Group Lead Job at Baxter (Skaneateles Falls)

New

Group Lead

In this pivotal role on our Manufacturing team, you will work collaboratively wi...

Location

United States , Skaneateles Falls

Salary:

27.00 USD / Hour

Baxter

Expiration Date

Until further notice

Requirements

High School Diploma/GED, Associates Degree preferred
2-4 years’ experience
good mechanical dexterity/eyesight, ability to read, write and use basic math
maintain a high degree of accuracy in performing repetitive tasks
ability to adapt to a changing work environment
work well with others and actively participate in team problem-solving activities
may be requested to work overtime, as needed
natural or corrected near-distance visual acuity of 20/25
ability to differentiate between colors
ability to lift 40lbs and work in various positions

Job Responsibility

Commit to a Zero-Harm workplace and ensure Safety policies are followed
Timely reporting of all safety incidents
Cultivate a collaborative environment while interacting and motivating a team of operators to achieve People/Quality/Delivery/Cost objectives
Ensure training and cross training on accurate procedures and operations of tools to develop operators and maintain flexibility
Use computer to update production targets, scrap transactions, order material
Knowledge of Excel/Word/SAP
Ensure all quality and regulatory policies are carried out
Review/Sign Device History Records, Training records and other quality documents
Assist your supervisor with employee appraisals

What we offer

Medical and dental coverage
Basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts
Educational assistance programs
Paid holidays
Paid time off ranging from 20 to 35 days
Family and medical leaves of absence
Paid parental leave

Fulltime

New

Principal Scientist: PKDM-BA (Small molecule bioanalysis group lead)

At Amgen, our shared mission—to serve patients—drives all that we do. It is key ...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree PhD OR PharmD OR MD and relevant post-doc where applicable and xx years of directly related experience
Master’s degree and xx years of directly related experience
Bachelor’s degree and xx years of directly related experience

Job Responsibility

Lead and mentor a team of scientists in the design, execution, and interpretation of bioanalytical studies
Develop, validate, and implement bioanalytical methods for quantitative measurement of drug candidates, metabolites, and biomarkers in biological matrices
Perform and supervise quantitative bioanalysis using LC-MS/MS and other advanced analytical platforms
Handle and process complex biological matrices (e.g., plasma, tissue homogenates, urine, bile) with robust extraction procedures to ensure accurate and reproducible results
Apply sound knowledge of extraction techniques (e.g., protein precipitation, liquid-liquid extraction, solid-phase extraction) to optimize bioanalytical workflows
Ensure compliance with regulatory guidelines and maintain high-quality documentation
Collaborate with PKDM project team representatives and BA scientists located at our US sites and ensure integration of bioanalytical data into project decision-making
Ensure data quality, integrity, reproducibility, and timely delivery of results while maintaining safety standards across all workflows
Mentor and develop team members, promoting a culture of scientific rigor and innovation
Contribute to strategic planning and allocation of bioanalytical resources

Fulltime

New

Principal Scientist: PKDM-BA (Small molecule in vitro ADME group lead)

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree PhD OR PharmD OR MD [and relevant post-doc where applicable] and directly related experience
Master's degree and directly related experience
Bachelor's degree and directly related experience

Job Responsibility

Involve and mentor a team of scientists in the design, execution, and interpretation of in vitro ADME studies
Develop, optimize, validate, and implement mechanistic in vitro assays to characterize drug metabolism, transporter interactions, and drug–drug interaction (DDI) risk
Design, establish, and validate robust high-throughput screening workflows to support compound profiling and lead optimization efforts
Oversee the execution and interpretation of a comprehensive suite of in vitro ADME assays, including: Metabolic stability assessments using liver microsomes, S9 fractions, and hepatocytes
Binding assays
CYP450 inhibition and induction studies
Transporter uptake and efflux assays
In vitro drug–drug interaction (DDI) evaluations
Manage and maintain cell culture platforms supporting ADME studies, including primary hepatocytes, immortalized cell lines, and transporter-transfected cell systems, ensuring model suitability and reproducibility
Supervise permeability and absorption studies using established in vitro models to assess compound absorption potential

Group Lead - Global PLM Chennai (Teamcenter)

The manufacture of wind energy plants in the on-shore segment has been our core ...

