry.
    • Technical Expertise:
      • Proficiency with Oracle Argus Safety Database.
      • Strong working knowledge of MedDRA, WHODrug, and global safety regulations (FDA, EMA, MHRA).
      • Understanding of ICH-GCP principles.
    • Preferred Experience: Early-phase oncology trials, immuno-oncology, and ATMPs.
    • Skills:
      • Strong communication and analytical skills.
      • Ability to work collaboratively in cross-functional teams.
      • Detail-oriented with problem-solving abilities.

    Location & Work Environment

    Pharmacovigilance Safety Specialist I role at Precision Medicine Group
    Pharmacovigilance Safety Specialist I role at Precision Medicine Group

    Application Process

    Interested candidates can apply directly via the company’s official listing here: Apply Now.

    FAQs

    Q1. Who can apply for the Safety Specialist I role?
    Candidates with a bachelor’s degree in Pharmacy, Nursing, Life Sciences, or related fields, along with 3+ years’ experience in clinical drug safety.

    Q2. Is Argus Safety Database experience mandatory?
    Yes, proficiency in Argus is required for this role.

    Q3. What therapeutic areas will I work on?
    You will gain exposure to oncology, immuno-oncology, and advanced therapy medicinal products.

    Q4. Is this role open to freshers?
    No, a minimum of 3 years’ clinical trial safety experience is required.

    Q5. Where is the role based?
    This role is based in Bengaluru, India.

    Call to Action

    Don’t miss this chance to advance your career in pharmacovigilance!
    Apply before the position closes to secure your spot with Precision Medicine Group.

    Summary Table

    Category Details
    Company Precision Medicine Group
    Vacancies Safety Specialist I
    Required Education B.Pharm, Nursing, Life Sciences, Biotechnology, Pharmacology
    Experience Minimum 3 years in drug safety (Pharma/CRO)
  • Apprentice – Asst Clinical Data Analyst at Fortrea

    Apprentice – Asst Clinical Data Analyst at Fortrea

    Apprentice Clinical Data Analyst – Fortrea, Bangalore, 2025

    Meta Description: Apply for Apprentice – Asst Clinical Data Analyst at Fortrea, Bangalore. Open for graduates in life sciences, IT & health sciences. Apply by Oct 10, 2025.

    Fortrea, a global leader in clinical research and healthcare innovation, is hiring apprentices for the role of Assistant Clinical Data Analyst in Bangalore, India. This position is part of Fortrea’s Early Careers program, offering a structured pathway for fresh graduates to enter the world of clinical data management, gain hands-on experience, and grow with mentorship from industry experts.

    Company Overview

    Fortrea is a trusted name in clinical research, dedicated to improving patient outcomes and accelerating medical innovation. With a strong global presence, Fortrea has been at the forefront of advancing healthcare solutions by combining technology, data-driven insights, and clinical expertise. The company values early talent, believing that curiosity, motivation, and innovation are key drivers of progress. Its Early Careers program is designed to nurture future leaders in life sciences and clinical research.

    Job Role & Responsibilities

    As an Apprentice – Assistant Clinical Data Analyst, you will gain exposure to data management workflows and clinical research operations. Your responsibilities include:

    • Following departmental Standard Operating Procedures (SOPs) and Work Instructions.
    • Completing all mandatory training within specified timelines.
    • Supporting assigned Data Management workflows and operational data flows.
    • Ensuring all data management activities comply with regulatory requirements and Good Clinical Practices (GCP).
    • Reviewing and resolving data queries within timelines, ensuring quality expectations are met.
    • Running diagnostics, reconciliation discrepancy listings, and other ancillary programs to support clinical trial data review.
    • Assisting with the review of external data edit checks, status reports, and listings.
    • Performing ongoing and final data consistency checks as defined in the Data Management Plan (DMP) and eCRF review manual.
    • Supporting tasks related to decommissioning/archiving, generating reports, and ad hoc project activities.

    Eligibility / Qualifications

    • Education: University/College degree in Life Sciences, Health Sciences, Information Technology, or related fields.
    • Skills Required:
      • Computer literacy and ability to work with data management tools.
      • Basic understanding of medical terminology and clinical research.
      • Knowledge of ICH-GCP principles.
      • Strong attention to detail and customer focus.
      • Ability to work collaboratively in a team.
    • Preferred Qualifications: Certification in allied health professions from accredited institutions.

