Post: Formulation R&D and QC Manager/supervisor in Pharma
No. of Posts: 02
Formulation Method development:
SCOPE: The Formulations development Scientist, product development provides support to the product development department by Dispensing and compounding of Dosage forms for clinical supplies. Additionally, the SCIENTIST product development is responsible for assisting in development and implementation of quality control systems and procedures.
SCOPE: The Formulations development Scientist, product development provides support to the product development department by Dispensing and compounding of Dosage forms for clinical supplies. Additionally, the SCIENTIST product development is responsible for assisting in development and implementation of quality control systems and procedures.
Duties/Responsibilities:
• Checking and identifying correct actives and excipients to overcome incompatibility
• Weighing/ dispensing of actives and excipients for making solid dosage forms
• Blending/ mixing of actives and excipients for making solid dosage forms
• Making the formulations by sophisticated instruments
• Film coating of Tablets, Capsule filling, Packaging of the dosage forms
• Check for Material Safety Data Sheets for all incoming materials before dispensing
• Formulation of Pharmaceuticals of Novel drug delivery systems
• Evaluation and modify existing processes as part of continuous improvement
• Equipment qualification, participate on technical team to justify, specifies and starts up new
• Development of Controlled Release Dosage forms
• Development of Batch Manufacturing records for processing of pharmaceuticals
• Assisting in analytical development work for pharmaceuticals
• Maintain and follow CGMP practices and OSHA regulations.
• processes.
• Checking and identifying correct actives and excipients to overcome incompatibility
• Weighing/ dispensing of actives and excipients for making solid dosage forms
• Blending/ mixing of actives and excipients for making solid dosage forms
• Making the formulations by sophisticated instruments
• Film coating of Tablets, Capsule filling, Packaging of the dosage forms
• Check for Material Safety Data Sheets for all incoming materials before dispensing
• Formulation of Pharmaceuticals of Novel drug delivery systems
• Evaluation and modify existing processes as part of continuous improvement
• Equipment qualification, participate on technical team to justify, specifies and starts up new
• Development of Controlled Release Dosage forms
• Development of Batch Manufacturing records for processing of pharmaceuticals
• Assisting in analytical development work for pharmaceuticals
• Maintain and follow CGMP practices and OSHA regulations.
• processes.
Quality control Manager:
Scope: The quality control provides support to the quality control department by performing functions, which aid assurance of GMP compliance. The quality control is responsible for assisting with quality control operations are performed according to written Sops, GMP and FDA guidelines. Additionally, the quality control is responsible for assisting in development and implementation of quality control systems and procedures.
Scope: The quality control provides support to the quality control department by performing functions, which aid assurance of GMP compliance. The quality control is responsible for assisting with quality control operations are performed according to written Sops, GMP and FDA guidelines. Additionally, the quality control is responsible for assisting in development and implementation of quality control systems and procedures.
Duties/Responsibilities:
• Maintain and follow cGMP practices and OSHA regulations.
• Preparation of standard operating procedures, for quality control activities
• Developing test methods or procedures and preparing the specifications and release
• Sampling and testing of all input raw materials, packaging material, in process tests and finished
• Calibration and maintenance of various instruments used in testing or analysis.
• Conducting stability studies.
• Providing support to validation activities.
• Training laboratory staff in line with GMP.
• Recording, reviewing and investigating out of specification results from the laboratory control mechanisms.
• Maintaining the reserve samples for raw materials, product contact materials and finished dosage forms.
• Maintain and follow cGMP practices and OSHA regulations.
• Preparation of standard operating procedures, for quality control activities
• Developing test methods or procedures and preparing the specifications and release
• Sampling and testing of all input raw materials, packaging material, in process tests and finished
• Calibration and maintenance of various instruments used in testing or analysis.
• Conducting stability studies.
• Providing support to validation activities.
• Training laboratory staff in line with GMP.
• Recording, reviewing and investigating out of specification results from the laboratory control mechanisms.
• Maintaining the reserve samples for raw materials, product contact materials and finished dosage forms.
Candidate Profile
UG - Any Graduate - Any Specialization, B.Pharma - Pharmacy
PG- M.Sc - Any Specialization, Chemistry, M.Pharma - Pharmacy
UG - Any Graduate - Any Specialization, B.Pharma - Pharmacy
PG- M.Sc - Any Specialization, Chemistry, M.Pharma - Pharmacy
Additional Information:
Experience: 0-2 Years
Qualification: B.Pharm, M.Pharm
Industry Type: Pharma/Biotech/Clinical Research
Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology
Location: Hyderabad
Last Date: 18th April, 2016
Experience: 0-2 Years
Qualification: B.Pharm, M.Pharm
Industry Type: Pharma/Biotech/Clinical Research
Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology
Location: Hyderabad
Last Date: 18th April, 2016
Send your CV to hr1.vsp@gmail.com
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