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Description
Kenvue is currently recruiting for:
Fixed Assets Accounting Analyst
This position reports to Fixed Assets Accounting, Senior Team Lead and is based in Paranaque, Philippines
This role will be part of the Global Services Finance team in the Fixed Assets Accounting process area.
The Global Services Finance organization provides best-in-class, cost-effective financial services, and compliance.
The Fixed Assets accounting team is responsible for the complete and accurate accounting for all the tangible and intangible fixed asset process flows (including leasing).
This includes but is not limited to ensuring accurate capitalization of assets including on-going impairment/UEL reviews, calculating, and posting depreciation/amortization, managing retirement/disposal postings, and ultimately ensuring accurate balance sheet reconciliations.
Who We Are
At Kenvue, we realize the extraordinary power of everyday care.
Built on over a century of heritage and rooted in science, we're the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON'S® and BAND-AID® that you already know and love.
Science is our passion; care is our talent.
Our global team is made up with 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers.
With expertise and empathy, being a Kenvuer means to have the power to impact life of millions of people every day.
We put people first, care fiercely, earn trust with science and solve with courage - and have brilliant opportunities waiting for you! Join us in shaping our future-and yours.
For more information, click here.
What You Will Do
Responsible for executing accounting and daily operations for Fixed Assets Accounting process area.
• Timely closing & execution of financial periods as per closing calendar and in accordance with SLA commitments, fully observing Compliance, Internal Audit & SOX requirements.
• Accountable for completeness, accuracy and validity of the actuals reported within process/entity scope.
• Deep expertise, fully knowledgeable of Worldwide Procedures and compliance requirements for respective areas.
• Regular focus on Balance Sheet reconciliations to minimize open items.
• On-the-job training for new team members / BPO partners.
• Support auditors and legal authorities with the execution of required activities.
• Understand, adhere, and execute per worldwide policies and procedures.
Identify compliance risks and recommend solutions.
• Ensure strong internal controls are in place, in order to achieve "adequate" internal and external audit ratings.
__PRESENT__PRESENT__PRESENT__PRESENT__PRESENT
Qualifications
What We Are Looking For
Required Qualifications:
• A minimum of a Bachelor's level degree or equivalent is required, preferably in accounting, finance, or related business discipline.
• At least 0-2 years of professional experience is required.
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Type: Permanent Location: Manila, PH-00
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:28
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Description
• Account for developing Medical Education strategy and plan including Disease education as well as Product education surrounding the relevant therapeutic area and product.
• Ensure the Medical Education strategy aligned with BU & company strategy through building an efficient cross-function collaboration network and communication models.
• Ensure succeed implementation of Medical Education events and programs in high-quality and high-compliance way; Work with MA team to provide guidance, support etc.
to ensure cascade and local education events execution successfully.
• Responsible for budget management to the relevant programs or TA to achieve finance target
• Develop TA KOLs and build interactive strategic cooperation with the KOLs and professional associations.
RESPONSIBILITIES
1.
Set clear performance objectives and provide accountable for key activities and deliverables.
2.
Respect to adherence to relevant Standard Operating Procedures (SOPs), and ensure similar adherence.
3.
Perform annual performance reviews to help support the creation of a diverse, high performing Medical Education team.
4.
Allocate time appropriately to conduct responsibilities and tasks such as status reports, expense reports, etc.
5.
Complete appraisal
6.
Respond in a timely manner to internal and external customer requests.
7.
Manage time and activities of self to correspond with the annual planning calendar.
8.
Communicate routinely and effectively to ensure effective integration of business plan.
9.
Effectively evaluate materials and programs from appropriate vendors and in-house departments.
Qualifications
RELATED EXPERIENCE:
• Bachelor and above degree.
Academic background with a scientific/medical or marketing degree is preferred
• 6-year or above working experience and 5-year or above Pharm industry/business experience
• More than 3-5 years or above of Marketing and/or Medical experience in the relevant therapeutic area
• 2-3 years above people management or functional line management experience
• A good understanding of the varying medical and marketing practices and perspectives across China, regional and overseas experience is a plus.
• Good planning and tracking skills.
• Strong oral and written communication skills.
Requirements:
1.
English writing and oral communication
2.
Flexibility for some domestic and international travels.
3.
Proven skills at developing and managing varied relationships within and outside the company.
4.
High customer and external industry insight
5.
Experienced in development of educational programmes.
6.
Skilled at understanding scientific data and translating it into effective education and communications materials.
7.
Strong and demonstrable presentation, communication and influencing skills that can impact at all levels.
8.
Organisational skills, project management, time-management skills
9.
Strong leadership, guide and reward high performance teams.
10.
Adherence to company policies...
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Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:27
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Description
Kenvue is currently recruiting for:
Production Planner - Mixing/Scheduling
This position reports into Plant Planning Manager and is based our plant in Mandra
Who We Are
At Kenvue, we realize the extraordinary power of everyday care.
Built on over a century of heritage and rooted in science, we're the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON'S® and BAND-AID® that you already know and love.
Science is our passion; care is our talent.
Our global team is made by 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers.
With expertise and empathy, being a Kenvuer means to have the power to impact life of millions of people every day.
We put people first, care fiercely, earn trust with science and solve with courage - and have brilliant opportunities waiting for you! Join us in shaping our future-and yours.
What You Will Do
Responsible for:
Maintain an optimized, executable and detailed production schedule at the lowest level of the hierarchy with consideration of time, resources and raw materials, managing short term exceptions as appropriate.
In this role, the Production Planner provides also support to the regional E2E plan organization and the supply sites with the key aim to ensure stock availability of the right products to the right locations at the right cost.
Moreover, work to provide relevant data to the regional E2E supply planning organization enabling an optimal decision making.
Key Responsibilities
• Responsible for the optimal scheduling for the SKUs in his portfolio, respecting customer requirements and inventory policies, avoiding any unnecessary production inefficiency
• Ensures the proper availability of the production materials and equipment, according to the production plan.
• Short term exceptions management due to materials / capacity / production, to ensure minimal deviation from the original schedule and minimum cost associated
• Is responsible for maintaining the production schedule and managing any issues, or unforeseen and/or anticipated constraints.
• Communication inside the organization:
• 1st point of contact for Manufacturing and Material Management team for short term criticalities
• Closely cooperate with supply planning organization
• Monitors and reports on schedule achievement and delays per machine.
• Organizes and coordinates weekly meetings with Production supervisors, in order to validate the production schedule.
• Works with the MPS Planner to resolve issues related material and human resources in a timely manner.
• Determines the optimal process sequence for production planning.