    Relevant Courses: B.Sc. Life Sciences, B.Sc. Nursing, B.Tech Biotechnology, B.Pharm, M.Pharm, Pharm.D, Clinical Research, Health Informatics, Information Technology.

    Location & Salary

    • Location: Bangalore, India (Hybrid – Office-based as per manager’s instructions)
    • Salary: Competitive apprenticeship stipend with additional benefits as per company policy.
    Apprentice - Asst Clinical Data Analyst at Fortrea
    Apprentice – Asst Clinical Data Analyst at Fortrea

    Application Process

    Apply online via Fortrea’s official career portal: Apply Here. The last date to apply is October 10, 2025. Submit a detailed resume highlighting your educational background, certifications, and technical skills. Apply early to secure your apprenticeship spot!

    FAQs

    Q1: Who can apply for this apprenticeship?
    A1: Fresh graduates in Life Sciences, Health Sciences, IT, or related fields with a keen interest in clinical data management.

    Q2: What is the last date to apply?
    A2: The application deadline is October 10, 2025.

    Q3: Is this role open for freshers?
    A3: Yes, this role is specifically designed for fresh graduates and early career professionals.

    Q4: What type of work environment is offered?
    A4: The role is hybrid, with a combination of office-based and remote work, depending on project needs.

    Q5: What skills will I gain?
    A5: Exposure to clinical data management, regulatory compliance, ICH-GCP practices, data review techniques, and teamwork skills.

    Why This Role Matters

    Starting your career as an Apprentice Clinical Data Analyst at Fortrea allows you to step into the world of clinical research while receiving structured training, mentorship, and growth opportunities. You’ll directly contribute to data accuracy, patient safety, and the success of global clinical trials—making a real impact on the future of healthcare.

    Apply now and be part of Fortrea’s mission to shape tomorrow’s healthcare breakthroughs!

    Vertical Summary Table

    Category Details
    Company Fortrea
    Vacancies Multiple (Apprenticeships, 2025)
    Required Education B.Sc Life Sciences, B.Pharm, M.Pharm, Pharm.D, Nursing, Biotechnology, IT, Health Informatics
    Experience Freshers and early career professionals

    Don’t miss this opportunity – Apply before October 10, 2025!

  • Omega Healthcare Hiring Trainee Medical Coders | Bangalore Freshers

    Omega Healthcare Hiring Trainee Medical Coders | Bangalore Freshers

    Omega Healthcare hiring Life Science & Paramedical freshers as Trainee Medical Coders in Bangalore. Immediate joiners preferred. Apply now!

    Omega Healthcare, a leading provider of healthcare outsourcing services, is inviting applications from fresh graduates in Life Sciences and Paramedical fields for the role of Trainee Medical Coder. This is a golden opportunity for freshers looking to start their career in the growing medical coding and healthcare documentation industry.

    Company Overview

    Omega Healthcare is one of the largest healthcare BPO and KPO companies in India, serving leading hospitals, insurance providers, and healthcare organizations globally. With a strong presence across multiple cities and thousands of professionals, Omega is a trusted name in medical coding, billing, and healthcare analytics. The company emphasizes continuous learning, career growth, and global exposure for its employees.

    Job Role & Responsibilities

    As a Trainee Medical Coder, selected candidates will:

    • Review and analyze medical records and documents.
    • Assign standard medical codes using ICD and CPT coding systems.
    • Ensure accuracy and compliance with healthcare regulations.
    • Work closely with healthcare professionals to support billing and reimbursement processes.
    • Learn industry best practices and coding guidelines under expert supervision.

    This role offers comprehensive training for freshers and a clear pathway to becoming a certified medical coder.

