Job Title: Project Manager II
Location (On-site, Remote, or Hybrid?): Pleasanton, CA (Onsite)
Contract Duration: Contract until 08/03/2027
Work Hours: 8AM - 5PM
Description:
Please note we are not looking for candidates with an IT background.
Manager is looking for a Manufacturing Engineering/Project Management.
Successful candidates so far have had a ME background but have transitioned to Project/Program management.
Job Title: Operator I
Location: Portland, OR (Onsite)
Contract Duration: 1 year
Work Hours: 4:00 AM - 2:30 PM M-Th.
Description:
This position is responsible for the production of high-quality medical devices within a manufacturing cell.Working under close supervision may perform a combination of assembly, repair, and test operations on pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical device assemblies.Performs routine assignments according to specified and standardized procedures.Work is closely and continually reviewed.Ensure that relevant job documentation for cell operations and functions is accurate and up to date.Be able to clearly communicate ideas, problems, and solutions to all levels of manufacturing management in both written and oral form.Maintain a positive attitude when interacting with internal and external customers such as tours.Follow safety guidelines and utilize appropriate safety devices when performing all operations.Participate in continuous improvement/quality initiatives in order to enhance production processes to achieve quality and profitability metrics.Maintain accurate records to ensure traveler and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products.Demonstrates a basic understanding of Lean Manufacturing.Participate with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations.Support all Divisional initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements Ability to read, comprehend, and follow written procedures; understand and follow verbal instructions - Understanding of and ability to utilize electronic data collection systems and computer software packages.Ability to prioritize work by determining the sequencing and timing of different jobs based on precedence and importance.Ability to handle and maneuver small components and parts.Ability to make critical decisions and judgments with minimal supervision.A high school degree or equivalent is required.Required dress code for tour during interview and on-the job:
Clothing must be non-shedding and free of frayed hems or loose threads.Tassels, fringes, glitter, sequins (sewn or glued on), and any other items that could become dislodges are not allowed on clothing.To verify a fabric can be worn: pull at the fabric tightly with your fingers, if fibers are dislodged, the garment may not be worn in the production area. Sweaters, sweater vests, loose fiber garments, loose knit, or fleece may not be worn.All clothing must be clean and free of visible contamination (sand, mud, dirt, lint, etc.).All clothing, from the waist up, must fit under the lab coat/gown. Turtle necks or high-necked clothing shall not stick out above the neck of the lab coat/gown.Sleeves shall not stick out beyond the cuff of the lab coat/gown. Caps, hats, scarves, or bandanas shall not be worn under the bouffant.Head wraps/scarves worn to accommodate customs:Must be covered by the bouffant and the tail end of the scarf must be fully covered by the lab coat/gown.Must be of tightly woven fabric, be clean, and laundered.Loose-fitting clothing shall not be worn around machinery or soldering/brazing torches.Shoes must be worn at all times in the production area.Stockings or socks are required.The heel of a shoe must not be pointed or higher than 2 inches.Sandals, clogs, slippers, and open-toe, or open-heel shoes are not allowed.Shoes with straps or weave where toes can be seen are not allowed.Changing shoes in the production area, other than a gowning room, is not allowed.Torsos, upper arms, and legs must be covered.Pants (above the ankle), skirts (above the ankle), skirts with slits, short shirts (above the navel), and sleeveless tops are not allowed.Skirts at the ankle are allowed, but full-length stockings, leggings, or pants must be worn under them.Nail polish, acrylic, artificial nails, or similar nail coatings are not allowed.Jewelry or body piercings that can pierce gloves or cannot be covered under gowning materials will not be permitted in the production area.Makeup shall not be worn.Lip balm in stick form is acceptable when applied outside of production areas and prior to hand washing.Scented personal use products shall not be worn, except deodorant. Lotions shall not be applied after hand washing.Cover any open or bleeding wound with a bandage.Don't wear anything that could be offensive.Company DescriptionTechLink Systems is a national provider of staffing services with offices all over the USA as well as development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified minority business that has been awarded 2017 TAPFIN Premier Partner, 2016 Manpower Excellence Award, 2016 TAPFIN Elite Partner, are a Known Tier Supplier for Agile 1, and have been ranked as a Top Women and Minority Owned Company since 2004 by several businesses including Philadelphia Business Journal, Diversity Business, Inc 5000, Inc 500, San Francisco Business Times, Diversity2000, and Los Angeles Business Journal.Job Title: Environmental Cleaning Specialist - 3rd shift Location (On-site, Remote, or Hybrid?): Sturgis, MI (onsite) Contract Duration: Contract until 06/01/2027 Working hours: 11:00 PM - 07:30 AM Total hours: 40 Description: This position is NonExempt. Hours over 40 will be paid at Time and a Half. Performs industrial cleaning of production areas. May include mixing chemical solutions/solvents to clean necessary work areas.