• Collaborates with Managers to find potential solutions to improve production productivity and efficiency.
• Provides alternative production schedules to assist in decision-making regarding uninterrupted operation planning.
• Is responsible ...
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Type: Permanent Location: Athens, GR-01
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:27
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Description
Kenvue is currently recruiting for: Senior Commercial Controller at CEE Business Intelligence Team
This position is based in Prague, Czech Republic
Who We Are:
At Kenvue, we realize the extraordinary power of everyday care.
Built on over a century of heritage and rooted in science, we're the house of iconic brands - including NEUTROGENA®, AVEENO®, LISTERINE® and JOHNSON'S® that you already know and love.
Science is our passion; care is our talent.
Our global team is made by 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers.
With expertise and empathy, being a Kenvuer means to have the power to impact life of millions of people every day.
We put people first, care fiercely, earn trust with science and solve with courage - and have brilliant opportunities waiting for you! Join us in shaping our future-and yours.
What You Will Do:
Key Responsibilities
* Lead a Team of Analysts supporting Kenvue business
* Support Sales and Brand & Shopper Activation Teams in the area of planning, analysis & process improvement
* Provide insights and recommendations based on sales, market data & sales force effectiveness analysis
* Prepare regular and ad hoc integrated data mining and analyses for commercial Teams to identify marketing opportunities
* Prepare reports and business cases to support operations & strategy of the Commercial Team
Qualifications
What We Are Looking For:
Required Qualifications
* Min 5 years of experience in analytical area (ideally in Finance, market research, sales effectiveness, revenue growth management)
* Strong business focus and very good understanding of P&L and finance in general
* Analytical thinking and ability to formulate insights supported with professional and persuasive attitude
* Advanced knowledge of MS Excel & ability to use and implement Business Intelligence solutions (SAP BW, Tableau, Power BI, SQL)
* Excellent English (written and verbal)
Desired Qualifications
* Experience in business planning process
* Project management skills
* People Leader's skills
* Good understanding of FMCG market
* Experience in working with market data analysis will be an asset (knowledge of Nielsen, IQVIA tools)
* Excellent Czech (written and verbal)
* Advance knowledge of SAP
What's In It For You:
* Competitive Benefit Package
* Paid Company Holidays, Paid Vacation, Volunteer Time & More!
* Learning & Development Opportunities
* A challenging and interesting job in one of the biggest global healthcare companies
Kenvue is proud to be an Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identify, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
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Type: Permanent Location: Prague, CZ-10
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:27
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Description
Kenvue is currently recruiting for:
Head of Czech & Slovakia
This position reports into the General Manager Central Eastern Europe and is based in Prague, Czech Republic
Who we are:
At Kenvue, we strive to realize the extraordinary power of everyday care.
Built on over a century of heritage and propelled forward by science, our iconic brands-including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON'S® and BAND-AID® -are category leaders trusted by millions of consumers who use our products to improve their daily lives.
Our employees share a digital-first mindset, an approach to innovation grounded in deep human insights, and a commitment to continually earning a place for our products in consumers' hearts and homes.
What will you do:
The Head of Czech & Slovakia will lead the delivery of sales, profit, cashflow and market share targets for the business.
Through leading in-country activation and commercial operation, in-line with the CEE and Central Europe Cluster strategies and priorities.
This leader will be responsible for continued development of the local talent pipeline and fostering strong employee engagement.
He/she will be key member of the Central Eastern Europe Leadership team.
Key Responsibilities
Main accountabilities
* Lead local country management team for Czech & Slovakia and represent these countries within the CEE Leadership Team
* Recruit, coach and develop local and regional high-potential talent in-line with our purpose and values to provide a robust succession plan
* Engage with local trade associations, customers, and government officials to shape current and future market opportunities
* Develop strong cross-country relationships across the CEE cluster and CE region and drive synergies (One team)
* Cultivate relationships with senior stakeholders and major customers
* Define, shape and model a high-performing culture
* Manage local legal and statutory issues effectively
Strategy and business planning
* Set vision and strategy for the Czech Republic & Slovakia and develop annual business plans in line with CEE and CE strategy execution.
* Ensure alignment of plans with the Central Eastern Europe functional leads (Finance, HR, SC, IT, Reg, etc)
* Identify and pursue growth opportunities aligned with global and CE strategies
* Foster a productive and inclusive climate and working relationship with the regional global functions based in Prague.
* Define resource allocation in-line with the cluster strategy
Business plan execution
* Ensure 100% compliance with HCC and legal frameworks
* Deliver sales and profit targets for Czech Republic & Slovakia, including direct responsibility of SG&A in line with corporate business plan targets
* Lead development and execution of local customer plans including JBPs for priority customers
* Lead development and delivery of brand-activation plans in-line with global brand strate...
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Type: Permanent Location: Prague, CZ-10
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:26
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Description
Manager, Supplier Climate Action Program
Kenvue is currently recruiting for a Manager Supplier Climate Action Program.
Who We Are:
At Kenvue, we believe there is extraordinary power in everyday care.
Built on over a century of heritage and propelled forward by science, our iconic brands-including NEUTROGENA®, AVEENO®, LISTERINE®, JOHNSON'S® and BAND-AID® -are category leaders trusted by millions of consumers who use our products to improve their daily lives.
Our employees share a digital-first mindset, an approach to innovation grounded in deep human insights, and a commitment to continually earning a place for our products in consumers' hearts and homes.
Join us in shaping our future--and yours.
What will you do:
As the Manager Supplier Climate Action Program you will play a key role supporting Kenvue's progress toward new climate goals.
Within the Global Procurement team, you will help establish and lead the reduction efforts of the Kenvue's greenhouse gas emissions across its supply chain (Scope 3).
Also, you will focus on enabling the integration of environmental data into procurement decision making and support the transition towards environmental sustainability.
In partnership with the Global ESG & Sustainability team, you will lead the supplier engagement program to drive reductions in Kenvue's supply chain (Scope 3) emissions.
In addition, in this role, you will be accountable to define and achieve clear milestones in conjunction with your Procurement and ESG counterparts and business stakeholders.
Key Responsibilities:
* Lead the implementation of Kenvue's Supplier Climate Program
* Facilitate the establishment of a forward-looking and industry-leading program to support the decarbonization efforts of Kenvue's supply chain
* Enable the integration of environmental footprint data into procurement decision making and support the progress towards reduction of Kenvue's Scope 3 GHG emissions
* Work with external partners or consultants in collecting supplier's environmental data and supporting the transition from estimated/proxy data to primary data, in close cooperation with the suppliers in scope
* Manage relevant internal and external stakeholders, especially the Procurement categories, to drive the reduction of Kenvue's scope 3 emissions: acting as the main point of contact and establishing regular communication and data exchange
* Ensure alignment across procurement categories and regions towards delivering the overall scope 3 targets
* Manage relationship with key internal stakeholders and business representatives within Procurement, R&D (Product Resiliency and Sustainability) Regional Supply Chain Operations and Global ESG & Sustainability
* Design and organize face to face or virtual workshops, trainings and webinars with internal stakeholders in line with Kenvue supplier engagement and Scope 3 emissions reduction targets
* Act as a key partner with the Global ESG...
