Manager- EU Compliance

Job Title:

EU Compliance Specialist

Business Unit:

Global Quality and Compliance

Job Grade

Manager-1

Location :

Paonta Sahib/

At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.

Are You Ready to Create Your Own Sunshine?

As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”

Key responsibilities:

The EU Compliance Specialist will be responsible for supporting EU-related activities in the Sun India DF site which manufacture products for the EU and UK markets.  Documents related to EU-products such as (but not limited to) Change Controls (including Temporary CC’s), Market Complaints, Investigations associated with Deviations, OOS/OOT shall be screened for robustness prior to sharing with the EU QP teams.   Supporting site compliance to EU-GMP Guidelines and their implementation, in addition to supporting ad-hoc requests from the EU Compliance Lead and/or EU QP and Compliance teams will be required.

Major Tasks & Responsibilities:

Travel Estimate

Job Requirements

Educational Qualification

Bachelor Degree in (Bio-) Chemistry, Pharmacy, Biotechnology or similar education

Experience

Tenure:  

• Tenure: Minimum 10 years
• Industry: (Bio) pharmaceutical, sterile manufacturing (as required per site)
• Content areas: Manufacturing, QA /QC. QA manufacturing operation

Technical skills/job specific competencies

• Experience on review of batch documentation and preparation for batch certification.

• Good experience and knowledge of QA/QC and EU regulatory compliance
• Good knowledge and experience in DF pharmaceutical processes and QA/QC operations.
• Good understanding of change control processes and interaction with regulatory affair processes.
• Capable of reviewing and assessing manufacturing and analytical technical documents and provide sound quality assessments on change controls, deviations and complaints.
• Experience working with electronic Document Management, electronic Training systems and e.g. Trackwise
• Understanding of risk assessment and risk management fundamentals/tools
• Experience interacting with external parties.

• Good knowledge of MS office and Windows based computer applications.

Behavioural Skills/Competencies (e.g. excellent communication skills, strong collaborator, Problem solving etc.)

• Strong interpersonal skills, excellent communication skills, good presentation, negotiations and influencing skills
• Ability to effectively manage multiple, complex priorities and quick shifting of those.
• Team player, task oriented and keen on working in a cross-cultural working environment.

Your Success Matters to Us

At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!

Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification.  It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job.  Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).