Job Title: Operator I
Location: Temecula, CA (onsite)
Contract Duration: until 04/13/2027
Working hours - 5AM - 1:30PM or 6AM - 2:20PM
Description:
Must have 6 months manufacturing experience (does not have to be medical that is a plus) not looking for warehouse, forklift drivers/ handlers, amazon
Must pass eye exam and color vision test.
Ask if they have any upcoming vacations or days off they will need during intake call.
Proficiency in English is required for speaking, reading, writing, and participating in training sessions led by an instructor.
Comfortable using microscopes.
Ability to follow policies and procedures.
Ability to read, write, and interpret information.
Ability to use microscopes.
Ability to add, subtract, multiply and divide.
Ability to use hand tools to manipulate, handle or feel.
Ability to sit/walk/stand for up to 10 hours a day.
Ability to intermittently crawl. Squat, climb, twist, bend, stoop, push or pull.
Must possess visual acuity, i.e., close, distance, and color vision, depth perception and the ability to adjust focus.
Ability to lift/carry items less than 50 pounds.
Job Title: Operator I
Location: Temecula, CA (onsite)
Contract Duration: until 04/13/2027
Working hours - 5AM - 1:30PM or 6AM - 2:20PM
Description & Qualifications:
Must have 6 months manufacturing experience (does not have to be medical that is a plus) not looking for warehouse, forklift drivers/ handlers, amazonMust possess visual acuity, i.e., close, distance, and color vision, depth perception and the ability to adjust focus.Must pass eye exam and color vision test.Must have proficiency in English is required for speaking, reading, writing, and participating in training sessions led by an instructor.Must have the following criterion:QC Inspector
Location: Temecula, CA (Onsite)
Payrate: $23.57/Hr
Schedule: Monday–Friday, 5:00 AM – 2:30 PM
Employment Type: Contract (Non-Exempt)
Overtime: Hours worked over 40 per week are paid at time-and-a-half.
Position Summary
We are seeking a detail-oriented QC Inspector to join our team in Temecula, CA. In this role, you will perform visual, dimensional, and functional inspections of products and components to ensure compliance with quality standards and documented procedures. The ideal candidate will have quality inspection experience, strong attention to detail, and the ability to work effectively in a fast-paced manufacturing environment.
Responsibilities
Perform visual, dimensional, and functional inspections according to established procedures and work instructions.Conduct testing using measurement and inspection equipment.Accurately record inspection and test results.Verify product compliance with quality standards and specifications.Follow quality policies, procedures, and documentation requirements.Identify and report nonconforming materials or products.Maintain organized inspection records and reports.Collaborate with production and quality teams to support manufacturing operations.Adhere to safety and quality guidelines at all times.Qualifications
Required
High School Diploma or equivalent.Previous experience performing quality inspections.Strong attention to detail and organizational skills.Good written and verbal communication skills.Basic computer proficiency, including Microsoft Word and Excel.Ability to work independently and as part of a team.Preferred
Experience inspecting medical device components.Experience using:Optical measurement equipmentHand toolsMeasurement gagesPressure and force gagesKnowledge of inspection sampling techniques.Additional Requirements
Ability to work in a fast-paced and changing environment.Strong follow-up and problem-solving skills.Willingness to work overtime, including weekends, as needed.Reliable attendance and punctuality.Why Apply?