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Type: Permanent Location: Prague, CZ-10
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:26
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Description
[職務ポジションの概要]
担当する得意先に対してKenvueの代表としてリーダーシップを発揮し,会社 対 会社の戦略的かつ強固な協働関係を構築し,戦略立案•実行し,継続的に競合よりも優れた店頭展開を実現する。
1.
中長期のストレッチなゴールを達成するために毎年売上を成長させる:担当得意先のセルアウトに責任を持つ
2.
毎年インストアシェアを増やしリーダーシップの地位を守るもしくは獲得することに貢献する
3.
KPIを達成する : 利益額および率,トレードファンドのROI,配荷•ディスプレイなどのセールスファンダメンタルズ
4.
毎月のセールスエスティメイト(セルアウト予測)の精度を±2%以内にする(Commitした数字をDeliverする)
[役割と責任]
担当得意先のキーアカウントおよび主要卸店との戦略的パートナーシップの構築 : (アドバンテージで上位3分の1を目標)
1.
得意先の戦略や価値を置くポイント(Customer Value)を明確に理解し,Win-Win関係を構築するためのSweet Spotを見つける
2.
得意先のDecision Mappingを理解し,Sweet SpotのDriveをベースにした協働関係構築のための戦略を策定する
3.
具体的に「いつ•誰と•どのような内容で」コンタクトを取るのかを含めた詳細な年間プランを作成する
質の高いジョイント•ビジネス•プランニング(JBP)の継続的実施
1.
個々の得意先にフィットし,その得意先が価値を置くものを中心に据えたセリングストーリー(バリュー•ドリブン•セリング)作成する
2.
中長期目標と戦略をベースにした継続したアプローチにするためPDCAサイクルを実行する
3.
得意先の期待値を超えるような,競合他社と差別化された質の高いJBP会議を社内のサポートを得ながら実行する
4.
クロージングとフォローアップの徹底し,質の高い店頭展開を実現する
担当得意先のセールスKPIの達成
KPIs : 配荷店舗数,ディスプレイ店舗数および質,価格
KPI対象 : 新製品, フォーカスアイテム=ヒーローSKU, ブランドトータルのパフォーマンス(配荷), プロモーションパック
会社全体のアクションへの貢献
プロジェクトリード:全社に良い影響を与えるためにプロジェクトに積極的に参加しリードする
[勤務地]
初期配属は東京または大阪を予定しています。
全国転勤のポジションのため今後,会社から転勤を命じられる場合はございます。
提出書類に希望勤務地を記載するようお願いいたします。
Qualifications
[職務に関連し必要とされる経験]
•コンシュマーグッズ業界の同様の部署ですくなとも3~5年の経験を積んでいること
• 新しいことにチャレンジし,失敗した後でも高い目標を達成した経験がある
[リーダーシップ行動,知識とスキル]
リーダーシップ行動
•インサイトに基づき,未着手のニーズを見出す
•現状を打破し,変化を主導し,対応する
•建設的な対話で人々のやる気を引き出ししオーナーシップを発揮できる
•結果に対する責任感と危機感を持ってビジネスに対峙できる
専門知識とスキル
•周囲を巻き込む力,戦略的関係構築,柔軟な問題解決能力,インサイトと実現力,ビジネス管理能力,人材育成力
•ショッパー,業界,競合,小売業,卸店等に関する知識
•英語でのコミュニケーションスキル : TOEIC 650点以上 (英語での会話を理解する必要がある)
•PCスキル --- Excel, Word, Powerpoint, Tableau (社内データソース) , i-Canvus (Intageマーケットデータ)
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Type: Permanent Location: Chiyoda, JP-13
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:25
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2406167034W REQUIREMENTS
* Student pursuing an degree in Engineering or a related field.
* Familiarity with project management terms and concepts, ability to prioritize tasks is a plus
* Ability to communicate ideas and information clearly, effectively and frequently
* Execute tasks in a timely manner without direct supervision
* Must be proficient with Microsoft Office Suite
* Detail-oriented, highly organized and able to manage multiple tasks.
* Ability to work independently as well as on a team.
* Must have completed two semesters in school by the start of the co-op (rising Sophomore or above)
* Must be familiar with basic statistics concepts/terminology (If not in an engineering application- other roles are acceptable (i.e.
budget management from a club, or any experience working with numbers)
Abiomed is an Equal Opportunity Employer committed to a diverse workforce.
Abiomed will not discriminate against any worker or job applicant on the basis of race, color, religion, gender, gender identity, national origin, ancestry, age, sexual orientation, gender identity, marital or civil partnership status, pregnancy, gender reassignment, non-job related mental or physical disability, genetic information, veteran status, military service, application for military service, or membership in any other category protected under law.
Abiomed maintains a drug-free workplace.
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Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:25
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2406167030W REQUIREMENTS
* Student pursuing an degree in Engineering or a related field.
* Familiarity with project management terms and concepts, ability to prioritize tasks is a plus
* Ability to communicate ideas and information clearly, effectively and frequently
* Execute tasks in a timely manner without direct supervision
* Must be proficient with Microsoft Office Suite
* Detail-oriented, highly organized and able to manage multiple tasks.
* Ability to work independently as well as on a team.
* Must have completed two semesters in school by the start of the co-op (rising Sophomore or above)
* Must be familiar with basic statistics concepts/terminology (If not in an engineering application- other roles are acceptable (i.e.
budget management from a club, or any experience working with numbers)
Abiomed is an Equal Opportunity Employer committed to a diverse workforce.
Abiomed will not discriminate against any worker or job applicant on the basis of race, color, religion, gender, gender identity, national origin, ancestry, age, sexual orientation, gender identity, marital or civil partnership status, pregnancy, gender reassignment, non-job related mental or physical disability, genetic information, veteran status, military service, application for military service, or membership in any other category protected under law.
Abiomed maintains a drug-free workplace.