    Eligibility / Qualifications

    • Education: Only Life Science and Paramedical graduates can apply.
    • Relevant Courses: B.Sc. Life Sciences, B.Sc. Nursing, B.Pharm, M.Pharm, BPT, MPT, Biotechnology, Microbiology, Biochemistry, Zoology, Botany, and other allied paramedical streams.
    • Skills Required:
      • Strong knowledge of Human Anatomy and Physiology.
      • Good communication skills (written & spoken).
      • Ability to learn and adapt quickly in a fast-paced environment.
    • Experience: Freshers only (Immediate joiners preferred).

    Location & Salary

    • Job Location: Bangalore, Karnataka
    • Salary Package: As per industry standards with performance-based incentives.
    • Benefits:
      • Structured medical coding training.
      • Certification support for CPC (Certified Professional Coder).
      • Healthcare benefits, growth opportunities, and a stable career path.
    Non-Certified Medical Coding Jobs for Freshers Omega Healthcare
    Non-Certified Medical Coding Jobs for Freshers Omega Healthcare

    Application Process

    Interested candidates can apply by filling out the official registration form here:
    👉 Apply Here

    📅 Apply immediately as limited seats are available for this fresher intake. Immediate joiners will be given priority.

    Why Join Omega Healthcare?

    • Be part of one of the largest and most trusted healthcare outsourcing firms.
    • Hands-on training in medical coding, one of the fastest-growing healthcare career paths.
    • Opportunity to earn global certifications like AAPC’s CPC.
    • Stable career growth with exposure to international healthcare standards.
    • Collaborative work culture with mentorship from experienced coders.

    FAQs

    1. Who can apply for this role?
    Only Life Science and Paramedical graduates are eligible.

    2. Is prior coding experience required?
    No, this role is open for freshers. Training will be provided.

    3. What is the job location?
    Bangalore, Karnataka.

    4. Is certification mandatory?
    Not initially. Omega will provide training and certification support.

    5. When should I apply?
    Apply immediately as applications are processed on a first-come-first-serve basis. Immediate joiners preferred.

    Summary Table

    Company Omega Healthcare
    Vacancies Trainee Medical Coder
    Required Education Life Sciences, Paramedical streams (Nursing, Pharmacy, Biotechnology, etc.)
    Experience Freshers only
    Location Bangalore, Karnataka
  • Project Associate Clinical Trials at Syngene

    Project Associate Clinical Trials at Syngene

    Project Associate Clinical Trials – Life Science/Pharmacology – Bangalore | Syngene Careers

    Apply now for Project Associate Clinical Trials at Syngene, Bangalore. Openings for MSc Life Science/Pharmacology graduates with 1–3 years’ experience.

    In today’s competitive healthcare and life sciences industry, securing a position at a global leader like Syngene International Ltd. can be a career-defining move. If you are a postgraduate in Life Sciences or Pharmacology with a passion for clinical operations, this Project Associate – Clinical Trials role in Bangalore offers a strong platform to grow your expertise in clinical research, regulatory compliance, and trial management.

    Company Overview

    Founded in 1993, Syngene International Ltd. is one of India’s leading contract research, development, and manufacturing organizations (CRDMO). With a strong global presence, Syngene partners with some of the world’s top pharmaceutical, biotechnology, and specialty chemical companies including Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife.

    Syngene is home to over 4,200 scientists, working across discovery, development, and manufacturing services, supporting end-to-end R&D. Its mission is to help clients accelerate time-to-market, reduce innovation costs, and improve global healthcare outcomes.

    Job Role & Responsibilities

    As a Project Associate – Clinical Trials, you will play a key role in ensuring smooth clinical operations and regulatory compliance. Your responsibilities will include:

    • Assisting Clinical Project Managers (CPMs) and Clinical Research Associates (CRAs) in maintaining site compliance and project tracking systems.
    • Supporting clinical teams with documentation, distribution, archiving, and reporting activities.
    • Preparing and handling Clinical Trial Supplies while maintaining accurate tracking records.
    • Managing and coordinating Case Report Forms (CRFs), data queries, and clinical data flow.
    • Acting as a central communication hub between internal teams, vendors, and investigators.
    • Supporting Quality Assurance (QA) during audits by providing access to Trial Master Files (TMFs).
    • Coordinating translations of study-related documents in collaboration with translation agencies.
    • Performing administrative tasks that support clinical trial execution.

