Abryl Inc-opening Quality Management Positions

Abryl Inc-opening Quality Management Positions

Abryl Inc-opening

Abryl Inc. is currently seeking qualified candidates to fill multiple positions in our Quality Management team. If you have the required experience and are passionate about ensuring top-notch quality in production, engineering, microbiology, or IT QA, we want to hear from you!

Positions Available:

  1. Production Quality Management Specialist
    • Experience: 4-7 years in QMS
    • Preferred Experience: Injectable experience
  2. Engineering Quality Management Specialist
    • Experience: 7-10 years in QMS
    • Preferred Experience: Injectable experience
  3. Microbiology Quality Management Specialist
    • Experience: 7-10 years in QMS
    • Preferred Experience: Injectable experience
  4. IT Quality Assurance Executive
    • Experience: 3-7 years in QA

Requirements:

  • Relevant experience as per the position applied for
  • Strong understanding of quality management systems
  • Proven track record of ensuring compliance with industry standards and regulations
  • Excellent communication and interpersonal skills
  • Ability to work collaboratively in a team environment

If you meet the qualifications and are interested in joining our dynamic team, please share your updated resume and any additional relevant documents to hr.2@abryl.in.

Abryl Inc. is committed to fostering an inclusive and diverse workplace. We encourage applicants from all backgrounds to apply.

Job Category: pharma
Job Type: Full Time
Job Location: Panchkula Haryana

Apply for this position

Allowed Type(s): .rtf

About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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