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Company Jobs - AstraZeneca Pharmaceuticals



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Pharmaceutical Sales Specialist - EQ PC - Salisbury, MD

Salisbury MD

Qualifications: Education: -Bachelors degree (any major) from an accredited college or university is required. Experience: - Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required - Demonstrated effective organizational and communication skills - Leadership, self--motivation and initiative - Demonstrated judgment and decision-making capability - Be results oriented with demonstrated time management skills - Ability to learn, analyze, understand and convey complex information - Demonstrated technical aptitude and computer skills are essential - A valid driver's license and safe driving record

Posted On - 4/16/2014 7:12:06 AM

Pharmaceutical Sales Specialist - PM PC1 - Waterbury, CT

Waterbury CT

Qualifications: Education: -Bachelors degree (any major) from an accredited college or university is required. Experience: - Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required - Demonstrated effective organizational and communication skills - Leadership, self--motivation and initiative - Demonstrated judgment and decision-making capability - Be results oriented with demonstrated time management skills - Ability to learn, analyze, understand and convey complex information - Demonstrated technical aptitude and computer skills are essential - A valid driver's license and safe driving record

Posted On - 4/16/2014 7:12:06 AM

Warehouse Logistic Analyst

Newark DE

Minimum Requirements: * Bachelor of Science in business, engineering or other related discipline. * Working knowledge of cGMP, SHE, SOX policies and regulations * Three (3) yrs. experience in Pharmaceutical and /or other industry distribution and logistics management or related disciplines * Proven ability to work effectively in a team environment along with the ability to plan, organize and deliver the desired business results * Working knowledge of warehouse management systems * Self motivated and the ability to work independently * Demonstrated strong influencing, interpersonal and communication skills * Strong knowledge of production supply chain principles * Excellent analytical and problem solving skills Preferred Background: * Experience in GMP or regulated environment, specifically responsible for material logistics. * Receiving and inventory control within a computer / automated warehouse. * Working knowledge of SAP / WM, EZbuy, Trackwise, Microsoft applications. * Experience working in a LEAN-manufacturing environment. * Experience with inventory control management.

Posted On - 4/16/2014 7:12:06 AM

Diabetes Sales Specialist - D3 - Montpelier, VT

Montpelier VT

Qualifications: Education: -Bachelors degree (any major) from an accredited college or university is required. Experience: - Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required - Demonstrated effective organizational and communication skills - Leadership, self--motivation and initiative - Demonstrated judgment and decision-making capability - Be results oriented with demonstrated time management skills - Ability to learn, analyze, understand and convey complex information - Demonstrated technical aptitude and computer skills are essential - A valid driver's license and safe driving record

Posted On - 4/16/2014 7:12:06 AM

Pharmaceutical Sales Specialist - ONC - Grand Rapids, MI

Grand Rapids MI

Qualifications: EDUCATION: Bachelors degree No Company Relocation Assistance Provided. EXPERIENCE: At least two years of documented, successful pharmaceutical sales, or at the discretion of those involved in the hiring process, related sales to physicians and hospitals such as medical equipment. Experience selling and knowledge of Oncology products or diseases preferred. Breast and lung cancer drug sales experience strongly preferred for Oncology positions. History of building and influencing customer relationships, and goal achievement Demonstrated clinical selling skills Demonstrated ability to manage PREP budget and to work through the PRA process ADDITIONAL SKILLS: Knowledge of medical office equipment, territory management direct and in-direct sales processes Possess excellent written and verbal communications skills, and presentation skills Problem solving skills Business administration skills Laptop computer skills Managed Care knowledge including prior authorization successes, demonstrated understanding of managed care contracting Proven ability to understand, internalize, and routinely present challenging scientific information Effective communication abilities to include strong group presentation skills Ability to freely accept, implement, and exchange best practices

