Job in Pharmaceutical Company GSK

THIS ROLE IS BASED IN JAMSHORO SITE

 Important Notice: 

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please directly apply through GSK portal. Date posted for this job is 29^th- May-2020

Job Purpose

Develop and execute Process Validation according to Validation Master Plan to meet cGMP requirements on time and quality.

Education & Education Levels

1. BS. in Pharmacy, Pharmaceutical Technology, Chemistry or equivalent scientific degree.

2. Desirable MS. Or Pharm-D

3. 0 -3 years operational experience in manufacturing / Quality and execution of process validation

Key Responsibilities

· Ensure that process validation activities are performed and are in line with the current GSK requirements and cGMP, handling any deviations associated to these activities

· Responsible to translate the critical process parameters and the process control strategy into a focused validation plan for process validation

· Perform risk assessments prior to validation activities

· Author the routine process validation protocols and reports, reviews Master Batch Records MBRs, associated change controls and perform execution at the shop floor

· Understand the potential risk areas/shortfalls and make sure that the validation program is always inspection ready

· Ensure on time delivery of validation KPIs, as required by Module

· Any other responsibility assigned from time to time as per business requirements

· Comply and ensure compliance to GMP (Good Manufacturing Practices), Quality and other related policies, guidelines and requirements as applicable by law and GSK Corporate Guidelines.

· Comply and ensure compliance to Environment, Health and Safety policies, guidelines and requirements as applicable by law and GSK Corporate Guidelines.

Any other responsibility assigned from time to time as per business requirements.

Please click on below link to apply for this job. This link will directly take you to GSK website. There you can signup and fill the job application form.

https://jobs.gsk.com/en-gb/jobs/252679?lang=en-us&source=APPLICANT_SOURCE-6-18