Perrigo Perrigo Company is dedicated to making lives better by bringing high quality and affordable self-care products that consumers trust everywhere they are sold. Help us do it. The Director of Consumer Insights will lead this new function within Perrigo that will primarily support the Consumer Self-Care Americas’ major business units. This newly created function will support the validation and prioritization of consumer driven innovation inclusive of products, programs, and messaging, developed by the Marketing organizations in support of our transformation to a self-care business. This team will unlock meaningful consumer insights that differentiate our products in order to meet consumer needs and expectations for Self-Care. The Director of Consumer Insights will oversee the company’s custom consumer research and product testing, and syndicated consumer research. The Director’s main responsibilities include: Support all existing business segments within Consumer Self-Care Americas, with a reporting structure into the SVP of OTC Business, and the company’s initiatives in innovation and new consumer brand development with innovative new products, segments and technologies. Field and lead consumer insight research, custom product research design, test market design, and advertising research. Oversee brand and store brand syndicated analysis to support the business segments as well as identify key consumer trends. Participate in the development of the applicable marketing strategic plans and analytical learning agendas Requirements: Bachelor’s degree in Business, Marketing or closely allied field, with a master’s degree preferred. Ten plus years of progressive marketing leadership experience specific to CPG (consumer and syndicated market data knowledge) and new product experience. Exceptional leadership and communication skills, including well-developed interpersonal skills and strong written communication skills. Sound financial management skills combined with strong negotiating experience are required. Superior leadership skills with ability to manage and develop teams and manage multiple projects. Demonstrated ability to manage senior executive relations and ability to collaborate and build relations with stakeholders across functional and organization lines, and enterprise-wide program development and management skills. Knowledge of and experience with technology tools to support the marketing function, including excellent computer skills. Equal Employment Opportunity/M/F/disability/protected veteran status. PI116176682
Dec 10, 2019
Perrigo Perrigo Company is dedicated to making lives better by bringing high quality and affordable self-care products that consumers trust everywhere they are sold. Help us do it. The Director of Consumer Insights will lead this new function within Perrigo that will primarily support the Consumer Self-Care Americas’ major business units. This newly created function will support the validation and prioritization of consumer driven innovation inclusive of products, programs, and messaging, developed by the Marketing organizations in support of our transformation to a self-care business. This team will unlock meaningful consumer insights that differentiate our products in order to meet consumer needs and expectations for Self-Care. The Director of Consumer Insights will oversee the company’s custom consumer research and product testing, and syndicated consumer research. The Director’s main responsibilities include: Support all existing business segments within Consumer Self-Care Americas, with a reporting structure into the SVP of OTC Business, and the company’s initiatives in innovation and new consumer brand development with innovative new products, segments and technologies. Field and lead consumer insight research, custom product research design, test market design, and advertising research. Oversee brand and store brand syndicated analysis to support the business segments as well as identify key consumer trends. Participate in the development of the applicable marketing strategic plans and analytical learning agendas Requirements: Bachelor’s degree in Business, Marketing or closely allied field, with a master’s degree preferred. Ten plus years of progressive marketing leadership experience specific to CPG (consumer and syndicated market data knowledge) and new product experience. Exceptional leadership and communication skills, including well-developed interpersonal skills and strong written communication skills. Sound financial management skills combined with strong negotiating experience are required. Superior leadership skills with ability to manage and develop teams and manage multiple projects. Demonstrated ability to manage senior executive relations and ability to collaborate and build relations with stakeholders across functional and organization lines, and enterprise-wide program development and management skills. Knowledge of and experience with technology tools to support the marketing function, including excellent computer skills. Equal Employment Opportunity/M/F/disability/protected veteran status. PI116176682
Perrigo Perrigo Company is dedicated to making lives better by bringing high quality and affordable self-care products that consumers trust everywhere they are sold. Help us do it. Job Overview: Position provides technical expertise and support to drug development programs executed by Strategic Partnership companies. The role assures Perrigo technical input into all aspects of drug development, FDA regulatory submissions and commercial product launch. As a result of the job responsibilities, this role may sit at a Perrigo site location or be remote, depending on the selected candidates qualifications and circumstances. Core Job Knowledge: Demonstrated hands-on experience in designing/developing at least two to three different types of dosage forms that include transdermal patches, metered-dose and dry powder inhalers, modified-release oral solids, and sterile dosage forms (ophthalmic solutions and suspensions, lyophilized injectables, pre-filled syringes and long-acting injectables), combination drug-device products. Hands-on experience in formulation/analytical development by quality-by design, scale-up and technical-transfer, process validation for the complex generics. Experience in working with CMOs and partnership companies in developing complex generics Ability to critically evaluate data, identify trends and draw accurate conclusions. Able to work through complex problems with a systematic approach. Competency in managing project milestones and timelines. Knowledgeable in FDA regulatory processes and ANDA data requirements. Strong interpersonal communication skills and well-developed collaborative management skills. Ability to work effectively across various drug development disciplines. Excellent writing skills in both technical and business