Imran Rashid
About
Imran Rashid is from Singapore. Imran works in the following industries: "Biotechnology". Imran is currently Strategic Account Manager, Life Sciences at Cytiva, located in Singapore. In Imran's previous role as a Biotech Sales Specialist, South East Asia and Taiwan at Pall Corporation, Imran worked in Singapore until Oct 2021. Prior to joining Pall Corporation, Imran was a Technical Applications Scientist, South East Asia and Taiwan at Pall Corporation and held the position of Technical Applications Scientist, South East Asia and Taiwan at Singapore. Prior to that, Imran was a Senior Manufacturing Biotechnologist at Roche, based in Singapore from Feb 2012 to Nov 2015.
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Imran Rashid's current jobs
- Manage accounts assigned by working with key customer partners, C-suite leaders for pre and post-sales for all products. - Develop account penetration strategies for strategic & growth accounts by collaborating with internal partners – Global Strategic Managers, Modality, Application & Service teams. - Prospecting for new opportunities in existing and new customers by qualifying leads and drive funnel growth for Bioprocess, Cell Gene Therapy and Alternative food segments. - Achieve annual and quarterly targets for Orders and Sales through forecasting and effective funnel management using commercial excellence tools. - Develop solution selling strategies to achieve maximum foot print with good commercial competence, customer orientation, and market intelligence
Imran Rashid's past jobs
- Manage monthly, quarterly and annual sales targets assigned. Sales targets are achieved via direct sales activity and channel partners with growth and mature customers in the region. - Establish strong relationships with customers, end-users and management to successfully position and promote Pall technology solutions and capabilities. - Provide technical expertise in various processing streams and promote the use of single - use technologies to develop and support solutions that meet or exceed the customers’ expectations. - Coordinate with various functional groups internally to assemble and direct an effective team strategy so that customer’s needs are addressed in a timely manner and sales opportunities are won. - Report and communicate all business opportunities, solution concepts and strategies through the CRM and the sales funnel.
- Manage and execute field trials as part of feasibility assessments and process optimization projects at all major Biotechnology and Pharmaceutical companies in Singapore and the APAC region. - Provide technical consultations to end users/management on clarification/harvesting, purification, single-use and continuous bioprocessing technologies that includes sterile, virus, tangential flow filtration, chromatography, filter integrity testing, steam-in-place and more. - Troubleshoot manufacturing and processing deviations, providing potential root causes, recommendations, and solutions in written technical reports for customers to make well-informed decisions. - Well versed and experienced in cGMP regulatory requirements, PDA technical reports, quality control, process validation qualifications, and up/downscale process optimization activities. - Support the commercial team to achieve annual sales targets through win-the spec, wallet-share and capacity expansion initiatives.
- Organize and prioritize assigned shift work activities to team members to ensure timely completion. - Prepare and operate equipment including fermentation and purification vessels, media solutions, buffers, single-use technologies, pool, pH and conductivity adjustments, raw materials sampling for Lucentis campaign while adhering to health, safety, cGMP and biochemical manufacturing guidelines. - Mentor new manufacturing hires on cGMP procedures, SOPs, batch records and safety watchouts. - Use automation systems for execution of process recipes, monitoring data trending process parameters. - Participate in root cause analysis with the discrepancy management team and various stakeholders to determine closure. - Ensure timely quality assurance review of batch records and supporting documentation to ensure compliance with GDP and cGMP standards. - Troubleshoot equipment issues, support and initiate process improvement efforts. - Proficient in quality, inventory and resource business management systems (Trackwise, SAP and RPMS).