Biocon Biologics Released Job Openings On 05/03/2022.Biocon Biologics is a globally recognized, innovation-led organization that is enabling access to high quality, advanced therapies for diseases that are chronic, where medical needs are largely unmet and treatment costs are high.
Vacancy Details:
Biocon Biologics Recruiting BE / B.Tech /ME / M.Tech /MSÂ Candidates with 00Â Years of Experience for MSAT ( Manufacturing Science And Technology ) Position.
Important Details :
- Location :India
- Course:Â Biotechnology, Chemical, Bio Process Engineering.
- No of Vacancies:Not Disclosed by Recruiter
- Details of Salary: Not Disclosed by Recruiter
- Opening date for online Application:05/03/2022
- Mode of application :Online
- How To Apply: jyothirmai.mondi101@biocon.com
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Job Description/Skills Required
MSAT team in Biocon Biologics plays an important role in achieving the manufacturing excellence by providing technical support to the manufacturing / operations teams to enable consistent manufacturing of safe and high-quality biological/biosimilar products. MSAT team bridge the efforts from process development to successful scale-up, validation and consistent manufacturing of high quality, cost effective therapeutic products of biological origin. MSAT team in Biocon Biologics is working on a mission to enable consistent supply of high-quality biosimilar products accessible and affordable across the globe through building multi-disciplinary expertise.
- Scheduling, planning, executing, monitoring and control of manufacturing operations.
- Coordinating with other departments for manufacturing activities.
- Implementing EHS policies in respective areas and ensuring the compliance.
- Ensuring cGMP compliance in respective areas, Investigating the deviations/non-conformities to identify the root-cause and CAPA.
- Preparation and review cGMP documents like SOP, batch manufacturing records, protocols and reports.
- Assessing and mitigating the risks with respect to product, process, operations, equipment, facility and personnel.
- Maintaining the equipment and facility in a state of compliance with effective calibration, preventive maintenance and validation programs.
- Working on continuous improvement programs for operational efficiency and better compliance.
- Authoring/ review of Continued Process Verification (CPV) protocol. Analysis of batch data and trends and summary of CPV report.
- Authoring/ review protocol and technical reports to support process changes, modifications, improvements and scale up to support implementation at manufacturing scale.
- Authoring study protocols and reports for any trials to support the same. Small scale purification.
- Authoring/ review of comparability protocols and reports.