writing. Education and Experience: Minimum B.S. degree in a scientific discipline and 8+ years of pharma industry experience. Responsibilities: Collaborate with partnership companies and CMOs to establish product development strategies, scale-up, data expectations for FDA submissions, develop project timelines / milestones and commercial launch planning. Provide recommendations for pilot, exhibit, bio, scale-up batch and process validation strategies that satisfy all bioequivalence, submission and commercial launch requirements Technical review of product development reports, product characterization data, batch records, process optimization and validation reports. Propose solutions to unexpected product formulation, manufacture and testing issues. Perform on-site visits to partner manufacturing facilities to audit data and records Research and review technical literature e.g., summary basis of approval, Drug Master Files, related FDA guidance, applicable patents, bench-marking technologies, etc. Draft and edit technical responses to FDA review questions and meeting packages Support due diligence assessments on new partnership opportunities for the Rx business Equal Employment Opportunity/M/F/disability/protected veteran status. PI116144936
Dec 08, 2019
Perrigo Perrigo Company is dedicated to making lives better by bringing high quality and affordable self-care products that consumers trust everywhere they are sold. Help us do it. Job Overview: Position provides technical expertise and support to drug development programs executed by Strategic Partnership companies. The role assures Perrigo technical input into all aspects of drug development, FDA regulatory submissions and commercial product launch. As a result of the job responsibilities, this role may sit at a Perrigo site location or be remote, depending on the selected candidates qualifications and circumstances. Core Job Knowledge: Demonstrated hands-on experience in designing/developing at least two to three different types of dosage forms that include transdermal patches, metered-dose and dry powder inhalers, modified-release oral solids, and sterile dosage forms (ophthalmic solutions and suspensions, lyophilized injectables, pre-filled syringes and long-acting injectables), combination drug-device products. Hands-on experience in formulation/analytical development by quality-by design, scale-up and technical-transfer, process validation for the complex generics. Experience in working with CMOs and partnership companies in developing complex generics Ability to critically evaluate data, identify trends and draw accurate conclusions. Able to work through complex problems with a systematic approach. Competency in managing project milestones and timelines. Knowledgeable in FDA regulatory processes and ANDA data requirements. Strong interpersonal communication skills and well-developed collaborative management skills. Ability to work effectively across various drug development disciplines. Excellent writing skills in both technical and business writing. Education and Experience: Minimum B.S. degree in a scientific discipline and 8+ years of pharma industry experience. Responsibilities: Collaborate with partnership companies and CMOs to establish product development strategies, scale-up, data expectations for FDA submissions, develop project timelines / milestones and commercial launch planning. Provide recommendations for pilot, exhibit, bio, scale-up batch and process validation strategies that satisfy all bioequivalence, submission and commercial launch requirements Technical review of product development reports, product characterization data, batch records, process optimization and validation reports. Propose solutions to unexpected product formulation, manufacture and testing issues. Perform on-site visits to partner manufacturing facilities to audit data and records Research and review technical literature e.g., summary basis of approval, Drug Master Files, related FDA guidance, applicable patents, bench-marking technologies, etc. Draft and edit technical responses to FDA review questions and meeting packages Support due diligence assessments on new partnership opportunities for the Rx business Equal Employment Opportunity/M/F/disability/protected veteran status. PI116144936
Perrigo Perrigo Company is dedicated to making lives better by bringing high quality and affordable self-care products that consumers trust everywhere they are sold. Help us do it. Perrigo Company plc is a leading global healthcare supplier that develops, manufactures and distributes over-the-counter (OTC) and prescription (Rx) pharmaceuticals, nutritional products, and active pharmaceutical ingredients (API). As a QC Chemist, you will perform analytical testing on samples relative to the release of Perrigo materials and product according to cGMP requirements. These positions vary, but will be off shift opportunities on 2nd, or Weekend rotations. Perrigo offers competitive wages, including off shift premiums, as well as a comprehensive benefit package that includes medical, dental, vision, a comprehensive wellness program with an onsite fitness center, tuition reimbursement, holiday time, paid time off and more! Responsibilities: Collect samples including raw material, finished product, process equipment and environmental. Test purchased materials and/or Perrigo manufactured products per cGMP requirements and participate in laboratory investigations. Operate laboratory equipment. Participate in internal and external quality audits. Maintain personal laboratory work area and assist with general laboratory cleaning. Participate in training and development. Qualifications: Bachelor of Science in a scientific discipline (Chemistry or Food Science preferred, Biology) which includes academic lab experience. Minimum of 1-2 years' experience working in a GMP/FDA regulated manufacturing environment. Good written and verbal communication skills, excellent documentation and organizational skills. Demonstrated critical thinking skills, attention to detail, and the ability to work independently and with others. Ability to take ownership of assigned tasks and responsibility for the results. Ability to work overtime as required. Equal Employment Opportunity/M/F/disability/protected veteran status. PI116053051
Dec 05, 2019