Consistent daytime schedule.Opportunity to work with a leading quality-focused manufacturing team.Overtime opportunities available.Company DescriptionTechLink Systems is a national provider of staffing services with offices all over the USA as well as development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified minority business that has been awarded 2017 TAPFIN Premier Partner, 2016 Manpower Excellence Award, 2016 TAPFIN Elite Partner, are a Known Tier Supplier for Agile 1, and have been ranked as a Top Women and Minority Owned Company since 2004 by several businesses including Philadelphia Business Journal, Diversity Business, Inc 5000, Inc 500, San Francisco Business Times, Diversity2000, and Los Angeles Business Journal.Job Title: QA /QC Inspector
Location: Temecula, CA (Onsite)
Contract Duration: Contract until 07/12/2027
Work Hours: 5:00am - 2:30pm
Description:
This This position is NonExempt. Hours over 40 will be paid at Time and a Half.Performs visual, dimensional, and functional inspection and testing according to documented policies and procedures.Records inspection and test data as prescribed by written instructions and proceduresEducation/Experience:
High School Diploma / 0-2 year’s related work experience preferred.
Top 5 skills/requirements:
Previous experience in Quality performing inspection.Prior medical device component inspection experience preferred.Experience with optical measurement equipment, hand tools, gages, pressure and force gage testing.Training and experience with inspection sampling techniques.Good communication and computer skills, including Microsoft Word and Excel.Additional skills to compliment the role:
Ability to work within a team and as an individual contributor in a fast-paced, changing environment.Strong organizational and follow-up skills, as well as attention to detail.Must be willing to work overtime as required, including weekendsAbility to maintain regular and predictable attendanceCompany DescriptionTechLink Systems is a national provider of staffing services with offices all over the USA as well as development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified minority business that has been awarded 2017 TAPFIN Premier Partner, 2016 Manpower Excellence Award, 2016 TAPFIN Elite Partner, are a Known Tier Supplier for Agile 1, and have been ranked as a Top Women and Minority Owned Company since 2004 by several businesses including Philadelphia Business Journal, Diversity Business, Inc 5000, Inc 500, San Francisco Business Times, Diversity2000, and Los Angeles Business Journal.Job Title: Operator I - 2nd Shift
Location: Liberty, SC (onsite)
Contract Duration: Contract until 06/28/2027
Work Hours: Monday-Thursday 5:30PM-3:30AM
Description:
Shift the focus more heavily on candidates who demonstrate:
This position is responsible for the production of high-quality medical devices assembly within a manufacturing environment. Working under close supervision, the employee may perform a combination of assembly, repair, and test operations on medical device assemblies used in implantable cardioverter defibrillators (ICDs). Prior manufacturing experience is not required; however, candidates must be able to follow instructions, work safely, and maintain consistent attendance.
