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QA Compliance Expert - Reg CMC Facilitator

3-7 years

Hyderabad / Secunderabad

1 vacancy

QA Compliance Expert - Reg CMC Facilitator

Sandoz

posted 5mon ago

Job Role Insights

Flexible timing

Job Description

Summary
Supporting product maintenance, and activities throughout the product life-cycle using regulatory strategies and documents related to CMC (Chemistry, Manufacturing & Control). This applies to sector-specific (global and local) products and is intended to ensure timely market supply in compliance with regulatory requirements. Supporting change - and inspection management within the QA Compliance Team.

About the Role:
Supporting product maintenance, and activities throughout the product life-cycle using regulatory strategies and documents related to CMC (Chemistry, Manufacturing & Control). This applies to sector-specific (global and local) products and is intended to ensure timely market supply in compliance with regulatory requirements. Supporting change - and inspection management within the QA Compliance Team.
Key Responsibilities:
  • Maintaining close cooperation with RA CMC to discuss regulatory requirements, strategies and knowledge of global product dossiers to stay up-to-date.
  • Conducting training to ensure appropriate knowledge and regulatory compliance.
  • Supporting the area in effective change control. Examination of reg. relevance and pre-evaluation amendments to Novartis products and customer products.
  • Contact person for regulatory matters and intermediary between RA CMC and production unit at strategy decisions and in the product life cycle.
  • Support of timely reviews of CMC documents for defined products; Support with and Identification of challenges in the course of regulatory compliance audits.
  • Implementation and overview of initiatives to improve (regulatory) compliance.
  • Coordination, guidance, and support in the preparation of CMC responses to health authorities for specific products.
Essential Requirements:
  • Advanced University or academic degree in chemistry, biology, pharmacy, engineering or equivalent.
  • Fluent English (German desired).
  • More than 3 years of experience in an operational GxP area, in Manufacturing, Development or QA or Regulatory Affairs; with a thorough knowledge of biologic drug substance manufacturing processes for recombinant proteins and/or nucleic acids.
  • Ability to speak up and to take Quality decisions during challenging situations.
Desirable Requirements:
  • Expertise in organization dynamics and culture, ability to gain trust and confidence at all levels in the organization, leadership, and project management experience.
  • Ability to work independently and effectively in international, complex, and multifaceted environments.
Skills Desired
Continuous Learning, Dealing With Ambiguity, Employee Performance Evaluations, Gmp Procedures, People Management, Qa (Quality Assurance), Quality Control (Qc) Testing, Quality Standards, Self-Awareness, Technological Expertise, Technological Intelligence

Employment Type: Full Time, Permanent

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What people at Sandoz are saying

3.0
 Rating based on 1 Facilitator review

Likes

Top Management is very supportive

  • Salary - Good
  • +2 more
Dislikes

Manager's are not so supportive and very poor in decision making

  • Job security - Poor
  • +1 more
Read 1 Facilitator review

What Sandoz employees are saying about work life

based on 425 employees
68%
52%
55%
93%
Flexible timing
Monday to Friday
No travel
Day Shift
View more insights

Sandoz Benefits

Submitted by Company
Competitive compensation
Pay equity
Pay for sustainable performance
Differentiated benefits and wellbeing programs
Values & integrity
Balanced rewards
Submitted by Employees
Free Transport
Health Insurance
Cafeteria
Job Training
Free Food
Soft Skill Training +6 more
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