Logistics And Warehousing Jobs in Schenectady

Our Crew Members create a warm and friendly shopping experience in our stores. We answer questions, offer suggestions, and ensure our customers know they are welcomed and cared for. We entertain customers and make grocery shopping an exciting adventure.

Some responsibilities may include:

• Working on teams to accomplish goals
• Operating the cash register in a fun and efficient manner
• Bagging groceries with care
• Stocking shelves
• Creating signage to inform and delight customers
• Helping customers find their favorite products

You'll learn a lot. You're not stuck doing one task here. Each Crew Member contributes to creating a WOW customer experience by participating in all aspects of the job.

If you have experience in art including penmanship, working with chalk, and large signage, that's a plus.

If you have a passion for people and a fervor for food, we'd love to meet you. We can teach you the rest.

Stores have the greatest need for people that can work evenings and weekends.

Trader Joe's is an equal-opportunity employer and is committed to hiring a diverse Crew.

2026 Summer College Internship Program

We are currently seeking rising Junior and Senior Undergraduate Students, as well as recent graduates looking for experience in the insurance industry for our Program.

Our part-time, 10-week, paid internship program provides students with immersive work experience, weekly professional development, mentorship from our leadership team, and more to gain experience in all areas of the insurance and business world.

Northeastern Insurance is an award-winning company located in the heart of the Capital Region in Latham, NY. Recognized as a 6-time winner of the Best Places to Work, we offer a dynamic and fun work environment with numerous growth opportunities. Our company has been ranked in the Top 10 for both Largest Property & Casualty Insurance Agencies and Fastest Growing Companies in the area for the past 3 years, and has been nationally recognized by Inc. Magazine for Fastest Growing Companies in the Northeast.

What’s in it for you?

Our comprehensive internship program will allow you the opportunity to gain hands-on experience, explore a wide range of career possibilities in the insurance industry, and develop real-world business skills. You'll apply classroom concepts through project work and client interaction, developing professional skills that will benefit your entire career. This internship offers a chance to find your niche in the insurance industry, giving insight into various roles and serving as a steppingstone into full-time careers in your desired field.

Our goal is to provide a broad understanding of the insurance industry and equip you with the tools necessary to build a solid foundation for a career in Client Management, Sales, and Marketing. If you are driven, passionate, and eager to learn in a dynamic team environment, this internship is the perfect opportunity for you!

The program will rotate through the following departments:

• Sales- gain hands-on experience in business development and revenue generation. Build communication, relationship-building, and business development skills by:

o Conducting prospect research

o Supporting lead generation

o Follow-up communications and pipeline management

• Customer Service/Account Management- this rotation emphasizes client experience, attention to detail, and long-term relationship management. Support client retention and service operations by:

o Assisting with policy reviews, renewals, and documentation

o Responding to client inquiries and service requests

o Learning policy coverage explanations and general insurance products knowledge

o Supporting cross-selling and client retention efforts

• Office Management- learn the operational side by:

o Supporting daily administrative processes

o Coordinating workflows across departments

o Maintaining client files and documentation systems

o Learning compliance and regulatory standards

o Assisting with reporting, data entry, and office logistics

• Marketing- gain insight into how marketing drives sales and strengthens brand visibility. Support brand growth and engagement initiatives by:

o Assisting with social media and email campaigns

o Conducting market research and competitive analysis

o Supporting event planning and community outreach

o Tracking marketing performance metrics

o Assisting with website and digital content updates

• And More!

We will count on you to:

• Be a dependable and accountable member of the team, committed to supporting a variety of office duties in client services
• Assist various departments in the company to attract and retain clients to grow/maintain our book of business
• Be open to learning about a variety of insurance products and how to apply business skills in real-life scenarios.

Qualifications:

• Business Majors
• Attention to detail and precise verbal/written communication skills
• Highly motivated and eager to learn
• Great work ethic and positive attitude
• Familiarity with Microsoft Office (Excel, Word, Outlook) is preferred

Work setting:

• In-person
• Office

Ability to commute/relocate:

• Latham, NY 12110: Reliably commute or planning to relocate before starting work (Required)

Pay: $20/hour

Visium Resources has been asked to identify qualified candidates for this Project Engineering Manager position located in Schenectady, NY. This position is a contract hire opportunity which is expected to be a hybrid work arrangement for a duration of one year. There will be some travel estimated to be one week per month. Prefer candidates who reside in the EST zone.

Summary

The Project Engineering Manager will execute the engineering portion of OTR (Order to Remittance) contracts that contain Balance of Plant (BOP) scope. Own the project control activity globally and drive consistent functional specifications and common global processes for projects implementation. Activities that are conducted to better understand or ultimately meet the expectations of the customer Impacts approaches, projects and programs in the functional area or affected business organization and ways of working. Impacts quality, efficiency and effectiveness of own team. Has significant input into priorities. Guided by professional practices and policies that are shaped by the role. The role has moderate autonomy, requiring high levels of operational judgment. Job will require some travel within the US, Latin America, and Globally as needed.

