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Day Shift Upstream Manufacturing Associate Jobs in Michigan

CJK Group

Manufacturing Associate - Press

Chelsea, MI · On-site

Manufacturing Associate- Press (We'll Train You!) 1st shift (7:00AM - 3:00PM) | Full-Time | ... You'll spend much of your day standing, walking, lifting, and moving materials. You should be ...

KFC

Manufacturing Assoc-TPI

Lanse, MI · On-site

Our Manufacturing Associates are self motivated, dependable, and work well with others. You must be ... day. You will work with fiberglass and a variety of chemicals.

Workforce Strategies

Manufacturing Associate

Ceresco, MI · On-site

$19.18 - $21.93/hr

... and 2nd shift. * Overtime opportunities to boost your earnings. * A $100 referral bonus for ... Apply now to start your journey with a company where every day is an opportunity to excel and ...

Workforce Strategies

Manufacturing Associate

East Leroy, MI · On-site

$19.18 - $21.93/hr

... and 2nd shift. * Overtime opportunities to boost your earnings. * A $100 referral bonus for ... Apply now to start your journey with a company where every day is an opportunity to excel and ...

Workforce Strategies

Manufacturing Associate

Bedford, MI · On-site

$19.18 - $21.93/hr

... and 2nd shift. * Overtime opportunities to boost your earnings. * A $100 referral bonus for ... Apply now to start your journey with a company where every day is an opportunity to excel and ...

WSI Talent

Manufacturing Associate

Battle Creek, MI · On-site

$19.18/hr

... and 2nd shift. * Overtime opportunities to boost your earnings. * A $100 referral bonus for ... Apply now to start your journey with a company where every day is an opportunity to excel and ...

CJK Group

Manufacturing Associate - Bindery

Chelsea, MI · On-site

Manufacturing Associate - Bindery 3rd Shift (We'll Train You!) 3rd Shift | Monday-Friday | 11:00 PM ... Comprehensive benefits after 30 days (medical, dental, vision, 401k) * Paid time off + holidays

CJK Group

Manufacturing Associate - Bindery

Chelsea, MI · On-site

Manufacturing Associate - Bindery 3rd Shift (We'll Train You!) 3rd Shift | Monday-Friday | 11:00 PM ... Comprehensive benefits after 30 days (medical, dental, vision, 401k) * Paid time off + holidays

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Day Shift Upstream Manufacturing Associate information

What is a day shift upstream manufacturing associate?

A Day Shift Upstream Manufacturing Associate is responsible for preparing and operating equipment to support the initial stages of biopharmaceutical production, typically involving cell culture, fermentation, and media preparation. Working during the day shift, they monitor processes, maintain sterile environments, and ensure production runs smoothly and efficiently. Their work is crucial in ensuring quality and consistency in the early phases of manufacturing biological products such as vaccines or therapeutic proteins.

What is the difference between Day Shift Upstream Manufacturing Associate vs Night Shift Upstream Manufacturing Associate?

AspectDay Shift Upstream Manufacturing AssociateNight Shift Upstream Manufacturing Associate
Work HoursTypically 8 AM - 4 PMTypically 8 PM - 4 AM
Work EnvironmentManufacturing floor during daytime operationsManufacturing floor during nighttime operations
Required SkillsSimilar technical skills, safety protocols, and certificationsSame technical skills, safety protocols, and certifications
Employer UsageCommonly used in biopharma and biotech manufacturingSame industry usage, different shift timing

The main difference between a Day Shift Upstream Manufacturing Associate and a Night Shift Upstream Manufacturing Associate lies in their working hours. Both roles require similar skills, certifications, and work environments, but they operate during different shifts. Employers in biopharma and biotech industries often employ both to ensure continuous production, with shift timing being the primary distinction.

What are the typical collaboration points between a day shift upstream manufacturing associate and other teams in a biomanufacturing facility?

Day Shift Upstream Manufacturing Associates frequently collaborate with downstream processing teams, quality control, and process engineering staff. Daily responsibilities often involve communicating batch progress, troubleshooting issues, and ensuring compliance with safety and GMP standards. Clear documentation and timely reporting to supervisors and quality teams are crucial for maintaining production flow. This cross-functional teamwork ensures efficient handoffs and rapid response to any process deviations, making collaboration a key part of the role.