Perrigo Perrigo Company is dedicated to making lives better by bringing high quality and affordable self-care products that consumers trust everywhere they are sold. Help us do it. Perrigo Company plc is a leading global healthcare supplier that develops, manufactures and distributes over-the-counter (OTC) and prescription (Rx) pharmaceuticals, nutritional products, and active pharmaceutical ingredients (API). As a QC Chemist, you will perform analytical testing on samples relative to the release of Perrigo materials and product according to cGMP requirements. These positions vary, but will be off shift opportunities on 2nd, or Weekend rotations. Perrigo offers competitive wages, including off shift premiums, as well as a comprehensive benefit package that includes medical, dental, vision, a comprehensive wellness program with an onsite fitness center, tuition reimbursement, holiday time, paid time off and more! Responsibilities: Collect samples including raw material, finished product, process equipment and environmental. Test purchased materials and/or Perrigo manufactured products per cGMP requirements and participate in laboratory investigations. Operate laboratory equipment. Participate in internal and external quality audits. Maintain personal laboratory work area and assist with general laboratory cleaning. Participate in training and development. Qualifications: Bachelor of Science in a scientific discipline (Chemistry or Food Science preferred, Biology) which includes academic lab experience. Minimum of 1-2 years' experience working in a GMP/FDA regulated manufacturing environment. Good written and verbal communication skills, excellent documentation and organizational skills. Demonstrated critical thinking skills, attention to detail, and the ability to work independently and with others. Ability to take ownership of assigned tasks and responsibility for the results. Ability to work overtime as required. Equal Employment Opportunity/M/F/disability/protected veteran status. PI116053051
Perrigo Perrigo Company is dedicated to making lives better by bringing high quality and affordable self-care products that consumers trust everywhere they are sold. Help us do it. This position will be the primary liaison for Perrigo and its Material or External Manufacturing Suppliers for Perrigo’s sites. The Supplier Relationship Manager (SRM) will work closely with our suppliers to ensure customer service, quality and supply chain standards are met for their assigned category through understanding of domestic and international logistics, shipment tracking etc. This position is responsible for coordinating procurement activities for required materials and execution of tactical procurement processes while complying with global procurement policies and procedures, and participating with global sourcing teams. A significant part of the Associate SRM position may require day-to-day activities that support material flow to the plants (MRP review, Purchase Order management, etc.). This position will require compliance with the Global Procurement RACI that outlines requirements regarding interaction with the global supply base (e.g., negotiation, communication, etc.). Requirements: Bachelor degree is required. Major in business, supply chain, materials management, or a related field are preferred. 1- 3 years of procurement/Perrigo experience in the Pharma, Food, or Medical Device industry is also preferred. Problem solving skills, sound decision making skills, and demonstrated ability to work independently, as well as on a team, and meet tight deadlines within a fast-paced environment are critical to the position’s success. The ideal candidate would have a good understanding of Good Distribution Practices and possess strong PC skills (word-processing, spreadsheet); SAP experience preferred. Excellent verbal and written communication skills, including proven ability to represent Perrigo in a professional manner. Demonstrated ability to prioritize, handle interruptions, and perform multiple tasks simultaneously to successfully meet daily goals is required. Equal Employment Opportunity/M/F/disability/protected veteran status. PI115841941
Nov 27, 2019
Perrigo Perrigo Company is dedicated to making lives better by bringing high quality and affordable self-care products that consumers trust everywhere they are sold. Help us do it. This position will be the primary liaison for Perrigo and its Material or External Manufacturing Suppliers for Perrigo’s sites. The Supplier Relationship Manager (SRM) will work closely with our suppliers to ensure customer service, quality and supply chain standards are met for their assigned category through understanding of domestic and international logistics, shipment tracking etc. This position is responsible for coordinating procurement activities for required materials and execution of tactical procurement processes while complying with global procurement policies and procedures, and participating with global sourcing teams. A significant part of the Associate SRM position may require day-to-day activities that support material flow to the plants (MRP review, Purchase Order management, etc.). This position will require compliance with the Global Procurement RACI that outlines requirements regarding interaction with the global supply base (e.g., negotiation, communication, etc.). Requirements: Bachelor degree is required. Major in business, supply chain, materials management, or a related field are preferred. 1- 3 years of procurement/Perrigo experience in the Pharma, Food, or Medical Device industry is also preferred. Problem solving skills, sound decision making skills, and demonstrated ability to work independently, as well as on a team, and meet tight deadlines within a fast-paced environment are critical to the position’s success. The ideal candidate would have a good understanding of Good Distribution Practices and possess strong PC skills (word-processing, spreadsheet); SAP experience preferred. Excellent verbal and written communication skills, including proven ability to represent Perrigo in a professional manner. Demonstrated ability to prioritize, handle interruptions, and perform multiple tasks simultaneously to successfully meet daily goals is required. Equal Employment Opportunity/M/F/disability/protected veteran status. PI115841941
Perrigo Perrigo Company is dedicated to making lives better by bringing high quality and affordable self-care products that consumers trust everywhere they are sold. Help us do it. This position will be the primary liaison for Perrigo and its Material or External Manufacturing Suppliers for Perrigo’s sites. The Supplier Relationship Manager (SRM) will work closely with our suppliers to ensure customer service, quality and supply chain standards are met for their assigned category through understanding of domestic and international logistics, shipment tracking etc. This position is responsible for coordinating procurement activities for required materials and execution of tactical procurement processes while complying with global procurement policies and procedures, and participating with global sourcing teams. A significant part of the Associate SRM position may require day-to-day activities that support material flow to the plants (MRP review, Purchase Order management, etc.). This position will require compliance with the Global Procurement RACI that outlines requirements regarding interaction with the global supply base (e.g., negotiation, communication, etc.). Requirements: Bachelor degree is required. Major in business, supply chain, materials management, or a related field are preferred. 1- 3 years of procurement/Perrigo experience in the Pharma, Food, or Medical Device industry is also preferred. Problem solving skills, sound decision making skills, and demonstrated ability to work independently, as well as on a team, and meet tight deadlines within a fast-paced environment are critical to the position’s success. The ideal candidate would have a good understanding of Good Distribution Practices and possess strong PC skills (word-processing, spreadsheet); SAP experience preferred. Excellent verbal and written communication skills, including proven ability to represent Perrigo in a professional manner. Demonstrated ability to prioritize, handle interruptions, and perform multiple tasks simultaneously to successfully meet daily goals is required. Equal Employment Opportunity/M/F/disability/protected veteran status. PI115841957