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Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:25
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l Support project daily production management work ; 支持项目日常生产管理工作。
l To operate machine in a safe and effective manner that ensures maximum performance and longevity of equipment ;
以安全和有效的方式操作机器,确保机器高效率持续运行。
l Comply with all aspects of good manufacturing practice to maintain full material and product traceability ;
遵守生产管理规范的所有方面,维护全部物料和产品的可追溯性。
l Work closely with engineers, modify the machine settings to compensate for product variations 。工程师紧密合作,产品变化时修改机器设置。
l According to the work order production plan , completes the material balance ;
根据工单生产计划需求,做好物料平衡。
l Others based on necessity; 根据需要其他相关工作。
l Other job assign by cell leader ;生产线主管安排的其他工作。l Good Working habit (5S), quality sense; 良好的工作习惯( 5S )与质量意识。
l Must have good experience in GMP manufacturer; 最好具备 GMP 相关生产经验。
l Good awareness of production safety; 良好的安全生产意识。
l Do the job according to the standard requirement, meet the requirement of productivity and quality 。执行标准化操作,满足产量和质量要求。
l Good team work spirit 。 良好团队合作精神。
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Type: Permanent Location: Suzhou, CN-32
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:24
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This role is dedicated to the overall cleaning process for all products made in Suzhou site, including IPC (In Process Clean) and Final Clean;
本岗位负责在苏州工厂所有产品的清洗工艺,包含过程清洗以及最终清洗;
• Lead and coordinate cleaning related activities cross Suzhou, sister sites, global Clean Virtual Team, and other global cleaning expert, ensure Suzhou cleaning technology comply to J&J standards and regulations.
主导和协调苏州和兄弟工厂,全球清洗虚拟团队以及其他全球清洗专家之间的项目,确保苏州的清洗技术符合强生的标准以及法规要求;
• It covers the creation and maintenance of the required cleaning processes to assure the expected quality, on time delivery and cost efficiency.
涵盖创造和维护要求的清洗工艺满足预期质量,按时交付以及成本效率
• Partner with cross functions to develop the quality system, validate equipment, processes, and products in order to guarantee full compliance with all regulations and quality standards.
与质量部门合作开发质量体系,验证设备,工艺确保符合法规和质量要求。
• It also covers any other project as deemed necessary (H&S, Environment, etc...).
同时包含一些必要的其他项目(环境健康等相关)Project management 项目管理
• Problem solving root cause analysis 问题解决根本原因分析
• Good communication and presentation skill好的沟通和表达技能
• Knowledge of lean production and six sigma精益生产和6西格玛知识
• Team work spirit 团队合作精神
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Type: Permanent Location: Suzhou, CN-32
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:24
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§ Facilities Management/ 设备管理 :
- Coordinates and communicates with business partners, clear understand the business requirements;
- 与业务伙伴进行沟通和协调,准确的了解业务需求。
- Develops and reviews procedures for preventive/predictive maintenance of utilities equipment.
Ensures that the required preventive/predictive maintenance is performed as per procedures ;
- 制定与审查公用设施预防性 / 预见性维护程序。
- Reviews the cause of major repairs with affected operations management to prevent recurrences ;
- 审查重大维修的原因及受影响业务的管理,防止其再发生。
- Analysis failures, breakdowns and repetitive repair causes; use this information and work with the site Facilities team to prioritize the utility systems to support the core businesses.
- 分析工作中出现的错误,故障及反复发生的故障的原因,结合相关信息协同厂区设备部团队利用公用设施系统优先为核心业务提供支持。
- Participates in continuous improvement teams and generates, develops, evaluates innovative ideas.
Recommends cost improvement projects.
Develops and implements energy conservation plans and projects ;
- 参与持续改善团队工作,协助生成,发展与评估革新型创意,提供成本改进项目,制定与实施能源节约计划与项目。
- Tracks and maintain performance metrics and provides data and recommendations to aid management in making decisions;
- 跟踪与维护绩效指标,提供数据和建议以协助管理层进行决议。
- Collects and reviews data concerning facility's specifications, company or government restrictions, pass them to regional MDD Facilities team to support the future development
- 收集和评议有关设施规格,公司或政府相关条款与法规的信息,将其提供给区域 MDD 设备团队,为将来发展提供支持。
- Participate in the department budget preparing and control in daily work.
- 参与部门预算编制与日常工作的管理。
- Support the regional/campus level Facility Strategy execution processes.
- 支持区域 / 厂区级别的相关设施战略执行事宜。
- Support the regional Facility facilities operations.
- 支持区域性设备设施运营工作
§ Project Delivery/ 项目交付 :
- Work with the regional and site MDD Facilities Project team to deliver the capital projects;
- 协同管理区域以及厂区 MDD 设备工程团队开展工程建设项目
- Manages project resources, including vendors and contractors;
- 管理项目资源,包括供应商与承包商;
- Provides project support including scoping/defining projects, developing projects metrics and reviewing project status and deliverables;
- 提供项目支持,包括项目范畴与定义的界定,制定工程测量指标,评估工程进度与成果。
§ EHS management/EHS 管理 :
- Be familiar with both J&J corporate EHS requirements as well as local code requirements; under ...
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Type: Permanent Location: Suzhou, CN-32
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:21
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• Acts as a pro-active sparring partner and single point of contact to the business combining intelligence on competitors, customers, strategies, and markets by challenging assumptions.
• Leverages insights of and actively contributes to the respective EMEA and MSM BI communities.
• Understands common key drivers of success in the therapeutic area and adapts regional strategies, according to local market conditions.
• Supports the respective BUs in the business planning and budget cycles.
• Supports benchmarking within MSM and EMEA.
• Interprets and presents market research results and data to generate high-impact, actionable recommendations to business partners.
• Plays a key role in discovering and exploiting business opportunities in existing and new areas and segments.
• Conducts advanced analyses of all relevant data and ensures that main messages are visualized appropriately.
• Supports EMEA BI in the development and improvement of forecasting models.
• Responsibility for one or more therapeutic area(s) in analyzing and interpreting market intelligence, competitive data, market research and customer needs and gather new data to derive trends, risks and opportunities.
• Subject matter expert for one or more of the core business processes as required.
• Local SOS go-to person: subject matter expert for EMEA PIMS processes and systems in Austria.
• Consulting, ad-hoc and project work on request• Academic background / working experience in business/mathematics/statistics/ informatics.
• Relevant experience in a comparable function.
• Deep knowledge of Pharma industry and Health Care Environment.
• Fluency English and German required.
• Highly agile (mental, results, learning, change and people agility as well as personal leadership ability).
• Advanced business acumen (result driven) and strategic thinking
• Strong analytical thinking capability and ability to translate insights into business recommendations.
• Strong communication and influencing skills.
• Ability to operate successfully in a matrix environment.
....Read more...
