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Associate Production Scientist Jobs in Ohio (NOW HIRING)

Description: QC/Production Associate I Title | QC/Production Associate I Department | Network ... High school diploma required; associates degree in chemistry, engineering, or natural sciences ...

QC Associate Scientist

Concord, OH · On-site

$75K - $80K/yr

... Associate Scientist to join their team in Lake County, OH! Location: Lake County, OH Salary: $75 ... Collaborate effectively with Quality Assurance, Production, and Technical teams. * Perform other ...

In this entry-level manufacturing position as a Production Associate with Avient you will be ... Innovation goes far beyond materials science; it's powered by the passion, creativity, and diverse ...

In this entry-level manufacturing position as a Production Associate with Avient you will be ... Innovation goes far beyond materials science; it's powered by the passion, creativity, and diverse ...

Weed Scientist

Marysville, OH · On-site

$77K - $90K/yr

The Weed Scientist will work to design & support a diverse portfolio of lawn & landscape products ... products and practices for the homeowner. Associates are expected to participate in our business ...

Weed Scientist

Marysville, OH · On-site

$77.20 - $90.80/hr

The Weed Scientist will work to design & support a diverse portfolio of lawn & landscape products ... products and practices for the homeowner. Associates are expected to participate in our business ...

Lead Data Scientist

Columbus, OH · On-site

$144K - $250K/yr

Focus and complete tasks in situations that have a speed or productivity metric * Maintain focus in ... New associate elected coverage begins on date of hire (with the exception of disability coverage ...

Lead Data Scientist

Columbus, OH · On-site +1

$144K - $250K/yr

Focus and complete tasks in situations that have a speed or productivity metric * Maintain focus in ... New associate elected coverage begins on date of hire (with the exception of disability coverage ...

We write admitted products in all 50 states and have a premium volume of $2.2 billion ... Headquartered in Amelia, Ohio, and with associates located across the United States, we are part of ...

We write admitted products in all 50 states and have a premium volume of $2.2 billion ... Headquartered in Amelia, Ohio, and with associates located across the United States, we are part of ...

We write admitted products in all 50 states and have a premium volume of $2.2 billion ... Headquartered in Amelia, Ohio, and with associates located across the United States, we are part of ...

We write admitted products in all 50 states and have a premium volume of $2.2 billion ... Headquartered in Amelia, Ohio, and with associates located across the United States, we are part of ...

We write admitted products in all 50 states and have a premium volume of $2.2 billion ... Headquartered in Amelia, Ohio, and with associates located across the United States, we are part of ...

We write admitted products in all 50 states and have a premium volume of $2.2 billion ... Headquartered in Amelia, Ohio, and with associates located across the United States, we are part of ...

Showing results 21-40

Associate Production Scientist information

What does an associate production scientist do?

An Associate Production Scientist is responsible for supporting the manufacturing and quality control processes in a laboratory or production facility, often within the biotechnology or pharmaceutical industries. Their duties typically include preparing reagents, operating laboratory equipment, ensuring compliance with safety and quality standards, and documenting production data. They work as part of a team to help produce products such as chemicals, pharmaceuticals, or biological materials, and may also assist in troubleshooting production issues. This role is crucial for maintaining efficient and accurate production workflows.

What are the key skills and qualifications needed to thrive as an associate production scientist, and why are they important?

To thrive as an Associate Production Scientist, you need a solid background in chemistry, biology, or a related scientific field, typically supported by a relevant bachelor's degree. Familiarity with laboratory equipment, safety protocols, and quality control systems such as GMP is essential, and experience with LIMS or similar data management tools is highly valued. Attention to detail, problem-solving abilities, and strong teamwork and communication skills help you excel in collaborative lab environments. These skills ensure accurate, efficient production of scientific materials and compliance with safety and quality standards.

What are some common challenges faced by associate production scientists, and how are they typically addressed?

Associate Production Scientists often encounter challenges such as troubleshooting laboratory equipment, ensuring strict adherence to quality control protocols, and meeting tight production deadlines. These challenges are usually addressed through ongoing training, collaboration with cross-functional teams, and following standardized procedures. Regular communication with senior scientists and production managers also helps resolve issues efficiently and fosters a supportive work environment where learning and problem-solving are encouraged.

What cities in Ohio are hiring for Associate Production Scientist jobs?

Cities in Ohio with the most Associate Production Scientist job openings:

QC/Production Associate I

SOFIE Co.

Oakwood, OH • On-site

$25 - $27/hr

Full-time

Re-posted 24 days ago


Key responsibilities

  • Operate radiosynthesizers and analytical equipment for drug production and quality control according to SOPs.

  • Perform synthesis, quality control processes, and basic maintenance of equipment while ensuring compliance with SOPs and cGMP documentation.

  • Assist with inventory management, troubleshooting equipment issues, and maintaining a clean, safe, and qualified working environment.


SOFIE rating

8.1

Company rating: 8.1 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

39th of 86 rated pharmaceutical


Job description

Description:
QC/Production Associate I
Title | QC/Production Associate I
Department | Network Operations
Reports To | Facility Manager
Compensation | $25-$27
Overview
The QC/Production Associate I will operate the radiosynthesizers for the production of drug product, as well as operate analytical equipment for the quality control of drug product.
Essential Duties and Responsibilities
  • Perform FDG and NaF synthesis according to SOFIE Standard Operating Procedures (SOPs):
  • Ensure all materials/reagents are accepted according to SOPs and within expiry
  • Ensure all equipment is appropriately qualified prior to use
  • Operate the synthesis unit according to SOPs
  • Learn the basic operational principles of the synthesis unit and assist in routine maintenance of the synthesis unit
  • Perform FDG and NaF quality control (QC) processes according to SOPs:
  • Assist with basic maintenance of QC equipment
  • Ensure all equipment is appropriately calibrated and qualified prior to use
  • Operate the QC equipment according to SOPs
  • Ensure completion of applicable cGMP documentation.
  • Assist with inventory management:
  • Maintain production/QC/cleaning supply levels as appropriate
  • Assist with inventory reporting
  • Perform material acceptance according to SOPs
  • Communicate with local and Network support resources to troubleshoot equipment, production, or QC issues.
  • Perform basic computer-controlled cyclotron operations for FDG and NaF production under the advisement of site Cyclotron and Facility Engineer.
  • Maintain a clean and safe working environment.
  • Perform radiation safety duties according to SOFIE's Corporate Radiation Compliance Program and site licensing requirements.
  • Maintain all qualification and validation requirements for entering ISO classified area.
  • Clean classified and non-classified areas according to SOPs.
  • Perform environmental monitoring of classified areas according to SOPs.
  • Report manufacturing metrics into data repository as required.
  • Complete cGMP documents as required and assist site and corporate Quality Assurance including, but not limited to:
  • Investigations
  • Corrective and Preventative Actions
  • Deviations
  • Out of Specifications
  • No or Atypical Yields
  • Manufacturing and QC Records
  • Logbooks
  • Attend internal meetings as required.
  • Other assigned duties as required.

Qualifications
  • High school diploma required; associates degree in chemistry, engineering, or natural sciences preferred.
  • Technical experience with computer-controlled automation preferred.
  • Efficient in the use of MS Office Suite required.
  • Ability to work various shifts and weekends required.
  • Ability to be detail-oriented, accountable, patient, organized, and work in a team environment required.
  • Ability to communicate professionally with colleagues and customers, have excellent attention to detail, and be dependable and responsible in a fast-paced, highly technical environment required.
  • Ability to lift ~50 lbs. required.
  • Up to 5% travel required.

What SOFIE employees say

Hours and flexibility

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