Quality Control Assistant

Company : Pharmaceutical & Medical Device Trading Company (MNC)

Position : QC Assistant

Job Location : Gandhidham (Gujarat)

Job Role :

To implement the release process for all products including review of batch documentation and samples, proper handling, communication and filing of supplier non-conformities. Review and control of kits and kits packing process. Executing the process as defined in SOP.

JOB RESPONSIBILITIES: WAREHOUSE QUALITY SEGMENT CONTACT: § Quality resource person for dedicated customer segments in close collaboration with other colleagues.

§ Perform quality checks on received orders including sampling and visual check of dosage form and in parallel with document review release the batches physically and administratively. § Collect, review, stamp and upload manufacturers COAs/COS or any other lot/batch related quality certificates for conformance to specifications as part of the QC release. § Random sampling and checking of kits during Kit packing activity and shipments. § Line clearance for packing process. § Report, handle and investigate product deviations internally and towards the manufacturer in close coordination with QA, Procurement, sales, and other relevant functions. § Ensuring configuring and placing data loggers at the time of dispatch. § Participate in meetings relating to segment updates. § Participate in meetings relating to deviations / product non- conformances/customer claims. § Communicate with suppliers for correction; follow up on documents and for resolving the non-conformities. § Involvement in Packaging material layout checking and testing. § Ensure compliance with GDP, ISO 9001, ISO 14001, local laws, and regulations. § Prepare and review QA/QC related SOPs and other documents in eQMS. § Archiving and review of control samples. § Any other duties or assignments related to QC function or assigned by reporting head

Desired Profile

Education:

Science graduate/ B. Pharm/M. Pharm Work experience:

Fresher or 1-2 years of experience in Production, Quality Control/ Quality Assurance department of formulation manufacturing in pharmaceutical company/ medical devices or hospital equipment. Should have Hands on Experience with QMS and GMP related issues. Competences: § Good English skills verbally and in writing. Should be well structured and systematic. Should be efficient and have a fast responsiveness. Should have good knowledge of computers excel/word. Should once trained be able to understand the features in our ERP system facilitating compliance in our document system. Should be proactive of nature and follow-up on own initiative in writing and verbally towards the manufacturer. Should maintain a positive attitude also when taking up unvarying tasks. Languages: Proficiency in English Travel activity: Shall be able to travel as and when required for supplier visit/Pre-shipment inspection of goods.

Contact Rina Arun +91 9904322770 rina@uhr.co.in