Penam Biosciences Pvt. Ltd. is a premier manufacturing facility specializing in liquid and freeze-dried sterile injectable products. Known for its integrity and commitment to quality, the company is dedicated to fostering positive growth for the community and its partners. Penam Biosciences Production / QC / ARD / Microbiology
Current Job Openings
Production (Injectable)
Position: QMS Executive
Vacancies: 2
Experience: 4–8 years
Qualifications: B.Pharma / M.Sc
Analytical Research and Development (AR&D)
Position: Analyst
Vacancies: 2
Experience: 4–8 years
Qualifications: M.Pharma / M.Sc
Microbiology
Position: QMS Executive
Vacancies: 2
Experience: 5–8 years
Qualifications: M.Sc in Microbiology
Quality Control
Positions:
Executive GLP
AMV
RM & PM
HPLC
Vacancies: 4
Experience: 3–6 years
Qualifications: M.Sc Chemistry / B.Pharma
Why Join Penam Biosciences?
Work at a state-of-the-art injectable manufacturing facility.
Be part of a team that values integrity and quality.
Opportunities for growth and professional development.
Precision For Medicine Hiring for Document Control Specialist
Document Control Specialist
Location: Pune, Maharashtra Experience: 1–3 years Qualification: B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, or Lifesciences background
About Precision For Medicine
Precision For Medicine is at the forefront of supporting life sciences companies with tailored solutions to accelerate clinical research and advance personalized medicine. With a global presence, the organization is committed to driving innovation in precision healthcare.
Role Overview
As a Document Control Specialist, you will play a crucial role in managing and maintaining controlled documents and providing administrative support to the quality assurance team.
Key Responsibilities
Quality Assurance and Document Management
Manage electronic document control workflows for Quality System Documents.
Track document lifecycles from creation to obsolescence.
Ensure documents comply with internal standards, formatting, and readability requirements.
Report documentation gaps to senior management and assist in revisions during system integration.
Assign training workflows for updated or new procedures.
Conduct periodic reviews and ensure document security.
Upload documents to the PLN portal or internal sites.
Training
Provide training to employees on the electronic quality management system.
Audit Support
Prepare and reconcile document requests for audits.
Ensure prompt responses to documentation needs.
Update procedure binders and compile training materials for audits.
Additional Duties
Perform tasks as assigned by management to meet organizational goals.
Qualifications and Skills
Minimum Requirements
Bachelor’s degree in a relevant field.
1–3 years of experience with ISO 9001/13485 standards.
Familiarity with quality systems and document control in clinical research organizations.
Additional Requirements
Document Control Certification (to be obtained within the first year).
Proficiency in Microsoft Office applications.
Strong organizational and administrative skills.
Ability to meet deadlines and adapt to shifting priorities.
Excellent communication skills, with fluency in English.
Why Join Us?
Work with a leading organization driving innovation in personalized healthcare.
Engage in meaningful projects that contribute to clinical research advancements.
Enjoy a collaborative and dynamic work environment.
How to Apply
Submit your application online to be part of this exciting journey.
Make an impact with Precision For Medicine—where innovation meets precision in healthcare!
Merck is a leading global science and technology company known for its innovation and dedication to advancing health and well-being. Operating in over 70 countries, Merck provides a vibrant and dynamic environment for professionals to grow their careers while contributing to groundbreaking scientific advancements. Fresher Hiring Merck for Analyst (Contract)
Position Details
Role: Analyst (Contract)
Team: Tender Management
Location: Electronic City, Bangalore
Experience Level: 0–2 years (Freshers are encouraged to apply!)
Eligibility Criteria
Educational Qualifications
M.Sc. in one of the following fields:
Molecular Biology
Chemistry
Biochemistry
Microbiology
Biotechnology
Fresher Hiring Merck for Analyst (Contract)
Preferred Skills
Strong knowledge in the relevant scientific disciplines.
Experience with laboratory equipment and handling is an advantage.
Why Join Merck?
Be part of a global leader in science and technology.
Work in a dynamic environment that fosters innovation and growth.
Contribute to cutting-edge advancements that improve lives globally.
How to Apply
Submit your application before the deadline via the link provided below:
Aculife Healthcare Pvt. Ltd. is a trusted name in the healthcare industry with over 30 years of excellence. Renowned for its innovation, growth, and reliability, Aculife is a market leader committed to delivering high-quality healthcare products and services that maximize customer value.
