The Zydus Group with an overarching purpose of empowering people with freedom to live healthier and more fulfilled lives, is an innovative, global Lifescience company that discovers, develops, manufactures, and markets a broad range of healthcare therapies. The group employs over 23000 people worldwide and is driven by its mission to unlock new possibilities in life-sciences through quality healthcare solutions that impact lives. The group aspires to become a global life-sciences company transforming lives through pathbreaking discoveries. The group has manufacturing sites and research facilities spread across five states of Gujarat, Maharashtra, Goa, Himachal Pradesh and Sikkim in India and in the US and Brazil.
Greetings from Zydus Pharmaceuticals !!!
LOOKING FOR TECHNICIANS AND ENGINEERS FOR OSD MANUFACTURING PLANT
We are looking for Below Engineering and Maintenance role for our OSD Manufacturing Plant based out of Ahmedabad
Engineering
Technician :
- Diploma/ITI/ ITI(Refrigeration) with 3 to 7 years of experience in Utility/HVAC + BMS/ Electrical (HT, LT panels)/ Process Equipment(Granulation, Compression, Packing )/ Instrumentation.
Engineers:
- Utility, HVAC+ BMS : B.E / B.Tech (Mechanical) having 3-7 Years of experience in Maintenance of AHU, Air Compressor, Chiller and Water system.
- Civil: B.E / B.Tech (Civil) having 8-12 Years in Civil, preparation, design , BOQ, Planning scheduling and supervision of all new projects.
- Process Equipment (Mechanical) having 3-7 Years experience in Maintenance of OSD equipment used in process such as Granulation, Compression, Packing Etc.
Candidate details
- The candidate should have exposure to USFDA.
- The candidate should be from Pharma industry only.
- The candidate should have knowledge of GDP/ GMP.
Interested candidate Please share your resume at [email protected]
Greetings from Zydus Pharmaceuticals!!!!
LOOKING FOR QMS LEAD FOR OSD MANUFACTURING FACILITY
We are looking for QMS Lead for our OSD Manufacturing Facility based out of Ahmedabad
- Education Qualification: M.Pharmacy/ B. Pharmacy
- Experience : 12-15 Years of experience in QMS .
Roles and Responsibilities:
- The candidate should be handling of Process investigation, Market complaint, Adverse drug events, incidents, CAPA & Change Controls in Trackwise system viz. Logging, Investigation , closure and effectiveness check with coordination of cross functional team and subject matter experts.
- Trending of various QMS tools like Market complaints, incidents and CAPA to assess any emerging trend and escalate to site management to recommended CAPA wherever applicable.
- Review of batch records and supporting document with respect to final batch release to market sale and prepare certificates of compliance.
- Performing Quality risk assessment triggered from various QMS tools and ensure the implementation and effectiveness of identified mitigation actions.
- Prepare Quality Matrix presentation by compiling various QMS data as per regulatory requirement and escalate to higher management team on monthly basis as a Site Quality council lead role.
- Perform Gap assessment for site QMS procedures to make in line with global policy to ensure enhancement of compliance as per updates on regulatory guidance.
- Handling of raw and packaging material vendor management activity like Qualification, periodic Qualification, onsite audits, supplier impact assessment and annual evaluation etc.
- Preparation of Quality technical agreements related to raw and packaging material vendors, service providers, customers and other Mylan entities.
- Participate in Cleaning validation activity viz. preparation and execution of validation protocols, equipment grouping, worst case molecule/product/equipment identification, CV metrix, CEHT/DEHT and annual evaluation.
- Review and approval of various packaging materials artworks by coordination with packaging development, sourcing and regulatory departments.
- Prepare audit compliance report for observation given by regulatory, customer & other corporate quality audits under guidance of HOD & co-ordination with concern department.
- Prepare and review of standard operating procedure pertaining to QMS system and implement at site by imparting training.
Candidate details:
- The candidate should be from Pharma(OSD) Industry only.
- The candidate should Have knowledge and Exposure of GDP/ GMP.
- The candidate should have good communication skills (Verbal & Written)
- The candidate should have Regulatory exposure(USFDA).
- The Candidate should have team under him in current assignment.
Interested candidate, Please share the resumes at my mail id [email protected]
Greetings from Zydus Pharmaceuticals!!!
LOOKING FOR PACKING OPERATOR FOR OSD MANUFACTURING FACILITY
We are looking for Primary Blister and CVC Line Bottle Packing operator based out of OSD manufacturing Facility Located in Ahmedabad.
- Education: Diploma
- Experience: 3-7 Years
Roles and Responsibilities:
- Setting, Cleaning operating & Troubleshooting of bottle packing Primary Equipment’s
- Handling CVC Bottle line and Blister packing.
- Handling of Track & Trace Equipment’s (BPO , LABELLING, 360DEGREE WITH HELPER CODE, 2D BULK BARCODE INSPECTION SYSTEM & ONLINE PALLET SYSTEM) and OPTEL.
- Handling & Modification of change parts.
- Participating of new Equipments installation & qualifications.
- Conducting trainings to contract employees.
- Coordinating with engineering team for Equipment PMP.
- SOP Preparations and modifications.
- Coordinating with vendors for new change parts.
Key Skill:
- Blister Packing
- CVC
- Track and Trace (Jekson)
- CAM Auto Cartonator
- Inkjet Printers (Domino)
- OPTEL
Candidate details:
- The candidate should have exposure to GDP/ GMP and Regulatory(USFDA)
- The person should have worked upon OSD Packing (Primary ).
Interested candidates please share your resume at [email protected].
Greetings from Zydus Pharmaceuticals !!!
LOOKING FOR OPERATOR IN OSD MANUFACTURING FACILITY IN AHMEDABAD
We are looking for Operators for OSD Manufacturing Facility based out of Ahmedabad for Multiple Areas:
Granulation
- Operating Granulation Machines like IGL, RMG, FBD, Blender ETC.
- Maintaining of daily documents and online BMR filling during Manufacturing process.
- Achieving of production target with essential GMPs, and in-process quality checks as per SOP and Manufacturing instruction.
- Activity involving like Line Clearance ,filling up the Batches EBR, Line Clearance Checklist on MES & Cleaning CIP & SIP check lists, Machine setting log cards, Environmental Monitoring & SOP Training Records & Equipment Calibration Log cards on MES etc.
Compression
- Operating Compression Machines of FETTE(3200i), FETTE (2200i), FETTE (P3030), GEA , Cadmach C100, C300 Machine
- Maintaining of daily documents and online BMR filling during Manufacturing process.
- Achieving of production target with essential GMPs, and in-process quality checks as per SOP and Manufacturing instruction.
- Activity involving like Line Clearance ,filling up the Batches EBR, Line Clearance Checklist on MES & Cleaning CIP & SIP check lists, Machine setting log cards, Environmental Monitoring & SOP Training Records & Equipment Calibration Log cards on MES etc.
Coating
- Operating Coating Machines of Ohara and continuous Coater.
- Maintaining of daily documents and online BMR filling during Manufacturing process.
- Achieving of production target with essential GMPs, and in-process quality checks as per SOP and Manufacturing instruction.
- Activity involving like Line Clearance ,filling up the Batches EBR, Line Clearance Checklist on MES & Cleaning CIP & SIP check lists, Machine setting log cards, Environmental Monitoring & SOP Training Records & Equipment Calibration Log cards on MES etc.
Above mentioned positions required to have Regulatory (USFDA) exposure. Interested candidate please share your resume at [email protected].
Regards
Team HR
ZPL- SEZ-II
