API Pharma Tech Private Limited

• Well acquainted with all activities pertaining to Parenteral formulation (Liquid and Lyophilized Formulations) development techniques from literature survey, patent evaluation for product under development.
• Knowledge about the handling of Cytotoxic materials.
• Knowledge about the regulatory guidelines, safety aspects, GLP and GMP.
• Knowledge about the qualification of instruments
• Write SOPs, Protocols and Reports
• Maintain laboratory SOPs in a state of compliance.
• Ensure equipment is adequately qualified and maintained in accordance with cGMP requirements.
• Perform, track and monitor stability testing as required.
• Produce deliverables for assigned projects in a timely manner.

We have opening in multiple department for multiple positions:
> Quality Control: 20 positions (incl. freshers and experienced candidates)
> Formulation R&D: 10 (incl. freshers and experienced candidates)
> Synthesis R&D: 10 (freshers)
>Procurement : 2 (Experienced candidates)

Please contact us more information.

Regards
V Prasant
Human Resource
API PHARMA TECH PRIVATE LIMITED
9679617228/8637085495
[email protected]
www.apipharmatech.com