Regulatory Jobs in Nalagarh

Acme Formulation - Nalagarh

Audit,Approval and monitoring of contract manufacturers,Supplier and outside Laboratories as per GMP. requirement. Exposure to Regulatory Audits will be preferred . . 15-16 Lacs PA INR

from: naukri.com - 14 days ago

Centrient Pharmaceuticals - Rupnagar, Punjab, India

Responsibilities: To participate in vendor qualification activities To participate in Internal/External audit activities To ensure compliance as per applicable regulatory requirement Release/rejection of finished

from: linkedin.com - More than 30 days ago

Venus Remedies (VRL) - Baddi

1) Exposure to work in Injectable pharma regulatory plant. 2) Review of all documents relating to the manufacturing, Packaging & analysis report prior to batch release. 3) Exposure of Serialization Not disclosed INR

from: naukri.com - 8 days ago

Glenmark Pharmaceuticals - Baddi

Prepare validation Protocol and Report as per guideline and regulatory requirement Preferred candidate profile . . Not disclosed INR

from: naukri.com - 22 days ago

Nalagarh, India

, and nasal formulations. This group of formulations requires meticulous attention to detail, stringent regulatory compliance, and a deep understanding of both the scientific and market landscape. Hence Not Mentioned

from: Monsterindia.com - More than 30 days ago

Acme Formulation - Baddi

for grant/renewal/ retention of Drugs Retail licenses. Provide necessary feed back to the central team based on day to day interaction with Regulatory Authorities. Follow up with CRI Kasauli regarding Drugs 8-10 Lacs PA INR

from: naukri.com - 15 days ago

C & E Limited - Baddi, Solan

processes specifically tailored to the leather chemicals industry. - Ensure adherence to quality standards and regulatory requirements in these processes. - Continuously optimize these processes to enhance 13-15 Lacs PA INR

from: naukri.com - 15 days ago

Nalagarh, India

, market potential, and strategic fit. Regulatory Compliance: Ensure that all R&D activities comply with relevant regulatory requirements and industry standards. Collaborate with regulatory affairs teams Not Mentioned

from: Monsterindia.com - More than 30 days ago

Syschem India - Kalka

as per SOPCandidate must be from API / Bulk Drug manufacturing/regulatory plant experience 1.5-4.25 Lacs PA INR

from: naukri.com - 27 days ago

Baddi, India

for Vendor Qualification/disqualification for Pharma division and other activities including GMP assessment and compliance as per regulatory requirements. Reporting to Head – QA Job Responsibilities To vendor Not Mentioned

from: Monsterindia.com - 8 days ago