Softgel Healthcare – Walk-In Interview for Quality Control / Quality Assurance / Analytical Development on 4th to 13th Aug’ 2023

Softgel Healthcare – Walk-In Interview for Quality Control / Quality Assurance / Analytical Development on 4th to 13th Aug’ 2023

Softgel Healthcare provides Outsourcing Solutions to the Pharmaceuticals and Nutraceuticals industry. The company, an associate of the reputed Madras Pharmaceuticals, has recently set up its state of the art and dedicated encapsulation facility for the manufacture of soft gelatin capsules. Softgel Healthcare Pvt. Ltd is conducting walk-in interviews, interested candidates to join in Quality Control / Regulatory Affairs / Analytical QA team can come & attend the interview.

Softgel Health Care Pvt. Ltd, conducting is the walk-in interview for Multiple Positions in Quality Control / Quality Assurance / Analytical Development on 9th to 13th Aug’ 2023 @ Pudupakkam, Tamilnadu.

  • Designation: Sr. Chemist/ Executive/ Sr. Executive
  • Department: – QA / QC & AD
  • Experience: 2-7 yrs
  • Qualification: M.Sc / B.Pharm / M.Pharm / B.Tech – Biochem, Biotech, Biomedical
  • Openings: 10
  • Job Location: Chennai (Kelambakkam)
  • Job Description:

Quality Assurance:

  • Monitoring the compliance of cGMP in warehouse, manufacturing and packing areas
  • To verify the functioning of QA systems on the shop floor during shift hours
  • Monitoring the Dispensing, manufacturing activities as per GMP requirements
  • Performing In process checks of manufacturing and packing activities as per the approved batch document record/ Batch manufacturing record and Batch packing record appropriately to ensure product quality
  • Sampling at different stages of manufacturing and packaging activity
  • Giving line clearance for the dispensing, manufacturing and packing
  • Ensuring cleanliness and traces of batch/ material/ product as applicable.
  • Preparing, Issuing, Monitoring and maintenance of BMR/BPR/BDR.
  • Preparation of Annual Product Quality Review.

AD

  • Maintenance of Laboratory Log books and documents
  • Developing of new methods and documentation of the same.
  • Summarization of stability data.
  • Review of Analytical method validation, Analytical method transfer and Comparative dissolution profile.
  • Maintenance of Column stocks and usage log book.
  • Review of Method Development (New product formulation) documents.
  • Review and Summarize the Stability data.
  • Support to regulatory queries.
  • Periodic Calibration and performance verification and preventive maintenance of HPLC, GC, dissolution apparatus.

Quality Control

  • Should prepare and review SPEC/MOA/ATR/ADS/GTP.
  • Should ensure proper care of colums, working Standards.
  • Responsible for testing of In- process/ Bulk Products/ Finished Products.
  • Documentation of all analysis performed
  • Handling QC related instruments.
  • Should analyse raw materials/stability samples/process validation.
  • Periodic Calibration and performance verification and preventive maintenance of HPLC, GC, dissolution apparatus.
  • Should ensure proper labelling of reagents, glasswares, mobile phase etc.
Walk-In Details:
  • Date: 4th August – 13th August, 2023
  • Time: 9.30 AM – 4.00 PM
  • Venue: Softgel Healthcare Pvt. Ltd, Survey No:20/1, Vandalur – Kelambakkam Road, Pudupakkam Village – 603 103, Tamil Nadu.
  • Phone: +91 73732 51777, +91 73732 52777,
  • Email: career@softgelhealthcare.com
Job Category: pharma
Job Type: Full Time
Job Location: Chennai (Kelambakkam)

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About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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