2-3

Pre formulation studies of Pharmaceutical & Medicinal Devices and to check the compatibility of the API with different excipients. Formulation development of Pharmaceutical & Medicinal Devices. Execution of successful technology transfer at commercial site.

Well-versed with QC related activities of Pharmaceutical Manufacturing Industry. Knowledge of CGMP & Safety Guidelines.

Experience in handling QC instruments like HPLC, LCMS, GC, UV -spectrophotometer, dissolution apparatus, KF, IPC-OES, IR spectrophotometer

Candidates having experience in monitoring and handling of shop-floor activities for Tablet, Capsule, Ointmnet, Ampoule, Vial and Injectable production operations, online documentation like log book & batch records and QMS

Filling machine Groninger, Optima, Dyno Truking filling and sealing machine, Bosch filling machine, Steam sterilizer Fedegree

2-8 years of experience in BMR, QMS, PQR, Qualification, AQA, ERP, Control Sample, Process Validation.

Identify and develop new business opportunities in global markets. Build and maintain strong relationship with international clients and partners Assist contract negotiation proposals and strategic planning for business growth.

Must know process validation cleaning validation verification and hold time studies. Candidate should also have exposure to EU, MHRA, and USFDA regulatory audits.

To Perform IPQA, To Perform Line Clearance, To withdrawn FG Sample, To support in Validation Activities