Type: Permanent Location: Wien-Umgebung, AT-1
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:21
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Johnson & Johnson Vision Care is recruiting for a Tooling Technician II located in Jacksonville , FL .
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
The Tooling Technician performs all responsibilities as a multi-skilled, multi-tasking individual in an empowered team.
Performs various required tasks including servicing the injection mold tooling used on the production lines.
Mold service includes assembly, disassembly, preventive, and reactive maintenance of the injection mold and offline subcomponents, required to deliver production-ready molds within tolerance and on time.
Supports projects to drive continuous improvement.
Maintains current knowledge and adheres to provisions of FDA, OSHA, GMP, MPs, ISO 9001, ISO 4001, equipment and process specifications.
Vigilant for maintaining compliance with Environmental Health and Safety policies and procedures.
Key Responsibilities:
* Intermediate Level Position qualified in Mold Services for visual inspections and limited repair of injection molds.
* Performs maintenance of cassettes including cleaning, visual inspections, and precision metrology.
* Maintains accurate records/documentation related to work in progress and quality checks.
* Assists with in-process quality checks on sub-assemblies and production-ready mold tooling assemblies.
* Assists with basic maintenance of tools or equipment and advises supervisor of needed repairs and issues.
* Responsible for using equipment for mold maintenance on more than one injection mold type to produce production-ready molds according to established specifications.
* Able to perform full disassembly and rebuild of cassettes used in injection molding.
* Assembles various components into cassettes using appropriate tools and equipment, in accordance with approved manufacturing procedures.
* Accountable for adhering to all quality and safety guidelines.
* Train associates to established procedures.
There is a pre-identified candidate for consideration.
However, all applications will still be reviewed.
* High school diploma or equivalent is required.
Vocational training, certification, and technical, or Associate's degree is preferred.
* 2 years college in technical discipline (or equivalent) preferred, or equivalent industrial experience emphasizing injection molding, mold fabrication, electro-mechanical, tool and die fabrication.
* 2 to 4 years of experience in a mold stacking environment or related field.
* Excell...
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Type: Permanent Location: Jacksonville, US-FL
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:20
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Johnson & Johnson Innovative Medicine is recruiting for a Senior Scientist, Discovery Data Science to help advance Artificial Intelligence/Machine Learning (AI/ML) for Drug Discovery.
The preferred location for this position is our R&D site in La Jolla - CA.
Consideration may be given to candidates located near other R&D sites in Spring House, PA or Beerse, Belgium.
Remote work options in the US may be considered on a case-by-case basis and if approved by the Company.
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Within Janssen R&D, the Therapeutics Discovery organization is continuing to build the key scientific expertise to bring ground-breaking new medicines to patients; we invest in medicinal chemistry, screening, and pharmacology, and in the computational and data science fields that inspire and inform them.
Many aspects of the drug discovery process are being partially virtualized: modelling methodologies prescreen existing or virtual molecules (including antibodies, degraders, etc.) for relevant properties, and focusing experimental bandwidth to make and test those molecules that hold the most promise.
The Senior Scientist will invent, internalize, and apply creative yet scientifically sound data science solutions to virtually assess molecules in the broadest possible sense.
The position's scope includes methodological innovation as well as crafting data generation, acquisition, and alliance strategies.
The successful candidate will be actively involved in method development and project support in collaboration with data science teams, computational and experimental protein scientists, computational and medicinal chemists, project biologists, toxicology and pharmacokinetics and IT colleagues.
Key responsibilities include:
* Contribute to developing data science applications with a focus on antibodies and targeted protein degradation discovery across different therapeutic areas and projects.
* Bridge between experimental and groundbreaking digital technologies, expertise in machine learning and artificial intelligence (AI) as applied to drug discovery.
* Interact in a team environment built on trust and collegiality.
* Communicate effectively and encourage colleagues to do so.
* Evaluate and make recommendations regarding the internalization, conceptualization and development of building of innovative technologies.
* Impact sound application of science within the company and beyond.
* Publish in peer-reviewed journals and prese...
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Type: Permanent Location: San Diego, US-CA
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:19
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Cilag AG, a member of the Johnson & Johnson Family of Companies, is recruiting for a Senior MRP Planner! Located in Schaffhausen, Switzerland, this role is a 12-month contract.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are less invasive, and solutions are personalized.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
The site in Schaffhausen with its strong R&D organization is uniquely positioned in the Large Molecule Platform Manufacturing Network to bring the most innovative break-through medicines fast to market.
Are you excited by the vision of building a world where disease is a thing of the past? Apply now and join us with this exciting opportunity!
The Senior MRP Planner ensures uninterrupted supply of direct materials to our production lines in time, quantity and quality and manages the relationship with assigned suppliers.
Key Responsibilities:
* Translate monthly plan cycle requirements into a supply plan and communicate to the assigned suppliers; manage the procure to pay cycle.
* Drive monthly S&OP supplier review to enhance supplier agility and flexibility and meet demand requirements while continuing to meet our inventory and reliability targets.
* Support resolution of Quality and Supplier Investigations in collaboration with quality teams, warehouse, and finance; ensure return or destruction of rejected materials.
* Proactively identify constraints or potential supply issues and report to appropriate escalation forums.
* Handle inbound material flow (freight, carrier, customs clearance partner, documents).
* Manage inventory of materials in scope (master data maintenance, slow moving and obsolescence, destruction avoidance, etc.), as well as phase-in, phase-out process.
* Drive continuous improvement projects simplifying processes, enhancing efficiency, deploying automation solutions, and leading our digitalization strategy.
* Train peers on new capabilities and become change agent.
Education :
* Minimum of a Bachelor's/University or equivalent degree is required; Supply Chain Management degree or related Business field is preferred
* Supply Chain Certification (e.g.
APICS) is preferred
* Continuous improvement and/or Lean training and/or certification is preferred
Experience and Skills:
Required:
* Minimum 4 years of relevant work experience
* Supply Chain Management experience (e.g., Planning, Logistics, or Manufacturing)
* Experience in a Planning/Purchasing role within a multi-national and fast-paced environment
* Profound knowledge of SAP MM (transactional and master da...
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Type: Permanent Location: Schaffhausen, CH-SH
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:18
-
About Johnson & Johnson
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in in pharmaceutical, and medical devices and diagnostics markets Janssen and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/ .
1.
포지션 : Associate QC Technician
2.
계열사 : 얀센백신 (Janssen Vaccines)
3.
근무지 : 인천 송도
4.
근무 형태 : Fixed Term
[Responsibilities]
General Laboratory Activity
• Compliance with laboratory safety requirements.
• Compliance with laboratory-related regulations and requirements.
