Excellent Opportunity For B. Pharma,M. Pharma Graduates At Unichem Laboratories

Unichem Laboratories Released Job Openings On 26/03/2022.Promoted by the late Mr. Amrut Mody, a pioneer of the Indian pharmaceuticals business, Unichem Laboratories has grown to become one of India’s most respected pharmaceutical companies. It is committed to deliver better health through superior products.Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for Unichem Laboratories Recruitment 2022 are provided below. Interested and eligible candidates can  submit application along with resume. 

Vacancy Details:

Unichem Laboratories Recruiting B.Pharma,M.Pharma Candidates with 5 – 8 years of Experience for Senior Officer / Executive QMS Position.Complete Details for the Senior Officer / Executive QMS as follows.

Important Details :

• Location : Ghaziabad
• No of Vacancies:NA
• Details of Salary: NA
• Opening date for online Application: 26/03/2022
• Mode of application :Online
• How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps

Related Job : Gland Pharma Walk In Interview On 28th March 2022 

Job Description/Skills Required

• Management and handling of deviations, change controls, market complaints, adverse drug reactions / events, CAPA, OOS, OOT, Risk Assessment.
• Coordinate and conduct required investigation for any reported OOS results / deviation / OOT results / product recall / market complaints / stability failures etc. and prepare detailed investigation report.
• Perform periodic review of change controls / deviation and CAPA.
• Maintain a track on implementation of suggested corrective and preventive actions against reported OOS results / deviation / OOT results / product recall / market complaints / stability failures / Audit outcomes or initiated for any improvements etc.
• Perform quality risk management (QRM) as team member.
• Prepare and evaluate trending of deviation control, change control and market complaints.
• Prepare the Standard Operating Procedure & study protocols.
• Perform Nitrosamine Risk Assessment and Elemental Impurity Risk Assessment for the drug products.
• Prepare Quality metrics, Special Implementation team & management review meeting report.
• Preparation of audit compliance review reports of Internal / External (regulatory, Customer) audits for updating of point wise compliance status and tracking of corrective action.
• Organize and coordinate the scheduled / unscheduled self-inspection.

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