Reliance life sciences is hiring for the below mentioned post as per the details provided below. Read the complete notification before applying:-
Post:- Young Professionals [81097616]
- Posted Date :18 Dec 2023
- Function/Business Area :Life Sciences
- Location :DALC – Navi Mumbai
Job Responsibilities :
To ensure manufacturing as per SOP and timely completion of projects.
1)Plan & Execution of product manufacturing :
- To facilitate Operation & changeover of process systems, debottlenecking of process hurdles
- Regular interaction with Operation team, QAD and supporting functions to achieve the desired targets
- Focus on plant goals in order to attain expected products over all batch yield
- Coordinate and monitor the manufacturing schedule to ensure proper utilisation of process units, utilities etc.
- Hands on experience with bioreactors ,chromatography,TFF,CIP systems
- Exposure on DCS control system would be preferable
- Scale up, scale down processing of both upstream and downstream process
- Upstream processing operations # seed bioreactors ,production bioreactors operations ,media and buffer preparation activities
- Downstream processing operations # Centrifugation, Microfiltration and Ultrafiltration skid systems.
2) Review & monitoring :
- To ensure the preparation of the cleaning / disinfectant solution and cleaning/fumigation of area/equipment as per the schedule and respective SOPs.
- To ensure entire manufacturing activities to be performed as per respective SOP’s /guidelines
- To ensure that on- line entries in GMP documents like BMRs, BPRs, log-books etc. are performed as per Good Documentation Practice.
- To ensure that all documents are updated/revised periodically to meet cGMP standards and as per QAD requirement
- Ability to mainly evaluate schedule in accordance to manufacturing processes, and determine the most efficient method of accomplishing goals in order to meet the targets.
- Supervise, coach and train new and current employees (i.e. job, safety, etc.) to meet performance expectations by providing strong leadership skill set.
3) GMP compliance, Validation and audit readiness
- To co-ordinate and support for timely completion of calibration, preventive maintenance, qualification/ validation revalidation of process units as per schedule.
- Ensure that safety, Good Manufacturing Practices (GMPs) and sanitation policies and procedures are met.
- Process systems and manufacturing area readiness for GMP.FDA,WHO and international audits
- Preparation of BMR#s and BPR#s
- Validation protocols preparation and its execution
Education Requirement :
- Graduate or Post graduate in Science, B.E in biotech engineering
Experience Requirement :
- Having minimum 0-1 years# experience.
- Demonstrated ability to effectively supervise, lead and build relationships at all levels within the company.
Skills & Competencies :
Safety Requirements:
Carrying out activities related to Occupational Health, Safety and Environment Management as per SOP
Awareness/Knowledge on the consequences of not following Standard Operating Procedures related to Occupational Health, Safety and Environment Management