Posted by Overview
Biocon Limited, publicly listed in 2004, is India’s largest and fully-integrated, innovation-led biopharmaceutical company. It is an emerging global biopharmaceutical enterprise serving customers in over 120 countries. Driven by a vision to enhance global healthcare through innovative and affordable biopharmaceuticals, we have enabled access to advanced therapies for diseases that are chronic, where medical needs are largely unmet and treatment costs are high.
Biocon Careers Opportunities for Graduate Freshers, Entry Level and Mid Level role in various domain such as Technology, Engineering, Finance, Legal, Business Operation, Sales, Marketing, HR, Healthcare and many more
Biocon Limited has partnered with Ministry of Skill Development and Start your Entrepreneurship (MSDE) to hire freshers as apprentices under National career with Apprenticeship Promotion Scheme (NAPS). Selected candidates will receive extensive on the job training for 6 to 12 months, which Biocon may be followed by full time employment opportunities based on available vacancies at the time.
Careers Opportunities for Entry Level 2025
JUNIOR EXECUTIVE (17305) – INDIA
Job Description:
1. Handling of Downstream operations for commercial batch manufacturing of PEG-GSCF (E.coli based product).
2. Handling of critical equipment like Chromatography columns and systems, Ultrafiltration and Di-filtration Systems , Process vessels etc
3. Well Versed with Protein purification concepts like , Chromatography, Filtration , centrifugation etc
4. Work in manufacturing team for 24 x7 hrs in 3 shifts.
5. Compliance to current GMP guidance and EHS policies.
6. Coordination with cross functional teams for completion of batches on time.
7. Adherence to Standard Operating Procedures, Operational Control Procedures.
Job Responsibilities
1. Handling of Downstream operations for commercial batch manufacturing of PEG-GSCF (E.coli based product).
2. Handling of critical equipment like Chromatography columns and systems, Ultrafiltration and Di-filtration Systems , Process vessels etc
3. Well Versed with Protein purification concepts like , Chromatography, Filtration , centrifugation etc
4. Work in manufacturing team for 24 x7 hrs in 3 shifts.
5. Compliance to current GMP guidance and EHS policies.
6. Coordination with cross functional teams for completion of batches on time.
7. Adherence to Standard Operating Procedures, Operational Control Procedures.
Qualifications
Qualification: B.Tech
Required Experience: 0 – 7 years
For more details to apply, Click here!
JUNIOR ASSOCIATE (17812) – Malaysia
Job Description:
1. To plan day to day shift activities in coordination with the superior to carry out production activity in order to achieve production targets.
2. To ensure that all production activities are carried out in compliance with the cGMP requirements by strictly adhering to the standard operating procedures and good documentation practices.
3. Ensures all team members strictly comply with cGMP procedures and immediately calls attention and corrects any member deviating procedures.
4. To record and maintain daily reports.
5. Responsible for reporting any kind of illness or any abnormal health condition to immediate superior so that appropriate action can be taken (BM/PDP/SOP/115).
6. Adherence to safety, health, hygiene and environmental measures.
7. Follow dedicated procedures to enter Drug Product building as per BM/PDP/SOP/001.
8. Follow dedicated procedures to enter Cleanroom area of Drug Product building as per BM/PDP/SOP/004.
9. Follow dedicated behaviour and hygiene as required in cleanroom area as per procedures (BM/PDP/SOP/146).
10. Ensures all team members are properly trained before assigning tasks (BM/PDP/SOP/105).
11. Strictly implements line clearance procedure as per BM/QA/SOP/026. Does not start line unless it is cleared to operate. Escalates any issue immediately to superior.
Qualifications
Qualification: B.Pharma
Required Experience: 1 – 3 years
For more details to apply, Click here!
ASSOCIATE (17848) – Malaysia
Job Description:
• Able to perform Calibration and Mapping Activities.
