Teva Pharmaceuticals
Overview
We are on a mission to make good health more affordable and accessible, helping millions worldwide enjoy healthier lives. We are the world’s leading manufacturer of generic medicines and proud producer of many products on the World Health Organization’s Essential Medicines List. Position Summary
The Quality Control Laboratory Planner is a high‑impact, self‑driven position responsible for leading advanced planning analytics, data modeling, and execution of QC budget & capacity related activities. The role involves participating in site planning meetings that influence QC commercial testing plan, understanding samples demands and corresponding standardized QC test scheduling, and helping QC leaders on the assignment of QC tests to be aligned on the business plan (E2E and NPL). The ideal candidate excels in data automation, visualization, and reporting using SAP, Power BI, VBA, and SQL, ensuring data accuracy, readiness, and timely decision‑making. Essential Areas of Responsibility
Support completion and documentation of the Annual Operating Plan (AOP) for QC Labs. Develop, validate, and submit monthly QC Samples Release Plan in coordination with QC and Supply Chain leaders. Serve as SME for data analysis, ensuring accuracy and integration. Manage and track project deliverables; assign tasks, ensure follow‑up, and elevate issues when needed. Utilize scheduling systems (Excel, Smart QC, LIMS 7) to create accurate QC lab schedules aligned with production. Ensure timely availability of materials, reagents, and consumables for QC testing. Drive development of dashboards and reports for sample inventory, KPIs, and QC release commitments. Maintain and communicate QC schedules, WIP sheets, and readiness with cross‑functional teams. Problem solve and negotiate corrective actions impacting QC testing and release schedules. Conduct capacity analyses to determine tools/resources needed; address constraints proactively. Connect QC Plans with Production Schedules to meet service and forecast goals. Provide weekly/monthly reports on operational metrics and QC performance. Ensure compliance with company policies, cGMP, SOPs, safety procedures, and mandatory training. Position Requirements
Education/Certification/Experience
Bachelor’s degree or equivalent in supply chain, engineering, data analytics, business, science, or related field. Minimum of 5 years progressive experience in a GMP regulated environment, preferably within pharmaceuticals experience in a supply chain or planning analytics role; or an equivalent combination of education and experience. Skills/Knowledge/Abilities
Demonstrated servant leadership and ability to maintain commitments by due dates. Ability to create, compose, and edit written materials. Ability to merge data from different digital sources into cohesive dashboards and reports. Demonstrated experience independently managing laboratory materials readiness. Conduct capacity analysis (RCCP) to determine projected need for resources (materials/machine/human). Advanced proficiency in SAP, Smart QC (scheduling software) and LIMS (Labware 7). Expert knowledge in Microsoft Excel for pivot tables, nested functions, modeling, and capacity projections. Able to manage multiple priorities and ensure appropriate follow‑ups. Highly organized and excellent time and project management skills with the ability to juggle a wide range. Skill levels in business, scientific and personal computer hardware and software applications. Skill levels in MS Office including proficiency in Word, PowerPoint, Excel, Access and SharePoint. Must be able to maintain the highest levels of confidentiality, integrity and discretion. Excellent verbal, written, and interpersonal skills required. Problem Solving
Exercises judgment within broadly defined practices and policies and selects methods and techniques (TLMS Problem Solving Standard, 5W, Fishbone Analysis, Kaizen events) for obtaining solutions. Demonstrates creative, collaborative approaches to problem‑solving and continuous improvement. Must be able to work independently and collaboratively within cross‑functional teams. Able to identify solutions to general problems through collaboration and creativity. Competitive Benefits Package
Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment. Retirement Savings: 401(k) with employer match up to 6% and an annual 3.75% defined contribution. Paid Time Off including vacation, sick/safe time, caretaker time and holidays. Company paid Life and Disability insurance. Additional benefits include, but are not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible, Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more. Internal Career Site
If you are a current Teva employee, please apply using the internal career site available on “Employee Central”. Application priority is given and you can see opportunities that are open exclusively to Teva employees. Use the following link to search and apply:
Internal Career Site . Teva’s Equal Employment Opportunity Commitment
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva’s policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws. Please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Request a reasonable accommodation by sending an email to disabilityassistance@tevapharm.com with the nature of your request and your contact information. Only inquiries concerning a request for a reasonable accommodation will be responded to from this email address. Important Notice to Employment Agencies
Teva Pharmaceuticals USA does not accept unsolicited assistance from agencies for employment opportunities. All CVs/resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre‑existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
