Jubilant Generics Hiring QC Executive - Chemistry & Pharma Apply

Jubilant Generics Hiring QC Executive – Chemistry & Pharma Apply

Jubilant Generics (JGL) is a wholly-owned subsidiary of Jubilant Pharma. JGL in India has Research & Development units at Noida and Mysore. It has two manufacturing facilities one at Mysore, Karnataka and another at Roorkee, Uttarakhand, engaged in APIs and Dosage manufacturing, respectively.

Job Title: Executive-Quality Control

Eligibility Criteria: M.Sc. (Chemistry) / B.Pharm

Experience Range: 3-6 years

Desirable Experience :

3-6 Years of experience in the Quality Control department and handling of all Instruments like HPLC, GC, UV, etc., from a regulatory reputed Pharmaceutical unit

Functional Skills :

  • Operating and troubleshooting skills on all major analytical equipment like HPLC, GC, UV, etc.
  • Good Knowledge of Regulatory guidelines like MHRA, MCC, ANVISA, USFDA, TGA, etc.
  • Good knowledge of Quality Systems (eg. Market complaint handling, handling of recalled or returned goods, OOS Investigations, Deviations, Change Controls, Quality Management review, etc.

Behavioral Skills :

  • Attention to detail
  • Data collection, management, and analysis
  • Problem analysis and problem solving
  • Customer service orientation
  • Willingness to learn and adapt to changes

General Awareness: Knows the fundamental or general understanding of concepts.

Working Knowledge: Has broad job knowledge; knows and applies the full range of concepts and practices

. Has broad/working knowledge of the subject. The candidate should use these concepts in day-to-day practices.

Functional Expert: The candidate is a certified functional expert with strong knowledge on concepts.

Mastery: The candidate is a subject matter expert and has command over the subject/ concepts.

Job Context:

To analyze the In-Process samples & finished product samples by ensuring compliance & also a recording of Analytical data & online documentation.

Challenges:

Calibration and Preventive Maintenance of instruments, Preparation of reference/working standards, method development/validation, maintaining cGMP and other compliances in area, correct recording, and measuring of results.

Area of Impact : (Dept. Location / Function or Business / Organisation)

Production, Warehouse, Quality Assurance, Technical Services

Apply Online

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