Biological E Limited Walk In Interview 2023. Biological E Limited Notification full details below..Interested and eligible candidates can attend interview on scheduled time and venue.Biological E Limited, the first private sector biological products company in India and the first pharmaceuticals company in South India was established in 1953.Originally incorporated as Biological Products Private Limited, and launched by Dr. Vijay Kumar Datla, Biological E (BE) today, is a leader in the vaccine market.
Vacancy details:
- Designation: Engineering – Executive / Senior Executive
- Qualification: B.Tech with minimum 7 Years and Diploma with 10 years’ experience.
- Experienced:06-11 Years
Job Description: Greeting from Biological E Limited !!!!
Important Details :
- Location: Shamirpet, Hyderabad/Secunderabad
- Post of date:28/03/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face To face Interview
- Interview Rounds of Interview: HR
Time and Venue
30th March , 10.00 AM – 4.00 PM
Biological E Limited. Pharma Division, Plot No.4, Phase-II, Alexandria Knowledge Park, Genome Valley, Kolthur Village, Shameerpet Mandal, R. R. District, Hyderabad, Telangana, India.
Contact – HR
Biological E. Limited invites Dynamic & Self-motivates candidates experienced, dynamic and self-motivated candidates for Engineering department at its Pharma SGI -USFDA Approved plant, Shamirpet, Hyderabad:
Roles and Responsibilities
Department: Engineering
Position: Executive/Sr. Executive
Qualification: B.Tech with minimum 7 Years and Diploma with 10 years’ experience.
JD of Instrumentation Engineer
- Must be experienced in Sterile injectable facility and equipment.
- Responsible for schedule activities i.e. Preventive maintenance, backup & restore, time synchronization etc.
- Participate in instrument calibration activity.
- Hand on experience in trouble shooting & maintenance of below following equipment:-
Vial filling machine (Make Steriline), Vial washing machine (Make Steriline), Vial
depyrogenation tunnel (Make Steriline), Automatic loading & unloading system (Truking),
Lyophilizer (Truking), Vial cap sealing machine (steriline), Steam sterilizer & terminal
terilization autoclave (Fedegari), Manufacturing vessel (DDE)
- Daily monitoring and documentation of Operation & Maintenance log sheets for the Instrumentation.
- Involving and executing of Installation and Operational qualification protocols, compile and archive it with the coordination of vendor.
- Monitoring of computer system validation activities for PA, PF and Admin.
- Responsible for preparing & training on SOPs related to instrumentation.
- Responsible for computer system admin activities for production & admin systems.
- Responsible for audit compliance related to instrumentation.
- Identify the operational issues related to instrumentation and rectify the same.
- Preparation of Basic and detail engineering for instrumentation and automation projects.
- Involving and executing of instrumentation and automation projects.
- Responsible to keeping the areas and documents ready for various regulatory inspections/audits and need based active participation during audits.
- To support the documentation related to Change Controls, CAPAs and Deviations etc., to comply as per the CGMP guidelines, site quality procedures.
- Responsible to execute the assigned projects.
- Ensure the requirements/ principles of CGMP, CGEP and CGDP are adhered during the execution of activities.
- Ensure safety precautions followed during the execution of activities.
JD of Mechanical Engineer
- Must be experienced in Sterile injectable facility and equipment.
- Hand on experience in trouble shooting & maintenance of below following equipment:-
- Vial filling machine (Make Steriline), Vial washing machine (Make Steriline), Vial depyrogenation tunnel (Make Steriline), Automatic loading & unloading system (Truking), Lyophilizer (Truking), Vial cap sealing machine (steriline), Steam sterilizer & terminal sterilization autoclave (Fedegari), Manufacturing vessel (DDE).
- Involving in all Equipments qualifications as part of mechanical.
- Involving in preparation of protocols along with QA.
- Involving and executing of Installation and Operational qualification protocols, compile and archive it with the coordination of vendor.
- Verification of drawings and making as-built with the coordination of vendor.
- Responsible to maintain spares for Process equipments.
- Addressing and rectification of mechanical breakdowns.
- Follow up with vendors for project execution, maintenance and break down activities.
- Responsible to prepare, SOPs, Preventive Maintenance Schedules and Preventive Maintenance checklists for Process Equipment.
- Performing of Preventive Maintenance Procedure for Production Formulation Process equipments.
- Raising and Closing of Engineering Change controls, Incidents, Deviations and CAPA etc. coordinating with cross functional teams to close the documents.
- Responsible for keeping the areas and documents ready for various regulatory inspections/audits.
- Responsible to impart the trainings for the team members and Vendors
- Ensure the Requirements /Principles of CGMP, CGEP and CGDP are adhered during the execution of activities.
- Ensure Safety precautions followed during the execution of activities.