Nov 27, 2019
Perrigo Perrigo Company is dedicated to making lives better by bringing high quality and affordable self-care products that consumers trust everywhere they are sold. Help us do it. This position will be the primary liaison for Perrigo and its Material or External Manufacturing Suppliers for Perrigo’s sites. The Supplier Relationship Manager (SRM) will work closely with our suppliers to ensure customer service, quality and supply chain standards are met for their assigned category through understanding of domestic and international logistics, shipment tracking etc. This position is responsible for coordinating procurement activities for required materials and execution of tactical procurement processes while complying with global procurement policies and procedures, and participating with global sourcing teams. A significant part of the Associate SRM position may require day-to-day activities that support material flow to the plants (MRP review, Purchase Order management, etc.). This position will require compliance with the Global Procurement RACI that outlines requirements regarding interaction with the global supply base (e.g., negotiation, communication, etc.). Requirements: Bachelor degree is required. Major in business, supply chain, materials management, or a related field are preferred. 1- 3 years of procurement/Perrigo experience in the Pharma, Food, or Medical Device industry is also preferred. Problem solving skills, sound decision making skills, and demonstrated ability to work independently, as well as on a team, and meet tight deadlines within a fast-paced environment are critical to the position’s success. The ideal candidate would have a good understanding of Good Distribution Practices and possess strong PC skills (word-processing, spreadsheet); SAP experience preferred. Excellent verbal and written communication skills, including proven ability to represent Perrigo in a professional manner. Demonstrated ability to prioritize, handle interruptions, and perform multiple tasks simultaneously to successfully meet daily goals is required. Equal Employment Opportunity/M/F/disability/protected veteran status. PI115841957
Perrigo Perrigo Company is dedicated to making lives better by bringing high quality and affordable self-care products that consumers trust everywhere they are sold. Help us do it. The Global Indirect Sourcing Manager is primarily responsible for the strategic sourcing and negotiation of multiple complex spend categories to ensure cost effectiveness and performance standards in direct alignment with Perrigo’s Global Procurement strategy, category management structure, supplier management methodology and performance objectives. Collaborates with the Global Stakeholders to deliver best value global products and solutions to the company and its clients. Responsibilities of the role include but are not limited to: Savings – Review and manage category spend and identify opportunities for cost improvements without negatively impacting quality of service Benchmark Best Practices and Industry trends with Internal and external business partners to build a pipeline of savings and value creation opportunities Develop the Sourcing category strategies Lead the engagement with the required internal stakeholders to drive main initiatives and projects Represent Procurement in multi-functional initiatives RFx Project Management - Responsible for the end to end management of the sourcing process through collaboration and consultation with business stakeholders. Contract Management – Partner with the Procurement Legal Team to manage contract redlines and Terms of Business. Implement Statements of Work for inbound services Supplier Performance Management - Monitor performance and delivery of contracted services within your categories Reporting - Spend analysis and Budgetary investigation Requirements for the role include: Bachelor's degree is required, in a business related field is highly preferred Minimum of 7 years experience in leading Procurement Organization Proven ability to manage high spend, high complexity Global RFx processes with demonstrable competency in all stages of the sourcing process for all categories of Indirect Procurement and specifically with experience of Marketing category Knowledge on best practices and main industry trends Ability to work under pressure with changing priorities and bold targets for deliveries in terms of Cost reductions, Innovation, Cash Flow and Value Creation Solid track record meeting substantial savings targets Strong negotiation and influencing skills High level understanding of Contract Terms and Conditions for Marketing agreements Excellent written and verbal communication skills Excellent organizational and problem-solving skills Ability to handle multiple tasks, with awareness of deadlines Ability to identify processes needing improvement, and to recommend improvement Advanced MS Office skills in Excel, Word, Power Point, Outlook SAP knowledge and navigation skills Equal Employment Opportunity/M/F/disability/protected veteran status. PI115675544
Nov 22, 2019