Posted On - 4/16/2014 7:12:06 AM

Diabetes Sales Specialist - DOV3 - Manchester, NH

Manchester NH

Qualifications: Education: -Bachelors degree (any major) from an accredited college or university is required. Experience: - Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required - Demonstrated effective organizational and communication skills - Leadership, self--motivation and initiative - Demonstrated judgment and decision-making capability - Be results oriented with demonstrated time management skills - Ability to learn, analyze, understand and convey complex information - Demonstrated technical aptitude and computer skills are essential - A valid driver's license and safe driving record

Posted On - 4/16/2014 7:12:06 AM

Diabetes Sales Specialist - D3 - Rapid City, SD

Rapid City SD

Qualifications: Education: -Bachelors degree (any major) from an accredited college or university is required. Experience: - Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required - Demonstrated effective organizational and communication skills - Leadership, self--motivation and initiative - Demonstrated judgment and decision-making capability - Be results oriented with demonstrated time management skills - Ability to learn, analyze, understand and convey complex information - Demonstrated technical aptitude and computer skills are essential - A valid driver's license and safe driving record

Posted On - 4/16/2014 7:12:06 AM

Diabetes Sales Specialist - D3 - Omaha N, NE

Omaha NE

Qualifications: Education: -Bachelors degree (any major) from an accredited college or university is required. Experience: - Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required - Demonstrated effective organizational and communication skills - Leadership, self--motivation and initiative - Demonstrated judgment and decision-making capability - Be results oriented with demonstrated time management skills - Ability to learn, analyze, understand and convey complex information - Demonstrated technical aptitude and computer skills are essential - A valid driver's license and safe driving record

Posted On - 4/16/2014 7:12:06 AM

Head of Diabetes Oral therapy

South East Cambridgeshire

Essential: Degree qualified, ideally with additional post-graduate qualification such as an MBA Significant pharmaceutical commercial experience with a strong performance track record Substantial experience in pharmaceutical marketing lead or sales management roles Desirable: Good experience of the UK market, with its unique NHS system In depth of knowledge of diabetes therapy area

Posted On - 4/16/2014 7:12:06 AM

Medical Science Director, Inflammation

Global Cambridgeshire

Accountabilities/Responsibilities: Clinical Trials Protection of human subjects in Clinical trials for all compounds the MSD is accountable for overseeing Adherence to the highest ethical standards of clinical trial conduct and GCP regulations concerning human subjects Ensuring delivery of clinical trials to time, cost and quality Global Product Team Ethical integrity of clinical plans Timely provision of medical/scientific strategies for clinical components of the TPP, TPC, Clinical development plans, and core labelling texts Design & Interpretation On behalf of the GPT, leads the design and interpretation activities; generates high quality design options that characterize benefit, risk, and value of medicinal products and focuses on reducing uncertainties for these, while adhering to design & interpretation best practices Leads discussions to identify the scientific direction and to identify the questions e.g. Design Remit which the next stage of the development programme needs to answer Ensures the alignment of program design activities with CPT (and therefore Global Product Team) objectives and requirements Ensures each clinical program has the proper expertise supporting its activities Accountable for the content and quality of all clinical program deliverables Accountable for all medical content of design & interpretation activities and, in particular, all activities involving assessment of the benefit and risk of the product Timely provision of scientific and medical components of commercial activities including the pricing & value strategy Benefit-risk assessments, risk management plans, and protection of human subjects in clinical studies Provides clear recommendations for clinical decision bodies and governance Together with the Director of Clinical Development, plans/decides resources for design & interpretation activities, and supports adherence to AZ standards Strategic leadership and supervision of team of physicians and scientists aligned to GPT and CPT objectives. Supports as appropriate within project during issue & crisis management as directed by VP Clinical GMed Minimum Requirements: Education and Experience Graduate of a recognized school of medicine with an M.D. degree or equivalent Demonstrated clinical research expertise in Rheumatology or Immunology Specialty training and board eligibility in Rheumatology or Immunology preferred Significant demonstrated leadership experience Extensive Drug Development experience Proven team leadership and collaboration skills. Broad influencing skills with ability to build effective relationships within Clinical Development and external environments. Requires focus on customer and business need. Willingness to travel nationally and internationally

