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CorroHealth Hiring for Medical Coder / Senior Coder

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CorroHealth Hiring for Medical Coder / Senior Coder

CorroHealth Hiring for Medical Coder / Senior Coder

Position: Medical Coder / Senior Coder
Location: On-site, Noida, Uttar Pradesh
Employment Type: Full-time
Eligibility: B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences
Experience Required: Minimum 1 year in HCC coding

Key Responsibilities

As a Medical Coder at CorroHealth, you will:

  • Review patient charts and ensure documentation accuracy and completeness.
  • Utilize current and active codes to maintain compliance with medical coding guidelines.
  • Handle complex coding scenarios with precision.
  • Follow up with payers for clarification on unclear documentation.
  • Ensure adherence to policies and guidelines for medical coding.
    CorroHealth Hiring for Medical Coder / Senior Coder

Desired Skills

  • Proficiency in HCC coding and ICD-10 codes.
  • Familiarity with the US healthcare system.
  • Strong skills in MS Office tools (Excel, PowerPoint, etc.).
  • Excellent written and verbal communication skills.
  • Ability to work independently and manage tasks efficiently.

Eligibility Criteria

  • Experience: Minimum 1 year in HCC coding.
  • Certification: Certified by AAPC or AHIMA.

How to Apply

Contact Details:

Start your career with CorroHealth and make a difference in the healthcare industry!

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Fresher Navitas Lifesciences Hiring for PV RA CDM

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Fresher Navitas Lifesciences Hiring for PV RA CDM

Fresher Navitas Lifesciences Hiring for PV RA CDM

Locations: Chennai, Bangalore, Manipal
Experience: 0–4 Years
Education: B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences
Application Mode: Email

Navitas Lifesciences invites talented individuals to explore exciting roles in Clinical Data Management, Pharmacovigilance (PV), Regulatory Affairs (RA), and Bioanalytical Sciences. Fresher Navitas Lifesciences Hiring for PV RA CDM

Open Positions

1. Clinical Data Analyst

Locations: Chennai & Bangalore
Responsibilities:

  • Create efficacy and safety tables, listings, and derived datasets.
  • Develop and validate SAS macros for project execution.
  • Manage multiple projects simultaneously, ensuring deadlines are met.
  • Lead teams with minimal supervision from biostatisticians.

Qualifications:

  • 2.5–3 years of experience in clinical data analytics.
  • Strong knowledge of clinical development and regulatory processes.
  • SAS certification is highly preferred.

2. Junior MICC Associate – Pharmacovigilance Support

Location: Bangalore
Responsibilities:

  • Handle inquiries via phone and email, performing case registrations.
  • Process individual case safety reports (ICSR) into safety databases.
  • Coordinate audits and ensure timely CAPA closures.
  • Comply with global and local data privacy regulations.

Qualifications:

  • 1–3 years of MICC experience.
  • Graduate or postgraduate degree in life sciences.
  • Familiarity with pharmacovigilance databases (e.g., MedDRA, WHO-DD).

3. Junior Regulatory Associate – Publishing and Submissions

Location: Chennai
Responsibilities:

  • Assist in regulatory submissions (IND, NDA, ANDA, DMF) in CTD/eCTD formats.
  • Support publishing and bookmarking of regulatory documents.
  • Ensure compliance with customer SOPs and company policies.

Qualifications:

  • 0–1 year of experience in regulatory affairs.
  • Familiarity with US-FDA, EMA, and other global regulatory bodies.

4. Bioanalytical Scientist

Location: Manipal
Responsibilities:

  • Develop and validate bioanalytical methods using LC-MS, HPLC, and GC-MS instruments.
  • Maintain calibration of sophisticated analytical instruments.
  • Ensure adherence to USFDA bioanalytical guidelines.

Qualifications:

  • 2–5 years of bioanalytical experience.
  • Bachelor’s degree in Pharma or a related field.
  • Strong expertise in LC-MS and HPLC operations.

How to Apply

Send your application via email to recruitment.chennai@navitaslifesciences.com. Ensure the subject line clearly states the position you are applying for.