Job Description:

Serves as the technical leader/manager to develop a scope of work and plan schedule and

monitor engineering activities for customer projects. Provide technical leadership and

interface with Proposal Management, Cost Estimating, Partners, Customers, Product

Engineering, Sourcing, Engineering sub-contractors.

* Developing specialized knowledge in their discipline. Serves as best practice/quality

resource. Has awareness of latest technical developments in own area. Contributes

towards strategy and policy development, and ensure delivery within area of responsibility.

* Has in-depth knowledge of best practices and how own area integrates with others; has

working knowledge of competition and the factors that differentiate them in the market.

* Uses judgment to make decisions or solve moderately complex tasks or problems in areas

of operational/product management, manufacturing, technology or engineering. Takes new

perspective on existing solutions. Uses technical experience and expertise for data

analysis to support recommendations. Uses multiple internal and limited external sources

outside of own function to arrive at decisions.

* Acts as a resource for colleagues with less experience. May lead small projects with

moderate risks and resource requirements. Explains difficult or sensitive information; works

to build consensus. Developing persuasion skills required to influence others on topics

within field.

* Own the engineering execution of BOP-scoped Projects from Contract signature until the

end of contractual obligations.

* Manage a cross functional Engineering team to master the risks and opportunities of the

Contract.

* Providing technical guidance and assistance to Project Management and internal

engineering teams.

* Reviewing Customer specifications and communicating contract and project requirements

to all design functions, utilizing internal documentation systems.

* Evaluating financial/schedule impact of Customer requested scope changes.

Providing technical support to Engineering, Sourcing, Vendors, and Installation teams to

ensure equipment meets all Customer requirements and business objectives.

* Enforce quality procedures and participate in their improvement.

* Assure the experience feedback by capturing issues (Lessons Learned).

Work in a matrix organization with numerous interfaces: In house with mainly the

Engineering departments of the various locations and In house with fellow PEM's and Project Coordinators. In house with project managers, quality, sourcing, logistics and scheduling. Externally with Customers, partners,

EPCs, and subcontractors

* Serve as Senior Project Engineering Manager, when assigned, to lead and facilitate a total

project solution across all product lines: Global technical project focal point... partner with

project manager for customer/EPC meetings, etc. Drive consistent project requirement flow

down across product lines. Drive-functional resolution to technical project issues from a system level across product lines. Respect of the contractual obligations while protecting the customer satisfaction. Management of technical risks of the project. Drive project profitability according to the assigned budgets.

Qualified candidates would have the following:

Required Qualifications

Bachelor's or higher degree in Engineering or any other related STEM program from an

accredited university or college.

A min of 6 years of experience or more of related industry experience with increasing

responsibilities.

Desired Characteristics

* Strong interpersonal and leadership skills.

* Demonstrated ability to lead programs/projects.

* Ability to document, plan, market, and execute programs.

* Demonstrates creativity and problem-solving capability.

* Willingness/ability to manage multiple priorities simultaneously.

* Excellent oral and written communication skills.

* Motivated and able to motivate others.

* Has a continuous improvement mind set.

* Demonstrates customer interface experience.

Technical superior training with experience in project/team management preferred, in the

field of energy or in the management of transverse teams.

* Demonstrates knowledge of Mechanical & electrical codes and compliance.

* Demonstrates knowledge of Turbo machinery, generator, electrical, controls and/or Power

Plant Accessory systems and equipment.

* Expertise in one of the disciplines (Mechanical/ Electrical / Process)

Department/Unit:

Work Shift:

Salary Range:

B. Pre-Study Initiation
1. Attend site pre-study visit/qualification visit meetings and Site Initiation Meeting, whether on site or remote  
2. Attend Investigator Meeting either remote or at location specified by the study sponsor (requires travel)   
3. Complete and submit new protocol feasibility questionnaires with research site information.  
4. Review confidentiality forms in conjunction with the ORA and obtain appropriate signatures 
5. Assist in study feasibility assessments by considering the patient population, time and personnel
requirements, competing trials, ability to maintain patient safety and confidentiality, fiscal soundness, and
logistical capabilities including interdepartmental needs, i.e. radiology, operating room, inpatient and
outpatient pharmacy.  
6. Prepare and submit pre-IRB approval documents for review and approval by the following institutional
committees as appropriate: Research Pharmacy, Value Analysis (VAMS), Antibiotic Sub-committee, Radiation
Safety Committee, Institutional Biosafety Committee, Departmental Review Committees  
7. Prepare and submit regulatory documents required by federal regulations to the Study sponsor/CRO prior to
site initiation and maintain during the course of the study  
a. 1572 (pharmaceutical trials) 
b. Statement of investigator (device trials) 
c. Financial Disclosure forms for PI and Sub Investigators (SI) 
d. CV and medical license for PI and Sub Investigators (SI) 
e. Current Human Subject Protection and Good Clinical Practice (GCP) training certificates for 
all personnel on the study   