Posted On - 4/16/2014 7:12:06 AM

Head of Diabetes Injectable therapy

South East Cambridgeshire

Essential: Degree qualified, ideally with additional post-graduate qualification such as an MBA Significant pharmaceutical commercial experience with a strong performance track record Substantial experience in pharmaceutical marketing lead or sales management roles Desirable: Good experience of the UK market, with its unique NHS system In depth of knowledge of diabetes therapy area

Posted On - 4/16/2014 7:12:06 AM

Corporate Affairs Associate/ Coordinator

Horizon Place (Luton) Bedfordshire

Accountabilities/Responsibilities - Provides professional and operational communications advice and support across the International and Europe CA functions contributing to enhanced reputation, achievement of CA and business objectives, positive media exposure and accessible, well presented publications - Responsible for supporting current, agreed and effective communications policies and guidelines - Produces and distributes accurate, timely and positive global leadership and regional communications within remit - Ensures contemporary, cost effective publications and web presence, including Intranet landing pages for International and Europe CA functions - Delivers high-level project management, including internal engagement events with external agencies and third party agencies - Researches relationships and supports meetings with external agencies and third party suppliers - Cross-functional management of internal and external relationships and customers needs - Content supervisor for Global Commercial/AVP SharePoint site - Provides administrative services to the VP, CA International and VP, CA Europe, coordinating complex meetings and off-site events, diary arrangements and travel in line with AZ policy - Co-ordinates, collates and communicates information at the detailed level, possibly of a technical or statistical nature - Ensures the production of reports or analyses, to meet quality standards, and provides interpretation of data - Reconciles figures or information from various sources, ensuring completeness and accuracy, and follow-up on discrepancies - Participates in establishing an understanding of (internal) customer requirements to ensure that planned activities and services meet needs, and in monitoring those services and activities to ensure requirements are fully met - Organises, controls and delivers specific clerical/administrative activities and coordinates the delivery of such above-market administrative support of the International and Europe Regional - Leads and motivates any assigned staff within defined parameters, ensuring they deliver their responsibilities effectively - May co-ordinate workflow management and mentors junior team members to ensure effective allocation of resources Minimum Requirements - Education and Experience Essential - Educated to degree level in relevant field or equivalent business experience - Proficient in one or more communication methods, media, web content etc - Prior Administrative experience - Ability to follow processes - Written and spoken communications - Specialist knowledge in relation to administrative/business support activities in the relevant Desirable - Professional communications experience and/or related qualification - Relevant vocational qualifications or equivalent experience - Team management skills

Posted On - 4/16/2014 7:12:06 AM

Stability Programme Manager - 12 month secondment

Alderley Park Cheshire

Accountabilities/Responsibilities For assigned products, through expert stability program knowledge and product overview: * Generate and maintain the Stability Master Plans and the supporting stability test protocol information (stability specifications, Stability Product Documents, stability packaging codes and packaging equivalencies, Global Stability QA system static data) * Ensure the global stability program fulfils all regulatory requirements, and is optimized and effective * Communicate of the Stability Master Plans to the Stability QC Centres * Translate stability sections in CMC documentation and Commitments into the Stability Master Plan * Assure the provision of accurate, submission ready stability data information that is in compliance with market specific Health Authority * Identify any issues that may result in stability related non-compliance with GMP, regulatory requirements or commitments * Maintain and update storage life records within S-Life * Seek opportunities for continuous improvement, across all aspects of global stability management Minimum Requirements - Education and Experience * University Degree in Chemistry or equivalent * Substantial experience in Pharmaceutical Production, Quality Assurance, Quality Control, Regulatory Affairs or Analytical or Formulation Development within R&D * Good awareness of pharmaceutical stability testing, stability management processes, regulatory requirements related to global stability management and cGMP * Knowledge of/ experience in analytical chemistry * Strong experience in use of IT Software (document and laboratory information management systems) * Understanding of the Operations Function. Skills & Capabilities * Strong communication skills (listening, verbal and written in English) * Excellent team working skills * Accurate and thorough information handling * Recognises different perspectives and is able to communicate well with others to influence positive outcomes.