• Theoretical knowledge and experience in PLC, DCS, SCADA, HMI and VFD’s
• Knowledge of Quality Management System and able to draft relevant documents
• Able to perform Computer System Validation
• Support validation activities that include FAT/SAT/DQ/IQ/OQ and PQ.
• Prepare and Review Planner, SOP, Checklist and other related documents of QMS.
• Execution of preventive maintenance of Field Instruments and Control System and its accessories as per schedule
• Keeping track of alarms and events and reporting to respective plant heads in case of abnormalities.
• Support mechanical team in troubleshooting of Instruments connected to control system
• Taking plant backup as regular intervals as per SOP and restore them whenever necessary
• Implementing plant security to prevent unauthorized access
• Creating login based security eg: Operator, Supervisor, Shift in Charge and etc as part of regulatory compliance
• To communicate relevant EHS issues to concerned personnel
Qualifications
Qualification: B.Pharma
Experience: 2 – 5 years
For more details to apply, Click here!
EXECUTIVE (17632) – INDIA
Role Description:
• Scheduling, planning, executing, monitoring and control of shift based manufacturing operations.
• Responsible for the downstream operations for the purification of cell culture processes for the production of monoclonal antibodies
• Preparation and review of cGMP documents like SOP, batch records, checklists, protocols and reports.
• Maintaining the equipment and facility in a state of compliance with effective calibration, preventive maintenance and validation programs.
• Organizing workflow by assigning responsibilities and preparing work schedules to meet the production targets.
• Managing and mentoring a small group of experienced employees for downstream operations.
• Analysing and resolving equipment, process and operational problems in an effective and timely manner.
• Coordinating with cross functional teams for the smooth functioning of operations to achieve the departmental objectives.
• Facing internal and external audits, ensuring highest level of compliance for cGMP and EHS norms.
Job Responsibilities
• Scheduling, planning, executing, monitoring and control of shift based manufacturing operations.
• Responsible for the downstream operations for the purification of cell culture processes for the production of monoclonal antibodies
• Preparation and review of cGMP documents like SOP, batch records, checklists, protocols and reports.
• Maintaining the equipment and facility in a state of compliance with effective calibration, preventive maintenance and validation programs.
• Organizing workflow by assigning responsibilities and preparing work schedules to meet the production targets.
• Managing and mentoring a small group of experienced employees for downstream operations.
• Analysing and resolving equipment, process and operational problems in an effective and timely manner.
• Coordinating with cross functional teams for the smooth functioning of operations to achieve the departmental objectives.
• Facing internal and external audits, ensuring highest level of compliance for cGMP and EHS norms.
Qualifications
Qualification: B.Tech
Experience: 1 – 7 years
For more details to apply, Click here!
JUNIOR ASSOCIATE (15952) – Malaysia
Qualification: B.Pharma
Required Experience: 1 – 5 years
Job Description:
1. To plan day to day shift activities in coordination with the superior to carry out production activity in order to achieve production targets.
2. To ensure that all production activities are carried out in compliance with the cGMP requirements by strictly adhering to the standard operating procedures and good documentation practices.
3. Ensures all team members strictly comply with cGMP procedures and immediately calls attention and corrects any member deviating procedures.
4. To record and maintain daily reports.
5. Responsible for reporting any kind of illness or any abnormal health condition to immediate superior so that appropriate action can be taken (BM/PDP/SOP/115).
6. Adherence to safety, health, hygiene and environmental measures.
7. Follow dedicated procedures to enter Drug Product building as per BM/PDP/SOP/001.
8. Follow dedicated procedures to enter Cleanroom area of Drug Product building as per BM/PDP/SOP/004.
9. Follow dedicated behaviour and hygiene as required in cleanroom area as per procedures (BM/PDP/SOP/146).
10. Ensures all team members are properly trained before assigning tasks (BM/PDP/SOP/105).
11. Strictly implements line clearance procedure as per BM/QA/SOP/026. Does not start line unless it is cleared to operate. Escalates any issue immediately to superior.