Sponsor Ad Sponsor Ad

Aykon Biosciences – Job Openings for Production, QA, QC and Regulatory Affairs Specialist [B.Pharm or M.Pharm]

Share With Your Friends

Aykon Biosciences Pvt. Ltd. invites dedicated professionals to join our team in Kheda, Gujarat. We are hiring for Quality Control, Quality Assurance, Production, and Regulatory Affairs roles to drive excellence in pharmaceutical manufacturing.

About Aykon Biosciences

Founded in 2021, Aykon Biosciences specializes in general liquid injectables (SVP) in ampoules and pre-filled syringes (PFS). Our Kheda facility adheres to cGMP standards, ensuring top-quality production for global markets.

Why Join Us?

Join a dynamic team committed to innovation and quality. Our collaborative environment offers career growth, exposure to advanced technologies, and the chance to impact healthcare worldwide.

Job Opportunities

We have eight openings across four critical roles: Quality Control, Quality Assurance, Production, and Regulatory Affairs. Each role is vital to our mission of delivering safe, effective pharmaceuticals.

Job Location

📍 Kheda, Gujarat
Address: Survey No. 86/1-2-3, Village Sarali, Ahmedabad–Indore Highway, Tal: Kathlal, Dist: Kheda, Gujarat-387630, India. A modern workplace awaits you.

Available Positions

Quality Control Specialist (2 Vacancies)

Qualifications

  • B.Pharm or M.Pharm from a recognized institution.
See also  AstraZeneca Hiring Regional Medical Advisors (R&I and CVRM) in Delhi | Pharmaceutical Careers in India

Experience

  • 1–2 years in quality control or related pharmaceutical fields.

Responsibilities

  • Conduct rigorous testing and inspection of products.
  • Ensure compliance with pharmaceutical standards and cGMP.
  • Maintain accurate quality documentation.
  • Support regulatory audits (e.g., USFDA, MHRA).

Skills

  • Expertise in quality testing and inspection techniques.
  • Strong analytical and documentation skills.
  • Familiarity with regulatory compliance.

Quality Assurance Specialist (2 Vacancies)

Qualifications

  • B.Pharm or M.Pharm from a recognized institution.

Experience

  • 2 years in quality assurance or related fields.

Responsibilities

  • Oversee quality protocols and regulatory compliance.
  • Ensure consistent manufacturing excellence.
  • Conduct internal audits and manage deviation reports.
  • Collaborate with teams to maintain cGMP standards.

Skills

  • Knowledge of quality management systems.
  • Strong problem-solving and communication skills.
  • Experience with regulatory audits.

Production Specialist (2 Vacancies)

Qualifications

  • B.Pharm or M.Pharm from a recognized institution.

Experience

  • 2 years in pharmaceutical production or related fields.

Responsibilities

  • Manage production processes for timely manufacturing.
  • Ensure adherence to quality standards and cGMP.
  • Optimize production efficiency and line operations.
  • Maintain safety and compliance during production.

Skills

  • Expertise in production management and process optimization.
  • Strong team coordination and technical skills.
  • Familiarity with pharmaceutical manufacturing regulations.

Regulatory Affairs Specialist (2 Vacancies)

Qualifications

  • B.Pharm or M.Pharm from a recognized institution.

Experience

  • 1–2 years in regulatory affairs or related fields.

Responsibilities

  • Coordinate with regulatory bodies for compliance.
  • Prepare regulatory documentation for market approvals.
  • Manage dossiers and handle regulatory queries.
  • Ensure adherence to USFDA, MHRA, and cGMP standards.

Skills

  • Knowledge of regulatory guidelines and submission processes.
  • Strong documentation and communication skills.
  • Ability to manage regulatory audits.

Why These Roles Matter

Each role ensures our products meet global standards, directly impacting patient safety and Aykon’s reputation for excellence in pharmaceutical manufacturing.

See also  Zasya Life Sciences Is Hiring Freshers for Research Associate – Synthetic Medicinal Chemistry

Benefits of Joining Aykon Biosciences

  • Competitive salary and benefits.
  • Exposure to advanced pharmaceutical technologies.
  • Collaboration with global regulatory bodies.
  • Supportive, innovative work culture.
  • Career growth opportunities.

Application Process

StepDetails
Step 1Submit your resume to careers@aykon.in.
Step 2HR reviews applications for eligibility.
Step 3Shortlisted candidates are contacted for interviews.
Step 4Final selection and offer process.

How to Apply

Send your resume to careers@aykon.in, specifying the role you’re applying for. Highlight relevant experience and qualifications. Applications are reviewed on a rolling basis—apply now!

Verified by Trusted HRs

The post is released by the Aykon Biosciences Official Webpage. Click here to visit the post

Aykon Biosciences - Job Openings for QA, QC  [B.Pharm or M.Pharm]

🔗Apply Now

Aykon Biosciences - Job Openings for Production and Regulatory Affairs Specialist [B.Pharm or M.Pharm]

About Our Facility

Our Kheda facility meets international regulatory standards, ensuring quality and reliability. Learn more at Aykon Biosciences.

Start Your Career with Us

Join Aykon Biosciences to make a global impact in pharmaceuticals. Apply today for a role in Quality Control, Quality Assurance, Production, or Regulatory Affairs and contribute to our mission.

Share With Your Friends

Connect with Us for Latest Job Alerts!

Join Now