Company Name: A Group of Industries
Job Location: Dhaka (Tejgaon Industrial Area)
Employment Status: Full-time
∎ Master of Science (MSc) in Chemistry
∎ Skills Required: Lab equipment, Laboratory Instrument
∎ 8 to 10 year(s)
∎ The applicants should have experience in the following area(s): Bio-Chemist/ Chemist
∎ The applicants should have experience in the following business area(s): Chemical Industries
∎ Responsible for managing the QC laboratory in accordance with cGMP, customer and company requirements. Lead, organize and maintain all department and laboratory processes, procedures and administrative duties.
∎ Act as liaison with external parties on matters relating to QC testing status, approvals, rejections, documentation status, and any other QC matters to support all internal departments and customers.
∎ Develop and implement systems designed to support assay development, stability, raw material and finished product testing.
∎ Facilitate the evaluation of new testing applications and instrumentation. Assist in the purchase and commission of analytical and microbiology instrumentation. Ensure there are efficient instruments for the workload of samples.
∎ Assure adequate communication of priorities exists between the lab and other departments and within the lab.
∎ Provide guidance to resolve problems with instruments, test methods, lab chemicals, standards, and samples.
∎ Assure that all raw materials, bulks, and finished goods are tested in accordance with all regulatory, Fagron, and customer requirements, as applicable.
∎ Prepare justification for new lab equipment. Prepare purchase orders and coordinate authorization and procurement. Arrange installation and qualification.
∎ Manages process optimization program that includes continual improvement programs for analyses, human capital development and management systems Overall responsible for
∎ Operate precision measuring tools.
∎ Overall responsible for stability programs and ensuring execution within required timelines. Continuous management, development and improvement of stability program.
∎ Overall responsibility to manage method validations/qualifications.
∎ Take lead responsibility with contract laboratories supporting outsourced testing, method development and assay validation activities.
∎ Investigate deviations and write exception documents as required, utilizing problem solving tools as needed. Demonstrate familiarity with product specifications, process reference files, code of federal regulations, and compendia requirements.
∎ Responsible for investigating and processing Deviations, Out of Specifications, and Out of Trend, QC events. Identify and report non-conformances/deviations/out-of-specification events.
∎ Age 35 to 40 years
∎ Only males are allowed to apply
∎ Ability to develop and lead a high performing team.
∎ Communicate clear work plans, coordinate staff schedules, training and standardize work hours among the staff when possible.
∎ Work with various staff members to evaluate and improve processes, through informal and formal channels.
∎ Ability to work on cross functional teams and apply influencing skills in a matrix environment
∎ Must be able to develop solutions for simple and complex problems, which require a high degree of ingenuity, creativity and innovation. Challenges are frequently unique and solutions may serve as precedent for future decisions, which effect the entire organization.
Compensation & Other Benefits:
∎ Provident fund
∎ Lunch Facilities: Partially Subsidize
∎ Festival Bonus: 2
∎ As per company policy
Application Deadline: 26 Feb 2021
∎ 27 Jan 2021
∎ A Group of Industries