Pharma IT

Implementation Manager...

Brussels, Belgium

Negotiable

Our leading International Healthcare client are looking for an experienced IT Implementation Manager to join them. You will have a proven successful project management in implementing SaaS solutions into the Pharma / Healthcare Industries. Major Accountabilities *Drive the implementation of a new global Medical Information system, including the oTranslate the business objectives into business requirements and roadmaps of capabilities. In collaboration with global IT, either develop or integrate and operate the specific solutions or ensure this is done to meet these goals oCoordinate the implementation of a SaaS solution, including the migration from old-to-new system oTogether with our Governance teams, ensure such solutions are trustworthy, secure, safe and compliant, which includes validation guidelines and GxP-relevant requirements Experience & Competencies Experience oProven project management success in a multinational environment. Diverse experiences (of which +5 years in IT) oExperience in managing a team of diverse internal & external competencies (2+ years) oAbility to operate and manage in a matrix-organization, with delivery partners in many places across the world. oProven track record of SaaS implementation, for a technology project oWorking experience in the pharmaceutical industry with GxP relevant projects, ideally in the area of medical affairs Competencies & attitude oBe agile by being able to perform at operational and tactical level oHave strong listening, communication, facilitation, influencing and analytical skills (having a consulting background or consultant attitude) oBe ready to challenge and be challenged oEmbrace diversity For further information please contact Nitin on +44 (0) 207 255 6655 or via email at nitinw@secrecruitment.com

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Lead Business Systems ...

West London

£60 - £65 per hour

Our leading International Healthcare company is looking for a Lead IT Business Analyst to join them on an initial 6 month contract. You will be experienced as a Lead IT Business Analyst across multiple concurrent project workstreams and at different phases in their lifecycle. You will also need to liaise and manage teams across multiple locations. There may also be some limited international travel required. The role is based in London and of course initially this will be a remote based role until current lockdown restrictions are relaxed. Pharmaceutical / Healthcare experience would be highly desirable. All deliverables are focused on the deployment of commercial IT solutions to the clients external customers and internal commercial user base. * User groups span Healthcare Professionals, Customer and Patient Services, Sales, Marketing, Supply Chain and Medical Affairs. * The commercial applications are predominantly built on Salesforce.com / Veeva, as well as Oracle ERP; these platforms enable Case Management, CRM, Order-to-Cash and Plan-to-Make business processes. The successful consultant will: * Assume IT Business Analyst responsibility through the full life-cycle of multiple critical IT projects supporting the ACE (Australia, Canada and Europe) region. * Ensure submission of high-quality deliverables on time, to budget and agreed meeting agreed quality criteria. * Independently engage a diverse group of stakeholders across dispersed geographies and time-zones. * Independently develop and maintain requisite project documentation to a high standard - in line with specified standards. * Complete all requisite analysis for critical ACE IT products and projects - Including business cases, requirements definition, testing, security and compliance assessments etc. * Participate in performance management and governance ceremonies. Including project status reviews and stand-ups. * Participate in design reviews and represent the 'Voice of the Customer' to ensure great Customer Experience. * Support the development of mitigation plans for project risks, issues and dependencies. * Engage independently with end-users and business partners to ensure all projects meet business objectives. * Support the procurement of 3rd party products and services (e.g. RFP). * Participate in UAT and secure business sign-off for IT projects and initiatives. * Complete value-affirmation activities with business stakeholders and identify areas for continual improvement. * Ensure regular communication with all relevant stakeholder groups in a consistent and timely manner.

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Operations Director

Liège, Belgium

€75000 - €90000 per annum + car, bonus, benefits

Operations Director This is a great role for an experienced pharmaceutical manufacturing operations expert, looking to play a crucial role in a global pharma manufacturing company. The role will require someone to be part of the site management committee and oversee all the operations across production and distribution of a biopharmaceutical manufacturing plant. You will be managing a team as well as operations, and ensuring all budgets, projects and timelines are met effectively and efficiently. Salary & Benefits: €90k plus benefits, car and bonus Role and responsibilities: *You will be responsible for implementing and managing the operating strategy of the site's production and warehouse in conjunction with the Site Leadership Team *Determination of short-term, mid-term and long-term strategy and goals, deploying an explaining these strategies to all departments *Control the budgets for the departments, managing and adjusting the resources required, both for equipment and personnel *Lead investigations on production issues *Implement problem solving actions relating to product quality, for example CAPAs *Documentation management - SOPs, deviations, work instructions etc. *Make sure that the processes in the manufacturing and warehouse departments are running efficiently and on time *Supervise and directly line manage a team of 5; 4 Production Managers and 1 Warehouse Manager Requires skills and qualifications: *Scientific Degree with extensive work experience is required *10+ years' in working in Operations, ideally in aseptic manufacturing, but certainly within GMP environments (pharma experience preferred) *Solid experience in management - line managing experienced professionals *Very good project management and budget management experience *You must be business fluent level in both French and English This is a great opportunity to work with a market leader in biopharmaceuticals. The role will play a key part on a site of around 150 people that are actively making a difference to people's lives every day. You will experience excellent career growth and development and be part of a best-in-class team making great strides in the medical world. To apply for this position and put yourself under immediate consideration, send your CV to john.spring@secpharma.com or call +44 (0) 207 255 6650

