Reliance Life Sciences is a medical biotechnology-led company engaged in research and development, manufacturing and marketing of differentiated medical products and services, used to treat patients primarily in intensive and critical care units in hospitals. Our core businesses are plasma proteins, biosimilars, and later generation oncology pharmaceuticals. In addition, we have initiatives in clinical research, molecular medicine, regenerative medicine, gene therapy, peptides and oligonucleotides…
- Vacancy details:
- Department: Young Professionals
- Experience: 0-1 years experience.
- Qualification: Graduate or Post graduate in Science, B.E in biotech engineering
- Salary: Not Disclosed
Job Description: Greeting from Reliance Life Sciences Pvt. Ltd .!!!!!
Important Details :
- Post of date :23/11/2024
- Location:Nashik
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
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 utilization 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 and BPR
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
Click here for APPLY
