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Vacancies for Scientist, Research Associate, Research Scientists, Analytical Scientists, Manager – Regulatory Affairs, Manager – Quality Assurance, QA Inspectors @ Parabolic Drugs

 

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Parabolic Drugs Limited is one of the fast growing API (Active Pharmaceutical Ingredients) and API intermediate manufacturing and marketing company in the SME segment, with increasing international presence and a strong R&D foundation, based at Chandigarh, India. Commissioned in 1998, PDL has two fully functional, state of the art manufacturing units, a WHO-GMP certified Unit based in Derabassi (Punjab) and a world class Semi Synthetic Penicillin manufacturing plant at Panchkula, (Haryana) with one of its products been approved for sales to USA, respectively.

Post: Scientist, Research Associate, Research Scientists, Analytical Scientists, Manager – Regulatory Affairs, Manager – Quality Assurance, QA Inspectors

Description:
Manager/Sr. Scientist/Scientists – (CRAMS & API): Ph. D./M.Sc. Organic Chemistry with 4 to 12 years of experience. Should have good communication & leadership skills and well versed with the latest development in area of synthetic chemistry and analytical instrumentation. Should have experience of developing small projects in lab and their scale up to pilot plant scale. Should be able to coordinate with peers in analytical, IPR, regulatory and production departments. Knowledge on IPR issues is also desired.

Research Associates/Chemists- (CRAMS &API): M.Sc. Organic Chemistry with 2 to 6 years of experience. The role demands an exposure to literature search, independently conducting the multi-step synthesis of small molecules and their characterization through the latest analytical techniques (UV, NMR, Mass Spectrometry, LC/MS).


Manager/Sr. Scientist/Scientists: Profile: PhD/M.Sc with 4-12 years experience in the area of organic synthetic chemistry having hands on experience on process development, scale up and commercialization of technologies

Research Associates/Chemists: Profile: M.Sc with 2-6 years experience in the area of cephalosporin chemistry. Having hands on experience on process development, scale up and commercialization of technologies.


Research Scientists: M.Sc with 4-8 years experience in the area of analytical method development. Should have good knowledge of chromatographic/spectroscopic techniques, GLPs, Regulatory.

Analytical Scientists: Profile: M.Sc with 4-6 years experience in the area of HPLC/GC method development and routine analysis. Should be aware of GLP and regulatory requirements.

Dy. Manager/Manager – Quality Control: B.Sc/ M.Sc with 10 to 12 years relevant experience. Shall be responsible for all QC operations, including raw material testing, stability study, documentation, validation & handling instrumentation related activities. To represent company for major regulatory audits. The person must have thorough knowledge of documentation as per GMP requirement. Good Communication, leadership and Computer Skills are desirable.

Manager – Regulatory Affairs: B.Sc./M.Sc. Chemistry 12-15 years relevant experience in looking after Regulatory Department of a reputed API manufacturing company. Shall be responsible for Regulatory Affairs function for regulated & Semi regulated markets. Prepare Dossier for various countries as per the guidelines of each country including CTD format. Organizing the required documents for US FDA submission. Respond to queries raised by regulatory authorities. Preparation of drug master files, site master files and dossiers. Review of specifications like RM, FP and Stability for regulatory compliance. Coordination with various departments like R&D, QC, QA & Production etc.

Manager – Quality Assurance: B.Sc./M.Sc Chemistry 12-15 years relevant experience with hands on  experience in complying with documentation and regulatory international agencies and others, training and development of quality assurance practices are essential attributes for success in this position. The incumbent should be a professionally qualified person having managed quality assurance function in a reputed Pharmaceutical Bulk Drug Company.

QA Inspectors: B.Sc./M.Sc Chemistry 2-3 years relevant experience in Quality Assurance and Regulatory Department of a reputed API manufacturing company. Should be well versed with Microsoft Office. Knowledge of LIMS/SAP is desirable.

Apply/Forward Your Resume At, hrd@parabolicdrugs.com

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