Location

India , Chennai

Salary:

Not provided

Nordex Group

Expiration Date

Until further notice

Requirements

A bachelor’s degree in engineering, computer science, or a comparable qualification
Solid experience working with Siemens Teamcenter in an engineering or industrial environment
Experience across operational PLM support, solution topics, and implementation or improvement initiatives
A strong delivery mindset, with the ability to structure work, set priorities, and follow up on execution
Experience working closely with teams, stakeholders, or service providers in a coordinated and goal‑oriented manner
The ability to keep teams focused and aligned in a dynamic and sometimes distracting environment
Very good communication skills, including the confidence to guide discussions, clarify expectations, and address issues early
Openness to combining leadership responsibilities with hands‑on contribution when needed
Fluent English
German or Spanish are a plus

Job Responsibility

Lead, coordinate, and prioritize the daily work of the local Global PLM team in Chennai, ensuring focus on agreed objectives and timely execution
Act as the main local point of contact for Global PLM activities in Chennai, providing direction, clarification, and escalation handling when needed
Ensure high‑quality operational support for PLM Teamcenter users, in coordination with the internal PLM team and the outsourced first‑level support provider
Coordinate, monitor, and continuously improve the collaboration with the external first‑level support team, leveraging local proximity and cultural alignment
Support and guide the System Architect and PLM Inhouse Consultants in their tasks, helping translate priorities into concrete actions
Contribute hands‑on to PLM topics when required, including analysis, solution discussions, and support of critical issues or initiatives
Coordinate local participation in PLM projects and improvements, ensuring alignment with global standards, architecture, and ways of working
Actively communicate status, risks, and needs to Global PLM management
Foster a collaborative, accountable, and delivery‑oriented team culture within the Chennai PLM team

Fulltime

Group Lead Mechanical Internals and Homologations

Location

India , Chennai

Salary:

Not provided

Nordex Group

Expiration Date

Until further notice

Requirements

Degree in Mechanical Engineering
+5 years preferred experience in the wind power industry
Design of mechanical parts

Job Responsibility

Lead and manage the team, fostering a collaborative and productive working environment
Lead and be responsible of mechanical internals in Nacelle and Hub
Optimize and refine processes and methods to increase efficiency
Planning, controlling and coordination of team tasks
Review of work results from team members
Mentor and support team members in their professional development and daily responsibilities
Represent the team and its deliverables to internal and external stakeholders
Handle performance management, workload distribution, and conflict resolution within the team
Promote a culture of continuous improvement and accountability

Fulltime

Medical Laboratory Scientist Group Lead

Medical Laboratory Scientist Group Lead - Mount Kisco, NY, Monday to Friday, 8:0...

Location

United States , Mount Kisco

Salary:

35.59 - 58.75 USD / Hour

Quest Diagnostics

Expiration Date

Until further notice

Requirements

Three (3) to five (5) years of clinical experience as a Medical Technologist within the designated discipline
Foreign educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation)
United States educated candidates must provide a detailed original transcript
Bachelor's Degree Medical Technology, Chemistry or Biology or Previously qualified as a Technologist under 42 CFR 493. 1433 published in March 14, 1990
Comprehensive theoretical and operational job knowledge in designated specialty required
Knowledge of organizational/departmental policies and procedures
Proven leadership and problem-solving skills
Must be detail-oriented, have the ability to work independently, establish work priorities for self and others and to handle several tasks simultaneously for maximum department efficiency
Ability to schedule and manage resources to meet department goals
Interpersonal skills necessary to deal courteously and effectively with supervisors, co-workers and clients

Job Responsibility

Demonstrate proficiency in all duties of a Medical Technologist I and II
Perform and report on assigned analytical tests in accordance with applicable Standard Operating Procedures (SOP) ensuring that applicable quality control requirements are met
Actively support and comply with laboratory policies and procedures for specimen handling and processing, test analysis, reporting and maintaining records of patient test results
Adhere to analytical schedules to maintain turnaround time of results including STATS or critical results to clients
Perform, review and document QC analysis to ensure accuracy of clinical data and proper instrument function
Make quality control decisions regarding the disposition of an assay or test
Review requests for validity checks and recommend an appropriate course of action taking into account the limitations of specimen requirements and the effects of time and the quality of additional and/or repeat testing
Serve as a technical resource for the department by investigating and resolving analytical testing problems, recommending a course of action in instances identified as beyond acceptable limits, and responding to non-routine/complex inquiries and/or requests from clients and sales representatives
Assist Lab Supervisor by monitoring workflow to meet testing schedules
distributing and reviewing work assignments

What we offer

Day 1 Medical, supplemental health, dental & vision for FT employees who work 30+ hours
Best-in-class well-being programs
Annual, no-cost health assessment program Blueprint for Wellness
healthyMINDS mental health program
Vacation and Health/Flex Time
6 Holidays plus 1 'MyDay' off
FinFit financial coaching and services
401(k) pre-tax and/or Roth IRA with company match up to 5% after 12 months of service
Employee stock purchase plan
Life and disability insurance, plus buy-up option

Fulltime

Manufacturing Group Lead- Compressed Work Week (CWW) Nights

Provide operational and people leadership for a manufacturing area, ensuring sus...