• Preparation/Revision of GMP documents (Test method documents, Lab notes (Worksheet), Procedures)
• Usage and Management of GMP documents / Assure that GMP documents are properly maintained and/or archived.
• Internal and external audit/inspection Preparation
• Other laboratory Support activity (e.g., housekeeping)
QC Laboratory Test Activity (Main Tasks)
• Perform QC tests (Release, Stability, and other tests) in compliance with GMP and corporate requirements/Procedures.
• Writing of analytical data.
• Perform Lab investigation when an issue occurs.
• Perform data integrity activity according to local regulations and JNJ internal.
• Utilizes electronic systems (LIMS, MES, LES, Empower, etc.) for execution and documentation of testing.
QC Laboratory Management
• Improvement of lab practice
• Perform maintenance for lab equipment.
• Preparation of GMP data in compliance with GMP and corporate requirements/Procedures.
• Keeps supervisor informed of task status and issues.
• Completes corrective and preventative actions (CAPA) as assigned.
[Requirements]
• Minimum College degree (in Chemistry, Chemical Engineering, Life Science, Pharmaceutical Engineering, or related fields)
• Minimal in written English and conversational spoken English is preferred.
• Interpersonal communication skills, persuasiveness, and an active desire to work with colleagues and external parties.
• Good knowledge of the application of Microsoft Office programs.
(Outlook, Excel, Word, and PowerPoint)
[Preferred Qualifications]
• About 1 year of experience in the pharmaceutical industrial experience in the QC department (analytical methods: product testing, raw material, chemical testing, method validation, bioassay).
• Skilled in performing basic testing within the functional laboratory is preferred.
• Experience in performing independent troubleshooting & basic root cause analysis skills is preferred.
• Knowledge and understanding of current Good Manufacturing Practices (cGMP) related to the QC labora...
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Type: Permanent Location: Seoul, KR-11
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:16
-
Cilag AG, a member of the Johnson & Johnson Family of Companies, is recruiting for a Senior MRP Planner! The role is located in Schaffhausen, Switzerland.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
The site in Schaffhausen with its strong R&D organization is uniquely positioned in the Large Molecule Platform Manufacturing Network to bring the most innovative break-through medicines fast to market.
Are you excited by the vision of building a world where disease is a thing of the past? Apply now and join us with this exciting opportunity!
The Senior MRP Planner ensures uninterrupted supply of direct materials to our production lines in time, quantity, and quality and manages the relationship with assigned suppliers.
Key Responsibilities:
* Translate monthly plan cycle requirements into a supply plan and communicate to the assigned suppliers; manage the procure to pay cycle.
* Drive monthly S&OP supplier review to enhance supplier agility and flexibility and meet demand requirements while continuing to meet our inventory and reliability targets.
* Support resolution of Quality and Supplier Investigations in collaboration with quality teams, warehouse and finance; ensure return or destruction of rejected materials.
* Proactively identify constraints or potential supply issues and report to appropriate escalation forums.
* Handle inbound material flow (freight, carrier, customs clearance partner, documents).
* Manage inventory of materials in scope (master data maintenance, slow moving and obsolescence, destruction avoidance, etc.), as well as phase-in, phase-out process.
* Drive continuous improvement projects simplifying processes, enhancing efficiency, deploying automation solutions and leading our digitalization strategy.
* Train peers on new capabilities and become change agent.
Education :
* Minimum of a Bachelor's/University or equivalent degree is required; Supply Chain Management degree or related Business field is preferred
* Supply Chain Certification (e.g.
APICS) is preferred
* Continuous improvement and/or Lean training and/or certification is preferred
Experience and Skills:
Required:
* Minimum 4 years of relevant work experience
* Supply Chain Management experience (e.g., Planning, Logistics, or Manufacturing)
* Experience leading/managing projects end to end (including design, charter, progress reporting, documentation of lessons learned, etc.)
* Experience in a Planning/Pur...
....Read more...
Type: Permanent Location: Schaffhausen, CH-SH
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:16
-
POSITION SUMMARY : Briefly state the objective of this position.
Why the job exists (2-3 sentence maximum)
MSL Manager will be responsible for engaging with identified KOLs in the Therapeutic area through appropriate high level scientific support for research activities, publications, education, consulting, and other medical Affairs initiatives.
MSL manager should deeply understand Therapeutic Area(s) and broader external market (competitors, healthcare, regulatory and reimbursement environments) so that they can differentiate organization, interprets and analyses scientific information, leading to stronger impact on business strategy.
Finally, they need to ensure effective communication across multifunctional teams in carrying out Medical Affairs tactics.
PRINCIPAL RESPONSIBILITIES may include but no limited to:
Define major accountabilities and/or activities.
List most complex or difficult parts of job first and indicate percentage of time required to perform each task.
% OF TIME
External Customer Engagement and Partnering
• Actively identify, develop, and engage key KOLs at regional level.
• Proactive and reactive communication/interpretation of medical/scientific data/information to KOLs.
• Through scientific interactions with KOLs, champion medical benefits of products and contribute to foster innovative therapeutic approaches to benefit patients
• Utilizes effective customer engagement strategies, skills, and technology to uncover deep actionable insights on treatment strategies, needs, and priorities that are relevant and important for mutually beneficial value to the customer and Janssen.
• Proactively builds a scientific informational resource network.
40%
Effectively Scientific Communication with internal/external customers
• To help customers and business partners stay abreast of significant advancements through timely identification and dissemination of emerging scientific and medical information from a multitude of sources.
• To respond to scientific queries of customers for approved products and products/indications in development, based on Medical Information documents e.g.
literatures, safety records, scientific FAQs etc.
• To organize and moderate advisory boards in cooperation with TA groups.
• To provide medical and product training and scientific support to Sales Representatives in coordination with Marketing team as appropriate.
• To collect insights from external customers and feedback timely to shape Brand/medical strategy
40%
Scientific Communication Effectiveness with external/internal customers
• To organize local or regional medical education activities including program development, speaker selection and support in collaboration with ME&MA as appropriate.
• To support national and regional medical educational events including material development, speaker selection and support in collaboration with ME&MAs.
• Support medical affairs program and activities at local and r...
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Type: Permanent Location: Shenyang, CN-21
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:15
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Janssen is an international pharmaceutical company belonging to the Johnson & Johnson Group and is engaged in the development of breakthrough drugs in the medical world.
Guided by Johnson & Johnson's Credo and values and with commitment to quality of life being at the forefront of its priorities, Janssen devotes considerable resources to developing drugs for the treatment of serious and life-threatening illnesses, as well as medicines that improve the quality of patients' lives.
