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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