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Senior Java Full Stack...

Brussels, Belgium

€500 - €600 per day

Senior JAVA Full Stack Engineer (minimum 7 years experience) Our leading International client are looking for a highly experienced Java Full Stack Developer. Scope: Build and maintain legacy application code with as end-goal transition to modern micro services architecture. Requirements Software: Excellent knowledge of Java 1.6. For future releases, Java 1.8+ (in general, we follow the LTS release of Java if technically possible). Excellent knowledge of GIT, ANT & MAVEN Excellent knowledge of JAVA EE5 EJB3 JAXB, XPath, Jaxen, JMS, IBM MQ Good knowledge of Plain JDBC & SQL, Struts 1.3.10 & JSP, Java Servlets, Apache POI for XLS, Json / Gson Being able to work with Testing: Junit 4, Mockito, Hamcrest, DbUnit, XML Unit Excellent knowledge of HMTL 5, especially Canvas, Javascript, CSS, Typescript Having knowledge of DevOps teams employing CI/CD pipelines. (Ansible / Bamboo) Having worked with Atlassian Tools (JIRA, Confluence, BitBucket, Bamboo) Good understanding of OWASP TOP 10 and secure code implementation Requirements English is mandatory, Dutch would be beneficial. Inquisitive and analytical mind with customer and end-user focus. Proven ability to work in a multi-cultural multi-functional environment where consensus is critical for success; Excellent oral and written communications skills. Candidate should Understand the underlying issues in most situations and relates some similarities between situations that are not obviously connected through the use of concepts, models or previous experiences. Candidate frequently identifies information gaps that are not immediately apparent and selects appropriate sources of information. If you are available soon and would be interested to know more then please contact Nitin on +44(0)207 255 6655 or via email at nitinw@secrecruitment.com.

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Senior GMP QA Manager

Zug, Switzerland

Swiss Franc140000 - Swiss Franc160000 per annum + benefits

Senior GMP QA Manager This is a fantastic opportunity to join a speciality pharmaceutical company in Switzerland, with a leading range of products in multiple therapy areas. The company has a global presence and has experienced dramatic accelerated growth in the past few years due to an increase in global demand for their products. This role will require an expert in Quality Assurance and pharmaceutical manufacturing to ensure global compliance with existing products on the market and also new products in development. Salary & Benefits: CHF 150k + benefits Role and responsibilities: *Ensure compliance to global cGMP standards for products including APIs, Bulk Drug Substances and Final Dosage Forms at external manufacturing partners (CMOs) *Provide QA support for Tech Transfer activities and manage process and method validation *Ensure GDP compliance, overseeing the distribution of pharmaceutical drug products across the world *Make sure that the internal QMS is inspection ready and functional at all times *Maintain the company documentation management system, authoring and updating QA procedures and policies *Oversee the risk management process - evaluation and mitigation *Mange the approval process for CMO documentation; CAPAs, change controls, customer complaints and deviations *Approve batch documentation according to GMP and GDP *Support supplier audits according to GMP and GDP Requires skills and qualifications: *Scientific Degree and background (ideally to Master's level minimum) *10+ years' experience in the pharmaceutical manufacturing industry with at least 5 years' experience in a QA Managerial role *Strong experience of working with various dosage forms including injectables, solid dosage forms and inhalation products *Expert knowledge in Tech Transfer activity *Fluent English as this is the company's main language This is a great role for an ambitious and dynamic QA Manager looking to join a fast growing and fast-paced company who have a solid track record in expanding into new markets with world-class products. If you are an expert in managing external suppliers relating to pharmaceutical manufacturing and want to take your career to the next stage, this is a perfect position for you. To apply for this position and put yourself under immediate consideration, send your CV to john.spring@secpharma.com or call +44 (0) 207 255 6600

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