The company is actively engaged in increasing awareness of various diseases and their therapeutic pathways, conducting educational and training activities for medical teams, and collaborating with various patient associations.
Whether serving as medical reps, product managers, team managers or medical consultants, Janssen Israel employees have highly rewarding collaborative relationships with medical staff and other health care professionals, and this contributes immensely to the sense of purpose, responsibility and involvement experienced by those who work at our company.
As Senior sales representative you will work with profession doctors in the medical centers, in the field of Gastroenterology, at a high scientific level and in a competitive market.
The position involves travelling, as well as using virtual conversations with our partners, marketing through digital communication channels.
The job includes leading regional projects also teamwork.
Location : Merkaz- Hasharon
#LI-LM5
* 2 years previous experience as a sales representative
* Experience working in a digital environment and marketing based on remote calls.
* Interpersonal communication and excellent teamwork skills
* High abilities in operating technological systems
* Capacity for intensive learning and analysis of scientific and professional material
* Independent ability to prioritize tasks
* English high level
* Valid driver's license - mandatory!
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Type: Permanent Location: Shefayim, IL-M
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:15
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POSITION SUMMARY : Briefly state the objective of this position.
Why the job exists (2-3 sentence maximum)
Develop medical strategy and medical projects, including clinical study design & operation; d etermination of the theme & high-quality medical content of national activities and expert discussion , collaboration for medical educational activities; u nderstanding recent progress in relevant therapeutic areas & products/competitors and sharing with cross-functions; communication and collaboration with internal and external customers; expert review and providing scientific input into the promotional/educational/project-based materials; providing TA or product related training/support.
PRINCIPAL RESPONSIBILITIES may include but no limited to:
Define major accountabilities and/or activities.
List most complex or difficult parts of job first and indicate percentage of time required to perform each task.
% OF TIME
1.
Lead development and execution of medical strategy:
1) Responsible for productive discussion with internal cross-functions including Global/AP, medical insights collection with key national external stakeholders including KOLs etc..
2) Responsible for exhaustive collection of information regarding the latest progress in therapeutic areas/products/competitors, existing knowledge gaps, scientific evidence gaps and clinical practice gaps.
3) Responsible for authoring the Medical Strategy after collection of input and insights from a wide cross-section of internal and external stakeholders.
4) Responsible for directing medical strategy and developing medical projects.
20%
2.
Lead clinical study management
1) Ensure the study is designed and operated in compliance with related SOP and other required regulations.
2) Design and compose clinical study protocols as required; submit concept/protocol for internal review and approval; manage the study budget and phasing; ensure the registration of the study online as required; present at investigator meeting if necessary.
3) Set up plan for CSR and publication; review study report; carry out medical monitoring during the clinical study.
4) MAO/CRO collaborations on study operation.
5) Collaborate with Statistician and Data Management team for SAP and data monitoring as required.
6) Ensure the AEs in the study are reported as required.
20%
3.
Determine the theme and high-quality medical content of national activities including advisory board and expert discussion; Contribute to the theme of medical educational activities and materials.
Closely work with ME/MSL team when necessary.
10%
4.
Understand the recent progress in literature/congress in relevant therapeutic areas and products/competitors , HCP perceptions; Generate insights from the above resources, then integrate and share with cross-functional team.
10%
5.
Establish good communication and cooperation with internal and external customers, including Global and Regional (AP) MAF, R&D (CD, RA, CDTL et al.), ME, MSL, M...
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Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:15
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Abiomed, part of Johnson & Johnson MedTech, is recruiting for a Sr.
Embedded Software Test Engineer lo cated in Danvers, MA.
The candidate is responsible for verifying and validating the performance-enhancing software used in ABIOMED's family of products.
We are looking for a motivated and energetic self-starter with a "make it happen" attitude who can thrive in a fast-paced, cutting-edge environment.
Responsibilities:
* Design, develop and execute manual test cases and protocols to verify software system design.
* Collaborate with software developers & other engineers to further enhance the capabilities of the test automation framework.
Collaborate with DevOps engineers to create new Jenkins jobs, test setup, and pipelines for continuous integration testing.
* Collaborate with cross-functional teams and technicians to design and develop test fixtures.
Provide guidance, mentorship, and supervision to junior test engineers.
Qualifications:
* B.S .
in computer science or electrical engineering; M.S.
preferred.
3 years of manual testing experience on an embedded product.
Experience in Python and windows shell programming.
* Working knowledge of using an oscilloscope, multimeter, and other software debugging tools.
Prior experience in designing fixtures and tools for test automation.
* Familiarity with behavior-driven software development & automation testing.
Familiarity with Jira, Jenkins, Jama, and other DevOps applications.
* Experience in the medical device industry is strongly preferred.
* Working knowledge of cardiovascular physiology would be a big PLUS.
* Willing to travel 5% of the time to meet with customers to assess product performance in the field and gather user needs.
* Highly collaborative with excellent communication and analytical skills.
Self -motivated and willing to learn and explore new technologies .
* Independent, efficient, and able to manage competing priorities.
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.care...
....Read more...
Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:14
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Abiomed, part of Johnson & Johnson MedTech, is recruiting for a Sr.
Embedded Software Test Engineer located in Danvers, MA.
The candidate is responsible for verifying and validating the performance-enhancing software used in ABIOMED's family of products.
We are looking for a motivated and energetic self-starter with a "make it happen" attitude who can thrive in a fast-paced, cutting-edge environment.
Responsibilities:
* Design, develop and execute manual test cases and protocols to verify software system design.
* Collaborate with software developers & other engineers to further enhance the capabilities of the test automation framework.
Collaborate with DevOps engineers to create new Jenkins jobs, test setup, and pipelines for continuous integration testing.
* Collaborate with cross-functional teams and technicians to design and develop test fixtures.
Provide guidance, mentorship, and supervision to junior test engineers.
Qualifications:
* B.S .
in computer science or electrical engineering; M.S.
preferred.
3 years of manual testing experience on an embedded product.
Experience in Python and windows shell programming.
* Working knowledge of using an oscilloscope, multimeter, and other software debugging tools.
Prior experience in designing fixtures and tools for test automation.
* Familiarity with behavior-driven software development & automation testing.
Familiarity with Jira, Jenkins, Jama, and other DevOps applications.
* Experience in the medical device industry is strongly preferred.
* Working knowledge of cardiovascular physiology would be a big PLUS.
* Willing to travel 5% of the time to meet with customers to assess product performance in the field and gather user needs.
* Highly collaborative with excellent communication and analytical skills.
Self -motivated and willing to learn and explore new technologies .
* Independent, efficient, and able to manage competing priorities.