    This position is best suited for detail-oriented professionals who can manage cross-functional coordination, documentation accuracy, and regulatory adherence.

    Eligibility / Qualifications

    To qualify for the Project Associate – Clinical Trials position at Syngene, you must have:

    • Education: Master’s degree in Life Sciences, Pharmacology, Biotechnology, or related fields. Relevant courses include MSc Life Sciences, MSc Pharmacology, MSc Biotechnology, MSc Clinical Research.
    • Experience: 1–3 years in clinical research or clinical operations.
    • Technical Skills:
      • Strong knowledge of ICH-GCP guidelines and Indian regulatory frameworks.
      • Proficiency in MS Word, Excel, and PowerPoint.
      • Experience in preparing SOPs (Standard Operating Procedures).
      • Familiarity with internal and external audits.
    • Behavioral Skills: Strong English communication skills, integrity, and teamwork.

    Location & Salary

    • Job Location: Bangalore, India
    • Salary: Competitive, based on experience and qualifications (industry standards for Clinical Research roles typically range between ₹4.5 LPA to ₹7.5 LPA for candidates with 1–3 years of experience).

    Application Process

    Interested candidates can apply directly through Syngene’s official career portal:

    👉 Apply Here

    Note: Early applications are encouraged as interviews are conducted on a rolling basis. Apply today to secure your spot!

    Why Join Syngene?

    • Work with global pharma and biotech leaders on cutting-edge projects.
    • Gain exposure to international regulatory standards and advanced trial methodologies.
    • Build a career in a fast-growing organization recognized for innovation and quality.
    • Inclusive workplace culture with equal opportunity policies.

    FAQs

    1. Who can apply for the Project Associate Clinical Trials role at Syngene?
    Candidates with a Master’s in Life Sciences, Pharmacology, or Biotechnology and 1–3 years’ experience in clinical operations are eligible.

    2. What skills are required for this position?
    Knowledge of ICH-GCP, regulatory guidelines, MS Office tools, SOP preparation, and audit handling are essential.

    3. What is the expected salary range?
    While Syngene does not disclose salaries publicly, typical ranges for similar positions in Bangalore are between ₹4.5 – ₹7.5 LPA.

    4. Where is this job located?
    The position is based at Syngene International’s Bangalore facility.

    5. How do I apply?
    Applications must be submitted via Syngene’s official careers page: Apply Here

    Summary Table

    Company Syngene International Ltd.
    Vacancies Project Associate – Clinical Trials
    Required Education Master’s in Life Sciences, Pharmacology, Biotechnology, Clinical Research
    Experience 1–3 years in Clinical Research / Operations
    Location Bangalore, India

    Call-to-Action:
    Don’t miss the opportunity to build a career with a global leader in life sciences research. Apply before the deadline to secure your place at Syngene International!

  • CRA – Clinical Research Associate | Syngene | Bangalore

    CRA – Clinical Research Associate | Syngene | Bangalore

    CRA – Clinical Research Associate | Syngene | Bangalore

    Apply for CRA (Clinical Research Associate) role at Syngene in Bangalore. 3–5 years’ experience required. Life Science/Pharmacology graduates. sydney sweeney porn

    Are you passionate about advancing clinical research and contributing to global healthcare innovations? Syngene International Ltd. is inviting applications for the position of Clinical Research Associate (CRA) in Bangalore. This is an excellent opportunity for life science professionals with hands-on experience in clinical research to grow with one of India’s leading CROs trusted by top global pharma and biotech companies.

    Company Overview

    Syngene International Ltd., incorporated in 1993, is a globally recognized, innovation-driven Contract Research Organization (CRO). With over 4,200 scientists, Syngene partners with leading pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical companies worldwide. Clients include industry giants such as Bristol-Myers Squibb, Amgen, Merck KGaA, GSK, Baxter, and Herbalife. The company’s mission is to accelerate R&D productivity, reduce time-to-market, and lower the cost of innovation while ensuring world-class compliance and quality.

    Job Role & Responsibilities

    As a Clinical Research Associate (CRA), you will play a pivotal role in ensuring the smooth conduct of clinical studies, site management, and compliance with international standards.