What are the key skills and qualifications needed to thrive as a day shift upstream manufacturing associate?

To excel as a Day Shift Upstream Manufacturing Associate, you typically need a background in biotechnology or life sciences, experience with aseptic techniques, and an understanding of Good Manufacturing Practices (GMP). Familiarity with bioreactors, cell culture systems, and process control software is commonly required, along with relevant safety or GMP certifications. Attention to detail, teamwork, and strong problem-solving abilities are valuable soft skills in this role. These competencies ensure the efficient and compliant production of high-quality biopharmaceuticals in a regulated manufacturing environment.
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Day Shift Upstream Manufacturing Associate jobs near you

Aseptic Manufacturing Associate (Weekdays)

Grand River Aseptic Manufacturing, Inc.

Grand Rapids, MI

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 15 days ago

Job description

Description

Aseptic Manufacturing Associate (Weekdays)


Agility, Impact, Methodology. Do you exhibit these values and wish to be around others that do too? Do you thrive in fast-paced environments where agility, adaptability, and high standards go hand in hand? Are you driven to make a meaningful impact, whether through your work, your support of others, or your commitment to your community? Are you motivated by a disciplined, science-based approach that ensures consistent excellence, safety, and integrity in everything you do? If these statements resonate with you, Grand River Aseptic Manufacturing (GRAM) welcomes you to apply to join our community of dedicated individuals improving lives every day!


Overview of this Position:

The Aseptic Manufacturing Associate (AMA) is responsible for performing various routine manufacturing tasks following established procedures and cGMP regulations under guidance of a production supervisor and/or senior management.


Shift Details: The primary location for this role is the Butterworth Facility, on shift A (Monday - Wednesday, and every other Thursday, from 6:00 am to 6:00 pm).


Non-Negotiable Requirements:

  • A bachelor's degree OR a high school diploma and 2+ years relevant work experience in a manufacturing, medical, and/or laboratory environment is required for a Level I role.
  • A bachelor's degree OR a high school diploma and 3+ years relevant work experience in a manufacturing, medical, and/or laboratory environment is required for a Level II role. Must also have experience working in a sterile manufacturing environment.
  • A bachelor's degree OR a high school diploma and 4+ years relevant work experience in a manufacturing, medical, and/or laboratory environment is required for a Level III role. Must also have experience working in a sterile manufacturing environment.
  • Qualification for use of a full-face respirator is required when working with hazardous chemicals. PAPR is required for working with hazardous chemicals during chemical dispense and addition activities.

Preferred Requirements:

  • Previous experience in pharmaceutical manufacturing or a laboratory environment is preferred.

Responsibilities Include (but are not limited to):

  • Perform equipment preparation, bulk drug formulation, and aseptic filling duties as needed.
  • Accurately document data and complete batch records as needed.
  • Perform cleaning and sanitization duties as instructed by the applicable procedure.
  • Successfully complete facility's aseptic gowning and manufacturing qualification program.
  • Perform duties in Grade 5, ISO 6, ISO 7, and ISO 8 cleanrooms.
Full job description available during formal interview process.


What Sets GRAM Apart from Other Employers:

BENEFITS starting day 1: Medical, prescription, dental, vision, life insurance, and disability benefits are available to you and your family on your first day of work, with the company paying a portion of the cost! Once eligible for the 401(k) program, all your contributions are immediately 100% vested, and you are immediately vested in GRAM contributions as well. We also offer generous off-shift premiums!

Paid VOLUNTEERISM starting day 1: GRAM encourages giving back to our community by offering 16 hours of paid volunteer time per calendar year!

PAID TIME OFF: You choose how to use this time for your vacation, sick, or mental health needs! PTO: Full-time employees accrue up to 104 hours of paid time off per calendar year, with this amount being prorated your first year. WELLNESS TIME OFF (WTO): In addition to PTO, employees earn 1 hour of wellness time off for every 30 hours worked, to use how you choose.

PAID HOLIDAYS: We offer 10 paid holidays per calendar year with immediate eligibility!

PAY: Depends on Experience and is discussed during the interview process.


If you meet the required criteria listed above, GRAM welcomes you to apply today!

Apply