Ultratech India Limited is an integrated pharmaceutical and life sciences company engaged in manufacturing pharmaceutical finished dosage forms, Active Pharmaceutical Ingredients and providing drug discovery solutions. Ultratech specializes in development and manufacturing of pulmonary drug delivery systems and offers a complete range of anti-asthmatic inhalation drugs in Dry Powder Inhalation and Pressurized Metered Dose Inhalation dosage forms.
Post : Quality Assurance Executive - 03
Job Description
• Phase-1 for 1 year : Preparation of new computerized QA documentation systems for the whole facility / SOPs / BMRs etc
• Phase-2: After 1 year to be part of QA team handling all routine QA compliances of API and Formulations plant and report directly to management
• Readiness to work in shifts from phase-2 onwards
• To ensure QA compliance of LL / third party manufacturing sites. Maintain and keep check on timely documentation of such sites. Remain responsible for audit of such sites. This could involve 2-3 day travelling to such units 5-6 times a year
Candidate Profile
• Should have worked in some unit as an active team member to prepare new documentation systems for facing WHO-GMP / US FDA audits
• Should have faced successful audits from US FDA or MHRA as an active team member
• Capability to create new cGMP documentation systems / SOPS / on their own
• Preferable if the person has worked in QC for some time
• Should have Worked in QA department of Formulations unit
Additional Information
Experience : Min 3 - 5 years in QA Documentation and faced USFDA Audit
Qualification : BSc Or B.Pharm / M.Pharm /
Location : Taloja, Navi Mumbai
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Quality Assurance
Salary : 3.60lacs p.a. - 4.7lacs p.a.
End Date : 25th June, 2021
E-Mail resume on hrd@ultratechindia.com
or
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