WORKING AT ANCILLARE

Founded in 2006, we support the clinical trial supply network globally. Today, we are a rapidly growing, entrepreneurial organization building upon our success and operational innovations to constantly meet the evolving needs of the life sciences industry.

卓越したスキルの専門家。
人類の福祉に貢献する誓い。


当社は、従業員が高品質のサービス、オペレーショナルエクセレンスを提供することを望み、誠実さ、協調、説明、革新、コミュニケーション、チームワークの文化を基盤とした価値観を支持します。

Entrepreneurial Environment

We have an entrepreneurial culture, which means our team members each accept the responsibility to respond quickly to challenges. As part of a growing company, you’ll join a self-motivated team of experts in a positive, innovative, high-energy workplace.

Proven Track Record

Our experience has helped us develop innovative business models for our clients. As a part of our team, you’ll be able to leverage new ideas and contribute to programs and services for our clients.

Rapid Growth

In order to pursue high-growth markets, we have invested in facilities, certifications and infrastructure to best serve our clients. We expect to continue to grow rapidly and are building the right team to help us get there.

Committed to Excellence

At Ancillare, you’ll find a company dedicated to innovation and client service, and this dedication motivates and energizes our corporate culture. Our team members are passionate about their areas of expertise, but remain flexible, adjusting processes and priorities to accommodate changes in scale, geographies, or regulations.

競争上のメリット

Ancillareは、従業員の生活の質は会社にとって非常に重要であると考えています。したがって、当社はあなたとご家族に、次のような競争上の報酬と複数の利益を提供します:

福祉と健康
  • HSA(医療貯蓄口座)付きSavings Plus HNOptionプラン、PPO(優先医療給付機構)プラン、HSA付き高額控除PPOプランを含む3つの医療プラン
  • デンタルPPOとDMO(データ管理事務所)プラン
  • ビジョンプラン

Financial Well-Being

金融福祉
  • 会社の匹敵分401 (k)退職プラン
  • 短期および長期障害
  • 生命保険および障害保険

個人的な利点
  • 有給休暇および祝日
    (24日間、毎年5日間繰り越し可能)
  • フレキシブルアワー
  • ジム割引プログラム
Background

現在の求人:

We are currently seeking a Project Manager to join our team in Horsham, PA (USA) to effectively managing the flow of products to global clinical trial locations for our clients as well as manage operations of the team based on approved timelines. This position will lead and assist a project team during protocol formulation and interface directly with clients, management, quality assurance, and logistics teams to manage all clinical and ancillary supply chain operations and processes.

Responsibilities:

  • Manage the scope of work for each project and the implementation of protocol requirements as given by the client and management.
  • Ensure all processes are implemented and completed according to all relevant SOPs, quality assurance, and logistics recommendations as well as the company’s strategic direction.
  • Serve as liaison and manage relationships between the organization and client to share all relevant information including recommendations, requirements and progress of project.
  • Ensure projects are completed based on timelines, budget, and scope of operations.
  • In collaboration with other departments assist in all functional areas of the project where needed to ensure completion.
  • Attend and or facilitate periodic teleconferences and study meetings.
  • Responsible for the management of study startup, day to day interactions with sites, study team and Ancillare team/s.
  • Collaborate with PM Team Leads and Portfolio Directors to assist in managing the project budget against actual expenses and current status.
  • Manage supply, resupply and disposition of study supplies (non-drug).
  • Collaborate with Supply Chain (logistics) to ensure that the regulatory requirements and necessary documents are in place before international shipments occur.
  • Coordinate and execute monthly status reports for client, partnering with IT and CPG for any special requests from client.
  • Partner with the client to gain project scope and timeline.
  • Interface with the quality assurance team and management team as needed.

Requirements:

  • Bachelor’s degree or equivalent Project Management work experience required.
  • PMP certification preferred.
  • Two to three years of experience working in Project Management.
  • Experience working in pharmaceutical or clinical supply highly desirable.

