Qureos Mentor

Reliance Life Science

<p></p><div><div><ul><div><p><b>Posted Date :</b></p>
<div>10 Sep 2025
</div></div><div><p><b>Function/Business Area :</b></p>
<div>Life Sciences
</div></div><div><p><b>Location :</b></p>
<div>DALC - Navi Mumbai
</div></div></ul></div><div><p><b>Job Responsibilities :</b></p>
<p>.</p>
<p>
To ensure manufacturing as per SOP and timely completion of projects.</p><p><b>
1)Plan &amp; Execution of product manufacturing :</b></p><p>
To facilitate Operation &amp; changeover of process systems, debottlenecking of process hurdles</p><p>
Regular interaction with Operation team, QAD and supporting functions to achieve the desired targets</p><p>
Focus on plant goals in order to attain expected products over all batch yield</p><p>
Coordinate and monitor the manufacturing schedule to ensure proper utilization of process units, utilities etc.</p><p>
Hands on experience with bioreactors ,chromatography, TFF,CIP systems</p><p>
Exposure on DCS control system would be preferable</p><p>
Scale up, scale down processing of both upstream and downstream process</p><p>
Upstream processing operations seed bioreactors ,production bioreactors operations ,media and buffer preparation activities</p><p>
Downstream processing operations Centrifugation, Microfiltration and Ultrafiltration skid systems.</p><p>
2) <b>Review &amp; monitoring</b> :</p><p>
To ensure the preparation of the cleaning / disinfectant solution and cleaning/fumigation of area/equipment as per the schedule and respective SOPs.</p><p>
To ensure entire manufacturing activities to be performed as per respective SOP's /guidelines</p><p>
To ensure that on- line entries in GMP documents like BMRs, BPRs, log-books etc. are performed as per Good Documentation Practice.</p><p>
To ensure that all documents are updated/revised periodically to meet cGMP standards and as per QAD requirement</p><p>
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.</p><p>
Supervise, coach and train new and current employees (i.e. job, safety, etc.) to meet performance expectations by providing strong leadership skill set.</p><p>
3) <b>GMP compliance, Validation and audit readiness</b></p><p>
To co-ordinate and support for timely completion of calibration, preventive maintenance, qualification/ validation revalidation of process units as per schedule.</p><p>
Ensure that safety, Good Manufacturing Practices (GMPs) and sanitation policies and procedures are met.</p><p>
Process systems and manufacturing area readiness for GMP.FDA,WHO and international audits</p><p>
Preparation of BMR and BPR</p><p>
Validation protocols preparation and its execution</p>
<p><b>Education Requirement :</b></p>
<ul><li>Graduate or Post graduate in Science, B.E in biotech engineering</li></ul>
<p><b>Experience Requirement :</b></p>
<ul><li>Having minimum 0-1 years experience.</li><li>
Demonstrated ability to effectively supervise, lead and build relationships at all levels within the company.</li></ul>
<p><b>Skills &amp; Competencies :</b></p>
<div></div><p><b>Safety Requirements:</b></p><p>
Carrying out activities related to Occupational Health, Safety and Environment Management as per SOP</p><p>
Awareness/Knowledge on the consequences of not following Standard Operating Procedures related to Occupational Health, Safety and Environment Management</p><p><br>
.</p></div></div><p></p>

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