We are excited to invite talented and enthusiastic individuals to join our Quality Control team at our manufacturing site in Sachana, Ahmedabad. Aculife Healthcare Hiring for Quality Control
Glenmark Life Sciences Hiring for Quality Control / Quality Assurance
About Glenmark Life Sciences
Glenmark Life Sciences Limited (GLS) is a leading developer and manufacturer of high-value Active Pharmaceutical Ingredients (APIs) in chronic therapeutic areas. We collaborate with 16 of the top 20 global generic pharmaceutical companies, expanding our reach and product offerings.
To support the growth of our manufacturing facilities, we are hiring passionate professionals for our API plant in Dahej, Gujarat. Glenmark Life Sciences Hiring for Quality Control / Quality Assurance
Walk-In Interview Details
Date: 26th November 2024 (Tuesday)
Time: 10:00 AM – 4:00 PM
Venue: Glenmark Life Sciences Limited, Dahej, Dist. – Bharuch, Gujarat
Current Openings
Department: Quality Control (QC) / Quality Assurance (QA)
Designation: Officer / Executive
Qualifications: B.Sc / M.Sc in relevant fields
Experience: 1 to 4 years of experience in QC and IPQA
Key Skills:
Knowledge of regulatory requirements, documentation, and cGMP standards
Preferred Candidates
Professionals with relevant experience in QC and QA roles
Exposure to regulatory audits and compliance
Documents to Bring
Updated resume
Educational certificates
Two passport-sized photographs
ID proof
Latest salary breakup and last 3 months’ salary slips
B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences graduates
Experience
1 to 2 Years
Salary
₹4 – ₹5.5 Lacs Per Year
Job Location
Chennai
Application Mode
Online Application
Elevate Your Career in Clinical Research with ICON plc
Are you ready to take the next step in your clinical research career? ICON plc, a global leader in healthcare intelligence and clinical research, is seeking a Clinical Trial Assistant to join their team in Chennai. This role offers the opportunity to contribute to innovative healthcare solutions and be part of a dynamic environment that values professional growth and excellence. ICON plc Hiring for Clinical Trial Assistant
About ICON plc
ICON plc is renowned for its commitment to healthcare intelligence and clinical research. With a focus on fostering a diverse and inclusive workplace, ICON empowers its employees to excel and contribute to advancing clinical development. Join a team that is passionate about innovation and shaping the future of healthcare. ICON plc Hiring for Clinical Trial Assistant
Key Responsibilities
As a Clinical Trial Assistant, your role will involve supporting the successful execution of clinical trials. Key responsibilities include:
Staying updated on ICH GCP guidelines and operational procedures.
Supporting multiple clinical studies and managing priorities effectively.
Maintaining study trackers, analyzing reports, and distributing dashboards to study teams.
Providing administrative support for both In-house and Field Study Operations (FSO) trials.
Managing and maintaining study systems like eTMF, CSAP, and CTMS.
Collaborating with SDS/SM for post-SAC activities and final archival.
Ensuring TMF Management for compliance through regular follow-ups.
Your attention to detail and organizational skills will ensure the seamless operation of clinical trials while adhering to quality standards.
ICON plc Hiring for Clinical Trial Assistant
Required Qualifications & Skills
To succeed in this role, you should have:
Technical/IT Skills: Proficiency in clinical trial management systems and the ability to leverage technology for trial operations.
ICH GCP Knowledge: Familiarity with Good Clinical Practice guidelines and quality standards for clinical studies.
Teamwork & Independence: Ability to work collaboratively as well as independently.
Communication Skills: Strong verbal and written communication skills for effective coordination.
Time Management: Ability to manage multiple tasks, meet deadlines, and maintain system updates.
Experience: 1-2 years of experience in clinical operations or a related field.
Benefits of Working at ICON
ICON plc values its employees and offers a range of benefits to support well-being and work-life balance:
Competitive Salary and annual leave entitlements for personal time.
A variety of health insurance plans for you and your family.
Retirement planning options to secure your future.
Access to the Global Employee Assistance Programme for 24/7 support.
Flexible benefits tailored to your needs, including gym memberships, childcare vouchers, and life assurance.
ICON plc Hiring for Clinical Trial Assistant
Why Join ICON?
By joining ICON, you’ll become part of a team that is dedicated to innovation, excellence, and improving healthcare globally. This position offers a unique opportunity to develop your skills, work in a supportive environment, and make a meaningful impact in clinical research. ICON plc Hiring for Clinical Trial Assistant
How to Apply
Submit your application online to become a part of ICON’s clinical research team in Chennai. Don’t miss this opportunity to advance your career with one of the industry’s leading organizations.
