Unison Pharmaceuticals Released Job Openings On 23/08/2022. Unison Pharmaceuticals is an Indian pharmaceutical company and the world’s largest producer of anti-retroviral drugs. Hetero’s business includes APIs, generics, biosimilars, custom pharmaceutical services, and branded generics.Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for Unison Pharmaceuticals Recruitment 2022 are provided below. Interested and eligible candidates can submit application along with resume.
Vacancy Details:
Unison Pharmaceuticals Recruiting B.Pharma,M.Pharma,M.Sc Candidates with 01-05+years of Experience for IPQA Officer Position.Complete Details for the IPQA Officer as follows.
Important Details :
- No of Vacancies:Not Disclosed by Recruiter
- Details of Salary: Not Disclosed by Recruiter
- Opening date for online Application: 23/08/2022
- Mode of application :Online
- How To Apply: Interested candidates may also email their resume to career@unisonpharmaceuticals.com
Related Job: Tata Consultancy Services(TCS) Hiring Graduate / Postgraduate in Lifesciences, Pharma, Medicine, Biotechnology
Job Description/Skills Required
1. IPQA Primary Packing
- Perform cleaning verification, document verification, Preventive maintenance status, instrument calibration status, change part verification related to area.
- Perform product related verification which includes; primary packing material verification, stereo verification and coding detail verification.
- Give line clearance based on above verifications.
- Perform camera challenge test at the beginning of the batch, end of the day/shift, start of the day/shift, end of the batch, power failure and machine breakdown.
- Perform leak test in various situations like; at a regular interval of 4 hours, temperature change in forming or sealing temperature, change in speed, machine breakdown, maintenance, power failure, foil roll change etc.
- In-process quality check at an interval of 2 hours which include; forming temperature, sealing temperature, machine speed, cutting, sealing, knurling, batch coding details, printed foil code verification, hologram quality and presence of hologram.
- Post batch completion, stereo impression verification, collection of stereo and destruction verification.
- Material return note which includes verification of left material and returning back to warehouse, destruction of rejected material.
- De-foiling activity verification which includes inspection of recovered tablets / capsules and weight verification (if recovered tablet weight is higher than 3% of total batch weight then deviation to be taken).
- Verification of reconciliation of packing materials document which include actual consumption details, destroyed material details and return material details (variation limit in reconciliation of primary packing material should not be more than 1 %).
2. Executed BPR review
- Review the executed BPR which include; crosschecking all pages available with issued copies, page reconciliation, line clearance and in process at each stage, yield verification at each stage, QC release at each stage, Environment monitoring records, material reconciliation verification, batch reconciliation verification, Deviation, OOS, OOT etc.
- Post review, send the BPR report to section head for approval.
3. Logbook Reviewer- Packing
- Daily review of logbooks available in primary packing area which are area cleaning logbook, equipment operation logbook, environment monitoring logbook, leak test operation logbook, weighing balance / analytical balance verification logbook, material in-out logbook etc.
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