    Key responsibilities include:

    • Performing site selection, initiation, monitoring, and close-out visits in line with SOPs, ICH-GCP, and regulatory guidelines.
    • Managing site activities for assigned clinical protocols and therapeutic areas.
    • Delivering protocol-related and study-specific training to site staff.
    • Ensuring compliance, quality, and integrity of trial data.
    • Addressing quality issues by implementing Corrective and Preventive Actions (CAPA).
    • Tracking regulatory approvals, Ethics Committee submissions, subject recruitment, CRF completion, and query resolution.
    • Maintaining accurate documentation including monitoring reports, follow-up letters, and action plans.
    • Assisting Clinical Project Managers in study tool development, team coordination, and project documentation.
    • Preparing for and supporting both internal and external audits.

    Eligibility / Qualifications

    To apply for this CRA role at Syngene, candidates must meet the following criteria:

    • Education: Master’s degree in Life Science, Pharmacology, Clinical Research, or related fields. Eligible courses include M.Sc. Pharmacology, M.Sc. Biotechnology, M.Sc. Biochemistry, M.Pharm Pharmacology, M.Sc. Clinical Research.
    • Experience: Minimum 3–5 years in core clinical research activities.
    • Technical Skills:
      • Strong knowledge of ICH-GCP guidelines and Indian regulatory requirements.
      • Proficiency in MS Office tools (Word, Excel, PowerPoint).
      • Knowledge of SOP development and compliance.
      • Experience in audit preparedness and facing regulatory inspections.
    • Behavioral Skills:
      • Strong communication skills in English.
      • Conflict resolution, stress management, empathy, and patience.

    Location & Salary

    • Job Location: Bangalore, India
    • Department: Clinical Operations – Discovery Services
    • Work Schedule: Full-time, 40 hours per week (IST)
    • Salary: Competitive package aligned with industry standards, commensurate with qualifications and experience.
    <img class=”size-full wp-image-123316″ src=”https://bpharmacyjobs.com/wp-content/uploads/2025/09/CRA-–-Clinical-Research-Associate-Syngene-Bangalore.webp” alt=”CRA – Clinical Research Associate | Syngene | Bangalore” width=”1200″ height=”675″ /> CRA – Clinical Research Associate | Syngene | Bangalore

    Application Process

    Interested candidates can apply online through Syngene’s career portal: Apply Here

    Applicants are encouraged to submit:

    • Updated resume
    • Cover letter highlighting clinical research experience
    • Relevant certifications and training documents

    Why Join Syngene?

    • Work with global pharma leaders and contribute to breakthrough discoveries.
    • Grow your career in an internationally accredited CRO.
    • Access to continuous professional development and structured learning.
    • Be part of a collaborative and innovation-driven team.

    FAQs

    1. What is the minimum experience required for this CRA role at Syngene?

    A minimum of 3–5 years in core clinical research activities is required.

    2. Can freshers apply for the CRA position?
    No. This role requires prior experience in clinical research operations.

    3. What qualifications are accepted for this role?
    A Master’s degree in Life Science, Pharmacology, Biotechnology, Biochemistry, M.Pharm, or related fields is mandatory.

    4. What does a CRA do at Syngene?
    A CRA ensures site selection, initiation, monitoring, compliance, and data integrity in clinical trials.

    5. Where is the job location?
    The position is based in Bangalore, India.

    6. Is remote work possible for this role?
    No, this is an on-site position within the Clinical Operations department.

    7. What is the salary range?
    Syngene offers a competitive compensation package in line with candidate expertise and market standards.

    Call to Action

    Don’t miss this opportunity to build your career with one of India’s leading CROs! Apply now and take the next step in your clinical research journey.
    👉 Apply before the position closes

    Summary Table

    Company Syngene International Ltd.
    Vacancies Clinical Research Associate (CRA)
    Required Education M.Sc. Life Sciences, M.Sc. Pharmacology, M.Pharm, M.Sc. Clinical Research, M.Sc. Biotechnology
    Experience 3–5 years in clinical research
  • Data, Systems & Document Associate Vacancy | Labcorp

    Data, Systems & Document Associate Vacancy | Labcorp

    Data, Systems & Document Associate Vacancy | Labcorp Bangalore

    Apply for Data, Systems & Document Associate role at Labcorp Bangalore. Open for Life Science graduates with 2+ years of experience.