Kickstart Your Career with GeBBS Healthcare Solutions
Are you a fresh graduate in life sciences looking to enter the world of medical coding? GeBBS Healthcare Solutions, a renowned healthcare outsourcing provider, is offering a fantastic opportunity for freshers to join their team as Non-Certified Medical Coders. The walk-in interview is your chance to step into a promising career path and gain specialized skills in medical coding. GeBBS Healthcare Hiring for Non Certified Medical Coders
About GeBBS Healthcare Solutions
GeBBS Healthcare Solutions is a global leader in healthcare outsourcing, providing services like medical coding, billing, and revenue cycle management. Known for its focus on quality and efficiency, GeBBS partners with leading healthcare organizations worldwide. Joining GeBBS means being part of an innovative team that contributes to improving the healthcare sector globally. GeBBS Healthcare Hiring for Non Certified Medical Coders
Job Responsibilities
As a Non-Certified Medical Coder, you will play a vital role in the revenue cycle management of healthcare organizations. Your key responsibilities include:
Analyzing Medical Records: Review patient records for accurate coding of diagnoses, procedures, and treatments.
Medical Coding: Apply knowledge of anatomy, physiology, and medical terminology to assign appropriate codes (CPT, ICD-10, HCPCS).
Adherence to Standards: Follow industry-specific guidelines and standards for accurate medical coding.
Specialization: Post-training, specialize in domains like Radiology, Anesthesia, Emergency Department, Evaluation & Management, or Home Health.
GeBBS Healthcare Hiring for Non Certified Medical Coders
Qualifications and Eligibility
Educational Requirements
Candidates must be graduates in life sciences (B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc).
Only graduates from 2020 or later are eligible.
Academic Criteria
No backlogs are allowed.
Carry xerox copies of your 10th, 12th, and degree mark sheets or provisional certificates.
Essential Skills
Basic knowledge of anatomy, physiology, and medical terminology.
Strong problem-solving and reasoning abilities.
Proficiency in English comprehension and communication.
Skills Required
To succeed in this role, you need:
A solid foundation in anatomy and physiology.
Familiarity with medical terminology.
Excellent analytical and reasoning skills.
Strong written and verbal communication abilities.
A willingness to learn and adapt to dynamic healthcare environments.
Selection Process
GeBBS Healthcare employs a rigorous selection process to identify top talent.
Written Test: Covers topics like anatomy, medical terminology, basic aptitude, reasoning, and English comprehension.
Technical Round: Includes in-depth questions on anatomy, physiology, and medical terminology.
Post-selection: Successful candidates will undergo comprehensive training, with opportunities to gain CPC (Certified Professional Coder) certification sponsored by the company. GeBBS Healthcare Hiring for Non Certified Medical Coders
GeBBS Healthcare Hiring for Non Certified Medical Coders
Walk-In Interview Details
Date: Monday, 10 AM onwards (Tuesday interviews if vacancies remain).
Updated resume with “Jay Dilip KadamEcn 81125” written at the top.
Xerox copies of:
Aadhaar and PAN cards.
10th, 12th, and degree mark sheets or provisional certificates.
Why Join GeBBS Healthcare Solutions?
Be part of a leading healthcare outsourcing company recognized globally.
Gain industry-relevant skills and hands-on experience in medical coding.
Work in a supportive environment that values work-life balance and flexibility.
Opportunity for career growth and certification sponsorship.
Don’t Miss Out!
This is your chance to begin a rewarding career in medical coding with GeBBS Healthcare Solutions. Head to the interview venue with your documents and seize the opportunity to join a company that values growth, innovation, and excellence in healthcare services. GeBBS Healthcare Hiring for Non Certified Medical Coders
B.Pharm, M.Pharm, M.Sc in Biotechnology, Microbiology, Life Sciences, Biochemistry, or related disciplines
Location
Bangalore
Skills Required
Analytical tools like HPLC, GC, spectroscopy; strong chemical principles; lab techniques
Job Type
Verified Internship
Application Method
Online application
Launch Your Research Career with Biocon’s R&D Internship
If you’re passionate about advancing pharmaceutical research and making a meaningful impact in biotechnology, Biocon’s R&D Internship Program offers the perfect platform to kickstart your career. Based in Bangalore, this opportunity is tailored for freshers eager to immerse themselves in cutting-edge research and development (R&D). Freshers Biocon Trainee RD
Why Join Biocon?