Posted On - 4/16/2014 7:12:06 AM

Device Quality Manager

Macclesfield Cheshire

Please note that the role will be based in either Macclesfield (UK) / Sodertalje (SE) / Ohio (US) Accountabilities/Responsibilities * Development and implementation of AZs approach for effective compliance management for commercialised AZ Devices and Combination Products, including maintenance of Design History files * Owner of the Quality Management System for Medical devices and combination products and ensure there is a robust process for reporting and analysis of quality metrics, as appropriate * Monitor emerging legislation, in relation to devices and where needed lead improvements to our quality management processes to assure future compliance with legislation. This may include leadership of change programmes to ensure Global Compliance with device related legislation * Ensure robust quality management processes are built into the device development processes, ensuring a robust regulatory strategy and to ensure that good quality Deign History files are transferred from Pharmaceutical Development and external partners to Operations sites * Support device sites and CMOs to ensure quality and robustness of Design History Files for commercial products and ensure a consistent approach is adopted * Support device teams in identification and delivery of continuous improvement initiatives (e.g. in response to product complaints) for their device portfolio and ensure robust change management and control processes are used * Work collaboratively with sites and CMOs to ensure effective resolution of complex device issues up to and including local management of device related IMTs. Manage alert processes to national regulators where serious non conformances are identified for products distributed in market, following the IMT decision making process * Lead and/or support sites and device teams to ensure a responsible and compliant approach to quality risk management is adopted, including design reviews, for all commercial devices * Provision of support to WWAG to audit sites and CMOs that manufacture devices, by ensuring device requirements and legislation are built into routine audits * Proactively support sites with preparations and management of device related external audits, including those from registered bodies e.g. G-MED. Ensure observations from external audits are acted upon to facilitate continuous improvement of the quality management system. All these activities will have a significant impact on the overall success of Operations as well as ensuring the quality and commercial viability of commercialised device products. The activities of the team help to ensure availability of all AstraZeneca device products to the commercial organisation. The role, therefore, has an impact on both financial and reputational aspects of the business. Minimum Requirements - Education and Experience * Likely to be educated to BSc level, with relevant experience in an appropriate discipline and have professional credibility within the business and industry * Experience in multiple areas of quality assurance within a Pharmaceutical manufacturing environment (including Medical Device and Combination Products) * Sound knowledge and understanding of the principles and concepts of quality and compliance management and device quality management systems * Knowledge of cGMP audit processes and procedures * Experience of participation in inspections from external regulatory bodies * Have an understanding of the overall drug and device development and commercialization process from development, launch and through life cycle management * Have a thorough understanding of principles, applications and management of SHE, cGMP, including a deep understanding of device standards and legislation * Experience in Operations and/or R&D, with a track record of successful delivery within a matrix organization * Evidence of excellent communication skills and building excellent relationships with customers Skills & Capabilities * Operates confidently as a part of a global organisation, with an integrating mindset, irrespective of function, geographical and company background to help to deliver an organisation prepared for future challenges and change. Demonstrates understanding of change management * Excellent team working and networking skills and ability to engage relevant AstraZeneca staff * Capable of making effective decisions, acting courageously and communicating with conviction * An excellent communicator with experience of interacting effectively across interfaces of discipline, culture, and expertise both internally and externally * Able to demonstrate the drive and energy to establish the role and make a difference * Demonstrate a high degree of personal credibility * Focus on delivery under pressure * Lead change effectively * Influencing skills to enable effective management of internal stakeholders and external partners * Good communication skills * Networking skills that enable the necessary links to be formed that allows the group to have high business impact * Work collaboratively across boundaries * Personal Technical capability development

