Open Vacancies At Boston Pharmaceutical Industries
Boston Pharmaceutical Industries is a leading Egyptian company that develops, produces and markets high-quality branded and generic pharmaceutical products. We are committed to secure the availability of safe and effective medicines in all therapeutic areas to our patients and our medical community.
Recently Boston Pharmaceutical Industries has launched a MEGA project to establish its Manufacturing Campus in the 10th of Ramadan city. The Campus includes a multiple state-of-the-art manufacturing facilities that will meet the highest standards of quality and safety.
And due to huge expansion & extension plan for Boston Pharmaceutical Group in the Egyptian market in the next 5 years, the group is looking forward to hire
1- External Manufacturing Specialists
Responsibilities
• Responsible for managing and handling all TOLL projects in a proactive manner.
• Prepare the supply plan and confirm it with the production planning team and manufacturers.
• Create/update and implement TOLL-related SOPs.
• Coordinate supply and business relationships with those who deal with toll manufacturing systems, material suppliers, and business partners.
• Coordinate with all concerned departments at the manufacturing sites (R&D, QA, QC, production planning) for stock holding processes and troubleshoot all bottlenecks that can affect delay or deviate the Production procedures to obtain timely and timely production dates.
• Coordination of contracts issuing of Toll manufacturing projects.
• Build a database showing the contact details of our manufacturer, Available capabilities, tools, etc.
• Provide all supply data for the weekly and monthly reviews/reports.
Job Requirements
• Bachelor’s degree in pharmaceutical/science/vet.
• Minimum 3 years of experience in handling toll manufacturing.
• Previous experience in pharmaceutical production (Pharma & Food supplement Experience is preferred)
• Excellent communication skills, attention to detail, problem-solving orientation, and ability to meet tight project deadlines while balancing multiple projects.
• Good English & Arabic language skills.
If you are interested and qualified for the job, please send your C.V to info@bostongroup-eg.com
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2-R&D Formulation Supervisor
Responsibilities:
• Implementing the designated formulations for new Humane, Supplements, Cosmetics, Antiseptics product & redeveloping the existing products
(Alternative raw materials, decreasing cycle time).
• Entail developing high quality robust products and processes that are scalable, stable and bioequivalent to the reference product, also Prepare manufacturing trial documentation for pilot / small production runs and scale-up operations based on ICH Q8 guidelines and QBD and support technology transfer for manufacturing processes from laboratory scale to production scale.
• Reporting, documenting, and summarizing the results of experimental trials and other data into a format that allows easy review by superiors. Also, assure that all formulation and process development activities are documented in the notebook as per company procedures GMP and cGLPs.
• Issuing Standard Operating Procedures (SOPs) for Routine work, handling with equipment or machines and manufacturing of new products. (Maintain confidentiality of data & company documents in R&D).
• Correlating the results of the performed trials and experiments and recommending changes in formulations & procedures so that optimal parameters can be achieved and simulation of the production conditions to ensure the applicability of proposed formulations & procedures.
• Work with Analytical Method Development, Regulatory Affairs, Quality Control, Quality Assurance and External Manufacturing etc. to expedite the development and approval of new products by EDA & NFSA (for dec. 645 has experiences in pharmaceutical development coping with CTD filling).
• Participate in investigations into product failure including quality, potency, visual characteristics and other to ensure involvement in all trouble-shooting activities,
Participate in managing and directing the research and development programs to meet organizational needs.
Requirements:
1- Pharmacists only.
2- Minimum 3 years’ experience. in the pharmaceutical industry.
3- Hands-on experience with Human and veterinary product and NFSA formulation.
If you are interested and qualified for the job, please send your C.V to
3-Export Manager
Job Description
• Can work in Human & Veterinary pharmaceuticals.
• Has good information about each market in the region. Distribution, competition, market shares.
• Plan and execute export strategy consistent with overall aims and requirements of the company.
• Facilitate all export documents starting from receiving the purchasing order from the export agents and ending with shipping of goods and sending the original documents.
• Negotiate and monitor export rates and services to reduce operating costs and increase profitability.
• Aware and Up to date to each country-specific regulations, requirements and standard operating procedures; including product registration, required product certificates, and test reports where need be.
• Direct and monitor the export operations from A to Z and have the knowledge of the details of the export business.
• Establish contact with distributors and sell the product portfolio and the story of the company.
• Negotiate contracts of sales, manage, renew and review contracts as required to enable effective trading.
• actively support Distributor with marketing activities with the goal to increase sales and to achieve Sales target in each country.
• Monitor all financial and currency processes and transactions
• input Distributors with all relevant information in the Sales Pipeline Tracker.
• Proven record of successful achievements of sales targets and driving growth.
• Design and implement strategic sales plans that expands company’s customers based and ensure its strong presence.
Job Requirements
• 10+ years of international experience in pharmaceutical Human & Vet industry as an export expert is a must.
• English language proficiency (Written and Spoken) is required.
• Second foreign language like French is preferred.
• Ability to meet and exceed the sales target.
• Organized and Methodological.
• Responsible, Flexible, Pro-active and Energetic person
• Leadership Skills, Positive attitude and presentable.
If you are interested and qualified for the job, please send your C.V to
info@bostongroup-eg.com
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4-External Manufacturing Manager
Summary:
In this role you will have responsibility for the operations of pilot and commercial drug product manufacturing in the Contract Manufacturing Network. Your remit will involve coordinating and leading all aspects of day-to-day operations, technology transfer, new technology introduction, issue resolution, relationship management and supply fulfilment at drug product manufacturing sites.
More specific responsibilities include:
• Establishes overall external manufacturing network strategy.
• Primary liaison between Boston Pharmaceutical’s internal functions and functional groups at the Contract Manufacturing sites or business partners.
• Coordinate all Manufacturing operations at contract and/or business partner
manufacturing sites, including but not limited to: scheduling of all batches, supply of materials, direct shipment of bulk and finished product at manufacturing site, track and monitor cycle times, technology transfer execution, validation activities, packaging changes, regulatory submission reviews and providing any required associated reports and technical expertise.
• Ensure the timely routing and review of all master manufacturing records (MRs),
standard operations procedures (SOPs), tech transfer reports, validation master
plans, and any other relevant documentation.
• Negotiate and review relevant contracts and agreements.
• Lead sub-team in continuous process improvements, system/equipment
implementation and/or strategy development
• Support all investigations which concern Contract Manufacturing or associated
shipping operations
• Ensure product integrity and company reputation by assisting in the monitoring of
cGMP compliance at drug product contract manufacturers.
• Will be the final business decision maker on all manufacturing sourcing decisions
(New CMO’s, pilot and commercial production needs).
• performs regular benchmarking to identify and implement industry best practices with regards to external supply management.
• Travel to contract manufacturers or business partners, as required
Requirements to be considered for the role:
• Bachelors/Master’s Degree (Pharmacist/ Chemist), additional competences in Business Administration, Supply Chain or related fields are a plus.
• Minimum 15 years of experience in increasingly responsible roles in the management of manufacturing or related activities, in the pharmaceutical sector.
• Experience in the management of outsourced activities either leading external manufacturing or working for a CMO highly valued.
• Demonstrated project leadership skills and ability to develop effective working processes and relationships with internal/external partners and cross-functional project teams.
• Good negotiation skills.
• Having a car is a must.
If you are interested and qualified for the job, please send your C.V to