Global Leader in Biotechnology
Established in 1978, Biocon is a pioneer in biotechnology and biopharmaceuticals. The company is a global name in biosimilars, generic formulations, and innovative healthcare solutions. With a mission to provide affordable and accessible healthcare, Biocon stands as a beacon of excellence and innovation. Freshers Biocon Trainee RD
Focus on Innovation
Biocon’s robust R&D infrastructure and state-of-the-art facilities offer unmatched opportunities for aspiring researchers to work on transformative projects that impact global healthcare. Freshers Biocon Trainee RD
Freshers Biocon Trainee RD
Role Overview: R&D Intern/Trainee
As an R&D Intern or Trainee, you’ll gain hands-on experience in various aspects of pharmaceutical research. This role is designed to empower you with practical skills while contributing to real-world projects. Freshers Biocon Trainee RD
Key Responsibilities
Experimentation and Analysis
Conduct experiments and tests in R&D laboratories under expert supervision.
Perform chemical synthesis, analysis, and characterization of compounds.
Data Management
Maintain accurate records of experimental findings.
Assist in the preparation of research reports, protocols, and presentations.
Collaborative Work
Collaborate with cross-functional teams to achieve project milestones.
Contribute to the development of innovative pharmaceutical solutions.
Qualifications and Eligibility
Biocon is looking for enthusiastic individuals who meet the following criteria:
Educational Background: B.Pharm, M.Pharm, or M.Sc in Biotechnology, Microbiology, Life Sciences, Biochemistry, or related fields.
Academic Excellence: A strong academic record and a keen interest in research and development.
Skills Required:
Proficiency in analytical tools like HPLC, GC, and spectroscopy.
Strong grasp of chemical principles and laboratory techniques.
Excellent documentation and communication skills.
What Makes This Internship Special?
Learning and Growth
This internship is your gateway to learning from industry leaders, working in high-tech facilities, and contributing to impactful projects. It provides an immersive environment to hone your technical skills and problem-solving abilities. Freshers Biocon Trainee RD
Networking Opportunities
As an intern at Biocon, you’ll interact with experts, peers, and mentors who can guide your professional journey and open doors to exciting career opportunities. Freshers Biocon Trainee RD
Work-Life Balance
Biocon values flexibility, time management, and a supportive work culture, ensuring interns can thrive in a balanced and enriching environment. Freshers Biocon Trainee RD
Freshers Biocon Trainee RD
Skills That Will Set You Apart
To excel in this role, focus on developing:
A proactive and innovative mindset.
Strong collaboration skills for working in team settings.
Mastery of laboratory and analytical techniques.
How to Apply
Applying for this role is straightforward:
Online Application Use the online Application Link to submit your application directly.
Prepare Your Resume Highlight your educational background, skills, and enthusiasm for research.
Joining Biocon as an R&D Intern/Trainee is more than just an internship – it’s a stepping stone to a promising career in the pharmaceutical industry. Gain hands-on experience, expand your professional network, and work on projects that redefine healthcare.
Apply today and become part of Biocon’s mission to transform lives through innovation.
Formulation Analytical Research, Formulation Research Development, Regulatory Affairs
Benefits
Transportation and canteen facilities provided
Application Method
Online application (via links provided)
Start Date
Within 1 month
Job Type
Verified Internship
Exciting Internship Opportunity at Eugia Pharma Specialities Ltd.
Looking for an exciting start to your career in Regulatory Affairs or Research and Development (R&D)? Eugia Pharma Specialities Ltd. offers a fantastic opportunity for freshers to gain real-world experience, enhance their skills, and set the stage for a rewarding career. Here’s everything you need to know about this incredible internship: Internship Eugia Pharma for Regulatory Affairs rd
About Eugia Pharma Specialities Ltd.
Eugia Pharma is a recognized leader in the pharmaceutical sector, known for innovation, excellence, and fostering young talent. This internship is specially designed for aspiring professionals eager to make their mark in R&D or Regulatory Affairs, providing both hands-on learning and industry exposure. Internship Eugia Pharma for Regulatory Affairs rd
Internship Eugia Pharma for Regulatory Affairs rd
Why Choose This Internship?
1. Hands-On Experience
This internship involves direct exposure to critical functions in Formulation Analytical Research, Formulation Research Development, and Regulatory Affairs, offering you a chance to work alongside seasoned professionals in the pharmaceutical industry. Internship Eugia Pharma for Regulatory Affairs rd
2. Attractive Benefits
In addition to the ₹12,000 stipend, the company provides transportation and canteen facilities, ensuring a seamless and comfortable work experience. Internship Eugia Pharma for Regulatory Affairs rd
3. Skill Development
You will gain valuable skills in time management, problem-solving, flexibility, and work-life balance, preparing you for the challenges of the professional world.
Key Details About the Role
Location
The internship will be based in Hyderabad, specifically in the Pashamylaram area, a hub for leading pharmaceutical companies.
Eligibility Criteria
Experience: Freshers with 0-1 year of experience are welcome.
