Rusan Pharma Ltd Recruitment 2020.Rusan Pharma Ltd. Notification full detailes below.Rusan Pharma Ltd. is a fully integrated global pharmaceutical company specializing in the treatment of ‘Addiction and Pain Management’.
Important Vacancy details:
- Post Name: Production / Quality Assurance
- Education:M.sc,Masters or PhD qualification in Organic Chemistry
- Experience: 5-12yrs
- Location: Kandla, Gandhidham (Gujarat),Ankleshwar (API)
- Openings: NA
Note:If interested candidates can share your resume to mentioned mail ID Below.
Job Description: Hiring For Production / Quality Assurance in Rusan Pharma Ltd.! If interested candidates can share your resume to mentioned mail IDcorporatehr@rusanpharma.com
Production – API (R&D) – Rusan Pharma ltd – Gandhidham
Opening for Manager – Production (API) with Rusan Pharma Ltd (R&D Center)
Location: Kandla, Gandhidham (Gujarat)
Exp : 5+ Years of Exp from R&D API Background
Profile: Manager Production in R & D
Candidate can apply only if wants to relocate at Gandhidham Location.
- Masters or PhD qualification in Organic Chemistry
Development, Technology transfer and production operation in API.
Expertiseinbuildingteambystreamliningmanufacturingoperationsusingprocedurestofacilitaterobustqualitymanagementsystemswithprocessoptimizationandcontrolrespectingquality,safety and process norms.
Route scouting, synthesis and scale-up of small organic molecules/intermediate
Plans and schedule synthesis campaigns to support large scale demands
Responsible & audit – the lab documentation in the PRD lab
Innovates solutions to synthetic/scale-up issues (chemical, physical, preparative, application specific and analytical), transfer results and involves in scale-up/production
Optimize process flows and methods of concerned working fields.
Plan, evaluate, document and analyse experiments, results and suggest improvements
Co-operates in cross functional project teams to ensure timely delivery.
Education and supporting of trainees as well as interns and ensure targeted safe work performance.
Stay up to date with scientific developments in the field of organic synthesis and organic process research & development percolate the developments to the peers in PRD lab.
Perform all project work to ensure effective and efficient on budget, on time delivery of the required amount of product of the required quality.
Carry out practical experiments and demonstrate understanding of organic chemistry, guided by line manager.
Use literature search engines to aid in selection of work plan with line manager.
Aid in the development of processes that are suitable and robust to transfer to pilot plant/kilo lab within budget and to the schedule assigned for that project.
Identify problems and propose potential solutions, with supervision where appropriate.
Document all experimental work fully and accurately in lab notebook.
Perform and interpret own routine analysis (eg NMR, HPLC, LCMS, KF).
Discuss the need for obtaining further analytical data with line manager.
Act as support chemist for project in kilo lab./pilot plant operations by ensuring clear communication of expectations of the process to operations or plant chemist.
Sr. Management – Quality Assurance – API – Rusan Pharma Ltd, Ankleshwar
Opening for Sr. Management – Corporate Quality Assurance – API (Ankleshwar) with Rusan Pharma Ltd
Qualification : M.sc
Exp : 12+ Years – API Background
Location : Ankleshwar (API)
Responsible for managing QA activities such as deviation management, change management, SOP compliance, batch release, supplier quality assurance, complaint handling and document review.
Preparation, Review and Maintaining corporate QMS SOPs. (Deviation, Change control, Audit Management, Complaints, Self Inspection, and document reviews).
Market complaints – Investigation, CAPA analysis, resolution of complaints & taking timely corrective action for critical and major categories.
Managing QA activities such as deviation management, change management, SOP compliance, batch release, supplier quality assurance, complaint handling and document review
preparation / review of various protocols and reports such as cleaning validation, process validation, validation master plan, computerized system validation, etc
Communication with international corporate colleagues on various subjects.
Preparing monthly and yearly reports with respect to QA activities and presenting the same to corporate QA.
Preparation of the site qualification and validation master plan for current year and tracking the progress plan on quarterly basis.
Preparation and Implementation of internal audit program.
Documentation, Validation & Qualification, Internal & External Audit, handling Customer Complaints and indepth knowledge of Regulatory requirements
Selection Process: The selection will be on the basis of Interview