Explore dynamic career opportunities with Navitas Lifesciences and contribute to innovative solutions in life sciences!

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Vgenomics Hiring for Bioinformatics Assistant

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Vgenomics Hiring for Bioinformatics Assistant

Location: Noida, India (In-office)
Experience: 1–3 Years
Education: Master’s degree in Bioinformatics, Computational Biology, Genomics, or related fields

Join Vgenomics, a biotech leader leveraging genomics and AI to revolutionize diagnostics for rare diseases. With 200+ research articles, 150+ US patents, and over 30 years of cumulative experience, Vgenomics is transforming the rare disease landscape. Vgenomics Hiring for Bioinformatics Assistant

Key Responsibilities

  • Analyze genomic and transcriptomic datasets for rare disease diagnostics.
  • Develop and optimize bioinformatics workflows and computational pipelines.
  • Collaborate with interdisciplinary teams to provide actionable insights.
  • Manage and curate large-scale genomic datasets.
  • Stay updated on the latest bioinformatics tools and methodologies.
  • Contribute to scientific publications, presentations, and grant proposals.

Mandatory Qualifications and Skills

Education:

  • Master’s degree in Bioinformatics, Computational Biology, Genomics, or related fields.

Experience:

  • 1–3 years in bioinformatics or genomics.
  • At least 1 research publication or equivalent project work.

Skills:

  • Expertise in NGS data analysis tools (e.g., GATK, HISAT2, STAR).
  • Proficiency in Python, R, or similar programming languages.
  • Familiarity with biological databases (e.g., Ensembl, UCSC, NCBI).
  • Strong computational and statistical skills for large-scale genomic data.
  • Knowledge of Linux/Unix systems and high-performance computing.
  • Hands-on experience in immuno-oncology.

Preferred Skills

  • Experience with cloud platforms (AWS, Google Cloud).
  • Familiarity with workflow managers like Nextflow or Snakemake.
  • Knowledge of machine learning applications in bioinformatics.
  • Expertise in structural bioinformatics or systems biology.

Why Work with Vgenomics?

  • Be part of cutting-edge innovations in genomics and diagnostics.
  • Collaborate with a world-class team of experts.
  • Contribute to impactful solutions for rare diseases.

Apply Online Now and take the next step in advancing your bioinformatics career!

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IKS Health Hiring for CDM

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IKS Health Hiring for CDM

IKS Health Hiring for CDM

Location: Airoli Mindspace, Thane-Belapur Road, Navi Mumbai
Experience: Freshers
Salary: ₹2.10 LPA (₹12,500 in-hand after deductions)
Qualifications: B.Pharm, B.Sc, M.Sc

Start your career in Clinical Data Management (CDM) with IKS Health, a leading healthcare solutions company. IKS Health Hiring for CDM

Walk-In Interview Details

  • Dates: Tuesday & Wednesday (26th & 27th November 2024)
  • Time: 10:00 AM sharp
  • Venue: Building 5, 2nd Floor, Airoli Mindspace, Thane-Belapur Road, Navi Mumbai

Position Highlights

Role: Clinical Data Management (CDM)

  • Shift: Day Rotational
  • Eligibility: Fresh graduates in B.Pharm, B.Sc, or M.Sc

Walk-In Process

  • Contact Person: HR Sophia John (📞 8291476149) (Note: Do not call for confirmations)
  • Gate Pass Instructions:
    • Send your name and phone number via SMS upon arrival at Mindspace Gate for gate pass issuance.

What to Bring

  • Updated CV
  • Relevant documents

Why Join IKS Health?

  • Excellent work-life balance
  • Opportunities for professional growth
  • Exposure to cutting-edge healthcare solutions

Don’t miss this opportunity to kick-start your career in Clinical Data Management!

Walk-In and Join Our Team!

