At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering
an environment where you grow at every step, take charge of your journey and
thrive in a supportive community.
ARE YOU READY TO CREATE YOUR OWN SUNSHINE?
As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every
day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and
lead with confidence. Additionally, demonstrate a team-oriented spirit, knowing
that we ‘Thrive together’ and support each other’s journeys.”
Key responsibilities:
* Ensure that batch production records are executed and reviewed in accordance
with established SOPs and cGMP regulations.
* To release / reject the Batch after complete review of batch and related
quality documentation.
* Conduct certification of BPR after completion of batch.
* Review and approve equipment qualification protocols and reports for
accuracy, completeness,
and traceability as well as adherence to protocol /
procedures.
* Review and approve Annual Product review reports for the products as per the
schedule.
* Track to completion all deviation and investigations related to product
release.
* Conduct thorough investigations into and complaints for products manufactured
at the site and ensure on-time closure of complaints.
* Run reports in electronic systems to ensure that all requirements related to
batch release are met.
* Work directly with planning, QC, other QA functions, and Regulatory Affairs
to ensure batches are released to meet supply chain requirements.
* Participate in self-audits of facility and equipment in partnership with
Manufacturing and Engineering to ensure readiness for operations.
* Identify continuous improvement opportunities to increase compliance, process
clarity, and operational efficiency.
* Review and approve Master Formula (Manufacturing / Packing Instruction) and
SOPs
📌 IPQA Head (Dewas)
🏢 Sun Pharmaceutical Industries
📍 Dewas
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