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10-12 years of relevant experience in Pharmaceutical analytical R & D.
Experience in handling analytical activities for new product development and reformulation will be preferred.
Additional Requirements:
Strong communication, coordination and follow-up skills
Problem-solving and decision-making ability
Leadership, ownership and accountability
Continuous improvement mindset
MS Office and report preparation
Ability to work under pressure and manage multiple operational requirements
Ziska Pharmaceuticals Limited, is one of the reputed pharmaceutical companies in Bangladesh. It is ISO 9001:2015 certified and has a fully GMP compliant factory which follows the USFDA guidelines. To support rapid expanding business, the company is looking for Manager, R & D (Analytical).
Job Location:
Shofipur, Gazipur
Key Responsibilities:
To Plan, Coordinate, review and oversee physical and chemical testing related to new product development and reformulation of existing products.
To conduct analytical testing required for pre-formulation studies and laboratory batch evaluation of new and reformulated products.
To develop, review, optimize and revise analytical methods and procedures considering accuracy, reliability, ease of execution, minimum consumption of reagents/solvents, laboratory safety and cost effectiveness.
To conduct accelerated, real-time, ongoing and in-use stability studies of new and reformulated products as per approved protocols and ensure timely analysis and evaluation of stability data.
To compile, analyze and interpret stability data and provide technical recommendations regarding product stability, trends, specifications and product development decisions.
To perform comparative analysis of innovator/leader products and own products during product development and stability studies and undertake testing of incoming materials and development batches as required.
To prepare, review and revise Standard Testing Procedures (STPs), analytical specifications and related documents and ensure their readiness for technology transfer to the validation/concerned department.
To ensure compliance with GLP and applicable quality requirements at all stages of analytical activities and implement relevant procedures and instructions of ISO 9001:2015 and ISO 14001:2015 within the area of responsibility.
To prepare, standardize and manage chemical reagents and working standards and ensure their proper documentation, safe storage, distribution, usage and disposition in accordance with established procedures.
To maintain accurate and complete records and documentation related to analytical testing, method development, stability studies, batch analysis, reagents, working standards and other product development activities while ensuring data integrity and traceability.
To provide technical guidance and coordinate analytical R&D activities with Formulation R&D, QA, QC, Validation, Production and other relevant functions, identify opportunities for continuous improvement and cost optimization.
To coordinate day-to-day analytical activities with R & D Executives and ensures effective utilization of laboratory resources.
Perform any other tasks assigned by Head of R & D/ Immediate Supervisor.
Work at office
Full time
Gazipur
Applications for this job are handled on the company's own website.
Ziska Pharmaceuticals Limited is one of the fastest growing Pharmaceutical companies in Bangladesh. It is ISO 9001:2015 certifed and has a fully GMP compliant factory which follows the USFDA guidelines. The phenomenal growth of ZISKA PHARMA offers suitable candidate not just a job but also the opportunity for rapid…
এই চাকরির জন্য বিজ্ঞাপনদাতা ব্যক্তি/প্রতিষ্ঠান আপনার কাছ থেকে কোন অর্থ চাইলে কিংবা নিয়োগ প্রক্রিয়া চলাকালীন কোন প্রকার হয়রানিমূলক (শারীরিক/মানসিক) আচরণ করলে অতিসত্বর আমাদেরকে জানান অথবা জবটি রিপোর্ট করুন। চাকরি পাওয়ার জন্য কোন ব্যক্তি/প্রতিষ্ঠানকে অর্থ প্রদান করবেন না। চাকরিকালীন কোন প্রকার হয়রানির (শারীরিক/মানসিক) সম্ভাবনা থাকলে সেখানে জয়েন করবেন না। কোন প্রকার অর্থ লেনদেন বা নিয়োগদাতা কর্তৃক হয়রানির দায়িত্ব Chakrie বহন করবে না।
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