f. 
IATA training certificates (if applicable for the study)  
8. Complete the delegation of authority/duty logs to indicate the site personnel involved with the study and
update as necessary throughout the course of the study with either new study personnel or personnel that is
no longer involved with the study.  
9. Prepare the patient informed consent (ICF) and assent (if applicable) by inserting the AMC required language
into the sponsors ICF template and submitting to the sponsor for approval prior to IRB submission  
10. Prepare for study site initiation visit 
a. Schedule visit and all required personnel (PI, sub-investigators, coordinators, research
manager, pharmacy, clinical nursing units, operating room staff, etc.) to be present 
b. Schedule study specific training visits,  
c. Ensure all study required items are on-site (tablets for questionnaires, lab supplies, devices,
study medication/investigational products, EKG machine, etc.) 

11. Develop original source data collection worksheets to comply with protocol specific data requirements to 
include adverse event logs, and medication logs to ensure all required patient data is collected.
 

C.      IRB
1. Prepare initial IRB submission documents to include: AMC Checklist, IRB application, study protocol, ICF,        
advertisements, Investigator Brochure, patient diaries (paper or screen shots), patient questionnaires,
other patient facing materials  
2. Submit the new protocol IRB submission to the ORA through the InfoEd portal and after approval submit
to the either WCG through Connexus Portal or approved IRB of record.   
3. Prepare and submit annual continuing review reports and site termination report to the IRB of record  
4. Prepare and submit any changes to the IRB approved study documents as requested by the study sponsor
to include protocol amendments, changes to the ICF, new versions of the Investigator Brochure, new or
changes to advertisements of patient facing materials 
5. Prepare and submit protocol deviations and/or violations to the study sponsor and IRB as necessary 
 

 
D. Patient Interactions
1. 
Participate in or conduct the informed consent process and HIPAA authorization, per AMC SOP, 
with research participants through discussion of the study protocol, procedures, timelines, risks, benefits
and answering any questions. Obtain the appropriate signatures and dates/time on the ICF form and
documents the process and file a copy in the patient’s medical record. Assures that patients sign any future
amended versions of the consent if applicable.  
2. Develop study schedule and required procedures, timelines, and deadlines with study patient and family,
the PI and research team.  
3. Coordinate patient follow-up study visits, treatments, testing, procedures, and schedules  

4. Conduct patient study visits and required assessments per each individual protocol  
5. Assess patients for eligibility using the study specific inclusion and exclusion criteria.  
6. Perform patient health assessments to include but not limited to: Vital signs, EKG, medication and medical
history review as required per protocol and as ordered by the PI/Sub-I,  
7. Obtain required biological specimens from patient, i.e., urine, sputum, etc.  
8. Perform blood draw to obtain blood specimens  
9. Administer study specific scales; i.e. stroke scales, mental assessments, etc.  
10. Administer questionnaires to be completed by the patient, i.e. quality of life questionnaires, pain scores,
etc., and review for completeness  
11. Perform POC testing as applicable per SOP, i.e. urine pregnancy, urine drug test, blood sugar, urinalysis  
12. Coordinate/schedule other study required procedures to be done, i.e. physical exam with study provider,
radiology, ultrasounds, echocardiograms, follow up study visits etc.  
13. Dispense to patient and train patient on completion of study diary, if applicable  
14. Review completed patient diaries with patient   
15. In conjunction with the provider, provide oral study mediation to the patient or set up/schedule
medication infusions or coordinate with nurse to administer study medication injection.  
16. Review oral study medication compliance with patient at each visit  
17. Collect required data from the patient   
18. Procedure Visit –Clinic procedure room, Operating room, Cath lab, Angio suite, etc. 
a. Ensure appropriate study medication or device is ordered for procedure 
b. Ensure appropriate study personnel are scheduled and present for procedure 
c. Transport study medication or device to appropriate location  
d. Review intra operative inclusion/exclusion criteria  
e. Randomize patient to treatment arm, if required 
f. Collect required data before, during and after the procedure 
g. Ensure study procedure requirements are followed  
h. Collect specimens as appropriate and send to sponsor as required   
19. Monitor and communicate on a continuous basis with patients and families to facilitate identification of
untoward side effects/adverse events and initiate and coordinate clinical care to manage and minimize
harm to research patient  
 
 

Thank you for your interest in Albany Medical Center!​

Albany Medical is an equal opportunity employer.

This role may require access to information considered sensitive to Albany Medical Center, its patients, affiliates, and partners, including but not limited to HIPAA Protected Health Information and other information regulated by Federal and New York State statutes. Workforce members are expected to ensure that:

Access to information is based on a “need to know” and is the minimum necessary to properly perform assigned duties. Use or disclosure shall not exceed the minimum amount of information needed to accomplish an intended purpose. Reasonable efforts, consistent with Albany Med Center policies and standards, shall be made to ensure that information is adequately protected from unauthorized access and modification.