Hikal Limited - Urgent Openings for Production & Quality Control - Apply Now
Openings For GMP Coordinator/ Officer /Jr. officer – Production (API)
Job description:
We are looking for Junior Officer / Officer for General Production activities who will be working in shifts. Also we are looking for GMP Co-ordinator at Officer level who will be responsible for complete documentation for day to day activity in production department . Their Job Responsibility in detail is attached for your reference.
Job Responsibility for Jr. Officer/Officer Production:
Qualification-B.Sc/ M.Sc- Chemistry or Diploma in Chemical Engineering
Qualification-B.Sc/ M.Sc- Chemistry or Diploma in Chemical Engineering
Experience: For Junior Officer Experience required is 2-3 years & for Officer - 3-5 years.
Job Description:
· To receive operating instructions for the shift from Shift Incharge.
· Maintains the Log Book as per shift activities.
· Operates the process ensuring that all parameters are strictly followed and are within the specified limits.
· Shall submit the in process / intermediate sample to QC lab for analysis as per the batch instruction.
· Responsible for maintaining Good House Keeping in all the areas of Production department.
· Ensures that the equipment are always clean from outside.
· Follow GMP and Safety Instructions during the work.
· Ensure use of appropriate safety apparels while on work and should be aware of the location of fire fighting equipment and know operation.
· Shall be responsible for operating all the utilities, equipment's as per the operating instructions and ensure that the process parameters are strictly followed.
· Report immediately to the Executive / Officer any deviations observed during the operation.
· Ready to work in powder processing area.
· Ready to work in shifts
Job Responsibility for GMP coordinator (Documentation):
Qualification-B.Sc / M.Sc- Chemistry / B.Tech (Chemical Engineering)
Experience: Officer - 4 to 5.5 years.
Job Description:
· Shall be responsible for issuance of BPCR, BCLR, RM indent book, TI sheet, PRF book, check list, registers etc from QA day to day based on production planning.
· Responsible for production related daily checklist, records and cGMP related documents (Usage log,accessories,production consumable registers) review & ensuring online entries.
· Shall be responsible for reviewing of completed validation/Commercial batches BPCR and BCLR and handing over QA.
· Shall co-ordinate with Production team and Assisting to maintain critical parameters (like temperature, pH, pressure etc.) during the validation batch processing.
· Coordinate with Engineering department for the completion of Preventive maintenance jobs monthly, quarterly & yearly on time.
· Shall be responsible for preparing & handling of Documents like CCIF, Deviation, OQ & PQ based on requirement.
· Shall be responsible for clean room activities like milling & sifting & final packing of material.
· Shall be responsible for filing and Maintaining of all documents pertaining to production and handing over QA once completed.
· Attending EHS & GMP training programme.
· Shall update any abnormality or deviations observed during the processing to Production head & QA.
· Shall maintain Good House Keeping in plant and cleanliness of the equipment during audit and Visits.
· Shall be responsible for training the production personnel's on GMP practices and updates.
Note : Interested candidates kindly share your CV at shikha_saxena@hikal.com or call at D : +91-8110421000 Extn: 8194 / 8195.
Required Candidate profile
1) Candidates who are interested to work in shifts should apply.
2) Candidates who are serving notice period or can join early are preffered.
3) Preffered only male candidates.
4) For GMP co-ordinator role relevant experience of documentation in production is required in API Pharma Industry.
5) Candidates who have experience in production department in pharma industry (API/Bulkdrugs ) should only apply.
Opening For QC Officer (Pharma API Industry Only)
Job description
We are looking for QC Officers having experience in Pharma (API / Bulkdrugs) industry who will be working in shifts.
Experience: 3-5 years
Qualification: B.Sc / M.Sc (Analytical / General chemistry), B.Pharm / M.Pharm
Job Responsibility of QC - Officer:
· Analysis of raw materials, In-process, intermediate, packing material and finished products by instruments like HPLC/GC.
· Analysis of raw materials, In-process, intermediate, packing material and finished products for wet analysis like Moisture content /Loss on drying/Sulfated ash/Titrations etc.
· Should handle the instrument like FTIR /UV-VIS etc..
· Should have Knowledge on CGMP /GLP and Data integrity practices.
· Should work in shifts.
Note: Interested candidates kindly share your CV at shikha_saxena@hikal.com or call at D : +91-8110421000 Extn: 8194 / 8195.
Required Candidate profile
1) Candidates who are interested to work in shifts should apply.
1) Candidates who are interested to work in shifts should apply.
2) Candidates who are serving notice period or can join early are preferred.
3) Prefer male candidates.
4) Candidates who have experience in QC department in Pharma industry (API / Bulk drugs ) should only apply.
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