    Labcorp, a global leader in clinical research and laboratory services, is hiring a Data, Systems, and Document Associate for its Bangalore location. This role is ideal for life science graduates with a passion for laboratory operations, data systems, and compliance-driven document management. If you have experience in LIMS, GxP environments, and document control, this opportunity will allow you to contribute directly to advancing healthcare and improving patient outcomes.

    Company Overview

    Labcorp is a leading global life sciences company that provides comprehensive laboratory and drug development services. With a mission to improve health and improve lives, Labcorp partners with top pharmaceutical, biotech, and healthcare organizations worldwide. The company is recognized for its excellence in clinical trials, laboratory operations, and technological innovation. Joining Labcorp means becoming part of a team committed to transforming healthcare through science, data, and innovation.

    Job Role & Responsibilities

    As a Data, Systems, and Document Associate at Labcorp, you will be responsible for supporting laboratory operations and ensuring compliance in data and document management. Key responsibilities include:

    • Reviewing study protocols for new test code setup in Laboratory Information Management System (LIMS).
    • Performing laboratory study setup activities and data collection within a GxP-compliant environment.
    • Authoring, revising, and retiring controlled documents such as Policies, SOPs, Guides, and Forms for the Global Immunology & Immunotoxicology (I&I) department.
    • Acting as the Analytical Processes/Working Document (AP/WD) Librarian and document coordinator.
    • Supporting administrative tasks related to the Learning Management System (LMS).
    • Coordinating and updating quarterly organizational charts for the Global I&I department.
    • Managing multiple assignments effectively while meeting deadlines.
    • Other responsibilities as assigned to support departmental needs.

    Eligibility / Qualifications

    To qualify for this role, candidates must meet the following requirements:

    • Education: Bachelor’s or Master’s degree in Life Sciences, Biotechnology, Microbiology, Biochemistry, or related fields.
    • Experience: Minimum 2+ years of relevant experience in laboratory operations, LIMS, or document management.
    • Technical Skills:
      • Experience with Laboratory Information Management Systems (LIMS), preferably Watson LIMS.
      • Understanding of GxP compliance and laboratory data collection.
      • Strong documentation, communication, and coordination skills.

    Location & Salary

    • Location: Bangalore, India.
    • Work Type: Full-time, On-site (Not Remote).
    • Salary: Competitive industry-standard compensation with performance incentives and employee benefits.
    Data, Systems & Document Associate Vacancy | Labcorp
    Data, Systems & Document Associate Vacancy | Labcorp

    Application Process

    Labcorp encourages diverse applicants to apply. The company is an Equal Opportunity Employer, committed to building a workforce of inclusion and belonging.

    👉 Apply directly here

    FAQs

    1. Who can apply for this role?
    Candidates with a Bachelor’s or Master’s degree in life sciences and at least 2 years of experience in LIMS, laboratory operations, or document management.

    2. Is Watson LIMS experience mandatory?
    No, it is highly desirable but not mandatory.

    3. What type of environment will I work in?
    A GxP-compliant laboratory environment supporting Global Immunology & Immunotoxicology operations.

    4. What is the job location?
    This position is based in Bangalore, India and is not remote.

    5. Does Labcorp encourage diverse applicants?
    Yes, Labcorp is an Equal Opportunity Employer and values inclusion, belonging, and diversity in its workforce.

    Job Summary Table

    Category Details
    Company Labcorp
    Vacancies Data, Systems, and Document Associate
    Required Education Bachelor’s/Master’s in Life Sciences, Biotechnology, Microbiology, Biochemistry
    Experience 2+ years in laboratory operations, LIMS, or document management
    Location Bangalore, India
  • Statistical Programmer Vacancy for Life Science Graduates | TCS

    Statistical Programmer Vacancy for Life Science Graduates | TCS

    Statistical Programmer Vacancy for Life Science Graduates | TCS Mumbai

    Apply now for TCS Statistical Programmer vacancies in Mumbai, Pune, Bangalore & Noida. Open for life-science/engineering graduates with 5–12 years’ experience.