Posted On - 4/16/2014 7:12:06 AM

Device Technical Director

Macclesfield Cheshire

Minimum Requirements - Education and Experience * Have an understanding of the overall drug and device development and commercialization process from development, launch and through life cycle management * Significant experience of working with devices as a device design engineer or device quality engineer working in product development and/or operations * Likely to be educated to PhD level or BSc with experience in an appropriate discipline and have professional credibility within the business and industry * Have understanding in the disciplines in Packaging and Device development, analytical, formulation and physical Science and global supply chain in order to identify appropriate solutions for management of devices and deliver value to the organisation * Have a thorough understanding of principles, applications and management of SHE, cGMP and medication device/combination product standards and legislation * Experience in Operations and/or R&D with a track record of successful delivery within a matrix organization * Evidence of excellent communication skills and building excellent relationships with customers. Skills & Capabilities * Operates confidently as a part of a global organisation, with an integrating mindset, irrespective of function, geographical and company background to help to deliver an organisation prepared for future challenges and change. Demonstrates understanding of change management * Excellent team working and networking skills and ability to engage relevant AstraZeneca staff * Capable of making effective decisions, acting courageously and communicating with conviction * An excellent communicator with experience of interacting effectively across interfaces of discipline, culture, and expertise both internally and externally * Able to demonstrate the drive and energy to establish the role and make a difference * Demonstrate a high degree of personal credibility * Focus on delivery under pressure * Lead change effectively * Influencing skills to enable effective management of internal stakeholders and external partners * Good communication skills * Networking skills that enable the necessary links to be formed that allows the group to have high business impact * Work collaboratively across boundaries * Personal Technical capability development

Posted On - 4/16/2014 7:12:06 AM

Device Technical Manager

Macclesfield Cheshire

Accountabilities/Responsibilities * The optimisation of Chemistry Manufacturing & Control (CMC) and Device related labelling activities for specified Drug Products in Devices in collaboration with Pharmaceutical Development (R&D) * Part of the development team for Device Products, ensure device quality and manufacturability are built into the development process to ensure good process robustness from launch * Support device sites to ensure quality and robustness of design history files and support sites will key device maintenance activities such as periodic risk reviews * Ensure risk assessment/management is fully built into the development and products maintenance processes * Immediate first line technical expertise to aid the resolution of potential product recall incidents * The provision of product technical expertise to Operations sites that manufacture devices and external partners via GES and central functions within Operations e.g. Global Supply Chain, Global Quality * Influence decisions at sites in respect to investments and asset utilisation * Programme management of a number of improvement initiatives and establishment of business processes and requisite supply chain and quality management for devices * Identification and delivery of continuous improvement initiatives for their device portfolio * Responsible for the device related technical support during the transfer of established products and major brands to external manufacturing partners in the region * The identification and delivery of device related technical support for any major change initiatives (e.g. sourcing and asset strategy driven changes) * Develop technical solutions to a diverse range of problems based on sound analytical and conceptual thinking All these activities will have a significant impact on the overall success of Operations as well as ensuring the commercial viability of current device products. The activities of the team help to ensure availability of all AstraZeneca device products to the commercial organisation. The role, therefore, has an impact on both financial and reputational aspects of the business. Minimum Requirements - Education and Experience * Have an understanding of the overall drug and device development and commercialization process from development, launch and through life cycle management * Experience of working with devices as a device design engineer or device quality engineer working in product development and/or operations * Likely to be educated to PhD or BSc level with experience in an appropriate discipline and have professional credibility within the business and industry * Have understanding in the disciplines in Packaging and Device development, analytical, formulation and physical Science and global supply chain in order to identify appropriate solutions for management of devices and deliver value to the organisation * Have a thorough understanding of principles, applications and management of SHE, cGMP and Device standards and legislation * Experience in Operations and/or R&D with a track record of successful delivery within a matrix organization * Evidence of excellent communication skills and building excellent relationships with customers Skills & Capabilities * Operates confidently as a part of a global organisation, with an integrating mindset, irrespective of function, geographical and company background to help to deliver an organisation prepared for future challenges and change. Demonstrates understanding of change management * Excellent team working and networking skills and ability to engage relevant AstraZeneca staff * Capable of making effective decisions, acting courageously and communicating with conviction * An excellent communicator with experience of interacting effectively across interfaces of discipline, culture, and expertise both internally and externally * Able to demonstrate the drive and energy to establish the role and make a difference * Demonstrate a high degree of personal credibility

