Regulatory Affairs Officer in PAR Laboratories for B. Pharm, M.Pharm 2 posts
As a dedicated manufacturer and marketer of Hormone products, the Company concentrated on the niche areas of operations. With its beginnings in Mumbai, PAR Laboratories has been providing quality hormones and contraceptive products to various markets around the world.
Post
Regulatory Affairs Oficer - 2
• studying scientific and legal documents
• gathering, evaluating, organising, managing and collating information in a variety of formats
• ensuring compliance with Government regulations
• maintaining familiarity with company product ranges
• planning, undertaking and overseeing product trials and regulatory inspections
• keeping up-to-date with changes in regulatory legislation and guidelines
• analyzing complicated information, including trial data
• offering advice about company policies, practices and systems
• obtaining marketing permission
• outlining requirements for labeling, storage and packaging
• using a variety of specialist computer applications
• liaising and negotiating with regulatory authorities
• providing advice about regulations to manufacturers/scientists
• writing comprehensible, user-friendly, clear product information leaflets and labels
• ensuring that quality standards are met and submissions meet strict deadlines
• Preparing documentation
Experience: 1-3 year
Qualification: B. Pharm, M.Pharm
Location: Gozaria, Gujarat
Industry Type: Pharma/Biotech/Clinical Research
Functional Area: DRA
End Date: 17th Oct, 2013
As a dedicated manufacturer and marketer of Hormone products, the Company concentrated on the niche areas of operations. With its beginnings in Mumbai, PAR Laboratories has been providing quality hormones and contraceptive products to various markets around the world.
Post
Regulatory Affairs Oficer - 2
Job Description
• studying scientific and legal documents
• gathering, evaluating, organising, managing and collating information in a variety of formats
• ensuring compliance with Government regulations
• maintaining familiarity with company product ranges
• planning, undertaking and overseeing product trials and regulatory inspections
• keeping up-to-date with changes in regulatory legislation and guidelines
• analyzing complicated information, including trial data
• offering advice about company policies, practices and systems
• obtaining marketing permission
• outlining requirements for labeling, storage and packaging
• using a variety of specialist computer applications
• liaising and negotiating with regulatory authorities
• providing advice about regulations to manufacturers/scientists
• writing comprehensible, user-friendly, clear product information leaflets and labels
• ensuring that quality standards are met and submissions meet strict deadlines
• Preparing documentation
Additional Information
Experience: 1-3 year
Qualification: B. Pharm, M.Pharm
Location: Gozaria, Gujarat
Industry Type: Pharma/Biotech/Clinical Research
Functional Area: DRA
End Date: 17th Oct, 2013
where to forward CV - hr.parlabs@gmail.com
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