Location

United States , Wilton

Salary:

Not provided

ASML

Expiration Date

Until further notice

Requirements

High School Diploma or equivalent
7+ years of experience in a complex manufacturing environment
Minimum of 3+ years people management and operational leadership experience
Strong working knowledge of manufacturing processes and quality standards
Familiarity with tools and equipment, hands-on experience preferred
Deep knowledge of production management, quality systems, and Lean Manufacturing
Proven track record of Lean Manufacturing implementation and sustainability
Lean Yellow Belt or equivalent
Minimum 5 years with skills such as: MS Office, SAP, ERP software

Job Responsibility

Oversees assigned workcenters on-shift production execution
Leads and provides input to module output through strategic awareness with two week to 13 week production horizon
Ensure sustained volume output, quality, and cost performance on-shift
Collaborates and Communications with off-shift peers to achieve performance targets
Lead and develop Team Leads, module specialists, and technicians
Responsible for meeting assigned area staffing requirements to ensure production targets are met
Responsible for employee performance management, talent development, assisting and supporting career development, and succession planning as needed
Translate Factory mission, vision, and objectives to working level goals for individuals and team
Executes tactical and strategic initiatives, cascades to team
Provide individual annual performance dialogues with regular development and performance check ins

Fulltime

Group Lead and Function Owner - Light Control and Automation

The Group Lead and Function Owner for Light Control directs the activities of th...

Location

United States , San Diego

Salary:

172500.00 - 258750.00 USD / Year

ASML

Expiration Date

Until further notice

Requirements

Requires minimum Bachelor’s degree in a relevant technical field such as Electrical, Mechanical, Chemical, Mechatronics, or Aerospace Engineering, with a Control Systems emphasis
PhD Degree is a plus
Requires 8 years of relevant work experience, or combination of industry experience and relevant doctoral research
Participated on a project team of moderate size and delivered a successful product, handling schedules, documentation, design processes, and final delivery
Experience designing complex algorithms and control systems
Experience in semiconductor equipment design is highly desirable
Previous experience managing a team is highly desirable
Excellent written and verbal communication skills
Strong people‑leadership skills, including coaching, feedback, team development, and fostering accountability
Advanced execution leadership, including coaching project leads and balancing between programs

Job Responsibility

Directs a group of control and algorithms engineers, technical architects, and project leads to deliver new and upgraded laser light control algorithms and automation in alignment with Program and Company objectives
Oversees the operation of the Light Control Function, including goal setting, work assignments, prioritization, project allocation, monitoring technical progress, ensuring quality of deliverables, and managing staffing, performance, and career development
Owns Light Control function roadmap and functional deliverables across the full product lifecycle, including concept development, requirements, implementation, verification, release readiness, and long‑term sustainment
Acts as function owner for Light Control by defining and enforcing functional policies, standards, and ways of working, and ensuring consistent implementation across projects and products
Applies deep technical expertise in control systems and automation to guide the team in meeting performance, reliability, and cost requirements
Collaborates with Light Control architects and project leads to align on requirements and scope, priorities, functional roadmaps, and delivery timelines
Participates in developing technology roadmaps and defining technical elements of the business strategy
Collaborates with Program to define project scope, estimate effort, resources, and schedules, and to align and negotiate resource allocations in support of Program objectives
Interprets, implements, and monitors changes to department methods, processes, and policies that affect the Light Control work group
Monitors and guides the quality of control designs and deliverables through disciplined reviews and verification activities

What we offer

Medical
Dental
Vision
Basic life insurance
401k plan
Eight (8) hours of vacation leave every month
Thirteen (13) paid holidays throughout the calendar year

Fulltime

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Group Lead

Group Lead

Principal Scientist: PKDM-BA (Small molecule bioanalysis group lead)

Principal Scientist: PKDM-BA (Small molecule in vitro ADME group lead)

Group Lead - Global PLM Chennai (Teamcenter)

Group Lead Mechanical Internals and Homologations

Medical Laboratory Scientist Group Lead

Manufacturing Group Lead- Compressed Work Week (CWW) Nights

Group Lead and Function Owner - Light Control and Automation

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