Education: Open to candidates with a B.Pharm, M.Pharm, M.Sc, or B.Sc degree. This inclusive eligibility makes it an excellent opportunity for recent graduates looking to step into the industry.
Stipend
A monthly stipend of ₹12,000 ensures you are compensated while gaining invaluable experience.
Start Date
The internship is set to begin within one month, making it a perfect choice for candidates ready to embark on their career journey immediately.
What Makes This Internship Unique?
Comprehensive Learning
This program is tailored to provide insights into both research and compliance aspects of the pharmaceutical industry. By working in the Regulatory Affairs and R&D departments, interns can explore diverse roles that strengthen their foundation.
Internship Eugia Pharma for Regulatory Affairs rd
Networking Opportunities
You will have the opportunity to connect with industry professionals, mentors, and peers, building a network that can benefit your long-term career growth.
Verified Opportunity
As a verified job listing, this internship ensures authenticity and offers a trusted platform for launching your career.
How to Apply?
Online Application Visit the Application Link to submit your application.
Via Naukri Portal Alternatively, check the job listing on Naukri Portal. Look for the “Intern with Us” option, and submit your details to get started.
Fresh graduates passionate about Regulatory Affairs and R&D.
Individuals eager to work in a dynamic environment and gain hands-on industry experience.
Candidates looking to enhance their career prospects with practical knowledge and professional mentorship.
Start Your Career Today!
This internship is an incredible opportunity to kickstart your career in a fast-growing and essential industry. Don’t miss the chance to work with Eugia Pharma Specialities Ltd., a company committed to nurturing fresh talent and setting them up for success.
Apply now and take the first step towards a fulfilling career in pharmaceutical research and development or regulatory affairs.
Fresher CRDS Trainee Clinical Research Coordinator
CRDS Clinical Research Services
Freshers
delhi, Chandigarh, Haryana
B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences
Verified Job
Email Application
Job highlights
Work/Life Balance
Time management
Flexibility
CRDS Clinical Research Services, headquartered in New Delhi, is a pioneering organization specializing in providing comprehensive clinical research solutions. We are committed to bridging the gap between cutting-edge medical advancements and healthcare delivery through robust clinical trials and research programs. Our collaborations with top-tier hospitals and institutions across India ensure impactful contributions to the healthcare sector. Fresher CRDS Trainee Clinical Research Coordinator
We are seeking Trainee Clinical Research Coordinators (CRC) to join our esteemed team at multiple hospitals. This is a golden opportunity for fresh graduates in life sciences to begin their career in clinical research and gain hands-on experience at premier medical institutions. Fresher CRDS Trainee Clinical Research Coordinator
Locations and Vacancies
AIIMS Delhi: 2 positions
Maharaja Agrasen Hospital, Punjabi Bagh West, New Delhi: 2 positions
Sarvodaya Hospital, Faridabad, Delhi: 2 positions
PGI, Rohtak, Haryana: 2 positions
PGI, Chandigarh: 2 positions
We are looking for immediate joiners to fill these roles.
Key Responsibilities of Trainee CRC
As a Trainee Clinical Research Coordinator, your role will include:
Clinical Trial Coordination
Assisting in the management of clinical trials at the assigned site.
Ensuring compliance with Good Clinical Practice (GCP) and ethical standards.
Data Management
Collecting, verifying, and entering clinical trial data.
Maintaining accurate and up-to-date clinical documentation.
Patient Interaction
Coordinating with patients for trial-related visits and procedures.
Educating participants about study protocols and obtaining informed consent.
Liaison Role
Communicating with investigators, sponsors, and site staff to ensure seamless trial operations.
Regulatory Compliance
Ensuring trial-related activities align with regulatory requirements and organizational policies.
Fresher CRDS Trainee Clinical Research Coordinator
see This Job
Qualifications
We welcome freshers with the following educational background:
B. Pharm / M. Pharm
B. Sc / M. Sc
Graduates in Life Sciences or related fields
If you have a passion for clinical research and a commitment to contributing to healthcare advancements, this role is perfect for you!
Essential Skills
Basic Knowledge of Clinical Research: Familiarity with GCP guidelines and clinical trial phases.
Organizational Skills: Ability to manage time and multitask efficiently.
Communication: Strong verbal and written communication skills to interact effectively with patients and professionals.
Attention to Detail: Ensuring accuracy in data collection and documentation.
Team Player: Ability to work collaboratively with multidisciplinary teams. Fresher CRDS Trainee Clinical Research Coordinator
How to Apply
If you meet the qualifications and are excited about starting your journey in clinical research, please send your updated CV to crds.hr@gmail.com with the subject line “Application for Trainee CRC Position.”
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