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We are on a mission to make good health more affordable and accessible, helping millions worldwide enjoy healthier lives. We are the world’s leading manufacturer of generic medicines and proud producer of many products on the World Health Organization’s Essential Medicines List. Position Summary
The Quality Control Laboratory Planner is a high‑impact, self‑driven position responsible for leading advanced planning analytics, data modeling, and execution of QC budget & capacity related activities. The role involves participating in site planning meetings that influence QC commercial testing plan, understanding samples demands and corresponding standardized QC test scheduling, and helping QC leaders on the assignment of QC tests to be aligned on the business plan (E2E and NPL). The ideal candidate excels in data automation, visualization, and reporting using SAP, Power BI, VBA, and SQL, ensuring data accuracy, readiness, and timely decision‑making. Essential Areas of Responsibility
Support completion and documentation of the Annual Operating Plan (AOP) for QC Labs. Develop, validate, and submit monthly QC Samples Release Plan in coordination with QC and Supply Chain leaders. Serve as SME for data analysis, ensuring accuracy and integration. Manage and track project deliverables; assign tasks, ensure follow‑up, and elevate issues when needed. Utilize scheduling systems (Excel, Smart QC, LIMS 7) to create accurate QC lab schedules aligned with production. Ensure timely availability of materials, reagents, and consumables for QC testing. Drive development of dashboards and reports for sample inventory, KPIs, and QC release commitments. Maintain and communicate QC schedules, WIP sheets, and readiness with cross‑functional teams. Problem solve and negotiate corrective actions impacting QC testing and release schedules. Conduct capacity analyses to determine tools/resources needed; address constraints proactively. Connect QC Plans with Production Schedules to meet service and forecast goals. Provide weekly/monthly reports on operational metrics and QC performance. Ensure compliance with company policies, cGMP, SOPs, safety procedures, and mandatory training. Position Requirements
Education/Certification/Experience
Bachelor’s degree or equivalent in supply chain, engineering, data analytics, business, science, or related field. Minimum of 5 years progressive experience in a GMP regulated environment, preferably within pharmaceuticals experience in a supply chain or planning analytics role; or an equivalent combination of education and experience. Skills/Knowledge/Abilities
Demonstrated servant leadership and ability to maintain commitments by due dates. Ability to create, compose, and edit written materials. Ability to merge data from different digital sources into cohesive dashboards and reports. Demonstrated experience independently managing laboratory materials readiness. Conduct capacity analysis (RCCP) to determine projected need for resources (materials/machine/human). Advanced proficiency in SAP, Smart QC (scheduling software) and LIMS (Labware 7). Expert knowledge in Microsoft Excel for pivot tables, nested functions, modeling, and capacity projections. Able to manage multiple priorities and ensure appropriate follow‑ups. Highly organized and excellent time and project management skills with the ability to juggle a wide range. Skill levels in business, scientific and personal computer hardware and software applications. Skill levels in MS Office including proficiency in Word, PowerPoint, Excel, Access and SharePoint. Must be able to maintain the highest levels of confidentiality, integrity and discretion. Excellent verbal, written, and interpersonal skills required. Problem Solving
Exercises judgment within broadly defined practices and policies and selects methods and techniques (TLMS Problem Solving Standard, 5W, Fishbone Analysis, Kaizen events) for obtaining solutions. Demonstrates creative, collaborative approaches to problem‑solving and continuous improvement. Must be able to work independently and collaboratively within cross‑functional teams. Able to identify solutions to general problems through collaboration and creativity. Competitive Benefits Package
Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment. Retirement Savings: 401(k) with employer match up to 6% and an annual 3.75% defined contribution. Paid Time Off including vacation, sick/safe time, caretaker time and holidays. Company paid Life and Disability insurance. Additional benefits include, but are not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible, Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more. Internal Career Site
If you are a current Teva employee, please apply using the internal career site available on “Employee Central”. Application priority is given and you can see opportunities that are open exclusively to Teva employees. Use the following link to search and apply:
Internal Career Site . Teva’s Equal Employment Opportunity Commitment
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva’s policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws. Please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Request a reasonable accommodation by sending an email to disabilityassistance@tevapharm.com with the nature of your request and your contact information. Only inquiries concerning a request for a reasonable accommodation will be responded to from this email address. Important Notice to Employment Agencies
Teva Pharmaceuticals USA does not accept unsolicited assistance from agencies for employment opportunities. All CVs/resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre‑existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
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