Perrigo Perrigo Company is dedicated to making lives better by bringing high quality and affordable self-care products that consumers trust everywhere they are sold. Help us do it. The Global Indirect Sourcing Manager is primarily responsible for the strategic sourcing and negotiation of multiple complex spend categories to ensure cost effectiveness and performance standards in direct alignment with Perrigo’s Global Procurement strategy, category management structure, supplier management methodology and performance objectives. Collaborates with the Global Stakeholders to deliver best value global products and solutions to the company and its clients. Responsibilities of the role include but are not limited to: Savings – Review and manage category spend and identify opportunities for cost improvements without negatively impacting quality of service Benchmark Best Practices and Industry trends with Internal and external business partners to build a pipeline of savings and value creation opportunities Develop the Sourcing category strategies Lead the engagement with the required internal stakeholders to drive main initiatives and projects Represent Procurement in multi-functional initiatives RFx Project Management - Responsible for the end to end management of the sourcing process through collaboration and consultation with business stakeholders. Contract Management – Partner with the Procurement Legal Team to manage contract redlines and Terms of Business. Implement Statements of Work for inbound services Supplier Performance Management - Monitor performance and delivery of contracted services within your categories Reporting - Spend analysis and Budgetary investigation Requirements for the role include: Bachelor's degree is required, in a business related field is highly preferred Minimum of 7 years experience in leading Procurement Organization Proven ability to manage high spend, high complexity Global RFx processes with demonstrable competency in all stages of the sourcing process for all categories of Indirect Procurement and specifically with experience of Marketing category Knowledge on best practices and main industry trends Ability to work under pressure with changing priorities and bold targets for deliveries in terms of Cost reductions, Innovation, Cash Flow and Value Creation Solid track record meeting substantial savings targets Strong negotiation and influencing skills High level understanding of Contract Terms and Conditions for Marketing agreements Excellent written and verbal communication skills Excellent organizational and problem-solving skills Ability to handle multiple tasks, with awareness of deadlines Ability to identify processes needing improvement, and to recommend improvement Advanced MS Office skills in Excel, Word, Power Point, Outlook SAP knowledge and navigation skills Equal Employment Opportunity/M/F/disability/protected veteran status. PI115675544
Perrigo Perrigo Company is dedicated to making lives better by bringing high quality and affordable self-care products that consumers trust everywhere they are sold. Help us do it. The primary responsibilities of the Sr. Financial Analyst for our Corporate FP&A role is to support global financial planning and review processes including annual and long term plans, monthly/quarterly business reviews, flex updates and preparation of earnings call information. This role requires strong collaboration with Business Unit CFO’s, Global Tax, Global Operations Finance, Investor Relations and Accounting and Reporting teams amongst others. Responsibilities: Playing a key role in the Perrigo Annual Planning processes. Duties include supporting the activities of all relevant global stakeholders, support in maintaining detail project plan, identifying and resolving issues and providing status updates to the Director and Manager of FP&A. This may also include interaction and collaboration with the Global Tax, Global Operations Finance functions, and Business Unit Finance leaders to appropriately forecast acquisitions and intercompany activity. Providing key support to the completion of the quarterly flex update process and consolidation of information for the Quarterly Business Unit reviews, including preparation of the analysis and supporting presentation to the Executive Committee. Preparation of monthly ad hoc analysis including: working capital trends, global departmental spend, departmental spend; etc. Supporting the CEO, CFO and Investor Relations team with the preparation of quarterly analyst call materials, reviewing what is prepared by other members and supporting the analysts in the aggregation of all materials received. Leading process improvements and strategic initiatives within functional area. Proven ability to analyze business process and provide suggestions for improvement. Acting as the Finance liaison to 1 or 2 global departments (Finance, HR, IT&S, Legal/Compliance). Prepares monthly analysis and review results with the representative Executive Committee member. Supports annual budget, quarterly flex and capital processes for the Global department. Provides additional analysis as requested Required Experience: Must possess comprehensive knowledge of financial planning and analysis with a thorough understanding of analytical methods in a variety of accounting and operational sources. Requires expert MS Excel skills along with PowerPoint and SAP experience. Hyperion Planning, Smartview and Essbase experience is strongly preferred. Excellent verbal and written communication skills and good management skills are essential. Must have displayed an ability to collaborate with others outside of their immediate team, and be able to influence and drive change without authority Must be able to adapt quickly to changing needs in a fluid environment, while displaying a strong commitment to deliver results in within required timelines. These skills are normally acquired through completion of a Bachelor’s degree in accounting in addition to an MBA or CPA with 3 - 5 or more years of progressive responsibility in finance with direct FP&A experience in a large company setting. Equal Employment Opportunity/M/F/disability/protected veteran status. PI115640269
Nov 21, 2019
Perrigo Perrigo Company is dedicated to making lives better by bringing high quality and affordable self-care products that consumers trust everywhere they are sold. Help us do it. The primary responsibilities of the Sr. Financial Analyst for our Corporate FP&A role is to support global financial planning and review processes including annual and long term plans, monthly/quarterly business reviews, flex updates and preparation of earnings call information. This role requires strong collaboration with Business Unit CFO’s, Global Tax, Global Operations Finance, Investor Relations and Accounting and Reporting teams amongst others. Responsibilities: Playing a key role in the Perrigo Annual Planning processes. Duties include supporting the activities of all relevant global stakeholders, support in maintaining detail project plan, identifying and resolving issues and providing status updates to the Director and Manager of FP&A. This may also include interaction and collaboration with the Global Tax, Global Operations Finance functions, and Business Unit Finance leaders to appropriately forecast acquisitions and intercompany activity. Providing key support to the completion of the quarterly flex update process and consolidation of information for the Quarterly Business Unit reviews, including preparation of the analysis and supporting presentation to the Executive Committee. Preparation of monthly ad hoc analysis including: working capital trends, global departmental