Technical Staff

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Division
Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing  organization (CDMO), offering end-to-end development and manufacturing  solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.
This enables us to offer a comprehensive range of services including Drug Discovery  Solutions, Process & Pharmaceutical Development services, Clinical Trial  Supplies, Commercial supply of APIs and Finished dosage forms. We also offer  specialized services like development and manufacture of Highly Potent APIs  and Antibody Drug Conjugation.
Our capability as an integrated service provider  & experience with various technologies enables us to serve Innovator and  Generic companies worldwide.
For more details, please visit : www.piramalpharmasolutions.com
Job Title
Technical Staff Job Description
Manufactured / Supervises quality products are being manufactured in conformance with c-GMP/safety and hygiene requirements on shift-to-shift basis. Maintains overall disciplines and productivity. Key Roles/Responsibilities:
• To take training before execute any manufacturing operation and use Ensur for training (If user Id available).
• To be committed when fill the document contemporaneous (online), Legible, Readable,
Accurate and Original.
• To be committed for GDP practices to avoid overwriting and errors, etc. in documents.
• Use self-login ID and password & do not share it to anyone.
• Follow instruction for new machine/methodology in accordance with the quality standards.
• Clean the equipment’s and line for Type A, B & D type in case of product / batch change and major mechanical related maintenance job.
• Visually check for the absence of any residue of previous product or any extraneous matter.
• Do status label as per SOP.
• Use appropriate personal protective equipment’s like face shield, Goggle, Hand gloves & nose mask during machine operation, machine cleaning and follow safety regulation.
• Know hazards associated with given product/ machine/equipment/ tools and adopt necessary protection against identified hazards.
• Identified the Hazards & report any near miss, unsafe act, unsafe condition to your supervisor immediately.
• To maintain good hygiene, safety practices and cGMP Practices.
• To set the parameter of machine as per defined in the BMR/SOP.
• Check the Raw material / SFG product name, batch number, weight of material, sieves, FBD bag, bellow and punch set as per BMR, if any mismatch inform to supervisor.
• Handle the rejection as per defined in the SOP.
• In case of any non-conformity or deviation inform the line supervisor immediately.
• Sending samples (SFG, FG, etc.) to different Customer.
• Participate in Validation activities as per the protocol.
• Review of executed BMR and BPR before submission to Client.
• Knowledge and involvement in SFTI & 6S Activities.
• Knowledge and involvement in ISO 14000 & 13485.
• Check and review the BMR before start of next operation.
• Any other activity from time to time which his supervisor / company feels appropriate.