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Zydus Lifesciences Hiring for QC / QA / Production / Engineering

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Zydus Lifesciences Hiring for QC / QA / Production / Engineering
Zydus Lifesciences Hiring for QC / QA / Production / Engineering

Location: Ahmedabad
Experience Required: 1–7 Years
Qualifications: B.Pharm, M.Pharm, B.Sc, M.Sc, ITI, Diploma

Zydus Lifesciences, a global leader in life sciences, is inviting talented professionals to join our team. With over 23,000 employees worldwide, we are committed to discovering, developing, and delivering healthcare solutions that improve lives. Zydus Lifesciences Hiring for QC / QA / Production / Engineering

Walk-In Interview Details

  • Date: 1st December 2024 (Sunday)
  • Time: 9:00 AM to 3:00 PM
  • Venue: Hotel Woodlands, N.H No. 8, Near Desai Automobiles, Balitha, Vapi

Open Positions

1. Quality Control – Analyst

  • Qualification: B.Sc. / M.Sc.
  • Experience: 3–7 years
  • Skills:
    • HPLC, GC
    • Dissolution apparatus
    • UV-visible spectrometer
    • Weight analysis
    • Stability studies
    • Good Laboratory Practices (GLP)

2. Engineering – Technical Assistant / Plant Operator

  • Qualification: ITI / Diploma
  • Experience: 2–7 years
  • Skills:
    • Process equipment maintenance
    • Utility operations
    • HVAC systems

3. Production – Plant Operator / Technical Assistant

  • Qualification: ITI / Diploma
  • Experience: 2–7 years
  • Skills:
    • Granulation
    • Compression
    • Coating
    • Wurster coating
    • Capsule filling

4. Production – FTE / FTA

  • Qualification: ITI / Diploma / B.Sc.
  • Experience: 1–3 years
  • Skills:
    • Granulation
    • Compression
    • Coating
    • Wurster coating
    • Capsule filling

5. Quality Assurance – IPQA

  • Qualification: B.Pharm / M.Pharm / M.Sc.
  • Experience: 2–8 years
  • Skills:
    • IPQA
    • Equipment qualification
    • Analytical QA
    • Validation activities

Why Join Zydus Lifesciences?

  • Work with an innovative global life sciences leader.
  • Contribute to impactful healthcare solutions.
  • Enjoy professional growth and development opportunities.

Don’t miss this opportunity to advance your career with Zydus Lifesciences!

Walk-In and Join Our Team!

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Biorasi Hiring for Clinical Project Associate

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Biorasi Hiring for Clinical Project Associate

Location: Mumbai
Experience Required: 1–2 Years
Salary: ₹4.5–6 Lacs per Year
Qualifications: B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Lifesciences

Biorasi, a full-service Clinical Research Organization (CRO), is renowned for its innovation, collaboration, and dedication to advancing life-changing therapies. We are growing and looking for passionate individuals to join our dynamic team and make a difference in clinical research. Biorasi Hiring for Clinical Project Associate

About the Role

The Clinical Project Associate will play a key role in supporting clinical trial operations, ensuring smooth execution of clinical studies. This position involves managing site operations, coordinating with vendors, and ensuring compliance with international GCP guidelines.

Key Responsibilities

Communication

  • Participate in meetings and teleconferences.
  • Develop and share agendas, minutes, and monthly status reports.
  • Track and document project updates and action items for stakeholders.

Site Management

  • Assist with site budget development, contract preparation, and payment administration.
  • Support Clinical Trial Managers (CTMs) in subject recruitment tracking and monitoring visit schedules.
Biorasi Hiring for Clinical Project Associate
Biorasi Hiring for Clinical Project Associate

Study Start-Up and Activation

  • Assist in developing project plans for site feasibility, selection, and activation.
  • Coordinate and review regulatory documentation for site initiation.

Document and Supplies Management

  • Collect, file, and archive essential documents in the Trial Master File.
  • Oversee the distribution and tracking of study supplies.

Study and Vendor Management

  • Maintain project trackers and systems like CTMS and study portals.
  • Support vendor identification, selection, management, and payment processing.

Compliance and Support

  • Ensure adherence to ICH GCP guidelines and local regulations.
  • Assist in resolving audit findings and preparing for audit readiness.

Your Profile

Qualifications

  • Associate’s or Bachelor’s degree in biomedical sciences or a related field.
  • Prior clinical research experience, preferably as a study coordinator or regulatory coordinator.