spend, departmental spend; etc. Supporting the CEO, CFO and Investor Relations team with the preparation of quarterly analyst call materials, reviewing what is prepared by other members and supporting the analysts in the aggregation of all materials received. Leading process improvements and strategic initiatives within functional area. Proven ability to analyze business process and provide suggestions for improvement. Acting as the Finance liaison to 1 or 2 global departments (Finance, HR, IT&S, Legal/Compliance). Prepares monthly analysis and review results with the representative Executive Committee member. Supports annual budget, quarterly flex and capital processes for the Global department. Provides additional analysis as requested Required Experience: Must possess comprehensive knowledge of financial planning and analysis with a thorough understanding of analytical methods in a variety of accounting and operational sources. Requires expert MS Excel skills along with PowerPoint and SAP experience. Hyperion Planning, Smartview and Essbase experience is strongly preferred. Excellent verbal and written communication skills and good management skills are essential. Must have displayed an ability to collaborate with others outside of their immediate team, and be able to influence and drive change without authority Must be able to adapt quickly to changing needs in a fluid environment, while displaying a strong commitment to deliver results in within required timelines. These skills are normally acquired through completion of a Bachelor’s degree in accounting in addition to an MBA or CPA with 3 - 5 or more years of progressive responsibility in finance with direct FP&A experience in a large company setting. Equal Employment Opportunity/M/F/disability/protected veteran status. PI115640269
Perrigo We strive to make lives better by bringing quality, affordable self-care products that consumers trust everywhere they are sold. Help us do it! The Allegan Michigan based Analytical Research and Development department, specializing in solid and liquid Over-the-Counter (OTC) product development, is looking to add a talented colleague to our New Product Development team. Our focus is on the development of analytical methods for small molecules in support of research and characterization of new and reformulated drug products. Chief techniques include HPLC/UPLC-UV stability-indicating methods with various separation chemistries. The individual will be responsible for development of assay, impurities, dissolution, and physical characterization methods for oral and nasal drug products. There is an expectation of both direct hands-on laboratory work as well as mentoring/training of colleagues. This is a great career move for someone who wants to be involved in the entire drug product life cycle, participating from initial concept to commercial production, with opportunities to contribute to a successful global pharmaceutical business focused on Quality, Affordable Self-Care Products. Major Duties and Responsibilities to include: Perform physical and chemical testing on raw materials, in-process and finished product samples with superior attention to detail and a focus on operational excellence. Clearly document and precisely execute analyses and experiments of moderate to high complexity. Analyze and properly interpret data, prepare reports, give presentations, or author other technical communications as necessary. Develop, validate and transfer analytical methods of varying complexity on the following platforms: HPLC, UPLC, GC, dissolution, and others as needed. Collaborate effectively with other departments and/or sites on project deliverables. Participate in/lead cross-functional teams at project-related meetings and technical discussions. Carry forward multiple concurrent projects and significantly contribute to product knowledge. Required Skills/Experience: Proficiency with a variety of analytical instruments for physical and chemical analyses, including but not limited to: HPLC, UPLC, GC, Dissolution. Ability to develop, trouble-shoot, and validate complex or innovative analytical methods which are robust and reliable, with minimal supervision, in a fast-paced and dynamic environment. Familiarity with calibration, maintenance, installation, and qualification of lab equipment. A working understanding of chemical structure at the molecular level. Judgement to make clear and concise decisions regarding project execution. Strong organizational, communication, and project management skills are a must. Passion for a team-oriented culture focused on shared ownership and responsibility. Familiarity with a variety of compendial references including the United States and European Pharmacopeia, as well as FDA Guidances and ICH Guidelines related to analytical methods validation and drug product development. Experience with statistical analyses of data and Design of Experiment concepts. Waters Empower software experience highly desired. The skills required for this role are normally acquired through completion of a: Bachelor’s degree in Chemistry or Pharmaceutical Sciences with 2-4 or more years of cGMP or cGLP laboratory experience , or Master's degree in Chemistry or Pharmaceutical Sciences with 1-2 or more years of experience in a cGMP or cGLP laboratory, or PhD degree in Chemistry or Pharmaceutical Sciences Equal Employment Opportunity/M/F/disability/protected veteran status. PI115605996
Nov 20, 2019
Perrigo We strive to make lives better by bringing quality, affordable self-care products that consumers trust everywhere they are sold. Help us do it! The Allegan Michigan based Analytical Research and Development department, specializing in solid and liquid Over-the-Counter (OTC) product development, is looking to add a talented colleague to our New Product Development team. Our focus is on the development of analytical methods for small molecules in support of research and characterization of new and reformulated drug products. Chief techniques include HPLC/UPLC-UV stability-indicating methods with various separation chemistries. The individual will be responsible for development of assay, impurities, dissolution, and physical characterization methods for oral and nasal drug products. There is an expectation of both direct hands-on laboratory work as well as mentoring/training of colleagues. This is a great career move for someone who wants to be involved in the entire drug product life cycle, participating from initial concept to commercial production, with opportunities to contribute to a successful global pharmaceutical business focused on Quality, Affordable Self-Care Products. Major Duties and Responsibilities to include: Perform physical and chemical testing on raw materials, in-process and finished product samples with superior attention to detail and a focus on operational excellence. Clearly document and precisely execute