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.career...
....Read more...
Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:14
-
Associate Manufacturing Operator DSP
Ben jij flexibel, kwaliteitsgericht, dynamisch en communicatief vaardig met een oplossingsgerichte mindset?
Wil je deel uitmaken van het grootste farmaceutisch bedrijf ter wereld?
Wil je een bijdrage leveren aan de gezondheidszorg?
Dan is de functie van Associate Manufacturing Operator DSP echt iets voor jou!
Janssen Biologics B.V.
in Leiden is opzoek voor de afdeling DSP naar een associate manufacturing operator DSP.
De werkzaamheden worden in ploegendiensten uitgevoerd, waarbij wij een sterke voorkeur hebben voor kandidaten die graag in de 24/7 dienst willen werken.
De Associate Manufacturing Operator is in opleiding om de kerntaken en de ondersteunende routinematige werkzaamheden op de afdeling Downstream Processing (DSP) uit te voeren.
De taken worden in eerste instantie onder begeleiding van een ervaren (Senior) Manufacturing Operator uitgevoerd.
Indien de operator een taak aantoonbaar goed beheerst, mag deze zelfstandig, zonder begeleiding gedaan worden.
Na een periode van training is promotie naar Manufacturing Operator mogelijk wanneer de operator de kerntaken minimaal 6 maanden achtereen volwaardig heeft uitgevoerd.
• De kerntaken: een voldoende groot takenpakket wat de operator in staat stelt om op dagelijkse basis werkzaamheden te verrichten.
Dit takenpakket wordt door de Manufacturing Supervisor vastgesteld en voorafgaand aan de training besproken met medewerker en trainer.
• Volwaardig: zelfstandig en volledig volgens de cGMP, EHSS en PE normen.
Wil je met ons meegroeien?
• Trainingen/opleidingen
• Toeslagen voor shiftdiensten
• Tijdelijk contract met mogelijkheid tot vast contract
• Pensioen regeling
• Reiskosten
• Teamuitjes
• Interne aandacht voor diversiteit
De kerntaak van Downstream Processing is het opzuiveren van monoklonale antilichamen met behulp van verschillende kolomchromatografie- en filtratietechnieken, o.a.:
Kolomchromatografie
• Ultrafiltratie/Diafiltratie
• Filtratie
• Virus verwijderstap
• In Process Testen (o.a.
HPLC, OD 280, pH)
Naast de kerntaken van de afdeling verricht de Associate Manufacturing Operator ondersteunende werkzaamheden, zoals:
• het bijhouden van documentatie en computersystemen
• "basic asset care": zorgdragen voor de netheid (5S), onderhoud en organisatie van de ruimtes en apparatuur
• sampling
• gebruik van de aanwezige Lean systemen
CGMP, EHS&S, EN LEAN
De werkzaamheden worden uitgevoerd onder strenge cGMP condities.
De operator draagt zorg voor een veilige, gezonde en duurzame werkomgeving.
De uitvoering van de taken, de organisatie van het werk en het continu verbeteren van de efficiëntie, effectiviteit, kwaliteit en cGMP- en EHSS-compliance worden ondersteund door Lean technieken en concepten.
De operator heeft een goede kennis van cGMP, EHSS en Lean, op het niveau dat bij deze functie past, is getraind in de interne procedures en volgt deze, als ook andere interne standaarden, altijd.
De ...
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Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:13
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De Associate Manufacturing Technician is in opleiding om de kerntaken en de ondersteunende, routinematige werkzaamheden op de afdeling Medium Preparatie uit te voeren.
De taken worden in eerste instantie onder begeleiding van een ervaren (Senior) Manufacturing Technician uitgevoerd.
Indien de Associate Manufacturing Technician een taak aantoonbaar goed beheerst, mag deze zelfstandig, zonder begeleiding gedaan worden.
Na een periode van training is promotie naar Manufacturing Technician mogelijk wanneer de Associate Manufacturing Technician de kerntaken 6 maanden achtereen volwaardig heeft uitgevoerd.
• De kerntaken: een voldoende groot takenpakket wat de operator in staat stelt om op dagelijkse basis werkzaamheden te verrichten.
Dit takenpakket wordt door de Manufacturing Supervisor vastgesteld en voorafgaand aan de training besproken met medewerker en trainer.
• Volwaardig: zelfstandig en volledig volgens de cGMP, EHSS en PE normen.
Essential Job Duties and Responsibilities
De kerntaak is het leveren van verschillende soorten media of buffers aan klanten, o.a.:
• Afwegen van grondstoffen
• Voorbereiden van de preparatie
• Preparatie
• In Proces Testen (o.a.
osmo, PH, conductiviteit, LAL)
• Filtratie
• Filtertesten
• SAP / GLims
• Schoonmaken van systemen (CIP, SIP)
Daarnaast verricht de Associate Manufacturing Technician ondersteunende, routinematige werkzaamheden zoals:
• het bijhouden van documentatie en computersystemen
• "basic asset care": zorgdragen voor de netheid (5S), onderhoud en organisatie van de ruimtes en apparatuur
• sampling
• gebruik van de aanwezige Lean systemen
CGMP, EHS&S, EN LEAN
De werkzaamheden worden uitgevoerd onder strenge cGMP condities.
De operator draagt zorg voor een veilige, gezonde en duurzame werkomgeving.
De uitvoering van de taken, de organisatie van het werk en het continu verbeteren van de efficiëntie, effectiviteit, kwaliteit en cGMP- en EHSS-compliance worden ondersteund door Lean technieken en concepten.
De operator heeft een goede kennis van cGMP, EHSS en Lean, op het niveau dat bij deze functie past, is getraind in de interne procedures en volgt deze, als ook andere interne standaarden, altijd.
De Associate Manufacturing Technician signaleert tekortkomingen en verbetermogelijkheden.
Hij/zij voert incidenteel verbeterinitiatieven uit die praktisch van aard zijn en geen support van andere afdelingen nodig hebben.Minimum Qualification
1.
Minimum opleiding: Procestechniek op MBO 2 niveau
2.
Minimum ervaring: 0 - 1 werkervaring
3.
Competenties
• Nederlandse spreek-, lees- en schrijfvaardigheid is een pre maar geen must, Engelse spreek- en leesvaardigheid
• Kwaliteitsgericht: Werkt precies en accuraat, volgt instructies en standaarden nauwgezet.
Weet wanneer hij/zij de hulp van anderen moet inschakelen.
• Samenwerking en communicatie: Toont respect en luistert naar anderen, brengt eigen ideeën in.
Is zich bewust van eigen gedrag en effect daarva...
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Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2024-04-22 07:55:13