Skills and Knowledge

  • Basic understanding of ICH GCP and global/local regulatory requirements.
  • Proficiency in MS Office tools like Word, PowerPoint, and Excel.
  • Strong written and oral communication skills in English.

Desired Attributes

  • Detail-oriented with excellent organizational skills.
  • Ability to manage multiple tasks while meeting deadlines.

Benefits

  • Work/Life Balance: Half-day Fridays, paid time off, and holidays.
  • Professional Growth: Employee bonus programs and career development opportunities.
  • Training: Ongoing training and development sessions.
  • Perks: Extensive country-specific benefits.

Why Join Biorasi?

At Biorasi, we offer a collaborative environment where you can grow professionally while contributing to groundbreaking clinical research projects.

Apply Now to join a team committed to innovation and making a difference in patient lives.

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Biorasi Hiring for Clinical Project Associate
Biorasi Hiring for Clinical Project Associate

Sri Krishna Pharmaceutical Hiring for Quality Control API

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Sri Krishna Pharmaceutical Hiring for Quality Control API

Sri Krishna Pharmaceuticals Ltd (SKPL), established in 1974, is a pioneer in the bulk manufacture of Acetaminophen (Paracetamol) in India. Today, SKPL is a vertically integrated manufacturer of essential APIs, PFIs, and finished dosage drugs, driving growth through innovative projects and expanded capacities. Sri Krishna Pharmaceutical Hiring for Quality Control API

Job Details

  • Department: Quality Control (API)
  • Role: HPLC, GC, GLP Testing
  • Experience: 2-5 Years
  • Eligibility: Male Candidates Only
  • Qualification: B.Sc, M.Sc, B.Pharm, M.Pharm
  • Location: IDA Uppal, Hyderabad

Interview Details

  • Dates: 26th & 27th November 2024
  • Timing: 10:00 AM to 1:00 PM
  • Venue:
    Sri Krishna Pharmaceuticals Ltd,
    IDA Uppal, Hyderabad, Telangana

How to Apply

Documents to Bring

  • Updated CV
  • Passport-size photo
  • Copies of educational certificates
  • Aadhar and PAN card
  • Latest CTC details
  • Last 3 months’ payslips
  • Last 3 months’ bank statements

Why Join Us?

  • Be part of a growing and innovative pharmaceutical team.
  • Work on exciting projects in a leading API manufacturing company.
  • Unlock opportunities to grow your career with industry leaders.

Elevate your career with Sri Krishna Pharmaceuticals – Apply now and be a part of our success story!
Sri Krishna Pharmaceutical Hiring for Quality Control API

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Fresher Officer/Executive Positions at Endoc Biotech

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Fresher Officer/Executive Positions at Endoc Biotech
Fresher Officer/Executive Positions at Endoc Biotech

Location: Rajkot, Gujarat
Company: Endoc Biotech Pvt Ltd
Experience: 0–5 years
Qualification: B.Sc. / M.Sc. / Diploma / B.E.
Job Type: Full-time

Endoc Biotech Pvt Ltd is hiring Officers/Executives for multiple positions in their production and ETP departments. If you’re looking to grow your career in the pharmaceutical industry, this is your chance to join a dynamic team. Fresher Officer/Executive Positions at Endoc Biotech

Available Positions

1. Production Officer/Executive

  • Qualification: B.Sc. / M.Sc. in Organic/Industrial Chemistry
  • Experience: 0–5 years in the pharma industry

2. Production Officer/Executive

  • Qualification: Diploma in Chemical / B.E. (Chemical)
  • Experience: 1–5 years in the pharma industry

3. ETP Officer/Executive

  • Qualification: Diploma / B.E. (Chemical / Environment), B.Sc. / M.Sc.
  • Experience: 0–5 years

Why Join Endoc Biotech Pvt Ltd?

  • Work/Life Balance
  • Time Management
  • Flexibility
  • Problem Solving Skills

How to Apply

Interested candidates can send their updated CVs to:
Email: Project@endocbiotech.com

Join Endoc Biotech Pvt Ltd and advance your career in a growing and innovative company!