analyses and experiments of moderate to high complexity. Analyze and properly interpret data, prepare reports, give presentations, or author other technical communications as necessary. Develop, validate and transfer analytical methods of varying complexity on the following platforms: HPLC, UPLC, GC, dissolution, and others as needed. Collaborate effectively with other departments and/or sites on project deliverables. Participate in/lead cross-functional teams at project-related meetings and technical discussions. Carry forward multiple concurrent projects and significantly contribute to product knowledge. Required Skills/Experience: Proficiency with a variety of analytical instruments for physical and chemical analyses, including but not limited to: HPLC, UPLC, GC, Dissolution. Ability to develop, trouble-shoot, and validate complex or innovative analytical methods which are robust and reliable, with minimal supervision, in a fast-paced and dynamic environment. Familiarity with calibration, maintenance, installation, and qualification of lab equipment. A working understanding of chemical structure at the molecular level. Judgement to make clear and concise decisions regarding project execution. Strong organizational, communication, and project management skills are a must. Passion for a team-oriented culture focused on shared ownership and responsibility. Familiarity with a variety of compendial references including the United States and European Pharmacopeia, as well as FDA Guidances and ICH Guidelines related to analytical methods validation and drug product development. Experience with statistical analyses of data and Design of Experiment concepts. Waters Empower software experience highly desired. The skills required for this role are normally acquired through completion of a: Bachelor’s degree in Chemistry or Pharmaceutical Sciences with 2-4 or more years of cGMP or cGLP laboratory experience , or Master's degree in Chemistry or Pharmaceutical Sciences with 1-2 or more years of experience in a cGMP or cGLP laboratory, or PhD degree in Chemistry or Pharmaceutical Sciences Equal Employment Opportunity/M/F/disability/protected veteran status. PI115605996
Perrigo Improve the well-being of as many patients and consumers as possible by developing, manufacturing and distributing high quality, affordable specialized prescription products. The attorney in this role will primarily provide legal counsel and risk assessment to the commercial and business development functions of Perrigo’s prescription pharmaceutical business, with a focus on contracting. This attorney will interact frequently with upper-level management within Perrigo, outside counsel, and Perrigo employees in the U.S., Israel and Ireland. This position is fast-paced during working hours, but with a good work-life balance. Responsibilities: Daily drafting, editing, and negotiation of a variety of commercial agreements, including agreements with research and development partners, distribution partners, contract manufacturing organizations, suppliers, and others. Types of agreements will include research and development collaborations, distribution agreements, license agreements, contract manufacturing agreements, raw material supply agreements, confidentiality agreements, and asset acquisition and divestiture agreements. Collaboration with outside counsel on drafting, editing, and negotiating the types of agreements mentioned above. Daily interactions with employees in the legal, procurement, business development and commercial functions of Perrigo’s prescription business. This role will also interact with Perrigo management, outside counsel, and legal counsel from company customers and business partners. Leadership in implementation of best practices for contracting within the prescription business, including creation of contract templates, preparation of contract guidance documents and training of employees in contracting. Qualified Candidates Will Have: Juris doctor degree from accredited law school and admission to a state bar (active and in good standing) Member of the Michigan state bar or eligibility for admission to the Michigan state bar (general or as in-house counsel) Minimum 3-5 years of legal experience in corporate or law firm environment Extensive experience drafting, editing and negotiating commercial contracts Extensive experience providing legal advice to businesses regarding editing and negotiation of commercial contracts Strong and assertive communication and negotiating skills regarding both legal and financial/commercial issues Excellent interpersonal skills and the ability to learn new legal topics independently and quickly Ability to adapt legal advice to a variety of business needs and situations and to anticipate unique legal issues that could impact the business Strong business judgment and skills to find creative solutions to legal issues and the ability to effectively balance legal risks against business interests Experience with the pharmaceutical industry preferred (particularly in quality, regulatory or business development) Ability to work independently with little supervision Equal Employment Opportunity/M/F/disability/protected veteran status. PI115439555
Nov 13, 2019
Perrigo Improve the well-being of as many patients and consumers as possible by developing, manufacturing and distributing high quality, affordable specialized prescription products. The attorney in this role will primarily provide legal counsel and risk assessment to the commercial and business development functions of Perrigo’s prescription pharmaceutical business, with a focus on contracting. This attorney will interact frequently with upper-level management within Perrigo, outside counsel, and Perrigo employees in the U.S., Israel and Ireland. This position is fast-paced during working hours, but with a good work-life balance. Responsibilities: Daily drafting, editing, and negotiation of a variety of commercial agreements, including agreements with research and development partners, distribution partners, contract manufacturing organizations, suppliers, and others. Types of agreements will include research and development collaborations, distribution agreements, license agreements, contract manufacturing agreements, raw material supply agreements, confidentiality agreements, and asset acquisition and divestiture agreements. Collaboration with outside counsel on drafting, editing, and negotiating the types of agreements mentioned above. Daily interactions with employees in the legal, procurement, business development and commercial functions of Perrigo’s prescription business. This role will also interact with Perrigo management, outside counsel, and legal counsel from company customers and business partners. Leadership in implementation of best practices for contracting within the prescription business, including creation of contract templates, preparation