Join Nectar Lifesciences Ltd as a Global Regulatory Affairs Manager (APIs) | Regulatory Affairs jobs | Apply Now
Explore top opportunities in the regulatory affairs sector, including prominent Regulatory Affairs jobs and Pharmaceutical jobs with Nectar Lifesciences Ltd (NLL), a leader in India’s pharma sector. This Regulatory Affairs Manager (APIs): Global role in Dera Bassi is an exciting opportunity for talented professionals, looking for B Pharm Jobs, to contribute to one of the top API manufacturers driving innovation in global regulatory compliance. Such regulatory affairs jobs are ideal if you’re aiming for a career in regulatory affairs. You can join NLL and take your B Pharm career to the next level in a world-class pharmaceutical environment.
- Job Position: Regulatory Affairs Manager (APIs): Global
- Location: Dera Bassi, Punjab, India
About the Company
Nectar Lifesciences Ltd (NLL) is a knowledge-driven organization leading India’s pharmaceutical industry. Ranked among the top midsized pharma companies, NLL is a trusted name in API manufacturing and has established a strong global position in the Cephalosporins segment within the Anti-Infective Therapeutic category. Operating across 45 countries, NLL runs 11 state-of-the-art manufacturing facilities in Punjab and Himachal Pradesh, complying with cGMP and EHS standards. For those seeking positions, regulatory affairs jobs at NLL as a publicly traded company with a subsidiary in Portugal, continue to redefine innovation and quality in pharmaceutical jobs and manufacturing excellence. Opportunities in regulatory affairs jobs are abundant and often require a commitment to precision and detail.
Job Description: Regulatory Affair Jobs
The Regulatory Affairs Manager (APIs): Global is a full-time, on-site position based in Dera Bassi. This role is ideal for professionals passionate to excel in global regulatory management. In the realm of regulatory careers, the manager will ensure compliance with international standards, oversee regulatory submissions, and work closely with internal teams to uphold NLL’s reputation for regulatory excellence and product quality.
Key Responsibilities for B Pharm Jobs
- Ensure full compliance with global regulatory requirements.
- Prepare and manage regulatory submissions for international markets.
- Oversee Quality System Management in line with cGMP and EHS guidelines.
- Stay updated with evolving global regulatory standards
- Collaborate across departments to maintain product and process compliance
- Manage communication and documentation with global regulatory authorities.
Qualifications
- Expertise in Regulatory Compliance, Regulatory Affairs, and Regulatory Requirements
- Proven experience in Regulatory Submissions and Quality Systems.
- Excellent written and verbal communication skills.
- Attention to detail and ability to work independently or in teams.
- Bachelor’s degree in Pharmacy, Chemistry, or related field (B Pharm preferred).
- Industry experience in pharmaceutical jobs is advantageous.
- Familiarity with global regulatory guidelines and international compliance standards