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Aurobindo Pharma Hiring for Production

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Aurobindo Pharma Hiring for Production
Aurobindo Pharma Hiring for Production

Location: Jadcherla Unit-VII
Department: Production – Oral Contraceptive Block
Company: Aurobindo Pharma
Experience: 2–10 years
Qualification: Diploma, ITI, B.Pharm, M.Pharm
Job Type: Full-time

Aurobindo Pharma, a global leader in the pharmaceutical industry, is looking for skilled professionals to join their Production – Oral Contraceptive Block team at the Jadcherla Unit-VII. We are committed to delivering high-quality, affordable generic medicines across more than 150 countries.
Aurobindo Pharma Hiring for Production

Key Responsibilities

As a Production – Oral Contraceptive Block professional, your responsibilities will include:

  • Handling Production Operations: Granulation, compression, and coating processes.
  • Compliance Management: Ensure adherence to SOPs and regulatory guidelines.
  • Maintaining Quality & Safety: Uphold high-quality and safety standards during production.

Requirements

  • Experience: Proven experience in pharmaceutical production (mandatory).
  • Skills: Strong attention to detail, ability to follow instructions, good teamwork, and communication skills.
  • Work Environment: Ability to perform in a fast-paced, dynamic work environment.

Why Join Aurobindo Pharma?

  • Work for a globally reputed pharmaceutical company.
  • Competitive compensation with comprehensive benefits.
  • Career growth opportunities and skill enhancement.
  • Work alongside a talented and diverse team of professionals.

How to Apply

Interested candidates can send their updated resumes to:
Email: shivashanker.ravula@aurobindo.com
Subject Line: “Production Department”

Join Aurobindo Pharma and be part of a team that is dedicated to improving health and accessibility globally!

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Aurobindo Pharma Hiring for Production
Aurobindo Pharma Hiring for Production

Regulatory and Start-Up Specialist 1 at IQVIA

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Regulatory and Start-Up Specialist 1 at IQVIA
Regulatory and Start-Up Specialist 1 at IQVIA

Location: Bengaluru, Karnataka
Company: IQVIA
Job Type: Full-Time
Experience: 1-2 years
Qualification: B.Pharm / M.Pharm / MSc / BSc

IQVIA is hiring a Regulatory and Start-Up Specialist 1 to join their team in Bengaluru, Karnataka. This role involves managing clinical operations and study start-up activities. Below are the details of the position: Regulatory and Start-Up Specialist 1 at IQVIA

Job Responsibilities

As a Regulatory and Start-Up Specialist 1, your key responsibilities will include:

  • Survey Build: Create electronic surveys listing required study documents.
  • Package Build: Develop and manage electronic packages for essential and regulatory documents.
  • Query Tracking: Monitor and track regulatory queries using electronic systems.
  • Informed Consent Form (ICF) Development: Design ICF templates in compliance with country-specific requirements.
  • Essential Document Review: Verify essential documents according to country regulations.
  • Transactional Activities: Support activities like Clinical Study Report (CSR) preparation and Trial Master File (TMF) oversight.
    Regulatory and Start-Up Specialist 1 at IQVIA

Qualifications

Educational Background

  • Bachelor’s degree in healthcare or a scientific field (preferred) or equivalent experience.

Experience

  • 1-2 years in clinical research with at least 1 year in study start-up activities.
  • Familiarity with ICF review, essential document verification, and regulatory submissions (IRB/IEC).

Skills

  • Proficiency in Excel.
  • Experience with systems like Vault Clinical or similar tracking tools.
Regulatory and Start-Up Specialist 1 at IQVIA
Regulatory and Start-Up Specialist 1 at IQVIA

Why Join IQVIA?

  • Work/Life Balance
  • Time Management
  • Flexibility
  • Problem-Solving

IQVIA is a global leader in clinical research and healthcare intelligence, providing innovative solutions that improve patient outcomes across the life sciences industry. Regulatory and Start-Up Specialist 1 at IQVIA

How to Apply

For more details and to apply, visit the IQVIA Careers website.

Don’t miss out on the chance to be part of a global leader in clinical research!

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Regulatory and Start-Up Specialist 1 at IQVIA
Regulatory and Start-Up Specialist 1 at IQVIA