of contract guidance documents and training of employees in contracting. Qualified Candidates Will Have: Juris doctor degree from accredited law school and admission to a state bar (active and in good standing) Member of the Michigan state bar or eligibility for admission to the Michigan state bar (general or as in-house counsel) Minimum 3-5 years of legal experience in corporate or law firm environment Extensive experience drafting, editing and negotiating commercial contracts Extensive experience providing legal advice to businesses regarding editing and negotiation of commercial contracts Strong and assertive communication and negotiating skills regarding both legal and financial/commercial issues Excellent interpersonal skills and the ability to learn new legal topics independently and quickly Ability to adapt legal advice to a variety of business needs and situations and to anticipate unique legal issues that could impact the business Strong business judgment and skills to find creative solutions to legal issues and the ability to effectively balance legal risks against business interests Experience with the pharmaceutical industry preferred (particularly in quality, regulatory or business development) Ability to work independently with little supervision Equal Employment Opportunity/M/F/disability/protected veteran status. PI115439555
Perrigo Perrigo Company is dedicated to making lives better by bringing high quality and affordable self-care products that consumers trust everywhere they are sold. Help us do it. Provides technical support to assigned projects, using robust scientific methods which comply with standard operating procedures and scientific standards. Works with limited direction. As appropriate, may serve as a project leader to manage analytical support for projects with supervision. Knowledge, Experience and Education : Demonstrated proficiency in the use of a variety of standard analytical instruments, such as HPLC, GC, Dissolution, UV-Vis and FTIR. Familiarity with a variety of compendial references, including USP or European Pharmacopeia. The ability to develop, document and execute analyses or experiments of moderate complexity, ensuring methods are robust and reliable. The ability to maintain high quality research documentation, analyze and interpret data, and prepare reports, qualification documents, SOPs or other technical reports is necessary. Must be able to work independently on multiple concurrent projects, and communicate effectively with interdisciplinary project teams. These skills are normally acquired through completion of a bachelor degree in Chemistry or Pharmaceutical Sciences combined with 1 to 3 years of relevant experience in a cGMP or cGLP laboratory. Responsibilities: With minimal supervision, create/update and document new/revised product specifications and test methods which are robust and meet regulatory requirements. Perform physical and chemical testing on raw material, in-process, finished product and stability samples. This includes documentation and review. Successfully investigate and resolve moderately-complex analytical problems, project issues and deviations. Accurately maintain all related documentation in compliance with SOPs. Assist in researching, preparing and reviewing technical documents, including but not limited to SOPs, drug master files, technical packages, vendor qualification, raw material and release and stability specifications, stability summaries, test methods, and certificates of analysis which conform to company standards. Attend and present data at project-related meetings, interact with other departments and outside testing laboratories to ensure proper analytical testing. Participate in cross-functional project teams, and exercise and build basic team effectiveness skills. Utilize skills, established procedures, new methodologies, and experience to complete tasks; and provide formal and informal mentoring to interns and Technicians. Develop, validate and transfer of complex and non-complex analytical methods. Equal Employment Opportunity/M/F/disability/protected veteran status. PI115439577
Nov 13, 2019
Perrigo Perrigo Company is dedicated to making lives better by bringing high quality and affordable self-care products that consumers trust everywhere they are sold. Help us do it. Provides technical support to assigned projects, using robust scientific methods which comply with standard operating procedures and scientific standards. Works with limited direction. As appropriate, may serve as a project leader to manage analytical support for projects with supervision. Knowledge, Experience and Education : Demonstrated proficiency in the use of a variety of standard analytical instruments, such as HPLC, GC, Dissolution, UV-Vis and FTIR. Familiarity with a variety of compendial references, including USP or European Pharmacopeia. The ability to develop, document and execute analyses or experiments of moderate complexity, ensuring methods are robust and reliable. The ability to maintain high quality research documentation, analyze and interpret data, and prepare reports, qualification documents, SOPs or other technical reports is necessary. Must be able to work independently on multiple concurrent projects, and communicate effectively with interdisciplinary project teams. These skills are normally acquired through completion of a bachelor degree in Chemistry or Pharmaceutical Sciences combined with 1 to 3 years of relevant experience in a cGMP or cGLP laboratory. Responsibilities: With minimal supervision, create/update and document new/revised product specifications and test methods which are robust and meet regulatory requirements. Perform physical and chemical testing on raw material, in-process, finished product and stability samples. This includes documentation and review. Successfully investigate and resolve moderately-complex analytical problems, project issues and deviations. Accurately maintain all related documentation in compliance with SOPs. Assist in researching, preparing and reviewing technical documents, including but not limited to SOPs, drug master files, technical packages, vendor qualification, raw material and release and stability specifications, stability summaries, test methods, and certificates of analysis which conform to company standards. Attend and present data at project-related meetings, interact with other departments and outside testing laboratories to ensure proper analytical testing. Participate in cross-functional project teams, and exercise and build basic team effectiveness skills. Utilize skills, established procedures, new methodologies, and experience to complete tasks; and provide formal and informal mentoring to interns and Technicians. Develop, validate and transfer of complex and non-complex analytical methods. Equal Employment Opportunity/M/F/disability/protected veteran status. PI115439577