Minimum Requirements:

  • Demonstrated Strong Project Management skills with the ability to effectively lead a team to successful project completion.
  • Ability to effectively communicate in English both written and verbal.
  • Demonstrated ability to effectively multitask and manage multiple projects simultaneously.
  • Detail oriented and organized; must be able to meet demanding deadlines and deliver quality work output within these tight timeframes.
  • Proven ability to effectively influence and collaboratively work across diverse groups with both internal and external stakeholders and business partners.
  • Understanding of clinical supply chain process desirable.
  • Proficient Microsoft Office Suite including Word, PowerPoint, Outlook and Excel.
  • Results oriented, confident, self-motivated and driven with solid negotiation skills.
  • Flexible and capable of managing and implementing change.
  • Strong analytical and problem solving skills.
  • Rigor to strictly adhere to company SOPs and regulatory compliance.
  • Understanding of key global regulations including GCP and GMP preferred.
  • Ability to mentor and train other members of the organization.
  • Must be able to work well both independently and in a team environment.
  • Must have a track record of dependability, consistency and reliability.
  • Able to travel internationally.

We are currently seeking a Proposal Associate II to join our team in Horsham, PA (USA) to manage the RFI/RFP responses, proposal, and quote process with little supervision. This full-time position, reporting directly to the Associate Director of Client Proposal Group (CPG) will prepare, and review proposals/quotes engaging Business Development, Project Management, Procurement, Logistics, and other functional departments as needed at the appropriate time and level to help ensure smooth transition of proposals from initial RFP through final proposal submission, award, and handoff to Project Management.

Responsibilities

Manage all RFI/RFP responses, proposal, and quote generation process with little supervision.

Communicate with multiple departments across the organization to ensure Ancillare and client expectations and needs are satisfactorily and consistently met and/or exceeded with respect to the quote preparation process.

Work with functional team members within business development and project management departments to conduct appropriate research, effectively communicate status, and prepare proposals, using strong relationship management skills.

Schedule and facilitate strategy meetings with functional leads to identify potential issues, client requirements, and key strategies to be addressed.

Record and communicate agreement on deliverables, strategies, and timelines from resulting from strategy meeting(s). Ensure adherence through meaningful communication and follow up.

Facilitate pricing discussions with key team members. Draft proposal budget reflecting agreed upon proposal components and strategies. Ensure accuracy, consistency and price competitiveness.

Recommend proposal and study conduct strategies as well as identify internal resources, within parameters of the position.

Keep management and leadership teams engaged and well informed to ensure effective proposal process as well as quality of input and outcome.

Craft meaningful proposals for clients by accurately reflecting strategic decisions and accurately capturing proposal details. Ensure accurate mapping to client budget specifications.

Participate in client calls related to requests for proposals, budget discussions, and requests for information as required.

Provide quality deliverables under tight timeframes and deadlines. Record and maintain all agreed upon metrics.

Work overtime as required during peak periods and/or to meet deadlines. Maintain regular and predictable attendance within prescribed guidelines.

Provide training and mentorship to new or junior level proposal staff as assigned.

Perform other duties as assigned.

Qualifications:

3+ years of direct proposal development and management experience in a CRO, pharmaceutical, or related environment preferred.

Bachelor’s degree in business or other related field required.

 Requirements:

Detail oriented and organized.

Ability to successfully work on multiple projects simultaneously.

Effective verbal and written English communication skills.

Proficient in the use of Microsoft Word, Excel, Outlook and PowerPoint.

Assist a project team during protocol formulation and supply to global investigator sites. Interface directly with management, quality assurance and supply chain teams to assist managing all clinical supply operations and processes.  Work effectively in a team environment to manage flow of products to global clinical trial locations as well as manage operations of the team based on approved timelines.  Perform all functions according to company SOPs and strategic direction.

Responsibilities:

  • Working in a collaborative style assist in managing the scope of work for the project including managing the implementation of protocol requirements as given by the customer and management.
  • Under the direction of Senior Project Management ensure that all processes are implemented and completed according to all relevant SOPs, quality assurance and supply chain recommendations, and company strategic direction.
  • Assist in all functional areas of the project as needed to ensure timely completion including supply, resupply and disposition of study supplies (non- drug).
  • Interface regularly with internal stakeholders including; quality assurance and supply chain to assist project management team in all functional areas of the project where needed to ensure on time and budget completion.
  • Serve as liaison as may be required to manage relationships between the organization and customer to communicate all relevant information including recommendations, requirements and progress of project.
  • Manage and provide regular status reports to Senior Project Management staff as required
  • Work towards ensuring projects are completed based on timelines, budget, and scope of operations.
  • Ability and desire to work a project to completion meeting and or exceeding timeline deliverables.
  • Enhance organization reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to the job.
  • Ability to work successfully individually or in a team.
  • Perform other duties as assigned.
  • Demonstrate and drive the Ancillare mission, values and strategy.
  • Ability to travel as may be required.