Key Responsibilities
Perform assembly, testing, and/or production tasks according to specified and/or standardized proceduresFollow all safety guidelines and utilize appropriate safety devices/PPE when performing operationsMaintain accurate records to ensure quality documents are correct, product and inventory are traceable, and quality issues can be addressed to ensure product qualityCommunicate issues, concerns, or improvement ideas to leadershipParticipate with the Manufacturing Supervisor in setting and monitoring individual goals and daily process performance metricsSupport team goals and production targetsDemonstrate a basic understanding of Lean Manufacturing principlesParticipate in continuous improvement effortsMaintain a positive and professional attitude when interacting with coworkersSupport divisional initiatives and comply with Quality Management Systems (QMS), Environmental Management Systems (EMS), and applicable regulatory requirementsBasic Qualifications/Requirements
Ability to read, understand, and follow detailed work instructionsAbility to understand and carry out verbal instructionsAbility to prioritize work by determining sequencing and timing based on precedence and importanceStrong attention to detail and qualityReliable attendance and punctuality are requiredAbility to follow all safety proceduresBasic computer skills (as applicable to role)- Understanding of and ability to utilize electronic data collection systems and computer software packagesWillingness to learn and take directionHigh school diploma or equivalent requiredWork Environment
Manufacturing/production settingMay require standing /sitting for extended periodsInvolves repetitive tasks and handling small componentsSpecific work attire and safety requirements will be provided during onboarding and training.Important Expectations
Attendance and reliability are critical for success in this roleMust be able to meet schedule requirements consistentlyMust comply with all safety, quality, and company policiesCompany DescriptionTechLink Systems is a national provider of staffing services with offices all over the USA as well as development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified minority business that has been awarded 2017 TAPFIN Premier Partner, 2016 Manpower Excellence Award, 2016 TAPFIN Elite Partner, are a Known Tier Supplier for Agile 1, and have been ranked as a Top Women and Minority Owned Company since 2004 by several businesses including Philadelphia Business Journal, Diversity Business, Inc 5000, Inc 500, San Francisco Business Times, Diversity2000, and Los Angeles Business Journal.We are currently hiring for a Fund Accountant (Corporate Actions Operations Analyst) opportunity with a leading financial services organization in Boston, MA.
Position: Fund Accountant (Corporate Actions Operations Analyst)
Location: Boston, MA (Hybrid)
Duration: Contract through 01/23/2027
Position Summary:
The Corporate Actions Operations Analyst will support daily corporate action processing activities, ensuring timely and accurate release of corporate action notices. This role requires strong attention to detail, analytical thinking, and the ability to thrive in a fast-paced operational environment while collaborating with multiple internal teams.
Key Responsibilities:
• Perform daily checklist tasks to ensure complete and accurate processing of corporate action notices
• Research and validate corporate actions using internal and external data sources
• Monitor daily production volumes and maintain quality standards
• Escalate issues and exceptions promptly
• Assist with reconciliation activities, including pricing, custody position, and cash breaks
• Follow up on open inquiries and support issue resolution
• Collaborate with internal departments to resolve operational issues
• Contribute to management reporting and process improvement initiatives
• Manage multiple priorities while meeting strict deadlines
Qualifications:
• Bachelor's degree or equivalent work experience
• Financial services industry experience preferred
• Understanding of Fund Accounting and Fund Administration functions preferred
• Strong proficiency in Microsoft Office, especially Excel
• Bloomberg experience is a plus
• Excellent analytical, problem-solving, and organizational skills
• Strong written and verbal communication skills
• Ability to work effectively in a team-oriented environment
• Detail-oriented with strong time management skills
• Ability to work U.S. holidays and overtime when required
We are currently seeking a QA/QC Inspector for an exciting long-term contract opportunity in Temecula, CA.
Position: QA/QC Inspector
Location: Temecula, CA (Onsite)
Schedule: Monday–Friday, 5:00 AM – 2:30 PM
Duration: Contract through 07/12/2027
Pay: Competitive hourly rate (OT paid at 1.5x for hours worked over 40)
Key Responsibilities:
• Perform visual, dimensional, and functional inspections according to established procedures
• Conduct testing and inspections using documented quality standards
• Record inspection and test results accurately
• Utilize optical measurement equipment, hand tools, gauges, pressure gauges, and force testing equipment
• Follow inspection sampling techniques and quality procedures
Qualifications:
• High School Diploma required
• Previous quality inspection experience required
• Medical device component inspection experience preferred
• Experience using measurement equipment, gauges, and testing tools
• Knowledge of inspection sampling methods
• Proficiency with Microsoft Word and Excel
• Strong communication, organizational, and attention-to-detail skills
• Ability to work independently and within a team environment
• Willingness to work overtime and weekends as needed