    Tata Consultancy Services (TCS), one of the world’s leading IT and consulting organizations, is inviting applications for the role of Statistical Programmer across multiple locations in India. If you are an experienced professional in life sciences or engineering with expertise in SAS programming, R, and clinical data standards, this is your chance to advance your career with a globally reputed company.

    Company Overview

    TCS is a global leader in IT services, consulting, and business solutions, trusted by top pharmaceutical, biotechnology, and healthcare organizations worldwide. With decades of experience in clinical research and data analytics, TCS offers an excellent platform for professionals in clinical programming, biostatistics, and statistical analysis to make a meaningful contribution to healthcare advancements. The company is recognized for its innovation-driven culture, strong learning environment, and commitment to employee growth.

    Job Role & Responsibilities

    As a Statistical Programmer at TCS, you will play a key role in clinical trial data analysis and programming deliverables. Your day-to-day responsibilities will include:

    • Collaborating with statisticians to design, review, and implement Statistical Programming Plans (SPPs).
    • Executing Statistical Analysis Plans (SAPs) to create ADaM datasets and generate Tables, Listings, and Figures (TLFs).
    • Developing and validating SAS/R programs for statistical analyses and clinical trial reporting.
    • Ensuring compliance with CDISC standards and preparing detailed programming documentation.
    • Performing quality checks to validate outputs and ensure accuracy.
    • Designing and implementing standard macros and utilities to streamline programming efficiency.
    • Partnering with clinical study teams, statisticians, and external stakeholders for seamless execution of programming deliverables.

    Eligibility / Qualifications

    To be considered for this role, candidates must meet the following requirements:

    • Educational Qualification: Graduate/Postgraduate in Life Sciences, Pharmacy, Biotechnology, Statistics, Computer Science, or Engineering disciplines. Acceptable degrees include B.Sc, M.Sc, B.Tech, M.Tech, B.Pharm, M.Pharm, MBBS, MD (Biostatistics), and related fields.
    • Experience: 5–12 years in statistical programming within clinical research, CROs, or pharma industry.
    • Technical Skills:
      • Proficiency in SAS programming (Base, Macro, SQL) and R.
      • Hands-on experience with ADaM, TLF, SAP, and CDISC standards.
      • Knowledge of therapeutic areas such as Oncology, Immunology, and Neuroscience.
      • Familiarity with clinical trial data handling, statistical methodologies, and documentation.

    Location & Salary

    • Job Locations: Mumbai, Pune, Bangalore, Noida.
    • Work Type: Full-time, On-site.
    • Salary: Competitive compensation package aligned with industry standards, including benefits such as healthcare, performance bonuses, and professional development opportunities.
    Statistical Programmer Vacancy for Life Science Graduates | TCS
    Statistical Programmer Vacancy for Life Science Graduates | TCS

    Application Process

    Interested applicants are encouraged to apply early to secure their spot. The hiring process typically takes 1 week for review.

    👉 Apply directly through LinkedIn

    FAQs

    1. Who can apply for the TCS Statistical Programmer role?
    Candidates with a graduate or postgraduate degree in life sciences, pharmacy, biotechnology, statistics, computer science, or engineering, along with 5–12 years of experience in statistical programming.

    2. What technical expertise is required?
    Applicants must have advanced skills in SAS programming, R, ADaM, CDISC standards, and TLF generation.

    3. Is prior experience in a specific therapeutic area mandatory?
    While not mandatory, familiarity with Oncology, Immunology, or Neuroscience is highly desirable.

    4. What locations are available for this job?
    This role is open in Mumbai, Pune, Bangalore, and Noida.

    5. How soon should I apply?
    Apply as soon as possible. Early applicants have a higher chance of being shortlisted.

    Job Summary Table

    Category Details
    Company Tata Consultancy Services (TCS)
    Vacancies Multiple Statistical Programmer openings
    Required Education Graduate/Postgraduate in Life Sciences, Pharmacy, Biotechnology, Statistics, Computer Science, Engineering
    Experience 5–12 years in statistical programming in clinical research/pharma/CROs
    Locations Mumbai, Pune, Bangalore, Noida