Qualifications:

  • Bachelor degree preferred, may consider equivalent work experience in lieu of degree.
  • PMP certification candidate preferred.
  • Prior project management experience or management/supervisory experience preferred.
  • Prior working experience in a pharmaceutical industry, ancillary supply or supply chain is highly desirable.

 Minimum Requirements:  

  • Ability to effectively communicate in English verbally and written.
  • Proven ability to effectively hear, understand and follow directions or instructions.
  • Ability to multitask and successfully manage multiple projects simultaneously, flexible and capable of managing and implementing change.
  • Flexibility to work under pressure while maintaining a professional demeanor, detail oriented and organized with strong analytical and problem solving skills.
  • Ability to prioritize, meet demanding deadlines and deliver quality work output within tight time frames.
  • Ability to effectively work collaboratively across diverse groups with both internal and external stakeholders and business partners.
  • Self –motivated, confident and results oriented with rigor to strictly adhere to company’s SOPs and regulatory compliance.
  • Must possess demonstrated Microsoft Office skills; Word, Excel, Outlook and Power Point.
  • Must have a track record of dependability, consistency a reliability.

現在、当社は新しい事業開発の機会を獲得し、既存のビジネスチャンスを維持し、成長させ、同社の使命、ビジョン、文化を確立し促進するために、事業開発ディレクターを募集しています。この役職では、事業関係を構築し、収益を上げ、顧客要求と提案に参加し、すべての顧客の成果物が期限内に確実に配送されるようにします。

職務内容:

  • 組織の事業開発業務と実行を計画、開発、整理、指導します。
  • 指定された顧客企業内の事業連絡先と関係を確立し、維持します。
  • 新たな潜在的顧客とのネットワークを構築し、新しいビジネスチャンスを推進し、事業のパイプラインを拡大します。
  • 測定基準と管理システムを実装して、事業開発の全体的な運用の進捗状況を正常に追跡するのを支援します。
  • 新しい収益源を発見し、既存の顧客との提携を促進します。
  • 顧客の要望に応え、一貫性のある卓越した品質とサービスを保証します。
  • 最初の連絡から概略見積もり/提案依頼の完了まで、実装と移行計画までの販売プロセスを管理します。
  • 必要に応じて新しい事業提案を取得、作成し、提示します。
  • Ancillareのシステム、品質、および専門サービスを強化します。
  • 顧客にAncillareのシステム説明を行います。
  • 顧客関係を管理し、すべてのニーズが十分に満たされ、完全に外部委託されていることを確認します。スポンサー企業との長期にわたる契約を確立します。
  • 顧客と協力し、プロジェクトや計画の仕様、タイムラインと要件を取得し、必要に応じて賞、新事業、タイムライン、その他の要件を他の部門/社内の対応部署に伝えます。
  • 顧客の要件と仕様を満たす計画を立てます。
  • 顧客と積極的でオープンなコミュニケーションを維持し、進行中の計画/プロジェクトのために顧客に最新の情報を提供し、顧客とAncillareの調整役として働きます。
  • 事業開発の取り組みや活動を管理、追跡し、経営幹部に報告します。
  • プロジェクト管理、調達、物流およびその他の部門(必要に応じて)と協調し、顧客が要求する計画/プロジェクトの運用面を確実に理解します。
  • 提案者のチームと連携し、法律や法令遵守を含め、顧客のニーズに対する会社の提案の正確さを確かめます。
  • 見本市、会議、その他のマーケティング・イベントに出席し、Ancillareとそのサービスに対する見識を高めます。

要件:

  • 学士号(またはそれ以上の学位)があればなお可。
  • 事業開発に最低でも7年間プロフェッショナルとして携わった経験(要証明)。
  • 製薬企業/バイオテクノロジー企業、開発業務受託機関、関連業界で5年以上の経験。
  • 製薬企業/バイオテクノロジー企業における関係があればなお可。
  • 優れたプレゼンテーション、対人関係、および人間関係スキル。
  • 口頭および書面における優れたコミュニケーション能力。
  • 優秀な事業開発業務実践的な知識。
  • 戦略的、戦術的、独立的に職務を遂行する能力。
  • 組織を支えるためのプロフェッショナルな物腰と態度を備えた強力なリーダーシップスキル。
  • 優れた交渉能力。
  • 必要に応じて、または勤務時間の最大70%まで移動する能力。
  • 組織された強力な記録保持と時間管理スキル。
  • 優れた独立意思決定と創造的な問題解決スキル。
  • 複数の業務を開発、組織、管理する能力。

We are currently seeking a Senior Information Technology Specialist for our global organization headquartered in Horsham, PA (USA).  This position’s primary function is to perform analysis, programming, hardware, software and network support for the organization’s IT operations.