Posted On - 4/16/2014 7:12:06 AM

Principal Scientist

Macclesfield Cheshire

Minimum Requirements * Strong scientific background such as PhD with extensive experience within the business and industry * Good knowledge of the regulatory requirements for Medical Devices and combination products (e.g. ISO13485, QSR) * Have a good understanding of the overall drug development process from discovery through to launch with an appreciation of how Pharmaceutical Development contributes to R&D and the broader business * Ability to analyse and interpret complex situations and provide clear strategic directions for others. Passionate in science with a drive to make an impact * Results-focus and ability to deliver projects through strategic influence and relationship management versus direct line management * Excellent team working and net working skills and encourages team effectiveness * Be an excellent communicator both internally and externally * Possess strength and independence of viewpoint and be willing to challenge others when appropriate * Constructively challenging ideas to achieve best outcome for AZ * Strong interpersonal, motivational, coaching and leadership skills - experience of leading multi-disciplinary teams, line and matrix * Excellent written and verbal communication skills, negotiation, collaboration and interpersonal skills Knowledge of the commercialization and lifecycle management of products * Good understanding/knowledge of the overall medicines development process and knowledge of how Pharm Dev contributes to the R&D and the broader business Please Note, interviews for this role are scheduled to take place on Thursday 25th April.

Posted On - 4/16/2014 7:12:06 AM

Diabetes Sales Specialist - D3 - Lincoln, NE

Lincoln NE

Qualifications: Education: -Bachelors degree (any major) from an accredited college or university is required. Experience: - Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required - Demonstrated effective organizational and communication skills - Leadership, self--motivation and initiative - Demonstrated judgment and decision-making capability - Be results oriented with demonstrated time management skills - Ability to learn, analyze, understand and convey complex information - Demonstrated technical aptitude and computer skills are essential - A valid driver's license and safe driving record

Posted On - 4/15/2014 7:11:25 AM

Sr. Analyst, Microbiology

West Chester OH

QUALIFICATIONS: Education BS in a scientific discipline with at least 5 years of related experience; pharmaceutical or biotech experience highly preferred. Experience/Skills * A minimum of 3 years direct experience in Microbiology is required with previous manufacturing experience. Experience in pharmaceutical operations is required. * Candidate must display strong interpersonal skills, along with strong organizational abilities. Solid technical writing and documentation skills are required; the ability to communicate effectively and interact with multi-disciplinary teams is required. REQUIREMENTS: Physical Demands Occasional overtime, shift work and weekends will be required. Manual Dexterity Unimpaired Manual Dexterity Audible/Visual Demands Vision equal to or better than 20/20 Environment Lab, Manufacturing and Office

Posted On - 4/15/2014 7:11:25 AM

Analyst II, IT

West Chester OH

Required Experience/Skills: * Bachelors degree in Computer Science, Information Technology, or a related field; or a combination of relevant education, certifications and/or work experience * Minimum 3 years experience in server and data center administration * Minimum 3 years experience with networked/distributed computing environment * Expert level skill working with server and workstation hardware configuration (HP Preferred) and server OS configuration (Windows 2003/2008, XP/7). * Proficiency in Active Directory, Various imaging and backup software (Commvault, Symantec BESR preferred), VMware and AntiVirus * Must understand TCP/IP and network hardware * Strong customer service skills * Excellent written, verbal and presentation skills Desired Experience/Skills: * Biopharmaceutical or regulated environment experience * Experience with Cisco IOS Physical Demands: * Ability to lift up to 50 pounds Environment: * Exposure to potentially hazardous chemicals, biohazards. Work performed in a manufacturing, laboratory or office environment

Posted On - 4/15/2014 7:11:25 AM

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