Responsibilities:

  • Provides support in monitoring and maintaining system and network efficiency.
  • Under the direction of IT Leadership and in consultation with users assist with systems software evaluations including functional specifications, acquisition and installation.
  • Provides support with network hardware and software installations.
  • Responsible for maintenance/upkeep of IT equipment, including but not limited to telephone system/s, copiers and scanners as directed.
  • Assists with analysis, programming, documentation, and maintaining functionality in Ancillare systems using appropriate tools.
  • Assists with special projects as needed.
  • Provides project status updates and timelines to IT Director and Senior Leadership.
  • Working collaboratively within the IT department to ensure responsive IT help desk service delivery, and partnering with other departments to promote company goals.
  • Promotes adherence to company SOP’s among various stakeholders, as directed by IT management.
  • Responds to off hour calls and is available to travel internationally as required.
  • Maintains regular and predictable attendance within prescribed guidelines.
  • Perform other duties as assigned.

Qualifications:

  • Bachelor’s degree in Computer Science or a related technical discipline required, can substitute the equivalent combination of education, technical certifications, and/or training.
  • Demonstrated working knowledge of Microsoft Dynamics Navision and/or Filemaker.
  • Demonstrated working experience and knowledge of web programming tools desired.
  • 2+ years prior experience performing analysis and programming.

Requirements:

  • Effective oral and written English communication skills.
  • Detail oriented and organized with sustained time management skills.
  • Proven ability to effectively communicate and collaboratively work across diverse groups with both internal and external business partners.
  • Extensive knowledge of Microsoft Office suite including Word, PowerPoint and Outlook.
  • Intermediate to proficient data entry/typing skill.
  • Ability to work sitting at a desk for prolonged periods of time.

現在、当社では、臨床試験提案プロセスの開始段階で、臨床試験の供給計画の専門知識と事業開発(BD)および中枢提案グループ(CPG)部門へのサポートを提供するペンシルバニア州ホーシャムのチームに加わる事業運営のシニアディレクターを募集しています。この役職は、顧客提案の開発段階の前と中途に、事業開発やポートフォリオ・ディレクターによって提供された顧客要求と協力し、戦略的方向性を提供する責任を担い、機会の徹底的な分析が確実に行われ、提案の正確さが高まり、提案の所要時間が短縮されるようにします。

職務内容:

  • 顧客要求(提案依頼)の完全な分析を行い、事業開発およびポートフォリオ・ディレクターに、認識された不備やギャップを助言します。
  • サプライチェーンの同僚と協力し、必要に応じて製品の発見と代替品の提案を行います。
  • プロジェクトは、RFPの受け取りから提案書の提出とプロジェクト引き継ぎを経て提案プロセスを管理します。
  • CPGの同僚と協力し、臨床試験の供給戦略の専門知識や、提案が開発された時の対象分野の専門知識を提供します。
  • 必要に応じてビッド・ディフェンス会合/電話会談に参加します。
  • 割り当てられた事業開発パートナーとの協力、顧客固有の要求の開発/改訂および実装の責任を負います。
  • 教育機会に参加し、業務知識を更新します。
  • 新しい要求、異なる要求に応えるためのオーナーシップを受け入れ、組織の評判を高め、業務に付加価値を加える機会を模索します。
  • タイムラインの成果物を完成、適合、または超過するプロジェクトを実行する能力と希望。
  • 製造管理および品質管理に関する基準(GMP)、医薬品の物流に関する基準(GDP)、医薬品の臨床試験の実施の基準(GCP)、および関連するGXPをすべての責任分野に適用します。
  • Ancillareの使命、価値観、戦略を実証し、推進します。
  • 出張が必要な場合があります。
  • 割り当てられた他の職務を遂行します。

資格:

  • 製薬企業/開発業務受託機関/外部委託製造業界で7年以上の経験。
  • プロジェクト管理経験。
  • 学士号を所持しており、臨床試験における同等の職務経験も考慮。
  • 大学院の学位、予防保守計画および/または研究室の参加経験あればなお可。

必要条件:

  • 臨床試験について明確に理解していること。
  • 書面と口頭の両方で実務的な英語コミュニケーションができること。
  • 能動的なリスニングと優れたコミュニケーション能力(口頭と書面の両方で、積極的に自信を持ってコミュニケーションをとれる能力)。
  • 卓越したプレゼンテーション能力。
  • 組織の全段階での交流、影響、協力関係の獲得できる優れた対人関係スキル。
  • 細部に気を配り、強力な分析能力と問題解決能力を備えている必要があります。
  • チーム内や個人貢献者として、最低限の監視で効果的に業務遂行する能力。
  • 他の職務との交流をリードし、 複数のプロジェクトを同時に複数の仕事を遂行および管理する能力。
  • プロフェッショナルな姿勢を維持しながら、重圧の下で柔軟に職務を遂行する能力。
  • 強力な分析スキルと問題解決テクニックを持ち、組織化され、結果重視で、自発性がある、厳しいガイドラインと締め切り下で、複数の仕事を遂行する能力。
  • 製品/供給品の知識と理解、製品供給に関連する費用、臨床試験環境での業務遂行。
  • 実証されたプロジェクト管理スキル。
  • Microsoft Office Suiteを効果的に使用し、情報を確保して提示する能力。
  • 信頼性、一貫性のある業務実績が必要。&

We are currently seeking an Information Technology Network Associate for our global organization headquartered in Horsham, PA (USA) to assist with performing network design and capacity planning. This position will develop, implement and maintain policies, procedures and associated training plans for network resource administration, appropriate use and disaster recovery.

Responsibilities (including but not limited to):

 Strategy & Planning:

      • Assist with performing network design and capacity planning
      • Develop, implement and maintain policies, procedures and associated training plans for network resource administration, appropriate use, and disaster recovery
      • Establish service level agreements with end users

Acquisition & Deployment:

      • Assist in installation, configuration, maintenance, and troubleshooting of end user workstation hardware, software, and peripheral devices.
      • Conduct research on network products, services, protocols, and standards in support of network procurement and development efforts.

Operational Management:

    • Manage servers, including e-mail, print and backup servers and their associated operating systems and software.
    • Manage security solutions, including firewall, anti-virus, and intrusion detection systems.
    • Manage all network hardware and equipment, including routers, switches, hubs, and UPSs.
    • Ensure network connectivity of all workstations.
    • Administer all equipment, hardware and software upgrades.
    • Perform network asset management, including maintenance of network component inventory and related documentation and technical specifications information.
    • Administer and maintain end user accounts, permissions, and access rights.
    • Perform server and security audits.
    • Perform system backups and recovery.
    • Monitor and test network performance and provide network performance statistics and reports.
    • Occasional inspection of cables in floors and ceilings.
    • Recommend, schedule, and perform network improvements, upgrades, and repairs.

Qualifications:

  • College diploma or university degree in the field of computer science and/or two years equivalent work experience.
  • Working technical knowledge of network and PC operating systems, including Windows 7and newer.
  • Working technical knowledge of networking hardware, protocols, and standards, including TCP/IP, IPSEC, VPN.
  • Hands-on hardware troubleshooting experience.
  • Working knowledge of HIPAA Security Rule.
  • Extensive working server support experience.
  • VMware VSphere 4 Platform.
  • Windows Server 2003, 2008, 2012.
  • SQL Server 2005/2008, SQL Reporting Services.
  • Exchange Server 2007/2010.
  • Symantec Backup Exec.

We are looking for an Accounts Receivable Specialist for our global headquarters based in Horsham, PA (USA) to communicate directly to client’s to collect payments on a timely manner. Perform accounts receivable tasks including collection efforts. Provide a high level of customer service to internal and external (sponsor) parties.

Responsibilities:

  • Review accounts receivable aging reports to determine and carry out appropriate collection efforts. Research and analyze accounts prior to contacting sponsor.
  • Maximize collection of accounts receivables while maintaining customer goodwill.
  • Identify billing deficiencies and determine the root cause for delayed payments, partial payments and disputed
  • Maintain files on all past due accounts, documenting details of actions to secure payment. Keep track of all written and phone communications with internal and external parties.
  • Track and report key Accounts Receivable metrics.
  • Compile information, prepare reports and escalate issue as agreed upon with Supervisor.
  • Ability and desire to work a project to completion meeting and or exceeding timeline.
  • Maintain regular and predictable attendance within prescribed guidelines. Work overtime and travel as
  • Perform other duties as assigned.

Qualifications:

  • Five years of direct accounts receivable experience required, ideally in a team setting.
  • High school diploma or equivalent required.
  • Associate degree or business school training a plus.

Requirements:

  • Ability to effectively communicate in English both written and verbal.
  • Must be detail oriented and well organized.
  • Excellent communication and interpersonal skills.
  • Extensive  knowledge  of  Microsoft Office suite including  Word,  Excel, Power Point and Outlook.
  • Working knowledge  of  general  ledger preferred.
  • Bank reconciliation experience highly desirable.
  • Data entry/typing skills.
  • Ability to work sitting at a desk for prolonged periods of time.

We are looking for a Material Handler for our Milton Keynes depot to pick and prepare orders for shipment to global clinical trial clients in a fast paced warehouse environment. This position will provide the highest level of customer service with safety, accuracy, timeliness and dependability of work.

Responsibilities:

  • Pick all customer orders in the timeline designated by the request.
  • Understand the flow for the warehouse and the bin locations for all products.
  • Safely operate company equipment after training requirements are satisfactorily met.
  • Pack all products for shipping, in appropriate containers and/or cartons, per product specifications and standard operating procedures.
  • Understand the types of products that will be picked.
  • Count and sort various product types.
  • Prepare orders for shipment utilizing carrier software when needed.
  • Adhere to all warehouse rules and guidelines per company policies, procedures and SOP’s.
  • Understand pick tickets and all documents related to the position.
  • Understand and follow all health and safety regulations.
  • Work overtime and travel as may be required.
  • Maintain regular and predictable attendance.
  • Perform additional duties and responsibilities as assigned.

Qualifications:

  • One to two years of pick/pack and/or warehouse experience preferred.
  • O Level GCSE, High school diploma/GED required but will consider prior equivalent work experience to substitute.

 Requirements:  

  • Ability to effectively communicate in English; read write, speak and understand.
  • Must be detail oriented and organized.
  • Ability to learn quickly and effectively utilize matching skills.
  • Ability to understand and effectively carry out verbal instructions.
  • Proven ability to follow standard operating procedures to perform picking/packing/shipping work.
  • Ability to safely operate machinery following the successful completion of training.
  • Valid driver’s license with a clear driving record preferred.
  • Ability to effectively work in a team environment or as an individual contributor.

Working Conditions: 

This position will be in a warehouse environment subject to changes in temperature.

Physical Requirements:

  • Sitting, walking, standing, and kneeling.
  • Communicating, hearing, seeing, reading, and speaking.
  • Lifting, stooping, climbing, bending, and reaching.
  • Working at variable heights occasionally.
  • Operating warehouse equipment/machinery.

We are currently seeking a Quality Assurance Specialist for our global organization headquartered in Horsham, PA (USA). This position reporting directly to the Director of Quality Assurance will provide support in implementing and maintaining the Quality Management System.  This support would include the development, review and revision of Standard Operating Procedures (SOPs), and associated documents.

Responsibilities:

  • Schedule and perform training on SOPs.
  • Investigate and document Issues, Deviations, and Complaints.
  • Manage and maintain Quality documentation files.
  • Manage and maintain Quality metrics.
  • Develop and review Change Control documentation.
  • Assist in managing quality improvements.
  • Planning and conducting internal audits.
  • Provide positive motivation to all areas to implement processes and achieve goals with respect to quality of products and services.
  • Maintain calibration system.

Requirements:

  • Minimum of three years of experience in a Quality Assurance role with experience writing SOPs.
  • Bachelor’s degree or equivalent work experience required.
  • Knowledge of quality systems such as CAPA, Change Control, and Deviations.
  • Demonstrated ability to effectively communicate both written and verbal across all levels of the organization.
  • Must have solid computer skills and proficient with Microsoft Office.
  • Knowledge of GXP guidelines preferred.
  • Knowledge of process/continuous improvement.
  • Demonstrated analytical skills and ability to satisfactorily problem solve and prioritize with little guidance.
  • Excellent organizational skills.
  • Ability to travel internationally and domestically as required.
  • Must be able to work independently.

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